Gianfranco Puoti - Publications

University of Naples, Napoli, Campania, Italy 

40 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Cracco L, Puoti G, Cornacchia A, Glisic K, Lee SK, Wang Z, Cohen ML, Appleby BS, Cali I. Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype. Acta Neuropathologica Communications. 11: 141. PMID 37653534 DOI: 10.1186/s40478-023-01631-9  0.619
2021 Brennecke N, Cali I, Mok TH, Speedy H, Genomics England Research Consortium, Hosszu LLP, Stehmann C, Cracco L, Puoti G, Prior TW, Cohen ML, Collins SJ, Mead S, Appleby BS. Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion. Viruses. 13. PMID 34578375 DOI: 10.3390/v13091794  0.708
2020 Cali I, Cracco L, Saracino D, Occhipinti R, Coppola C, Appleby BS, Puoti G. Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a Seven-Octapeptide Repeat Insertion. Frontiers in Cellular Neuroscience. 14: 150. PMID 32733203 DOI: 10.3389/Fncel.2020.00150  0.725
2020 Nemani SK, Xiao X, Cali I, Cracco L, Puoti G, Nigro M, Lavrich J, Bharara Singh A, Appleby BS, Sim VL, Notari S, Surewicz WK, Gambetti P. A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease. Acta Neuropathologica Communications. 8: 85. PMID 32560672 DOI: 10.1186/S40478-020-00966-X  0.768
2020 Rossi F, Bruno G, Fratta M, Colavito D, Casertano S, Sampaolo S, Oliva M, Puoti G. Expanding the spectrum of SPTLC1-related disorders beyond hereditary sensory and autonomic neuropathies: a novel case of the distinct "S331 syndrome". Journal of the Peripheral Nervous System : Jpns. PMID 32470188 DOI: 10.1111/Jns.12394  0.355
2020 Bruno G, Puoti G, Oliva M, Colavito D, Allegorico L, Napolitano F, Sampaolo S. A novel missense mutation in CAV3 gene in an Italian family with persistent hyperCKemia, myalgia and hypercholesterolemia: Double-trouble. Clinical Neurology and Neurosurgery. 191: 105687. PMID 32004987 DOI: 10.1016/J.Clineuro.2020.105687  0.364
2020 Cali I, Puoti G, Smucny J, Curtiss PM, Cracco L, Kitamoto T, Occhipinti R, Cohen ML, Appleby BS, Gambetti P. Co-existence of PrP types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics. Scientific Reports. 10: 1503. PMID 32001774 DOI: 10.1038/S41598-020-58446-0  0.731
2019 Vola E, Russo C, Macera A, Del Vecchio W, Puoti G, Caranci F, Elefante A. Unusual CLIPPERS presentation and role of MRI examination in the proper diagnostic assessment: A case report. European Journal of Radiology Open. 6: 212-214. PMID 31198819 DOI: 10.1016/J.Ejro.2019.05.005  0.342
2019 Saracino D, D'Armiento FP, Conforti R, Napolitano M, Elefante A, Sampaolo S, Puoti G. Dramatic neurological debut in a case of Köhlmeier-Degos disease. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 31183675 DOI: 10.1007/S10072-019-03952-X  0.465
2019 Oliva M, Capaldo G, D'Amico A, Colavito D, Elefante A, Straccia G, Ugga L, Puoti G. A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 30607525 DOI: 10.1007/S10072-018-3684-8  0.313
2016 Coppola C, Saracino D, Puoti G, Lus G, Dato C, Le Ber I, Pariente J, Caroppo P, Piccoli E, Tagliavini F, Di Iorio G, Rossi G. A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations. Neurobiology of Aging. PMID 27814992 DOI: 10.1016/J.Neurobiolaging.2016.10.008  0.41
2016 Bonda DJ, Manjila S, Mehndiratta P, Khan F, Miller BR, Onwuzulike K, Puoti G, Cohen ML, Schonberger LB, Cali I. Human prion diseases: surgical lessons learned from iatrogenic prion transmission. Neurosurgical Focus. 41: E10. PMID 27364252 DOI: 10.3171/2016.5.Focus15126  0.723
2015 Imbriani P, Marfia GA, Marciani MG, Poleggi A, Pocchiari M, Puoti G, Caltagirone C, Pisani A. Heidenhain variant in two patients with inherited V210I Creutzfeldt-Jakob disease. The International Journal of Neuroscience. PMID 26268049 DOI: 10.3109/00207454.2015.1047017  0.477
2015 Del Pilar-Morales EA, Cali I, Chapas J, Bertrán-Pasarell J, Puoti G, Gambetti P, Nobo U. Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient. Puerto Rico Health Sciences Journal. 34: 40-3. PMID 25856877  0.733
2015 Xiao X, Cali I, Yuan J, Cracco L, Curtiss P, Zeng L, Abouelsaad M, Gazgalis D, Wang GX, Kong Q, Fujioka H, Puoti G, Zou WQ. Synthetic Aβ peptides acquire prion-like properties in the brain. Oncotarget. 6: 642-50. PMID 25460507 DOI: 10.18632/Oncotarget.2819  0.54
2015 Ghoshal N, Perry A, McKeel D, Schmidt RE, Carter D, Norton J, Zou WQ, Xiao X, Puoti G, Notari S, Gambetti P, Morris JC, Cairns NJ. Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old. Alzheimer Disease and Associated Disorders. 29: 173-6. PMID 24845762 DOI: 10.1097/Wad.0000000000000049  0.66
2014 Puoti G, Lerza MC, Ferretti MG, Bugiani O, Tagliavini F, Rossi G. A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms. Journal of Alzheimer's Disease : Jad. 42: 939-47. PMID 25024321 DOI: 10.3233/Jad-140717  0.387
2014 Strianese D, Napoli M, Russo C, D'Errico A, Scotti N, Puoti G, Bonavolontà G, Tranfa F, Briganti F. Coexistence of cavernous hemangioma and other vascular malformations of the orbit. A report of three cases. The Neuroradiology Journal. 27: 223-31. PMID 24750713 DOI: 10.15274/Nrj-2014-10016  0.472
2013 Puoti G, Elefante A, Saracino D, Capasso A, Cotrufo R, Anello CB. New-onset refractory status epilepticus mimicking herpes virus encephalitis. Case Reports in Neurology. 5: 162-7. PMID 24163672 DOI: 10.1159/000355273  0.358
2013 Xiao X, Cali I, Dong Z, Puoti G, Yuan J, Qing L, Wang H, Kong Q, Gambetti P, Zou WQ. Protease-sensitive prions with 144-bp insertion mutations. Aging. 5: 155-73. PMID 23515139  0.741
2012 Elefante A, Puoti G, Senese R, Coppola C, Russo C, Tortora F, de Divitiis O, Brunetti A. Non-alcoholic acute Wernicke's encephalopathy: role of MRI in non typical cases. European Journal of Radiology. 81: 4099-104. PMID 22954409 DOI: 10.1016/J.Ejrad.2012.08.006  0.48
2012 Hamlin C, Puoti G, Berri S, Sting E, Harris C, Cohen M, Spear C, Bizzi A, Debanne SM, Rowland DY. A comparison of tau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob disease. Neurology. 79: 547-52. PMID 22843257 DOI: 10.1212/Wnl.0B013E318263565F  0.694
2012 Puoti G, Bizzi A, Forloni G, Safar JG, Tagliavini F, Gambetti P. Sporadic human prion diseases: molecular insights and diagnosis. The Lancet. Neurology. 11: 618-28. PMID 22710755 DOI: 10.1016/S1474-4422(12)70063-7  0.734
2011 Gambetti P, Puoti G, Zou WQ. Variably protease-sensitive prionopathy: a novel disease of the prion protein. Journal of Molecular Neuroscience : Mn. 45: 422-4. PMID 21584652 DOI: 10.1007/S12031-011-9543-1  0.658
2011 Gambetti P, Puoti G, Kong Q, Zou W. A New Prion Disease: Protease-Sensitive Prionopathy Neurodegeneration: the Molecular Pathology of Dementia and Movement Disorders: Second Edition. 350-353. DOI: 10.1002/9781444341256.ch35  0.366
2010 Bugiani O, Giaccone G, Rossi G, Mangieri M, Capobianco R, Morbin M, Mazzoleni G, Cupidi C, Marcon G, Giovagnoli A, Bizzi A, Di Fede G, Puoti G, Carella F, Salmaggi A, et al. Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP. Archives of Neurology. 67: 987-95. PMID 20697050 DOI: 10.1001/Archneurol.2010.178  0.616
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, 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  0.724
2010 Ghoshal N, Cairns NJ, Puoti G, Gambetti P, Morris JC. P1-050: Protease-sensitive prionopathy in a cognitively normal 93-year-old Alzheimer's & Dementia. 6: S188-S188. DOI: 10.1016/J.Jalz.2010.05.597  0.501
2008 Mauro C, Giaccone G, Piscosquito G, Lavorgna A, Nigro M, Di Fede G, Leonardi A, Coppola C, Formisano S, Tagliavini F, Cotrufo R, Puoti G. A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings. Journal of Neurology, Neurosurgery, and Psychiatry. 79: 1395-8. PMID 19010951 DOI: 10.1136/Jnnp.2007.142976  0.466
2007 Di Fede G, Giaccone G, Limido L, Mangieri M, Suardi S, Puoti G, Morbin M, Mazzoleni G, Ghetti B, Tagliavini F. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease. Journal of Neuropathology and Experimental Neurology. 66: 124-30. PMID 17278997 DOI: 10.1097/Nen.0B013E3180302060  0.477
2005 Puoti G, Giaccone G, Mangieri M, Limido L, Fociani P, Zerbi P, Suardi S, Rossi G, Iussich S, Capobianco R, Di Fede G, Marcon G, Cotrufo R, Filippini G, Bugiani O, et al. Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc. Journal of Neuropathology and Experimental Neurology. 64: 902-9. PMID 16215462 DOI: 10.1097/01.Jnen.0000183346.19447.55  0.465
2004 Puoti G, Limido L, Cotrufo R, Di Fede G, Tagliavini F. Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques. Neurology. 62: 1239; author reply 1. PMID 15079047  0.411
2004 Puoti G, Fede GD, Cotrufo R, Tucci C, Capuano G, Giaccone G, Tagliavini F. P3-382 Insertional mutation in the prion protein gene presenting with Schizophrenia Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81531-8  0.324
2003 Pietrini V, Puoti G, Limido L, Rossi G, Di Fede G, Giaccone G, Mangieri M, Tedeschi F, Bondavalli A, Mancia D, Bugiani O, Tagliavini F. Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene. Neurology. 61: 1288-91. PMID 14610142  0.423
2000 Puoti G, Rossi G, Giaccone G, Awan T, Lievens PM, Defanti CA, Tagliavini F, Bugiani O. Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation. Annals of Neurology. 48: 269-70. PMID 10939584 DOI: 10.1002/1531-8249(200008)48:2<269::Aid-Ana24>3.0.Co;2-V  0.439
2000 Rossi G, Giaccone G, Giampaolo L, Iussich S, Puoti G, Frigo M, Cavaletti G, Frattola L, Bugiani O, Tagliavini F. Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene. Neurology. 55: 405-10. PMID 10932276  0.431
2000 Giaccone G, Canciani B, Puoti G, Rossi G, Goffredo D, Iussich S, Fociani P, Tagliavini F, Bugiani O. Creutzfeldt-Jakob disease: Carnoy's fixative improves the immunohistochemistry of the proteinase K-resistant prion protein. Brain Pathology (Zurich, Switzerland). 10: 31-7. PMID 10668893 DOI: 10.1111/J.1750-3639.2000.Tb00240.X  0.348
2000 Giaccone G, Iussich S, Puoti G, Rossi G, Goffredo D, Tagliavini F, Bugiani O. Topographic distribution of PRPRES in Creutzfeldt-Jakob disease as revealed by immunohistochemistry Neurobiology of Aging. 21: 54. DOI: 10.1016/S0197-4580(00)82919-X  0.415
2000 Puoti G, Giaccone G, Rossi G, Canciani B, Bugiani O, Tagliavini F. Sporadic creutzfeldt-Jakob disease coexistence of biochemically distinct types of PRPSC in the same brain Neurobiology of Aging. 21: 149. DOI: 10.1016/S0197-4580(00)82473-2  0.429
1999 Puoti G, Giaccone G, Rossi G, Canciani B, Bugiani O, Tagliavini F. Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain. Neurology. 53: 2173-6. PMID 10599800  0.371
Show low-probability matches.