Gianfranco Puoti - Publications

University of Naples, Napoli, Campania, Italy 

38 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
2020 Dato C, Elefante A, Coppola C, Melone MAB, Lus G, Costagliola A, Bruno G, Puoti G. "Borderline" idiopathic CD4 T-cell lymphocytopenia presenting with atypical progressive multifocal leukoencephalopathy. Journal of Neuroimmunology. 349: 577420. PMID 33032014 DOI: 10.1016/j.jneuroim.2020.577420  0.4
2020 Negro A, Paolucci A, Russo C, Di Stasi M, Guerriero P, Arrigoni F, Bruno F, Pagnini F, Angileri SA, Palumbo P, Masciocchi C, Puoti G, Tortora F, Caranci F. Predictive factors of volumetric reduction in lumbar disc herniation treated by O2-O3 chemiodiscolysis. Acta Bio-Medica : Atenei Parmensis. 91: 89-97. PMID 32945283 DOI: 10.23750/abm.v91i8-S.9975  0.4
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  0.72
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  0.72
2020 Bruno G, Miele G, Abbadessa G, Di Pietro A, Russo C, Negro A, Bonavita S, Puoti G. Atypical progressive multifocal leukoencephalopathy in a kidney transplant recipient with improving symptoms after immunocompetence recovery. Le Infezioni in Medicina. 28: 87-90. PMID 32172266  0.4
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  0.72
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  0.4
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  0.4
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  0.4
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
2011 Zou WQ, Xiao X, Yuan J, Puoti G, Fujioka H, Wang X, Richardson S, Zhou X, Zou R, Li S, Zhu X, McGeer PL, McGeehan J, Kneale G, Rincon-Limas DE, et al. Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain. The Journal of Biological Chemistry. 286: 15095-105. PMID 21393248 DOI: 10.1074/Jbc.M110.199356  0.72
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  0.72
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  0.72
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  0.72
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  0.72
2008 Barbarulo AM, Pappatà S, Puoti G, Prinster A, Grossi D, Cotrufo R, Salvatore M, Trojano L. Rehabilitation of gesture imitation: a case study with fMRI. Neurocase. 14: 293-306. PMID 18766981 DOI: 10.1080/13554790802363688  0.72
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  0.72
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  0.72
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  0.72
2003 Puoti G, Carrara F, Sampaolo S, De Caro M, Vincitorio CM, Invernizzi F, Zeviani M. Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son. Journal of Medical Genetics. 40: 858-63. PMID 14627683  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
1997 Scuotto A, Cappabianca S, Melone MB, Puoti G. MRI "fogging" in cerebellar ischaemia: case report. Neuroradiology. 39: 785-7. PMID 9406204 DOI: 10.1007/s002340050506  0.72
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