| Year |
Citation |
Score |
| 2024 |
Mammana A, Baiardi S, Rossi M, Quadalti C, Ticca A, Magliocchetti F, Bernhardt A, Capellari S, Parchi P. Improving protocols for α-synuclein seed amplification assays: analysis of preanalytical and analytical variables and identification of candidate parameters for seed quantification. Clinical Chemistry and Laboratory Medicine. PMID 38456740 DOI: 10.1515/cclm-2023-1472 |
0.441 |
|
| 2024 |
Bentivenga GM, Mammana A, Baiardi S, Rossi M, Ticca A, Magliocchetti F, Mastrangelo A, Poleggi A, Ladogana A, Capellari S, Parchi P. Performance of a seed amplification assay for misfolded alpha-synuclein in cerebrospinal fluid and brain tissue in relation to Lewy body disease stage and pathology burden. Acta Neuropathologica. 147: 18. PMID 38240849 DOI: 10.1007/s00401-023-02663-0 |
0.54 |
|
| 2023 |
Mastrangelo A, Mammana A, Parchi P. Tracking neurodegenerative diseases in biofluids: Combining pathology and pathophysiology markers is the way. Cell Chemical Biology. 30: 1340-1342. PMID 37977130 DOI: 10.1016/j.chembiol.2023.10.018 |
0.309 |
|
| 2023 |
Gonzalez-Ortiz F, Karikari TK, Bentivenga GM, Baiardi S, Mammana A, Turton M, Kac PR, Mastrangelo A, Harrison P, Capellari S, Zetterberg H, Blennow K, Parchi P. Levels of plasma brain-derived tau and p-tau181 in Alzheimer's disease and rapidly progressive dementias. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37858957 DOI: 10.1002/alz.13516 |
0.555 |
|
| 2023 |
Mastrangelo A, Vacchiano V, Zenesini C, Ruggeri E, Baiardi S, Cherici A, Avoni P, Polischi B, Santoro F, Capellari S, Liguori R, Parchi P. Amyloid-Beta Co-Pathology Is a Major Determinant of the Elevated Plasma GFAP Values in Amyotrophic Lateral Sclerosis. International Journal of Molecular Sciences. 24. PMID 37762278 DOI: 10.3390/ijms241813976 |
0.5 |
|
| 2023 |
Carrer T, Bonato G, Sandre M, Emmi A, Campagnolo M, Musso G, Carecchio M, Parchi P, Antonini A. Rapidly progressive multiple system atrophy in a patient carrying LRRK2 G2019S mutation. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 37752324 DOI: 10.1007/s10072-023-07056-5 |
0.323 |
|
| 2023 |
Bentivenga GM, Baiardi S, Righini L, Ladogana A, Capellari S, Sabattini E, Parchi P. Rapidly progressive dementia due to intravascular lymphoma: A prion disease reference center experience. European Journal of Neurology. PMID 37738529 DOI: 10.1111/ene.16068 |
0.559 |
|
| 2023 |
Bentivenga GM, Baiardi S, Mastrangelo A, Zenesini C, Mammana A, Polischi B, Capellari S, Parchi P. Diagnostic and prognostic value of cerebrospinal fluid SNAP-25 and neurogranin in Creutzfeldt-Jakob disease in a clinical setting cohort of rapidly progressive dementias. Alzheimer's Research & Therapy. 15: 150. PMID 37684653 DOI: 10.1186/s13195-023-01300-y |
0.56 |
|
| 2023 |
Abu-Rumeileh S, Halbgebauer S, Bentivenga GM, Barba L, Baiardi S, Mastrangelo A, Oeckl P, Steinacker P, Mammana A, Capellari S, Otto M, Parchi P. High diagnostic performance of plasma and cerebrospinal fluid beta-synuclein for sporadic Creutzfeldt-Jakob disease. Annals of Clinical and Translational Neurology. PMID 37553789 DOI: 10.1002/acn3.51873 |
0.528 |
|
| 2023 |
Baiardi S, Mammana A, Capellari S, Parchi P. Human prion disease: molecular pathogenesis, and possible therapeutic targets and strategies. Expert Opinion On Therapeutic Targets. 1-14. PMID 37334903 DOI: 10.1080/14728222.2023.2199923 |
0.627 |
|
| 2023 |
Vacchiano V, Mastrangelo A, Zenesini C, Baiardi S, Avoni P, Polischi B, Capellari S, Salvi F, Liguori R, Parchi P. Elevated plasma p-tau181 levels unrelated to Alzheimer's disease pathology in amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 37012065 DOI: 10.1136/jnnp-2022-330709 |
0.558 |
|
| 2023 |
Baiardi S, Mammana A, Dellavalle S, Rossi M, Redaelli V, Colaizzo E, Di Fede G, Ladogana A, Capellari S, Parchi P. Defining the phenotypic spectrum of sporadic Creutzfeldt-Jakob disease MV2K: the kuru plaque type. Brain : a Journal of Neurology. PMID 36883639 DOI: 10.1093/brain/awad074 |
0.628 |
|
| 2022 |
Tarozzi M, Baiardi S, Sala C, Bartoletti-Stella A, Parchi P, Capellari S, Castellani G. Genomic, transcriptomic and RNA editing analysis of human MM1 and VV2 sporadic Creutzfeldt-Jakob disease. Acta Neuropathologica Communications. 10: 181. PMID 36517866 DOI: 10.1186/s40478-022-01483-9 |
0.58 |
|
| 2022 |
Mastrangelo A, Mammana A, Baiardi S, Tiple D, Colaizzo E, Rossi M, Vaianella L, Polischi B, Equestre M, Poleggi A, Capellari S, Ladogana A, Parchi P. Evaluation of the impact of CSF prion RT-QuIC and amended criteria on the clinical diagnosis of Creutzfeldt-Jakob disease: a 10-year study in Italy. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 36428087 DOI: 10.1136/jnnp-2022-330153 |
0.574 |
|
| 2022 |
Baiardi S, Quadalti C, Mammana A, Dellavalle S, Zenesini C, Sambati L, Pantieri R, Polischi B, Romano L, Suffritti M, Bentivenga GM, Randi V, Stanzani-Maserati M, Capellari S, Parchi P. Diagnostic value of plasma p-tau181, NfL, and GFAP in a clinical setting cohort of prevalent neurodegenerative dementias. Alzheimer's Research & Therapy. 14: 153. PMID 36221099 DOI: 10.1186/s13195-022-01093-6 |
0.503 |
|
| 2022 |
Bartoletti-Stella A, Tarozzi M, Mengozzi G, Asirelli F, Brancaleoni L, Mometto N, Stanzani-Maserati M, Baiardi S, Linarello S, Spallazzi M, Pantieri R, Ferriani E, Caffarra P, Liguori R, Parchi P, et al. Dementia-related genetic variants in an Italian population of early-onset Alzheimer's disease. Frontiers in Aging Neuroscience. 14: 969817. PMID 36133075 DOI: 10.3389/fnagi.2022.969817 |
0.6 |
|
| 2022 |
Gelpi E, Baiardi S, Nos C, Dellavalle S, Aldecoa I, Ruiz-Garcia R, Ispierto L, Escudero D, Casado V, Barranco E, Boltes A, Molina-Porcel L, Bargalló N, Rossi M, Mammana A, ... ... Parchi P, et al. Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease. Acta Neuropathologica Communications. 10: 114. PMID 35978418 DOI: 10.1186/s40478-022-01415-7 |
0.613 |
|
| 2022 |
Vacchiano V, Bartoletti-Stella A, Rizzo G, Avoni P, Parchi P, Salvi F, Liguori R, Capellari S. Frequency of Parkinson's Disease Genes and Role of in Amyotrophic Lateral Sclerosis: An NGS Study. Genes. 13. PMID 35893043 DOI: 10.3390/genes13081306 |
0.521 |
|
| 2022 |
Poleggi A, Baiardi S, Ladogana A, Parchi P. The Use of Real-Time Quaking-Induced Conversion for the Diagnosis of Human Prion Diseases. Frontiers in Aging Neuroscience. 14: 874734. PMID 35547619 DOI: 10.3389/fnagi.2022.874734 |
0.397 |
|
| 2022 |
Cazzaniga FA, Bistaffa E, De Luca CMG, Portaleone SM, Catania M, Redaelli V, Tramacere I, Bufano G, Rossi M, Caroppo P, Giovagnoli AR, Tiraboschi P, Di Fede G, Eleopra R, Devigili G, ... ... Parchi P, et al. PMCA-Based Detection of Prions in the Olfactory Mucosa of Patients With Sporadic Creutzfeldt-Jakob Disease. Frontiers in Aging Neuroscience. 14: 848991. PMID 35401151 DOI: 10.3389/fnagi.2022.848991 |
0.341 |
|
| 2022 |
Abu-Rumeileh S, Barschke P, Oeckl P, Baiardi S, Mammana A, Mastrangelo A, Al Shweiki MR, Steinacker P, Ladogana A, Capellari S, Otto M, Parchi P. Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt-Jakob Disease. International Journal of Molecular Sciences. 23. PMID 35216166 DOI: 10.3390/ijms23042051 |
0.52 |
|
| 2022 |
Baiardi S, Mammana A, Rossi M, Ladogana A, Carlà B, Gambetti P, Capellari S, Parchi P. Phenotypic Heterogeneity of Variably Protease-Sensitive Prionopathy: A Report of Three Cases Carrying Different Genotypes at Codon 129. Viruses. 14. PMID 35215959 DOI: 10.3390/v14020367 |
0.708 |
|
| 2022 |
Halbgebauer S, Abu-Rumeileh S, Oeckl P, Steinacker P, Roselli F, Wiesner D, Mammana A, Beekes M, Kortazar-Zubizarreta I, Perez de Nanclares G, Capellari S, Giese A, Castilla J, Ludolph AC, Žáková D, ... Parchi P, et al. Blood β-Synuclein and Neurofilament Light Chain During the Course of Prion Disease. Neurology. PMID 35110380 DOI: 10.1212/WNL.0000000000200002 |
0.596 |
|
| 2021 |
Vacchiano V, Mastrangelo A, Zenesini C, Masullo M, Quadalti C, Avoni P, Polischi B, Cherici A, Capellari S, Salvi F, Liguori R, Parchi P. Plasma and CSF Neurofilament Light Chain in Amyotrophic Lateral Sclerosis: A Cross-Sectional and Longitudinal Study. Frontiers in Aging Neuroscience. 13: 753242. PMID 34744694 DOI: 10.3389/fnagi.2021.753242 |
0.545 |
|
| 2021 |
Areškevičiūtė A, Lund EL, Capellari S, Parchi P, Pinkowsky CT. The First Sporadic Creutzfeldt-Jakob Disease Case with a Rare Molecular Subtype VV1 and 1-Octapeptide Repeat Deletion in . Viruses. 13. PMID 34696491 DOI: 10.3390/v13102061 |
0.642 |
|
| 2021 |
Ximelis T, Marín-Moreno A, Espinosa JC, Eraña H, Charco JM, Hernández I, Riveira C, Alcolea D, González-Roca E, Aldecoa I, Molina-Porcel L, Parchi P, Rossi M, Castilla J, Ruiz-García R, et al. Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease. Alzheimer's Research & Therapy. 13: 176. PMID 34663460 DOI: 10.1186/s13195-021-00912-6 |
0.361 |
|
| 2021 |
Quadalti C, Calandra-Buonaura G, Baiardi S, Mastrangelo A, Rossi M, Zenesini C, Giannini G, Candelise N, Sambati L, Polischi B, Plazzi G, Capellari S, Cortelli P, Parchi P. Neurofilament light chain and α-synuclein RT-QuIC as differential diagnostic biomarkers in parkinsonisms and related syndromes. Npj Parkinson's Disease. 7: 93. PMID 34635674 DOI: 10.1038/s41531-021-00232-4 |
0.504 |
|
| 2021 |
Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, ... ... Parchi P, et al. Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification. Acta Neuropathologica. PMID 34324063 DOI: 10.1007/s00401-021-02350-y |
0.785 |
|
| 2021 |
Mastrangelo A, Baiardi S, Zenesini C, Poleggi A, Mammana A, Polischi B, Ladogana A, Capellari S, Parchi P. Diagnostic and prognostic performance of CSF α-synuclein in prion disease in the context of rapidly progressive dementia. Alzheimer's & Dementia (Amsterdam, Netherlands). 13: e12214. PMID 34222611 DOI: 10.1002/dad2.12214 |
0.559 |
|
| 2021 |
Rossi M, Baiardi S, Teunissen CE, Quadalti C, van de Beek M, Mammana A, Maserati MS, Van der Flier WM, Sambati L, Zenesini C, Caughey B, Capellari S, Lemstra A, Parchi P. Diagnostic Value of the CSF α-Synuclein Real-Time Quaking-Induced Conversion Assay at the Prodromal MCI Stage of Dementia With Lewy Bodies. Neurology. PMID 34210822 DOI: 10.1212/WNL.0000000000012438 |
0.495 |
|
| 2021 |
Vacchiano V, Mometto N, Bartoletti-Stella A, Rizzo G, Abu-Rumeileh S, Salvi F, Parchi P, Liguori R, Capellari S. The clinical spectrum of multisystem proteinopathy: Data from a neurodegenerative cohort. Journal of the Neurological Sciences. 426: 117478. PMID 34020145 DOI: 10.1016/j.jns.2021.117478 |
0.49 |
|
| 2021 |
Mammana A, Baiardi S, Quadalti C, Rossi M, Donadio V, Capellari S, Liguori R, Parchi P. RT-QuIC Detection of Pathological α-Synuclein in Skin Punches of Patients with Lewy Body Disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 34002890 DOI: 10.1002/mds.28651 |
0.528 |
|
| 2021 |
Abu-Rumeileh S, Parchi P. Cerebrospinal Fluid and Blood Neurofilament Light Chain Protein in Prion Disease and Other Rapidly Progressive Dementias: Current State of the Art. Frontiers in Neuroscience. 15: 648743. PMID 33776643 DOI: 10.3389/fnins.2021.648743 |
0.389 |
|
| 2021 |
Bartoletti-Stella A, Vacchiano V, De Pasqua S, Mengozzi G, De Biase D, Bartolomei I, Avoni P, Rizzo G, Parchi P, Donadio V, Chiò A, Pession A, Oppi F, Salvi F, Liguori R, et al. Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum. Journal of Neurology. PMID 33770234 DOI: 10.1007/s00415-021-10521-w |
0.49 |
|
| 2021 |
Hermann P, Appleby B, Brandel JP, Caughey B, Collins S, Geschwind MD, Green A, Haïk S, Kovacs GG, Ladogana A, Llorens F, Mead S, Nishida N, Pal S, Parchi P, et al. Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease. The Lancet. Neurology. 20: 235-246. PMID 33609480 DOI: 10.1016/S1474-4422(20)30477-4 |
0.367 |
|
| 2021 |
Sarapura-Castro E, Cosentino C, Landman J, Landman A, Torres L, Nuñez Y, Capellari S, Parchi P, Cornejo-Olivas M. Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families. Clinical Neurology and Neurosurgery. 202: 106490. PMID 33454496 DOI: 10.1016/j.clineuro.2021.106490 |
0.544 |
|
| 2020 |
Jones E, Hummerich H, Viré E, Uphill J, Dimitriadis A, Speedy H, Campbell T, Norsworthy P, Quinn L, Whitfield J, Linehan J, Jaunmuktane Z, Brandner S, Jat P, Nihat A, ... ... Parchi P, et al. Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study. The Lancet. Neurology. 19: 840-848. PMID 32949544 DOI: 10.1016/S1474-4422(20)30273-8 |
0.697 |
|
| 2020 |
Abu-Rumeileh S, Baiardi S, Ladogana A, Zenesini C, Bartoletti-Stella A, Poleggi A, Mammana A, Polischi B, Pocchiari M, Capellari S, Parchi P. Comparison between plasma and cerebrospinal fluid biomarkers for the early diagnosis and association with survival in prion disease. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 32928934 DOI: 10.1136/Jnnp-2020-323826 |
0.596 |
|
| 2020 |
Candelise N, Baiardi S, Franceschini A, Rossi M, Parchi P. Towards an improved early diagnosis of neurodegenerative diseases: the emerging role of in vitro conversion assays for protein amyloids. Acta Neuropathologica Communications. 8: 117. PMID 32711575 DOI: 10.1186/S40478-020-00990-X |
0.461 |
|
| 2020 |
Rossi M, Candelise N, Baiardi S, Capellari S, Giannini G, Orrù CD, Antelmi E, Mammana A, Hughson AG, Calandra-Buonaura G, Ladogana A, Plazzi G, Cortelli P, Caughey B, Parchi P. Correction to: Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies. Acta Neuropathologica. PMID 32556961 DOI: 10.1007/S00401-020-02170-6 |
0.51 |
|
| 2020 |
Bartoletti-Stella A, De Pasqua S, Baiardi S, Bartolomei I, Mengozzi G, Orio G, Pastorelli F, Piras S, Poda R, Raggi A, Maserati MS, Tarozzi M, Liguori R, Salvi F, Parchi P, et al. Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases. Neurobiology of Aging. PMID 32507413 DOI: 10.1016/J.Neurobiolaging.2020.05.004 |
0.598 |
|
| 2020 |
Melis M, Molari A, Floris G, Vascellari S, Balestrino L, Ladogana A, Poleggi A, Parchi P, Cossu G, Melis M, Orrù S, Defazio G. Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect. Neurogenetics. PMID 32458274 DOI: 10.1007/S10048-020-00618-1 |
0.437 |
|
| 2020 |
Mantovani P, Riccioli LA, Giannini G, Milletti D, Sorenson TJ, Maserati MS, Oppi F, Elder BD, Cevoli S, Cortelli P, Palandri G, Agati R, Calandra-Buonaura G, Capellari S, ... ... Parchi P, et al. Anterior callosal angle: a new marker of idiopathic normal pressure hydrocephalus? World Neurosurgery. PMID 32348895 DOI: 10.1016/J.Wneu.2020.04.085 |
0.505 |
|
| 2020 |
Rossi M, Candelise N, Baiardi S, Capellari S, Giannini G, Orrù CD, Antelmi E, Mammana A, Hughson AG, Calandra-Buonaura G, Ladogana A, Plazzi G, Cortelli P, Caughey B, Parchi P. Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies. Acta Neuropathologica. PMID 32342188 DOI: 10.1007/S00401-020-02160-8 |
0.607 |
|
| 2020 |
Raggi A, Bartoletti-Stella A, Parchi P, Capellari S. First case of an gene mutation causing frontotemporal dementia preceded by adult onset psychiatric symptoms. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-3. PMID 32290710 DOI: 10.1080/21678421.2020.1752251 |
0.595 |
|
| 2020 |
Baiardi S, Rizzi R, Capellari S, Bartoletti-Stella A, Zangrandi A, Gasparini F, Ghidoni E, Parchi P. Gerstmann-Sträussler-Scheinker disease ( p.D202N) presenting with atypical parkinsonism. Neurology. Genetics. 6: e400. PMID 32274419 DOI: 10.1212/Nxg.0000000000000400 |
0.582 |
|
| 2020 |
Abu-Rumeileh S, Oeckl P, Baiardi S, Halbgebauer S, Steinacker P, Capellari S, Otto M, Parchi P. CSF Ubiquitin Levels Are Higher in Alzheimer's Disease than in Frontotemporal Dementia and Reflect the Molecular Subtype in Prion Disease. Biomolecules. 10. PMID 32218217 DOI: 10.3390/biom10040497 |
0.616 |
|
| 2020 |
Mammana A, Baiardi S, Rossi M, Franceschini A, Donadio V, Capellari S, Caughey B, Parchi P. Detection of prions in skin punch biopsies of Creutzfeldt-Jakob disease patients. Annals of Clinical and Translational Neurology. PMID 32141717 DOI: 10.1002/Acn3.51000 |
0.608 |
|
| 2020 |
Abu-Rumeileh S, Vacchiano V, Zenesini C, Polischi B, de Pasqua S, Fileccia E, Mammana A, Di Stasi V, Capellari S, Salvi F, Liguori R, Parchi P. Diagnostic-prognostic value and electrophysiological correlates of CSF biomarkers of neurodegeneration and neuroinflammation in amyotrophic lateral sclerosis. Journal of Neurology. PMID 32100123 DOI: 10.1007/S00415-020-09761-Z |
0.562 |
|
| 2020 |
Abu-Rumeileh S, Halbgebauer S, Steinacker P, Anderl-Straub S, Polischi B, Ludolph AC, Capellari S, Parchi P, Otto M. CSF SerpinA1 in Creutzfeldt-Jakob disease and frontotemporal lobar degeneration. Annals of Clinical and Translational Neurology. PMID 31957347 DOI: 10.1002/Acn3.50980 |
0.631 |
|
| 2019 |
Abu-Rumeileh S, Steinacker P, Polischi B, Mammana A, Bartoletti-Stella A, Oeckl P, Baiardi S, Zenesini C, Huss A, Cortelli P, Capellari S, Otto M, Parchi P. CSF biomarkers of neuroinflammation in distinct forms and subtypes of neurodegenerative dementia. Alzheimer's Research & Therapy. 12: 2. PMID 31892365 DOI: 10.1186/S13195-019-0562-4 |
0.647 |
|
| 2019 |
Saijo E, Metrick MA, Koga S, Parchi P, Litvan I, Spina S, Boxer A, Rojas JC, Galasko D, Kraus A, Rossi M, Newell K, Zanusso G, Grinberg LT, Seeley WW, et al. 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathologica. PMID 31616982 DOI: 10.1007/S00401-019-02080-2 |
0.344 |
|
| 2019 |
Bongianni M, Ladogana A, Capaldi S, Klotz S, Baiardi S, Cagnin A, Perra D, Fiorini M, Poleggi A, Legname G, Cattaruzza T, Janes F, Tabaton M, Ghetti B, Monaco S, ... ... Parchi P, et al. α-Synuclein RT-QuIC assay in cerebrospinal fluid of patients with dementia with Lewy bodies. Annals of Clinical and Translational Neurology. PMID 31599499 DOI: 10.1002/Acn3.50897 |
0.754 |
|
| 2019 |
Puopolo M, Catelan D, Capellari S, Ladogana A, Sanguedolce A, Fedele A, Aprile V, Turco GL, Colaizzo E, Tiple D, Vaianella L, Parchi P, Biggeri A, Pocchiari M. Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy. Neuroepidemiology. 1-7. PMID 31563913 DOI: 10.1159/000503234 |
0.624 |
|
| 2019 |
Minikel EV, Kuhn E, Cocco AR, Vallabh SM, Hartigan CR, Reidenbach AG, Safar JG, Raymond GJ, McCarthy MD, O'Keefe R, Llorens F, Zerr I, Capellari S, Parchi P, Schreiber SL, et al. -Domain-specific quantification of prion protein in cerebrospinal fluid by targeted mass spectrometry. Molecular & Cellular Proteomics : McP. PMID 31558565 DOI: 10.1074/Mcp.Ra119.001702 |
0.631 |
|
| 2019 |
Areškevičiūtė A, Broholm H, Melchior LC, Bartoletti-Stella A, Parchi P, Capellari S, Scheie D, Lund EL. Molecular Characterization of the Danish Prion Diseases Cohort With Special Emphasis on Rare and Unique Cases. Journal of Neuropathology and Experimental Neurology. PMID 31553446 DOI: 10.1093/Jnen/Nlz089 |
0.696 |
|
| 2019 |
Baiardi S, Pizza F, Polischi B, Moresco M, Abu-Rumeileh S, Plazzi G, Parchi P. Cerebrospinal fluid biomarkers of neurodegeneration in narcolepsy type 1. Sleep. PMID 31552425 DOI: 10.1093/Sleep/Zsz215 |
0.339 |
|
| 2019 |
Abu-Rumeileh S, Baiardi S, Polischi B, Mammana A, Franceschini A, Green A, Capellari S, Parchi P. Diagnostic value of surrogate CSF biomarkers for Creutzfeldt-Jakob disease in the era of RT-QuIC. Journal of Neurology. PMID 31541342 DOI: 10.1007/S00415-019-09537-0 |
0.578 |
|
| 2019 |
Giannini G, Palandri G, Ferrari A, Oppi F, Milletti D, Albini-Riccioli L, Mantovani P, Magnoni S, Chiari L, Cortelli P, Cevoli S, Agati R, Calandra-Buonaura G, Capellari S, Parchi P, et al. A prospective evaluation of clinical and instrumental features before and after ventriculo-peritoneal shunt in patients with idiopathic Normal pressure hydrocephalus: The Bologna PRO-Hydro study. Parkinsonism & Related Disorders. 66: 117-124. PMID 31358442 DOI: 10.1016/J.Parkreldis.2019.07.021 |
0.545 |
|
| 2019 |
Minikel EV, Vallabh SM, Orseth MC, Brandel JP, Haïk S, Laplanche JL, Zerr I, Parchi P, Capellari S, Safar J, Kenny J, Fong JC, Takada LT, Ponto C, Hermann P, et al. Age at onset in genetic prion disease and the design of preventive clinical trials. Neurology. PMID 31171647 DOI: 10.1212/Wnl.0000000000007745 |
0.62 |
|
| 2019 |
Areškevičiūtė A, Høgh P, Bartoletti-Stella A, Melchior LC, Nielsen PR, Parchi P, Capellari S, Broholm H, Scheie D, Lund EL. A Novel Eight Octapeptide Repeat Insertion in PRNP Causing Prion Disease in a Danish Family. Journal of Neuropathology and Experimental Neurology. PMID 31107536 DOI: 10.1093/Jnen/Nlz037 |
0.604 |
|
| 2019 |
Mitolo M, Stanzani-Maserati M, Capellari S, Testa C, Rucci P, Poda R, Oppi F, Gallassi R, Sambati L, Rizzo G, Parchi P, Evangelisti S, Talozzi L, Tonon C, Lodi R, et al. Predicting conversion from mild cognitive impairment to Alzheimer's disease using brain H-MRS and volumetric changes: A two- year retrospective follow-up study. Neuroimage. Clinical. 23: 101843. PMID 31071594 DOI: 10.1016/J.Nicl.2019.101843 |
0.562 |
|
| 2019 |
Rossi M, Kai H, Baiardi S, Bartoletti-Stella A, Carlà B, Zenesini C, Capellari S, Kitamoto T, Parchi P. The characterization of AD/PART co-pathology in CJD suggests independent pathogenic mechanisms and no cross-seeding between misfolded Aβ and prion proteins. Acta Neuropathologica Communications. 7: 53. PMID 30961668 DOI: 10.1186/S40478-019-0706-6 |
0.62 |
|
| 2019 |
Vallabh SM, Nobuhara CK, Llorens F, Zerr I, Parchi P, Capellari S, Kuhn E, Klickstein J, Safar JG, Nery FC, Swoboda KJ, Geschwind MD, Zetterberg H, Arnold SE, Minikel EV, et al. Prion protein quantification in human cerebrospinal fluid as a tool for prion disease drug development. Proceedings of the National Academy of Sciences of the United States of America. PMID 30936307 DOI: 10.1073/Pnas.1901947116 |
0.622 |
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| 2019 |
Rossi M, Baiardi S, Parchi P. Understanding Prion Strains: Evidence from Studies of the Disease Forms Affecting Humans. Viruses. 11. PMID 30934971 DOI: 10.3390/V11040309 |
0.511 |
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| 2019 |
Tiple D, Poleggi A, Mellina V, Morocutti A, Brusa L, Iani C, Colaizzo E, Vaianella L, Baiardi S, Ladogana A, Parchi P, Pocchiari M. Clinicopathological features of the rare form of Creutzfeldt-Jakob disease in R208H-V129V PRNP carrier. Acta Neuropathologica Communications. 7: 47. PMID 30898147 DOI: 10.1186/S40478-019-0699-1 |
0.434 |
|
| 2019 |
Abu-Rumeileh S, Giannini G, Polischi B, Albini-Riccioli L, Milletti D, Oppi F, Stanzani-Maserati M, Capellari S, Mantovani P, Palandri G, Cortelli P, Cevoli S, Parchi P. Revisiting the Cerebrospinal Fluid Biomarker Profile in Idiopathic Normal Pressure Hydrocephalus: The Bologna Pro-Hydro Study. Journal of Alzheimer's Disease : Jad. PMID 30883350 DOI: 10.3233/Jad-181012 |
0.585 |
|
| 2019 |
Baiardi S, Abu-Rumeileh S, Rossi M, Zenesini C, Bartoletti-Stella A, Polischi B, Capellari S, Parchi P. Antemortem CSF A42/A40 ratio predicts Alzheimer's disease pathology better than A42 in rapidly progressive dementias. Annals of Clinical and Translational Neurology. 6: 263-273. PMID 30847359 DOI: 10.1002/Acn3.697 |
0.527 |
|
| 2019 |
Nonno R, Notari S, Di Bari MA, Cali I, Pirisinu L, d'Agostino C, Cracco L, Kofskey D, Vanni I, Lavrich J, Parchi P, Agrimi U, Gambetti P. Variable Protease-Sensitive Prionopathy Transmission to Bank Voles. Emerging Infectious Diseases. 25: 73-81. PMID 30561322 DOI: 10.3201/Eid2501.180807 |
0.826 |
|
| 2019 |
Bommarito G, Cellerino M, Prada V, Venturi C, Capellari S, Cortelli P, Mancardi GL, Parchi P, Schenone A. A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrhea. European Journal of Neurology. 25: e91-e92. PMID 29984897 DOI: 10.1111/Ene.13665 |
0.592 |
|
| 2018 |
Baiardi S, Rossi M, Capellari S, Parchi P. Recent advances in the histo-molecular pathology of human prion disease. Brain Pathology (Zurich, Switzerland). PMID 30588685 DOI: 10.1111/Bpa.12695 |
0.689 |
|
| 2018 |
Bartoletti-Stella A, Corrado P, Mometto N, Baiardi S, Durrenberger PF, Arzberger T, Reynolds R, Kretzschmar H, Capellari S, Parchi P. Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease. Molecular Neurobiology. PMID 30446946 DOI: 10.1007/S12035-018-1421-1 |
0.619 |
|
| 2018 |
Baiardi S, Redaelli V, Ripellino P, Rossi M, Franceschini A, Moggio M, Sola P, Ladogana A, Fociani P, Magherini A, Capellari S, Giese A, Caughey B, Caroppo P, Parchi P. Prion-related peripheral neuropathy in sporadic Creutzfeldt-Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 30355606 DOI: 10.1136/Jnnp-2018-319221 |
0.651 |
|
| 2018 |
Vicente-Pascual M, Rossi M, Gámez J, Lladó A, Valls J, Grau-Rivera O, Ávila Polo R, Llorens F, Zerr I, Ferrer I, Nos C, Parchi P, Sánchez-Valle R, Gelpí E. Variably protease-sensitive prionopathy presenting within ALS/FTD spectrum. Annals of Clinical and Translational Neurology. 5: 1297-1302. PMID 30349865 DOI: 10.1002/Acn3.632 |
0.47 |
|
| 2018 |
Abu-Rumeileh S, Mometto N, Bartoletti-Stella A, Polischi B, Oppi F, Poda R, Stanzani-Maserati M, Cortelli P, Liguori R, Capellari S, Parchi P. Cerebrospinal Fluid Biomarkers in Patients with Frontotemporal Dementia Spectrum: A Single-Center Study. Journal of Alzheimer's Disease : Jad. PMID 30320576 DOI: 10.3233/Jad-180409 |
0.575 |
|
| 2018 |
Abu-Rumeileh S, Redaelli V, Baiardi S, Mackenzie G, Windl O, Ritchie DL, Didato G, Hernandez-Vara J, Rossi M, Capellari S, Imperiale D, Rizzone MG, Belotti A, Sorbi S, Rozemuller AJM, ... ... Parchi P, et al. Sporadic Fatal Insomnia in Europe: Phenotypic features and diagnostic challenges. Annals of Neurology. PMID 30048013 DOI: 10.1002/Ana.25300 |
0.566 |
|
| 2018 |
Poleggi A, van der Lee S, Capellari S, Puopolo M, Ladogana A, De Pascali E, Lia D, Formato A, Bartoletti-Stella A, Parchi P, van Duijn C, Pocchiari M. Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the gene. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 30032116 DOI: 10.1136/Jnnp-2018-318756 |
0.625 |
|
| 2018 |
Baiardi S, Capellari S, Bartoletti Stella A, Parchi P. Unusual Clinical Presentations Challenging the Early Clinical Diagnosis of Creutzfeldt-Jakob Disease. Journal of Alzheimer's Disease : Jad. PMID 30010123 DOI: 10.3233/Jad-180123 |
0.615 |
|
| 2018 |
Capellari S, Baiardi S, Rinaldi R, Bartoletti-Stella A, Graziano C, Piras S, Calandra-Buonaura G, D'Angelo R, Terziotti C, Lodi R, Donadio V, Pironi L, Cortelli P, Parchi P. Two novel truncating mutations broaden the spectrum of prion amyloidosis. Annals of Clinical and Translational Neurology. 5: 777-783. PMID 29928661 DOI: 10.1002/Acn3.568 |
0.597 |
|
| 2018 |
Quadri M, Mandemakers W, Grochowska MM, Masius R, Geut H, Fabrizio E, Breedveld GJ, Kuipers D, Minneboo M, Vergouw LJM, Carreras Mascaro A, Yonova-Doing E, Simons E, Zhao T, Di Fonzo AB, ... ... Parchi P, et al. LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study. The Lancet. Neurology. PMID 29887161 DOI: 10.1016/S1474-4422(18)30179-0 |
0.641 |
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| 2018 |
Zerr I, Parchi P. Sporadic Creutzfeldt-Jakob disease. Handbook of Clinical Neurology. 153: 155-174. PMID 29887134 DOI: 10.1016/B978-0-444-63945-5.00009-X |
0.434 |
|
| 2018 |
Abu-Rumeileh S, Capellari S, Parchi P. Rapidly Progressive Alzheimer's Disease: Contributions to Clinical-Pathological Definition and Diagnosis. Journal of Alzheimer's Disease : Jad. PMID 29710713 DOI: 10.3233/Jad-171181 |
0.652 |
|
| 2018 |
Bartoletti-Stella A, Baiardi S, Stanzani-Maserati M, Piras S, Caffarra P, Raggi A, Pantieri R, Baldassari S, Caporali L, Abu-Rumeileh S, Linarello S, Liguori R, Parchi P, Capellari S. Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing. Neurobiology of Aging. PMID 29525180 DOI: 10.1016/J.Neurobiolaging.2018.02.006 |
0.625 |
|
| 2018 |
Giannoccaro MP, Bartoletti-Stella A, Piras S, Casalena A, Oppi F, Ambrosetto G, Montagna P, Liguori R, Parchi P, Capellari S. The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance. Journal of Alzheimer's Disease : Jad. 62: 687-697. PMID 29480190 DOI: 10.3233/Jad-170913 |
0.553 |
|
| 2018 |
Race B, Williams K, Hughson AG, Jansen C, Parchi P, Rozemuller AJM, Chesebro B. Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein. Acta Neuropathologica Communications. 6: 13. PMID 29458424 DOI: 10.1186/S40478-018-0516-2 |
0.464 |
|
| 2018 |
Iaccarino L, Presotto L, Bettinardi V, Gianolli L, Roiter I, Capellari S, Parchi P, Cortelli P, Perani D. An in vivo 11C-PK PET study of microglia activation in Fatal Familial Insomnia. Annals of Clinical and Translational Neurology. 5: 11-18. PMID 29376088 DOI: 10.1002/Acn3.498 |
0.535 |
|
| 2018 |
Abu-Rumeileh S, Capellari S, Stanzani-Maserati M, Polischi B, Martinelli P, Caroppo P, Ladogana A, Parchi P. The CSF neurofilament light signature in rapidly progressive neurodegenerative dementias. Alzheimer's Research & Therapy. 10: 3. PMID 29368621 DOI: 10.1186/S13195-017-0331-1 |
0.561 |
|
| 2018 |
Franceschini A, Strammiello R, Capellari S, Giese A, Parchi P. Regional pattern of microgliosis in sporadic Creutzfeldt-Jakob disease in relation to phenotypic variants and disease progression. Neuropathology and Applied Neurobiology. PMID 29345730 DOI: 10.1111/Nan.12461 |
0.657 |
|
| 2018 |
Cali I, Cohen ML, Haїk S, Parchi P, Giaccone G, Collins SJ, Kofskey D, Wang H, McLean CA, Brandel JP, Privat N, Sazdovitch V, Duyckaerts C, Kitamoto T, Belay ED, et al. Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study. Acta Neuropathologica Communications. 6: 5. PMID 29310723 DOI: 10.1186/S40478-017-0503-Z |
0.741 |
|
| 2017 |
Rossi M, Saverioni D, Di Bari M, Baiardi S, Lemstra AW, Pirisinu L, Capellari S, Rozemuller A, Nonno R, Parchi P. Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature. Acta Neuropathologica Communications. 5: 87. PMID 29169405 DOI: 10.1186/S40478-017-0496-7 |
0.66 |
|
| 2017 |
Bartoletti-Stella A, Gasparini L, Giacomini C, Corrado P, Terlizzi R, Giorgio E, Magini P, Seri M, Baruzzi A, Parchi P, Brusco A, Cortelli P, Capellari S. Messenger RNA processing is altered in autosomal dominant leukodystrophy. Human Molecular Genetics. 26: 3868. PMID 28934398 DOI: 10.1093/hmg/ddx225 |
0.424 |
|
| 2017 |
Franceschini A, Baiardi S, Hughson AG, McKenzie N, Moda F, Rossi M, Capellari S, Green A, Giaccone G, Caughey B, Parchi P. High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions. Scientific Reports. 7: 10655. PMID 28878311 DOI: 10.1038/S41598-017-10922-W |
0.605 |
|
| 2017 |
Baiardi S, Magherini A, Capellari S, Redaelli V, Ladogana A, Rossi M, Tagliavini F, Pocchiari M, Giaccone G, Parchi P. Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type). Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28668775 DOI: 10.1136/Jnnp-2017-315942 |
0.605 |
|
| 2017 |
Giannoccaro MP, Bartoletti-Stella A, Piras S, Pession A, De Massis P, Oppi F, Stanzani-Maserati M, Pasini E, Baiardi S, Avoni P, Parchi P, Liguori R, Capellari S. Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature. Journal of Neurology. PMID 28620717 DOI: 10.1007/S00415-017-8540-X |
0.59 |
|
| 2017 |
Terlizzi R, Valentino ML, Bartoletti-Stella A, Columbaro M, Piras S, Stanzani-Maserati M, Quadri M, Breedveld GJ, Bonifati V, Martinelli P, Parchi P, Capellari S. Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28543767 DOI: 10.1002/Mds.27049 |
0.536 |
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| 2017 |
Lattanzio F, Abu-Rumeileh S, Franceschini A, Kai H, Amore G, Poggiolini I, Rossi M, Baiardi S, McGuire L, Ladogana A, Pocchiari M, Green A, Capellari S, Parchi P. Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels. Acta Neuropathologica. PMID 28205010 DOI: 10.1007/S00401-017-1683-0 |
0.635 |
|
| 2016 |
Rumeileh SA, Lattanzio F, Maserati MS, Rizzi R, Capellari S, Parchi P. Diagnostic Accuracy of a Combined Analysis of Cerebrospinal Fluid t-PrP, t-tau, p-tau, and Aβ42 in the Differential Diagnosis of Creutzfeldt-Jakob Disease from Alzheimer's Disease with Emphasis on Atypical Disease Variants. Journal of Alzheimer's Disease : Jad. PMID 27886009 DOI: 10.3233/Jad-160740 |
0.594 |
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| 2016 |
Vita MG, Tiple D, Bizzarro A, Ladogana A, Colaizzo E, Capellari S, Rossi M, Parchi P, Masullo C, Pocchiari M. Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 27634418 DOI: 10.1111/Neup.12343 |
0.628 |
|
| 2016 |
McGuire LI, Poleggi A, Poggiolini I, Suardi S, Grznarova K, Shi S, de Vil B, Sarros S, Satoh K, Cheng K, Cramm M, Fairfoul G, Schmitz M, Zerr I, Cras P, ... ... Parchi P, et al. CSF RT-QuIC is a robust and reliable test for sporadic CJD: An international study. Annals of Neurology. PMID 27130376 DOI: 10.1002/Ana.24679 |
0.332 |
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| 2016 |
Cescatti M, Saverioni D, Capellari S, Tagliavini F, Kitamoto T, Ironside J, Giese A, Parchi P. Analysis of conformational stability of abnormal prion protein aggregates across the spectrum of Creutzfeldt-Jakob disease prions. Journal of Virology. PMID 27122583 DOI: 10.1128/Jvi.00144-16 |
0.637 |
|
| 2016 |
Takeuchi A, Kobayashi A, Parchi P, Yamada M, Morita M, Uno S, Kitamoto T. Distinctive properties of plaque-type dura mater graft-associated Creutzfeldt-Jakob disease in cell-protein misfolding cyclic amplification. Laboratory Investigation; a Journal of Technical Methods and Pathology. PMID 26878132 DOI: 10.1038/Labinvest.2016.27 |
0.398 |
|
| 2016 |
Minikel EV, Vallabh SM, Lek M, Estrada K, Samocha KE, Sathirapongsasuti JF, McLean CY, Tung JY, Yu LP, Gambetti P, Blevins J, Zhang S, Cohen Y, Chen W, Yamada M, ... ... Parchi P, et al. Quantifying prion disease penetrance using large population control cohorts. Science Translational Medicine. 8: 322ra9. PMID 26791950 DOI: 10.1126/Scitranslmed.Aad5169 |
0.742 |
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| 2015 |
Baiardi S, Capellari S, Ladogana A, Strumia S, Santangelo M, Pocchiari M, Parchi P. Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings. Journal of Alzheimer's Disease : Jad. PMID 26682685 DOI: 10.3233/Jad-150668 |
0.644 |
|
| 2015 |
Kobayashi A, Parchi P, Yamada M, Mohri S, Kitamoto T. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 26669818 DOI: 10.1111/Neup.12270 |
0.446 |
|
| 2015 |
Bartoletti-Stella A, Gasparini L, Giacomini C, Corrado P, Terlizzi R, Giorgio E, Magini P, Seri M, Baruzzi A, Parchi P, Brusco A, Cortelli P, Capellari S. Messenger RNA processing is altered in autosomal dominant leukodystrophy. Human Molecular Genetics. 24: 2746-56. PMID 25637521 DOI: 10.1093/Hmg/Ddv034 |
0.559 |
|
| 2015 |
Kobayashi A, Parchi P, Yamada M, Brown P, Saverioni D, Matsuura Y, Takeuchi A, Mohri S, Kitamoto T. Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology? Journal of Virology. 89: 3939-46. PMID 25609817 DOI: 10.1128/Jvi.03183-14 |
0.423 |
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| 2015 |
Scontrini A, Di Bonaventura C, Fiorelli M, Tiple D, Colaizzo E, Ladogana A, Parchi P, Pocchiari M. Creutzfeldt-Jakob disease masked by head trauma and features of Wilson's disease. The International Journal of Neuroscience. 125: 312-4. PMID 25485669 DOI: 10.3109/00207454.2014.992428 |
0.429 |
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| 2015 |
Alafuzoff I, Pikkarainen M, Neumann M, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Bugiani O, Ferrer I, Gelpi E, Gentleman S, Giaccone G, Graeber MB, Hortobagyi T, Ince PG, ... ... Parchi P, et al. Erratum to: Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium. Journal of Neural Transmission (Vienna, Austria : 1996). 122: 973-4. PMID 25418279 DOI: 10.1007/S00702-014-1337-5 |
0.301 |
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| 2015 |
Alafuzoff I, Pikkarainen M, Neumann M, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Bugiani O, Ferrer I, Gelpi E, Gentleman S, Giaccone G, Graeber MB, Hortobagyi T, Ince PG, ... ... Parchi P, et al. Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium. Journal of Neural Transmission (Vienna, Austria : 1996). 122: 957-72. PMID 25239189 DOI: 10.1007/S00702-014-1304-1 |
0.303 |
|
| 2014 |
Cardone F, Principe S, Schininà ME, Maras B, Capellari S, Parchi P, Notari S, Di Francesco L, Poleggi A, Galeno R, Vinci R, Mellina V, Almonti S, Ladogana A, Pocchiari M. Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt-Jakob disease patients. Biochemical and Biophysical Research Communications. 454: 289-94. PMID 25450391 DOI: 10.1016/J.Bbrc.2014.10.051 |
0.793 |
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| 2014 |
D'Angelo R, Rinaldi R, Parchi P, Cirignotta F. Wait and see: a 5 year history of 'recurrent dementia'. Bmj Case Reports. 2014. PMID 25410032 DOI: 10.1136/Bcr-2014-205991 |
0.341 |
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| 2014 |
Pizza F, Vandi S, Liguori R, Parchi P, Avoni P, Mignot E, Plazzi G. Primary progressive narcolepsy type 1: the other side of the coin. Neurology. 83: 2189-90. PMID 25355832 DOI: 10.1212/Wnl.0000000000001051 |
0.354 |
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| 2014 |
Damato V, Cuccagna C, Costantini EM, Gaudino S, Colosimo C, Parchi P, Servidei S, Luigetti M. Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: pitfalls and tips in the diagnosis. Journal of the Neurological Sciences. 346: 343-4. PMID 25201717 DOI: 10.1016/J.Jns.2014.08.026 |
0.344 |
|
| 2014 |
Bacchelli E, Ceroni F, Pinto D, Lomartire S, Giannandrea M, D'Adamo P, Bonora E, Parchi P, Tancredi R, Battaglia A, Maestrini E. A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. Journal of Neurodevelopmental Disorders. 6: 17. PMID 25050139 DOI: 10.1186/1866-1955-6-17 |
0.312 |
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| 2014 |
Bonora E, Graziano C, Minopoli F, Bacchelli E, Magini P, Diquigiovanni C, Lomartire S, Bianco F, Vargiolu M, Parchi P, Marasco E, Mantovani V, Rampoldi L, Trudu M, Parmeggiani A, et al. Maternally inherited genetic variants of CADPS2 are present in autism spectrum disorders and intellectual disability patients. Embo Molecular Medicine. 6: 795-809. PMID 24737869 DOI: 10.1002/Emmm.201303235 |
0.324 |
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| 2014 |
Moghadam KK, Pizza F, La Morgia C, Franceschini C, Tonon C, Lodi R, Barboni P, Seri M, Ferrari S, Liguori R, Donadio V, Parchi P, Cornelio F, Inzitari D, Mignarri A, et al. Narcolepsy is a common phenotype in HSAN IE and ADCA-DN. Brain : a Journal of Neurology. 137: 1643-55. PMID 24727570 DOI: 10.1093/Brain/Awu069 |
0.457 |
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| 2014 |
Cortelli P, Fabbri M, Calandra-Buonaura G, Capellari S, Tinuper P, Parchi P, Lugaresi E. Gait disorders in fatal familial insomnia. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 420-4. PMID 24375448 DOI: 10.1002/Mds.25786 |
0.712 |
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| 2013 |
Poggiolini I, Saverioni D, Parchi P. Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions. International Journal of Cell Biology. 2013: 910314. PMID 24454379 DOI: 10.1155/2013/910314 |
0.431 |
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| 2013 |
Vita MG, Gaudino S, Di Giuda D, Sauchelli D, Alboini PE, Gangemi E, Bizzarro A, Scaricamazza E, Capellari S, Parchi P, Masullo C. R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease. Journal of Neurology. 260: 2650-2. PMID 23979103 DOI: 10.1007/S00415-013-7078-9 |
0.645 |
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| 2013 |
Saverioni D, Notari S, Capellari S, Poggiolini I, Giese A, Kretzschmar HA, Parchi P. Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions. The Journal of Biological Chemistry. 288: 27972-85. PMID 23897825 DOI: 10.1074/Jbc.M113.477547 |
0.766 |
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| 2013 |
Mattsson N, Andreasson U, Persson S, Carrillo MC, Collins S, Chalbot S, Cutler N, Dufour-Rainfray D, Fagan AM, Heegaard NH, Robin Hsiung GY, Hyman B, Iqbal K, Kaeser SA, Käser SA, ... ... Parchi P, et al. CSF biomarker variability in the Alzheimer's Association quality control program. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 9: 251-61. PMID 23622690 DOI: 10.1016/J.Jalz.2013.01.010 |
0.324 |
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| 2013 |
Parchi P, Capellari S. Prion disease: diagnostic value of cerebrospinal fluid markers. Nature Reviews. Neurology. 9: 10-1. PMID 23208112 DOI: 10.1038/Nrneurol.2012.253 |
0.612 |
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| 2013 |
Gelpi E, Soler Insa JM, Parchi P, Saverioni D, Yagüe J, Nos C, MartÃnez-Saez E, Ribalta T, Ferrer I, Sanchez-Valle R. Atypical neuropathological sCJD-MM phenotype with abundant white matter Kuru-type plaques sparing the cerebellar cortex. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 33: 204-8. PMID 22862687 DOI: 10.1111/J.1440-1789.2012.01341.X |
0.407 |
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| 2013 |
Vita MG, Gaudino S, Giuda D, Sauchelli D, Alboini PE, Gangemi E, Bizzarro A, Scaricamazza E, Capellari S, Parchi P, Masullo C. Erratum to: R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease Journal of Neurology. 260: 3199-3199. DOI: 10.1007/S00415-013-7164-Z |
0.645 |
|
| 2012 |
Durrenberger PF, Fernando FS, Magliozzi R, Kashefi SN, Bonnert TP, Ferrer I, Seilhean D, Nait-Oumesmar B, Schmitt A, Gebicke-Haerter PJ, Falkai P, Grünblatt E, Palkovits M, Parchi P, Capellari S, et al. Selection of novel reference genes for use in the human central nervous system: a BrainNet Europe Study. Acta Neuropathologica. 124: 893-903. PMID 22864814 DOI: 10.1007/S00401-012-1027-Z |
0.542 |
|
| 2012 |
Parchi P, de Boni L, Saverioni D, Cohen ML, Ferrer I, Gambetti P, Gelpi E, Giaccone G, Hauw JJ, Höftberger R, Ironside JW, Jansen C, Kovacs GG, Rozemuller A, Seilhean D, et al. Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA. Acta Neuropathologica. 124: 517-29. PMID 22744790 DOI: 10.1007/S00401-012-1002-8 |
0.726 |
|
| 2012 |
Jansen C, Parchi P, Capellari S, Ibrahim-Verbaas CA, Schuur M, Strammiello R, Corrado P, Bishop MT, van Gool WA, Verbeek MM, Baas F, van Saane W, Spliet WG, Jansen GH, van Duijn CM, et al. Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects. Plos One. 7: e36333. PMID 22558438 DOI: 10.1371/Journal.Pone.0036333 |
0.672 |
|
| 2012 |
Parchi P, Saverioni D. Molecular pathology, classification, and diagnosis of sporadic human prion disease variants. Folia Neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences. 50: 20-45. PMID 22505361 |
0.419 |
|
| 2012 |
Cerullo F, Del Nonno F, Baiocchini A, Parchi P, Cesari M, Gambassi G. Creutzfeldt-Jakob disease: an under-recognized cause of dementia. Journal of the American Geriatrics Society. 60: 156-7. PMID 22239296 DOI: 10.1111/J.1532-5415.2011.03756.X |
0.441 |
|
| 2012 |
Popova SN, Tarvainen I, Capellari S, Parchi P, Hannikainen P, Pirinen E, Haapasalo H, Alafuzoff I. Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L family. Acta Neurologica Scandinavica. 126: 315-23. PMID 22211828 DOI: 10.1111/J.1600-0404.2011.01628.X |
0.663 |
|
| 2011 |
Jansen C, Parchi P, Capellari S, Strammiello R, Dopper EG, van Swieten JC, Kamphorst W, Rozemuller AJ. A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient. Journal of Neuropathology and Experimental Neurology. 70: 698-702. PMID 21760536 DOI: 10.1097/Nen.0B013E3182270C54 |
0.69 |
|
| 2011 |
Giaccone G, Arzberger T, Alafuzoff I, Al-Sarraj S, Budka H, Duyckaerts C, Falkai P, Ferrer I, Ironside JW, Kovács GG, Meyronet D, Parchi P, Patsouris E, Revesz T, Riederer P, et al. New lexicon and criteria for the diagnosis of Alzheimer's disease. The Lancet. Neurology. 10: 298-9; author reply . PMID 21435593 DOI: 10.1016/S1474-4422(11)70055-2 |
0.4 |
|
| 2011 |
Parchi P, Strammiello R, Giese A, Kretzschmar H. Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future. Acta Neuropathologica. 121: 91-112. PMID 21107851 DOI: 10.1007/S00401-010-0779-6 |
0.521 |
|
| 2011 |
Capellari S, Strammiello R, Saverioni D, Kretzschmar H, Parchi P. Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis. Acta Neuropathologica. 121: 21-37. PMID 20978903 DOI: 10.1007/S00401-010-0760-4 |
0.702 |
|
| 2011 |
Jansen C, Parchi P, Jelles B, Gouw AA, Beunders G, van Spaendonk RM, van de Kamp JM, Lemstra AW, Capellari S, Rozemuller AJ. The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau deposits. Neuropathology and Applied Neurobiology. 37: 549-53. PMID 20874730 DOI: 10.1111/J.1365-2990.2010.01126.X |
0.553 |
|
| 2011 |
Jansen C, Voet W, Head MW, Parchi P, Yull H, Verrips A, Wesseling P, Meulstee J, Baas F, van Gool WA, Ironside JW, Rozemuller AJ. A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature. Acta Neuropathologica. 121: 59-68. PMID 20198483 DOI: 10.1007/S00401-010-0656-3 |
0.469 |
|
| 2011 |
Parchi P, Capellari S, Gambetti P. Fatal Familial and Sporadic Insomnia Neurodegeneration: the Molecular Pathology of Dementia and Movement Disorders: Second Edition. 346-349. DOI: 10.1002/9781444341256.ch34 |
0.469 |
|
| 2011 |
Budka H, Head MW, Ironside JW, Gambetti P, Parchi P, Tagliavini F. Sporadic Creutzfeldt-Jakob Disease Neurodegeneration: the Molecular Pathology of Dementia and Movement Disorders: Second Edition. 322-335. DOI: 10.1002/9781444341256.Ch32 |
0.681 |
|
| 2010 |
Parchi P, Cescatti M, Notari S, Schulz-Schaeffer WJ, Capellari S, Giese A, Zou WQ, Kretzschmar H, Ghetti B, Brown P. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease. Brain : a Journal of Neurology. 133: 3030-42. PMID 20823086 DOI: 10.1093/Brain/Awq234 |
0.817 |
|
| 2010 |
Masullo C, Bizzarro A, Guglielmi V, Iannaccone E, Minicuci G, Vita MG, Capellari S, Parchi P, Servidei S. An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 31: 837-9. PMID 20730466 DOI: 10.1007/S10072-010-0388-0 |
0.635 |
|
| 2010 |
Zou WQ, Puoti G, Xiao X, Yuan J, Qing L, Cali I, Shimoji M, Langeveld JP, Castellani R, Notari S, Crain B, Schmidt RE, Geschwind M, Dearmond SJ, Cairns NJ, ... ... Parchi P, et al. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Annals of Neurology. 68: 162-72. PMID 20695009 DOI: 10.1002/Ana.22094 |
0.836 |
|
| 2010 |
Zou WQ, Langeveld J, Xiao X, Chen S, McGeer PL, Yuan J, Payne MC, Kang HE, McGeehan J, Sy MS, Greenspan NS, Kaplan D, Wang GX, Parchi P, Hoover E, et al. PrP conformational transitions alter species preference of a PrP-specific antibody. The Journal of Biological Chemistry. 285: 13874-84. PMID 20194495 DOI: 10.1074/Jbc.M109.088831 |
0.302 |
|
| 2010 |
Notari S, Moleres FJ, Hunter SB, Belay ED, Schonberger LB, Cali I, Parchi P, Shieh WJ, Brown P, Zaki S, Zou WQ, Gambetti P. Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States. Plos One. 5: e8765. PMID 20098730 DOI: 10.1371/Journal.Pone.0008765 |
0.823 |
|
| 2010 |
Jansen C, Parchi P, Capellari S, Vermeij AJ, Corrado P, Baas F, Strammiello R, van Gool WA, van Swieten JC, Rozemuller AJ. Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP. Acta Neuropathologica. 119: 189-97. PMID 19911184 DOI: 10.1007/S00401-009-0609-X |
0.668 |
|
| 2010 |
Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, et al. Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease. Alzheimer Disease and Associated Disorders. 24: 104-7. PMID 19571726 DOI: 10.1097/Wad.0B013E3181Ad378C |
0.602 |
|
| 2009 |
Jansen C, van Swieten JC, Capellari S, Strammiello R, Parchi P, Rozemuller AJ. Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology. Journal of Neurology, Neurosurgery, and Psychiatry. 80: 1386-9. PMID 19917818 DOI: 10.1136/Jnnp.2008.169359 |
0.681 |
|
| 2009 |
Lodi R, Parchi P, Tonon C, Manners D, Capellari S, Strammiello R, Rinaldi R, Testa C, Malucelli E, Mostacci B, Rizzo G, Pierangeli G, Cortelli P, Montagna P, Barbiroli B. Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study. Brain : a Journal of Neurology. 132: 2669-79. PMID 19755520 DOI: 10.1093/Brain/Awp210 |
0.585 |
|
| 2009 |
Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, Langeveld JP, Parchi P, Safar JG, Zou WQ, Gambetti P. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. Brain : a Journal of Neurology. 132: 2643-58. PMID 19734292 DOI: 10.1093/Brain/Awp196 |
0.795 |
|
| 2009 |
Parchi P, Strammiello R, Notari S, Giese A, Langeveld JP, Ladogana A, Zerr I, Roncaroli F, Cras P, Ghetti B, Pocchiari M, Kretzschmar H, Capellari S. Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification. Acta Neuropathologica. 118: 659-71. PMID 19718500 DOI: 10.1007/S00401-009-0585-1 |
0.799 |
|
| 2009 |
Mancuso M, Siciliano G, Capellari S, Orsucci D, Moretti P, Di Fede G, Suardi S, Strammiello R, Parchi P, Tagliavini F, Murri L. Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 30: 417-20. PMID 19597763 DOI: 10.1007/S10072-009-0118-7 |
0.679 |
|
| 2009 |
Baldin E, Capellari S, Provini F, Corrado P, Liguori R, Parchi P, Montagna P, Cortelli P. A case of fatal familial insomnia in Africa. Journal of Neurology. 256: 1778-9. PMID 19526349 DOI: 10.1007/S00415-009-5205-4 |
0.561 |
|
| 2009 |
Manners DN, Parchi P, Tonon C, Capellari S, Strammiello R, Testa C, Tani G, Malucelli E, Spagnolo C, Cortelli P, Montagna P, Lodi R, Barbiroli B. Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob disease. Neurology. 72: 1425-31. PMID 19380702 DOI: 10.1212/Wnl.0B013E3181A18846 |
0.561 |
|
| 2009 |
La Morgia C, Parchi P, Capellari S, Lodi R, Tonon C, Rinaldi R, Mondini S, Cirignotta F. 'Agrypnia excitata' in a case of sporadic Creutzfeldt-Jakob disease VV2. Journal of Neurology, Neurosurgery, and Psychiatry. 80: 244-6. PMID 19151026 DOI: 10.1136/Jnnp.2008.149344 |
0.594 |
|
| 2009 |
Ragno M, Scarcella MG, Cacchiò G, Capellari S, Di Marzio F, Parchi P, Trojano L. Striatal [123I] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease. Acta Neurologica Scandinavica. 119: 131-4. PMID 18638039 DOI: 10.1111/J.1600-0404.2008.01075.X |
0.583 |
|
| 2009 |
Parchi P, Notari S, Weber P, Schimmel H, Budka H, Ferrer I, Haik S, Hauw JJ, Head MW, Ironside JW, Limido L, Rodriguez A, Ströbel T, Tagliavini F, Kretzschmar HA. Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium. Brain Pathology (Zurich, Switzerland). 19: 384-91. PMID 18624793 DOI: 10.1111/J.1750-3639.2008.00187.X |
0.72 |
|
| 2008 |
Kovacs GG, Alafuzoff I, Al-Sarraj S, Arzberger T, Bogdanovic N, Capellari S, Ferrer I, Gelpi E, Kövari V, Kretzschmar H, Nagy Z, Parchi P, Seilhean D, Soininen H, Troakes C, et al. Mixed brain pathologies in dementia: the BrainNet Europe consortium experience. Dementia and Geriatric Cognitive Disorders. 26: 343-50. PMID 18849605 DOI: 10.1159/000161560 |
0.616 |
|
| 2008 |
Rizzo G, Martinelli P, Manners D, Scaglione C, Tonon C, Cortelli P, Malucelli E, Capellari S, Testa C, Parchi P, Montagna P, Barbiroli B, Lodi R. Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease. Brain : a Journal of Neurology. 131: 2690-700. PMID 18819991 DOI: 10.1093/Brain/Awn195 |
0.607 |
|
| 2008 |
Notari S, Strammiello R, Capellari S, Giese A, Cescatti M, Grassi J, Ghetti B, Langeveld JP, Zou WQ, Gambetti P, Kretzschmar HA, Parchi P. Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 283: 30557-65. PMID 18753138 DOI: 10.1074/Jbc.M801877200 |
0.818 |
|
| 2008 |
Ferrer I, Martinez A, Boluda S, Parchi P, Barrachina M. Brain banks: benefits, limitations and cautions concerning the use of post-mortem brain tissue for molecular studies. Cell and Tissue Banking. 9: 181-94. PMID 18543077 DOI: 10.1007/S10561-008-9077-0 |
0.305 |
|
| 2008 |
Alafuzoff I, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Braak H, Bugiani O, Del-Tredici K, Ferrer I, Gelpi E, Giaccone G, Graeber MB, Ince P, Kamphorst W, King A, ... ... Parchi P, et al. Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium. Brain Pathology (Zurich, Switzerland). 18: 484-96. PMID 18371174 DOI: 10.1111/J.1750-3639.2008.00147.X |
0.341 |
|
| 2008 |
Capellari S, Parchi P, Cortelli P, Avoni P, Casadei GP, Bini C, Baruzzi A, Lugaresi E, Pocchiari M, Gambetti P, Montagna P. Sporadic fatal insomnia in a fatal familial insomnia pedigree. Neurology. 70: 884-5. PMID 18332347 DOI: 10.1212/01.Wnl.0000287140.94379.52 |
0.717 |
|
| 2008 |
Cortelli P, Perani D, Montagna P, Gallassi R, Tinuper P, Provini F, Avoni P, Ferrillo F, Anchisi D, Moresco RM, Fazio F, Parchi P, Baruzzi A, Lugaresi E, Gambetti P. Pre-symptomatic diagnosis in fatal familial insomnia: Serial neurophysiological and 18FDG-PET studies (Brain (March 2006) 129: part 3 (668-675) doi: 10.1093/brain/awl003) Brain. 131: 1161. DOI: 10.1093/Brain/Awn067 |
0.491 |
|
| 2007 |
Notari S, Capellari S, Langeveld J, Giese A, Strammiello R, Gambetti P, Kretzschmar HA, Parchi P. A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule. Laboratory Investigation; a Journal of Technical Methods and Pathology. 87: 1103-12. PMID 17893675 DOI: 10.1038/Labinvest.3700676 |
0.795 |
|
| 2007 |
Ferrer I, Armstrong J, Capellari S, Parchi P, Arzberger T, Bell J, Budka H, Ströbel T, Giaccone G, Rossi G, Bogdanovic N, Fakai P, Schmitt A, Riederers P, Al-Sarraj S, et al. Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe study. Brain Pathology (Zurich, Switzerland). 17: 297-303. PMID 17465988 DOI: 10.1111/J.1750-3639.2007.00073.X |
0.531 |
|
| 2007 |
Magherini A, Pentore R, Galassi G, Stucchi CM, Capellari S, Parchi P. MV2 subtype of sporadic Creutzfeldt-Jakob disease presenting as corticobasal syndrome. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 898-9. PMID 17393534 DOI: 10.1002/Mds.21426 |
0.623 |
|
| 2007 |
Ferrer I, Santpere G, Arzberger T, Bell J, Blanco R, Boluda S, Budka H, Carmona M, Giaccone G, Krebs B, Limido L, Parchi P, Puig B, Strammiello R, Ströbel T, et al. Brain protein preservation largely depends on the postmortem storage temperature: implications for study of proteins in human neurologic diseases and management of brain banks: a BrainNet Europe Study. Journal of Neuropathology and Experimental Neurology. 66: 35-46. PMID 17204935 DOI: 10.1097/Nen.0B013E31802C3E7D |
0.342 |
|
| 2006 |
Cali I, Castellani R, Yuan J, Al-Shekhlee A, Cohen ML, Xiao X, Moleres FJ, Parchi P, Zou WQ, Gambetti P. Classification of sporadic Creutzfeldt-Jakob disease revisited. Brain : a Journal of Neurology. 129: 2266-77. PMID 16923954 DOI: 10.1093/Brain/Awl224 |
0.804 |
|
| 2006 |
Alafuzoff I, Pikkarainen M, Al-Sarraj S, Arzberger T, Bell J, Bodi I, Bogdanovic N, Budka H, Bugiani O, Ferrer I, Gelpi E, Giaccone G, Graeber MB, Hauw JJ, Kamphorst W, ... ... Parchi P, et al. Interlaboratory comparison of assessments of Alzheimer disease-related lesions: a study of the BrainNet Europe Consortium. Journal of Neuropathology and Experimental Neurology. 65: 740-57. PMID 16896308 DOI: 10.1097/01.Jnen.0000229986.17548.27 |
0.35 |
|
| 2006 |
Cortelli P, Perani D, Montagna P, Gallassi R, Tinuper P, Provini F, Federica P, Avoni P, Ferrillo F, Anchisi D, Moresco RM, Fazio F, Parchi P, Baruzzi A, Lugaresi E, et al. Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies. Brain : a Journal of Neurology. 129: 668-75. PMID 16399807 DOI: 10.1093/Brain/Awl003 |
0.703 |
|
| 2005 |
Capellari S, Cardone F, Notari S, Schininà ME, Maras B, Sità D, Baruzzi A, Pocchiari M, Parchi P. Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene. Neurology. 64: 905-7. PMID 15753435 DOI: 10.1212/01.Wnl.0000152837.82388.De |
0.811 |
|
| 2004 |
Chrétien F, Le Pavec G, Vallat-Decouvelaere AV, Delisle MB, Uro-Coste E, Ironside JW, Gambetti P, Parchi P, Créminon C, Dormont D, Mikol J, Gray F, Gras G. Expression of excitatory amino acid transporter-1 (EAAT-1) in brain macrophages and microglia of patients with prion diseases. Journal of Neuropathology and Experimental Neurology. 63: 1058-71. PMID 15535133 DOI: 10.1093/Jnen/63.10.1058 |
0.605 |
|
| 2004 |
Castellani RJ, Colucci M, Xie Z, Zou W, Li C, Parchi P, Capellari S, Pastore M, Rahbar MH, Chen SG, Gambetti P. Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease. Neurology. 63: 436-42. PMID 15304573 DOI: 10.1212/01.Wnl.0000135153.96325.3B |
0.825 |
|
| 2004 |
Notari S, Capellari S, Giese A, Westner I, Baruzzi A, Ghetti B, Gambetti P, Kretzschmar HA, Parchi P. Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD. The Journal of Biological Chemistry. 279: 16797-804. PMID 14754888 DOI: 10.1074/Jbc.M313220200 |
0.802 |
|
| 2004 |
Kong Q, Surewicz WK, Petersen RB, Zou W, Chen SG, Gambetti P, Parchi P, Capellari S, Goldfarb L, Montagna P, Lugaresi E, Piccardo P, Ghetti B. 14 Inherited Prion Diseases Cold Spring Harbor Monograph Archive. 41: 673-775. DOI: 10.1101/087969693.41.673 |
0.762 |
|
| 2003 |
Gambetti P, Kong Q, Zou W, Parchi P, Chen SG. Sporadic and familial CJD: classification and characterisation. British Medical Bulletin. 66: 213-39. PMID 14522861 DOI: 10.1093/Bmb/66.1.213 |
0.66 |
|
| 2003 |
Zou WQ, Capellari S, Parchi P, Sy MS, Gambetti P, Chen SG. Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 278: 40429-36. PMID 12917418 DOI: 10.1074/Jbc.M308550200 |
0.725 |
|
| 2003 |
Gambetti P, Parchi P, Chen SG. Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia. Clinics in Laboratory Medicine. 23: 43-64. PMID 12733424 DOI: 10.1016/S0272-2712(02)00065-3 |
0.693 |
|
| 2003 |
Korth C, Kaneko K, Groth D, Heye N, Telling G, Mastrianni J, Parchi P, Gambetti P, Will R, Ironside J, Heinrich C, Tremblay P, DeArmond SJ, Prusiner SB. Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene. Proceedings of the National Academy of Sciences of the United States of America. 100: 4784-9. PMID 12684540 DOI: 10.1073/Pnas.2627989100 |
0.553 |
|
| 2003 |
Schininá ME, Maras B, Cardone F, Mancone C, Principe S, Di Bari MA, Parchi P, Pocchiari M. Prion protein allotype profiling by mass spectrometry Pure and Applied Chemistry. 75: 317-323. DOI: 10.1351/Pac200375020317 |
0.402 |
|
| 2002 |
Capellari S, Parchi P, Wolff BD, Campbell J, Atkinson R, Posey DM, Petersen RB, Gambetti P. Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene. Neurology. 59: 1628-30. PMID 12451210 DOI: 10.1212/01.Wnl.0000035533.86833.28 |
0.751 |
|
| 2002 |
Beaudry P, Parchi P, Peoc'h K, Desbordes P, Dartigues JF, Vital A, Vital C, Capellari S, Gambetti P, Delasnerie-Lauprêtre N, Mary JY, Laplanche JL. A French cluster of Creutzfeldt-Jakob disease: a molecular analysis. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 9: 457-62. PMID 12220376 DOI: 10.1046/J.1468-1331.2002.00456.X |
0.629 |
|
| 2001 |
Gambetti P, Parchi P, Capellari S, Russo C, Tabaton M, Teller JK, Chen SG. Mechanisms of phenotypic heterogeneity in prion, Alzheimer and other conformational diseases. Journal of Alzheimer's Disease : Jad. 3: 87-95. PMID 12214077 DOI: 10.3233/Jad-2001-3113 |
0.831 |
|
| 2001 |
Belay ED, Gambetti P, Schonberger LB, Parchi P, Lyon DR, Capellari S, McQuiston JH, Bradley K, Dowdle G, Crutcher JM, Nichols CR. Creutzfeldt-Jakob disease in unusually young patients who consumed venison. Archives of Neurology. 58: 1673-8. PMID 11594928 DOI: 10.1001/Archneur.58.10.1673 |
0.71 |
|
| 2001 |
Hannah EL, Belay ED, Gambetti P, Krause G, Parchi P, Capellari S, Hoffman RE, Schonberger LB. Creutzfeldt-Jakob disease after receipt of a previously unimplicated brand of dura mater graft. Neurology. 56: 1080-3. PMID 11320182 DOI: 10.1212/Wnl.56.8.1080 |
0.662 |
|
| 2000 |
Chen SG, Zou W, Parchi P, Gambetti P. PrP(Sc) typing by N-terminal sequencing and mass spectrometry. Archives of Virology. Supplementum. 209-16. PMID 11214924 DOI: 10.1007/978-3-7091-6308-5_20 |
0.458 |
|
| 2000 |
Parchi P, Zou W, Wang W, Brown P, Capellari S, Ghetti B, Kopp N, Schulz-Schaeffer WJ, Kretzschmar HA, Head MW, Ironside JW, Gambetti P, Chen SG. Genetic influence on the structural variations of the abnormal prion protein. Proceedings of the National Academy of Sciences of the United States of America. 97: 10168-72. PMID 10963679 DOI: 10.1073/Pnas.97.18.10168 |
0.71 |
|
| 2000 |
Capellari S, Parchi P, Russo CM, Sanford J, Sy MS, Gambetti P, Petersen RB. Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain. The American Journal of Pathology. 157: 613-22. PMID 10934164 DOI: 10.1016/S0002-9440(10)64572-5 |
0.764 |
|
| 2000 |
Parchi P, Capellari S, Gambetti P. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia. Microscopy Research and Technique. 50: 16-25. PMID 10871544 DOI: 10.1002/1097-0029(20000701)50:1<16::Aid-Jemt4>3.0.Co;2-Y |
0.773 |
|
| 2000 |
Parchi P, Brown P, Capellari S, Ghetti B, Gibbs CJ, Gambetti PL. Transmission to non-human primates indicates that kuru as well as the ataxic (VV2) or kuruplaque (MV2) variants of sporadic Creutzfeldt-Jakob disease are caused by the same strain of prions Neurobiology of Aging. 21: 57. DOI: 10.1016/S0197-4580(00)82481-1 |
0.609 |
|
| 2000 |
Chen SG, Parchi P, Gambetti P. 38. Prion diseases including bovine spongiform encephalopathy (mad cow disease) Facts, Research and Intervention in Geriatrics. 2000: 491-502. |
0.365 |
|
| 1999 |
Worrall BB, Herman ST, Capellari S, Lynch T, Chin S, Gambetti P, Parchi P. Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 671-4. PMID 10519879 DOI: 10.1136/Jnnp.67.5.671 |
0.733 |
|
| 1999 |
Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Annals of Neurology. 46: 224-33. PMID 10443888 DOI: 10.1002/1531-8249(199908)46:2<224::Aid-Ana12>3.0.Co;2-W |
0.759 |
|
| 1999 |
Parchi P, Capellari S, Chin S, Schwarz HB, Schecter NP, Butts JD, Hudkins P, Burns DK, Powers JM, Gambetti P. A subtype of sporadic prion disease mimicking fatal familial insomnia. Neurology. 52: 1757-63. PMID 10371520 DOI: 10.1212/Wnl.52.9.1757 |
0.765 |
|
| 1999 |
Hainfellner JA, Parchi P, Kitamoto T, Jarius C, Gambetti P, Budka H. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. Annals of Neurology. 45: 812-6. PMID 10360778 DOI: 10.1002/1531-8249(199906)45:6<812::Aid-Ana20>3.0.Co;2-2 |
0.648 |
|
| 1999 |
Gambetti P, Parchi P. Insomnia in prion diseases: sporadic and familial. The New England Journal of Medicine. 340: 1675-7. PMID 10341282 DOI: 10.1056/Nejm199905273402111 |
0.594 |
|
| 1999 |
Goedert M, Spillantini MG, Crowther RA, Chen SG, Parchi P, Tabaton M, Lanska DJ, Markesbery WR, Wilhelmsen KC, Dickson DW, Petersen RB, Gambetti P. Tau gene mutation in familial progressive subcortical gliosis. Nature Medicine. 5: 454-7. PMID 10202939 DOI: 10.1038/7454 |
0.608 |
|
| 1999 |
Arnold SE, Trojanowski JQ, Parchi P. Protease resistant prion proteins are not present in sporadic "poor outcome" schizophrenia. Journal of Neurology, Neurosurgery, and Psychiatry. 66: 90-2. PMID 9886461 DOI: 10.1136/Jnnp.66.1.90 |
0.33 |
|
| 1999 |
Gambetti P, Petersen RB, Parchi P, Chen SG, Capellari S, Goldfarb L, Gabizon R, Montagna P, Lugaresi E, Piccardo P, Ghetti B. 13 Inherited Prion Diseases Cold Spring Harbor Monograph Archive. 38: 509-583. DOI: 10.1101/087969547.38.509 |
0.76 |
|
| 1999 |
Gold M, Rojiani AM, Parchi P, Gambetti P, Gibbs CJ, Kenney K. SPORADIC CREUTZFELDT-JAKOB DISEASE (sCJD) - A SOUTHWEST FLORIDA EXPERIENCE Journal of Neuropathology and Experimental Neurology. 58: 552. DOI: 10.1097/00005072-199905000-00182 |
0.609 |
|
| 1998 |
Padovani A, D'Alessandro M, Parchi P, Cortelli P, Anzola GP, Montagna P, Vignolo LA, Petraroli R, Pocchiari M, Lugaresi E, Gambetti P. Fatal familial insomnia in a new Italian kindred. Neurology. 51: 1491-4. PMID 9818894 DOI: 10.1212/Wnl.51.5.1491 |
0.693 |
|
| 1998 |
Ghorayeb I, Series C, Parchi P, Sawan B, Guez S, Laplanche JL, Capellari S, Gambetti P, Vital C. Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case. Neurology. 51: 271-4. PMID 9674819 DOI: 10.1212/Wnl.51.1.271 |
0.657 |
|
| 1998 |
Parchi P, Petersen RB, Chen SG, Autilio-Gambetti L, Capellari S, Monari L, Cortelli P, Montagna P, Lugaresi E, Gambetti P. Molecular pathology of fatal familial insomnia. Brain Pathology (Zurich, Switzerland). 8: 539-48. PMID 9669705 DOI: 10.1111/J.1750-3639.1998.Tb00176.X |
0.833 |
|
| 1998 |
Dorandeu A, Wingertsmann L, Chrétien F, Delisle MB, Vital C, Parchi P, Montagna P, Lugaresi E, Ironside JW, Budka H, Gambetti P, Gray F. Neuronal apoptosis in fatal familial insomnia. Brain Pathology (Zurich, Switzerland). 8: 531-7. PMID 9669704 DOI: 10.1111/J.1750-3639.1998.Tb00175.X |
0.648 |
|
| 1998 |
Parchi P, Chen SG, Brown P, Zou W, Capellari S, Budka H, Hainfellner J, Reyes PF, Golden GT, Hauw JJ, Gajdusek DC, Gambetti P. Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease. Proceedings of the National Academy of Sciences of the United States of America. 95: 8322-7. PMID 9653185 DOI: 10.1073/Pnas.95.14.8322 |
0.703 |
|
| 1998 |
Vital C, Gray F, Vital A, Parchi P, Capellari S, Petersen RB, Ferrer X, Jarnier D, Julien J, Gambetti P. Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits. Neuropathology and Applied Neurobiology. 24: 125-30. PMID 9634208 DOI: 10.1046/J.1365-2990.1998.00098.X |
0.68 |
|
| 1998 |
Parchi P, Capellari S, Chin S, Powers JM, Schwarz HB, Burns DK, Gambetti P. FATAL SPORADIC INSOMNIA (THALAMIC FORM OF SPORADIC CREUTZFELDT-JAKOB DISEASE) Journal of Neuropathology and Experimental Neurology. 57: 518. DOI: 10.1097/00005072-199805000-00216 |
0.657 |
|
| 1997 |
Pierangeli G, Parchi P, Barletta G, Chiogna M, Lugaresi E, Cortelli P. Power spectral analysis of heart rate and diastolic blood pressure variability in migraine with and without aura. Cephalalgia : An International Journal of Headache. 17: 756-60; discussion 7. PMID 9399005 DOI: 10.1046/J.1468-2982.1997.1707756.X |
0.465 |
|
| 1997 |
Chen SG, Parchi P, Brown P, Capellari S, Zou W, Cochran EJ, Vnencak-Jones CL, Julien J, Vital C, Mikol J, Lugaresi E, Autilio-Gambetti L, Gambetti P. Allelic origin of the abnormal prion protein isoform in familial prion diseases. Nature Medicine. 3: 1009-15. PMID 9288728 DOI: 10.1038/Nm0997-1009 |
0.825 |
|
| 1997 |
Capellari S, Vital C, Parchi P, Petersen RB, Ferrer X, Jarnier D, Pegoraro E, Gambetti P, Julien J. Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family. Neurology. 49: 133-41. PMID 9222181 DOI: 10.1212/Wnl.49.1.133 |
0.752 |
|
| 1997 |
Cortelli P, Perani D, Parchi P, Grassi F, Montagna P, De Martin M, Castellani R, Tinuper P, Gambetti P, Lugaresi E, Fazio F. Cerebral metabolism in fatal familial insomnia: relation to duration, neuropathology, and distribution of protease-resistant prion protein. Neurology. 49: 126-33. PMID 9222180 DOI: 10.1212/Wnl.49.1.126 |
0.733 |
|
| 1997 |
Castellani RJ, Parchi P, Madoff L, Gambetti P, McKeever P. Biopsy diagnosis of Creutzfeldt-Jakob disease by western blot: a case report. Human Pathology. 28: 623-6. PMID 9158712 DOI: 10.1016/S0046-8177(97)90086-1 |
0.723 |
|
| 1997 |
Parchi P, Capellari S, Chen SG, Petersen RB, Gambetti P, Kopp N, Brown P, Kitamoto T, Tateishi J, Giese A, Kretzschmar H. Typing prion isoforms. Nature. 386: 232-4. PMID 9069279 DOI: 10.1038/386232A0 |
0.558 |
|
| 1997 |
Montagna P, Parchi P, Cortelli P, Tinuper P, Avoni P, Capellari S, Plazzi G, Gallassi R, Cevoli S, Gambetti P, Lugaresi E. 3-12-22 Fatal familial insomnia: Two clinicopathological phenotypes related to a polymorphism at codon 129 of the prion protein gene Journal of the Neurological Sciences. 150: S157-S158. DOI: 10.1016/S0022-510X(97)85620-1 |
0.675 |
|
| 1996 |
Telling GC, Parchi P, DeArmond SJ, Cortelli P, Montagna P, Gabizon R, Mastrianni J, Lugaresi E, Gambetti P, Prusiner SB. Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity. Science (New York, N.Y.). 274: 2079-82. PMID 8953038 DOI: 10.1126/Science.274.5295.2079 |
0.728 |
|
| 1996 |
Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AA, Trojanowski JQ, Petersen RB, Gambetti P. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Annals of Neurology. 39: 767-78. PMID 8651649 DOI: 10.1002/Ana.410390613 |
0.803 |
|
| 1996 |
Sima AA, Defendini R, Keohane C, D'Amato C, Foster NL, Parchi P, Gambetti P, Lynch T, Wilhelmsen KC. The neuropathology of chromosome 17-linked dementia. Annals of Neurology. 39: 734-43. PMID 8651645 DOI: 10.1002/Ana.410390609 |
0.343 |
|
| 1996 |
Castellani R, Parchi P, Stahl J, Capellari S, Cohen M, Gambetti P. Early pathologic and biochemical changes in Creutzfeldt-Jakob disease: study of brain biopsies. Neurology. 46: 1690-3. PMID 8649571 DOI: 10.1212/Wnl.46.6.1690 |
0.756 |
|
| 1996 |
Petersen RB, Parchi P, Richardson SL, Urig CB, Gambetti P. Effect of the D178N mutation and the codon 129 polymorphism on the metabolism of the prion protein. The Journal of Biological Chemistry. 271: 12661-8. PMID 8647879 DOI: 10.1074/Jbc.271.21.12661 |
0.658 |
|
| 1996 |
Chen SG, Parchi P, Brown P, Roos RP, Vnencak-Jones CL, Gambetti P. FATAL FAMILIAL INSOMNIA AND FAMILIAL CREUTZFEDT-JAKOB DISEASE Journal of Neuropathology and Experimental Neurology. 55: 636. DOI: 10.1097/00005072-199605000-00135 |
0.337 |
|
| 1996 |
Parchi P, Capellari S, Sima AA, DʼAmato C, McKeever P, Mikol J, Brion S, Brown P, Chen SG, Petersen RB, Gambetti P. CREUTZFELDT-JAKOB DISEASE (CJD) WITH 178ASN MUTATION IN THE PRION PROTEIN GENE Journal of Neuropathology and Experimental Neurology. 55: 635. DOI: 10.1097/00005072-199605000-00132 |
0.652 |
|
| 1996 |
Parchi P, Petersen RB, Gambetti P. New topics in familial prion diseases Seminars in Virology. 7: 181-187. DOI: 10.1006/Smvy.1996.0023 |
0.674 |
|
| 1995 |
Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features. Brain Pathology (Zurich, Switzerland). 5: 43-51. PMID 7767490 DOI: 10.1111/J.1750-3639.1995.Tb00576.X |
0.73 |
|
| 1995 |
Créange A, Gray F, Cesaro P, Adle-Biassette H, Duvoux C, Cherqui D, Bell J, Parchi P, Gambetti P, Degos JD. Creutzfeldt-Jakob disease after liver transplantation. Annals of Neurology. 38: 269-72. PMID 7654078 DOI: 10.1002/Ana.410380223 |
0.594 |
|
| 1995 |
Chen SG, Teplow DB, Parchi P, Teller JK, Gambetti P, Autilio-Gambetti L. Truncated forms of the human prion protein in normal brain and in prion diseases. The Journal of Biological Chemistry. 270: 19173-80. PMID 7642585 DOI: 10.1074/Jbc.270.32.19173 |
0.588 |
|
| 1995 |
Parchi P, Castellani R, Cortelli P, Montagna P, Chen SG, Petersen RB, Manetto V, Vnencak-Jones CL, McLean MJ, Sheller JR. Regional distribution of protease-resistant prion protein in fatal familial insomnia. Annals of Neurology. 38: 21-9. PMID 7611720 DOI: 10.1002/Ana.410380107 |
0.735 |
|
| 1995 |
Parchi P, Gambetti P. Human prion diseases. Current Opinion in Neurology. 8: 286-93. PMID 7582044 DOI: 10.1097/00019052-199508000-00007 |
0.614 |
|
| 1995 |
Créange A, Gray F, Cesaro P, Bell J, Parchi P, Gambetti P, Degos J-. CREUTZFELDT-JAKOB DISEASE AFTER LIVER TRANSPLANT Journal of Neuropathology and Experimental Neurology. 54: 449. DOI: 10.1097/00005072-199505000-00168 |
0.521 |
|
| 1995 |
Castellani R, Parchi P, Stahl J, Cohen M, Gambetti P. BIOPSY DIAGNOSIS OF CREUTZFELDT-JAKOB DISEASE BY IMMUNOBLOT ANALYSIS Journal of Neuropathology and Experimental Neurology. 54: 448. DOI: 10.1097/00005072-199505000-00164 |
0.686 |
|
| 1995 |
Parchi P, Castellani R, Capellari S, Petersen RB, Chen SG, Younq K, Farlow M, Troianowski JQ, Sima A, Ghetti B, Gambetti P. PROTEASE-RESISTANT PRION PROTEIN IN SPORADIC CREUTZFELDT-JAKOB DISEASE (CJD) Journal of Neuropathology and Experimental Neurology. 54: 416. DOI: 10.1097/00005072-199505000-00035 |
0.732 |
|
| 1994 |
Montagna P, Cortelli P, Monari L, Pierangeli G, Parchi P, Lodi R, Iotti S, Frassineti C, Zaniol P, Lugaresi E. 31P-magnetic resonance spectroscopy in migraine without aura. Neurology. 44: 666-9. PMID 8164822 DOI: 10.1212/Wnl.44.4.666 |
0.664 |
|
| 1994 |
Cortelli P, Parchi P, Sforza E, Contin M, Pierangeli G, Barletta G, Lugaresi E. Cardiovascular autonomic dysfunction in normotensive awake subjects with obstructive sleep apnoea syndrome. Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society. 4: 57-62. PMID 8054838 DOI: 10.1007/Bf01828839 |
0.469 |
|
| 1994 |
Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Proceedings of the National Academy of Sciences of the United States of America. 91: 2839-42. PMID 7908444 DOI: 10.1073/Pnas.91.7.2839 |
0.74 |
|
| 1994 |
Sforza E, Parchi P, Contin M, Cortelli P, Lugaresi E. Do autonomic cardiovascular reflexes predict the nocturnal rise in blood pressure in obstructive sleep apnea syndrome? Blood Pressure. 3: 295-302. PMID 7866593 DOI: 10.3109/08037059409102277 |
0.461 |
|
| 1993 |
Parchi P, Cortelli P, Pierangeli G, Contin M, Barletta G, Lugaresi E. Atropine test in patients with Autonomic Failure (AF) Journal of the Autonomic Nervous System. 43: 99-100. DOI: 10.1016/0165-1838(93)90271-U |
0.436 |
|
| 1992 |
Cortelli P, Parchi P, Contin M, Sforza E, Lugaresi A, Pasquali R, Lugaresi E. Isolated failure of noradrenergic transmission in a case with orthostatic hypotension and hyperactivity of gastro-colic reflex. Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society. 2: 177-82. PMID 1323364 DOI: 10.1007/Bf01818959 |
0.487 |
|
| 1991 |
Cortelli P, Parchi P, Contin M, Pierangeli G, Avoni P, Tinuper P, Montagna P, Baruzzi A, Gambetti PL, Lugaresi E. Cardiovascular dysautonomia in fatal familial insomnia. Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society. 1: 15-21. PMID 1821660 DOI: 10.1007/Bf01826053 |
0.501 |
|
| 1991 |
Cortelli P, Pierangeli G, Parchi P, Contin M, Baruzzi A, Lugaresi E. Autonomic nervous system function in migraine without aura. Headache. 31: 457-62. PMID 1774161 DOI: 10.1111/J.1526-4610.1991.Hed3107457.X |
0.473 |
|
| 1991 |
Pierangeli G, Barletta G, Parchi P, Chiogna M, Gambera M, Cortelli P, Lugaresi E. Heart-Rate Variability in Migraine without Aura: A Preliminary Study. Cephalalgia. 11: 181-182. DOI: 10.1177/0333102491011S1198 |
0.441 |
|
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