| Year |
Citation |
Score |
| 2024 |
Giannini G, Minardi R, Barletta G, Cani I, Cecere A, Baldelli L, Fiorentino A, Guaraldi P, Sambati L, Capellari S, Cortelli P, Carelli V, Calandra-Buonaura G. The Degree of Cardiovascular Autonomic Dysfunction is not Different in GBA-Related and Idiopathic Parkinson's Disease Patients: A Case-Control Instrumental Evaluation. Journal of Parkinson's Disease. PMID 38306061 DOI: 10.3233/JPD-230334 |
0.323 |
|
| 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 |
0.505 |
|
| 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 |
0.525 |
|
| 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 |
0.47 |
|
| 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 |
0.531 |
|
| 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 |
0.535 |
|
| 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 |
0.497 |
|
| 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 |
0.605 |
|
| 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 |
0.531 |
|
| 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 |
0.602 |
|
| 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 |
0.558 |
|
| 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 |
0.545 |
|
| 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 |
0.473 |
|
| 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, ... Capellari S, 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 |
0.583 |
|
| 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, ... ... Capellari S, 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 |
0.59 |
|
| 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 |
0.501 |
|
| 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 |
0.488 |
|
| 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 |
0.697 |
|
| 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, et al. Blood β-Synuclein and Neurofilament Light Chain During the Course of Prion Disease. Neurology. PMID 35110380 DOI: 10.1212/WNL.0000000000200002 |
0.567 |
|
| 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 |
0.518 |
|
| 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 |
0.622 |
|
| 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 |
0.479 |
|
| 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, ... ... Capellari S, 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 |
0.78 |
|
| 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 |
0.53 |
|
| 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 |
0.463 |
|
| 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 |
0.459 |
|
| 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 |
0.499 |
|
| 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, ... Capellari S, 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 |
0.462 |
|
| 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 |
0.519 |
|
| 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, ... ... Capellari S, 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 |
0.687 |
|
| 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 |
0.572 |
|
| 2020 |
Romagnoli M, Stanzani Maserati M, De Matteis M, Capellari S, Carbonelli M, Amore G, Cantalupo G, Zenesini C, Liguori R, Sadun AA, Carelli V, Park JC, La Morgia C. Chromatic Pupillometry Findings in Alzheimer's Disease. Frontiers in Neuroscience. 14: 780. PMID 32848556 DOI: 10.3389/Fnins.2020.00780 |
0.309 |
|
| 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 |
0.482 |
|
| 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, ... Capellari S, 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 |
0.583 |
|
| 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, 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 |
0.532 |
|
| 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 |
0.589 |
|
| 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 |
0.583 |
|
| 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 |
0.613 |
|
| 2020 |
Calandra-Buonaura G, Sambati L, Baschieri F, Vitiello M, Contin M, Tonon C, Capellari S, Provini F, Cortelli P. The Bologna motor and non-motor prospective study on parkinsonism at onset (BoProPark): study design and population. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 32219591 DOI: 10.1007/S10072-020-04305-9 |
0.319 |
|
| 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 |
0.589 |
|
| 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 |
0.586 |
|
| 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 |
0.537 |
|
| 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 |
0.607 |
|
| 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 |
0.627 |
|
| 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 |
0.6 |
|
| 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 |
0.606 |
|
| 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 |
0.68 |
|
| 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 |
0.553 |
|
| 2019 |
Stanzani Maserati M, Mitolo M, Medici F, D'Onofrio R, Oppi F, Poda R, De Matteis M, Tonon C, Lodi R, Liguori R, Capellari S. Color Choice Preference in Cognitively Impaired Patients: A Look Inside Alzheimer's Disease Through the Use of Lüscher Color Diagnostic. Frontiers in Psychology. 10: 1951. PMID 31507498 DOI: 10.3389/Fpsyg.2019.01951 |
0.302 |
|
| 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 |
0.521 |
|
| 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 |
0.602 |
|
| 2019 |
Giorgio E, Lorenzati M, Rivetti di Val Cervo P, Brussino A, Cernigoj M, Della Sala E, Bartoletti Stella A, Ferrero M, Caiazzo M, Capellari S, Cortelli P, Conti L, Cattaneo E, Buffo A, Brusco A. Allele-specific silencing as treatment for gene duplication disorders: proof-of-principle in autosomal dominant leukodystrophy. Brain : a Journal of Neurology. PMID 31143934 DOI: 10.1093/Brain/Awz139 |
0.349 |
|
| 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 |
0.586 |
|
| 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 |
0.536 |
|
| 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 |
0.599 |
|
| 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 |
0.594 |
|
| 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 |
0.561 |
|
| 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 |
0.501 |
|
| 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 |
0.578 |
|
| 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 |
0.669 |
|
| 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 |
0.599 |
|
| 2018 |
Contin M, Lopane G, Mohamed S, Calandra-Buonaura G, Capellari S, De Massis P, Nassetti S, Perrone A, Riva R, Sambati L, Scaglione C, Cortelli P. Clinical pharmacokinetics of pramipexole, ropinirole and rotigotine in patients with Parkinson's disease. Parkinsonism & Related Disorders. PMID 30446407 DOI: 10.1016/J.Parkreldis.2018.11.007 |
0.309 |
|
| 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 |
0.631 |
|
| 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 |
0.551 |
|
| 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, et al. Sporadic Fatal Insomnia in Europe: Phenotypic features and diagnostic challenges. Annals of Neurology. PMID 30048013 DOI: 10.1002/Ana.25300 |
0.544 |
|
| 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 |
0.613 |
|
| 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 |
0.596 |
|
| 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 |
0.581 |
|
| 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, ... ... Capellari S, 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 |
0.629 |
|
| 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 |
0.633 |
|
| 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 |
0.612 |
|
| 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 |
0.531 |
|
| 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 |
0.506 |
|
| 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 |
0.537 |
|
| 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 |
0.638 |
|
| 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 |
0.639 |
|
| 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 |
0.389 |
|
| 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 |
0.582 |
|
| 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 |
0.586 |
|
| 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 |
0.576 |
|
| 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 |
0.516 |
|
| 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 |
0.612 |
|
| 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 |
0.571 |
|
| 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 |
0.608 |
|
| 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 |
0.614 |
|
| 2016 |
Terlizzi R, Calandra-Buonaura G, Zanigni S, Barletta G, Capellari S, Guaraldi P, Donadio V, Cason E, Contin M, Poda R, Tonon C, Sambati L, Gallassi R, Liguori R, Lodi R, et al. A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings. Autonomic Neuroscience : Basic & Clinical. PMID 26896090 DOI: 10.1016/J.Autneu.2016.02.005 |
0.302 |
|
| 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, ... ... Capellari S, et al. Quantifying prion disease penetrance using large population control cohorts. Science Translational Medicine. 8: 322ra9. PMID 26791950 DOI: 10.1126/Scitranslmed.Aad5169 |
0.731 |
|
| 2016 |
Donadio V, Incensi A, Capellari S, Rizzo G, Pantieri R, Stanzani Maserati M, Devigili G, Eleopra R, Montini F, Baruzzi A, Liguori R. 45. Skin nerve α-synuclein deposits as possible new biomarker for Dementia with Lewy bodies Clinical Neurophysiology. 127: e334. DOI: 10.1016/J.Clinph.2016.10.057 |
0.317 |
|
| 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 |
0.625 |
|
| 2015 |
Calandra-Buonaura G, Doria A, Lopane G, Guaraldi P, Capellari S, Martinelli P, Cortelli P, Contin M. Pharmacodynamics of a low subacute levodopa dose helps distinguish between multiple system atrophy with predominant Parkinsonism and Parkinson's disease. Journal of Neurology. PMID 26566913 DOI: 10.1007/S00415-015-7961-7 |
0.307 |
|
| 2015 |
Bartoletti-Stella A, Chiaro G, Calandra-Buonaura G, Contin M, Scaglione C, Barletta G, Cecere A, Garagnani P, Tieri P, Ferrarini A, Piras S, Franceschi C, Delledonne M, Cortelli P, Capellari S. A patient with PMP22-related hereditary neuropathy and DBH-gene-related dysautonomia. Journal of Neurology. 262: 2373-81. PMID 26410747 DOI: 10.1007/S00415-015-7896-Z |
0.387 |
|
| 2015 |
Giannoccaro MP, Donadio V, Incensi A, Pizza F, Cason E, Di Stasi V, Martinelli P, Scaglione C, Capellari S, Treglia G, Liguori R. Skin biopsy and I-123 MIBG scintigraphy findings in idiopathic Parkinson's disease and parkinsonism: A comparative study. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 986-9. PMID 25778097 DOI: 10.1002/Mds.26189 |
0.306 |
|
| 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 |
0.54 |
|
| 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 |
0.787 |
|
| 2014 |
Antelmi E, Rizzo G, Fabbri M, Capellari S, Scaglione C, Martinelli P. Arylsulphatase A activity in familial parkinsonism: a pathogenetic role? Journal of Neurology. 261: 1803-9. PMID 24989669 DOI: 10.1007/S00415-014-7425-5 |
0.359 |
|
| 2014 |
Ferrera D, Canale C, Marotta R, Mazzaro N, Gritti M, Mazzanti M, Capellari S, Cortelli P, Gasparini L. Lamin B1 overexpression increases nuclear rigidity in autosomal dominant leukodystrophy fibroblasts. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 28: 3906-18. PMID 24858279 DOI: 10.1096/Fj.13-247635 |
0.306 |
|
| 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 |
0.7 |
|
| 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 |
0.633 |
|
| 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 |
0.754 |
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| 2013 |
Giorgio E, Rolyan H, Kropp L, Chakka AB, Yatsenko S, Di Gregorio E, Lacerenza D, Vaula G, Talarico F, Mandich P, Toro C, Pierre EE, Labauge P, Capellari S, Cortelli P, et al. Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expression. Human Mutation. 34: 1160-71. PMID 23649844 DOI: 10.1002/Humu.22348 |
0.37 |
|
| 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 |
0.591 |
|
| 2013 |
Sambati L, Agati R, Bacci A, Bianchi S, Capellari S. Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 34: 1235-8. PMID 22729508 DOI: 10.1007/S10072-012-1129-3 |
0.422 |
|
| 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 |
0.633 |
|
| 2012 |
Cortelli P, Terlizzi R, Capellari S, Benarroch E. Nuclear lamins: functions and clinical implications. Neurology. 79: 1726-31. PMID 23071165 DOI: 10.1212/Wnl.0B013E31826Ea887 |
0.319 |
|
| 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 |
0.518 |
|
| 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 |
0.659 |
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| 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 |
0.651 |
|
| 2011 |
Marconi S, Rizzo G, Capellari S, Scaglione C, Cortelli P, Martinelli P, Bonazza S. Eating disorder as a psychiatric onset of juvenile Huntington's disease. The American Journal of Psychiatry. 168: 1120-1. PMID 21969052 DOI: 10.1176/Appi.Ajp.2011.11020312 |
0.325 |
|
| 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 |
0.679 |
|
| 2011 |
Bonazza S, La Morgia C, Martinelli P, Capellari S. Strio-pallido-dentate calcinosis: a diagnostic approach in adult patients. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 32: 537-45. PMID 21479613 DOI: 10.1007/S10072-011-0514-7 |
0.35 |
|
| 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 |
0.688 |
|
| 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 |
0.528 |
|
| 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 |
0.433 |
|
| 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 |
0.808 |
|
| 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 |
0.622 |
|
| 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, ... ... Capellari S, 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 |
0.828 |
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| 2010 |
Fusco D, Vargiolu M, Vidone M, Mariani E, Pennisi LF, Bonora E, Capellari S, Dirnberger D, Baumeister R, Martinelli P, Romeo G. The RET51/FKBP52 complex and its involvement in Parkinson disease. Human Molecular Genetics. 19: 2804-16. PMID 20442138 DOI: 10.1093/Hmg/Ddq181 |
0.3 |
|
| 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 |
0.657 |
|
| 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 |
0.584 |
|
| 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 |
0.668 |
|
| 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 |
0.559 |
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| 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 |
0.79 |
|
| 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 |
0.67 |
|
| 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 |
0.534 |
|
| 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 |
0.533 |
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| 2009 |
Rizzo G, Marconi S, Capellari S, Scaglione C, Martinelli P. Benign tremulous parkinsonism in a patient with dardarin mutation. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1399-401. PMID 19373934 DOI: 10.1002/Mds.22544 |
0.351 |
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| 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 |
0.568 |
|
| 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 |
0.564 |
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| 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 |
0.595 |
|
| 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 |
0.587 |
|
| 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 |
0.809 |
|
| 2008 |
RodrÃguez-MartÃnez AB, Alfonso-Sánchez MA, Peña JA, Sánchez-Valle R, Zerr I, Capellari S, Calero M, Zarranz JJ, de Pancorbo MM. Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation. Neurogenetics. 9: 109-18. PMID 18347820 DOI: 10.1007/S10048-008-0120-X |
0.325 |
|
| 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 |
0.709 |
|
| 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 |
0.785 |
|
| 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 |
0.5 |
|
| 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 |
0.603 |
|
| 2005 |
Zaidi SI, Richardson SL, Capellari S, Song L, Smith MA, Ghetti B, Sy MS, Gambetti P, Petersen RB. Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding. Journal of Alzheimer's Disease : Jad. 7: 159-71; discussion 1. PMID 15851854 DOI: 10.3233/Jad-2005-7209 |
0.619 |
|
| 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 |
0.807 |
|
| 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 |
0.819 |
|
| 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 |
0.793 |
|
| 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 |
0.751 |
|
| 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 |
0.709 |
|
| 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 |
0.745 |
|
| 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 |
0.609 |
|
| 2002 |
Taratuto AL, Piccardo P, Reich EG, Chen SG, Sevlever G, Schultz M, Luzzi AA, Rugiero M, Abecasis G, Endelman M, Garcia AM, Capellari S, Xie Z, Lugaresi E, Gambetti P, et al. Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease. Neurology. 58: 362-7. PMID 11839833 DOI: 10.1212/Wnl.58.3.362 |
0.719 |
|
| 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 |
0.824 |
|
| 2001 |
Mastrianni JA, Capellari S, Telling GC, Han D, Bosque P, Prusiner SB, DeArmond SJ. Inherited prion disease caused by the V210I mutation: transmission to transgenic mice. Neurology. 57: 2198-205. PMID 11756597 DOI: 10.1212/Wnl.57.12.2198 |
0.472 |
|
| 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 |
0.697 |
|
| 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 |
0.645 |
|
| 2000 |
Capellari S, Zaidi SI, Long AC, Kwon EE, Petersen RB. The Thr183Ala Mutation, Not the Loss of the First Glycosylation Site, Alters the Physical Properties of the Prion Protein. Journal of Alzheimer's Disease : Jad. 2: 27-35. PMID 12214108 DOI: 10.3233/Jad-2000-2104 |
0.383 |
|
| 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 |
0.695 |
|
| 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 |
0.753 |
|
| 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 |
0.763 |
|
| 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 |
0.585 |
|
| 1999 |
Capellari S, Zaidi SI, Urig CB, Perry G, Smith MA, Petersen RB. Prion protein glycosylation is sensitive to redox change. The Journal of Biological Chemistry. 274: 34846-50. PMID 10574957 DOI: 10.1074/Jbc.274.49.34846 |
0.401 |
|
| 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 |
0.721 |
|
| 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 |
0.751 |
|
| 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 |
0.756 |
|
| 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 |
0.749 |
|
| 1999 |
Tarauto A, Piccardo P, Reich F, Sevlever G, Schultz M, Leuzzi A, Ruggiero M, Abecassis G, Engelmann M, Garcia AM, Capellari S, Lugaresi E, Gambetti P, Dlouhy SR, Ghetti B. INSOMNIA IN FAMILIAL CREUTZFELDT JAKOB DISEASE (FCJD), E200K, WITH THALAMIC INVOLVEMENT Journal of Neuropathology and Experimental Neurology. 58: 551. DOI: 10.1097/00005072-199905000-00179 |
0.398 |
|
| 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 |
0.638 |
|
| 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 |
0.828 |
|
| 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 |
0.686 |
|
| 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 |
0.665 |
|
| 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 |
0.637 |
|
| 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 |
0.826 |
|
| 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 |
0.742 |
|
| 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 |
0.531 |
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| 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 |
0.664 |
|
| 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 |
0.795 |
|
| 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 |
0.74 |
|
| 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 |
0.639 |
|
| 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 |
0.717 |
|
| 1994 |
Tinuper P, Plazzi G, Monari L, Sangiorgi S, Pellissier JF, Cerullo A, Provini F, Capellari S, Baruzzi A, Lugaresi E. Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsy. Epilepsia. 35: 332-5. PMID 7908874 DOI: 10.1111/J.1528-1157.1994.Tb02440.X |
0.698 |
|
| 1992 |
Plazzi G, Tinuper P, Monari L, Capellari S, Sangiorgi S, Montagna P, Provini F, Cerullo A, Pellissier JF, Baruzzi A, Lugaresi E. Arylsulphatase A (ASA) pseudodeficiency (PD) and Lafora bodies (LB) in a patient with non progressive myoclonic epilepsy | EPILESSIA MIOCLONICA NON PROGRESSIVA CON CORPI DI LAFORA E PSEUDODEFICIENZA DI ARILSULFATASI A Bollettino - Lega Italiana Contro L'Epilessia. 195-196. |
0.638 |
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