Gianfranco Puoti

University of Naples, Napoli, Campania, Italy 
"Gianfranco Puoti"
Mean distance: 17.19 (cluster 28)
Cross-listing: Neuropathology Tree

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Coppola C, Saracino D, Puoti G, et al. (2016) A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations. Neurobiology of Aging
Bonda DJ, Manjila S, Mehndiratta P, et al. (2016) Human prion diseases: surgical lessons learned from iatrogenic prion transmission. Neurosurgical Focus. 41: E10
Imbriani P, Marfia GA, Marciani MG, et al. (2015) Heidenhain variant in two patients with inherited V210I Creutzfeldt-Jakob disease. The International Journal of Neuroscience
Del Pilar-Morales EA, Cali I, Chapas J, et al. (2015) Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient. Puerto Rico Health Sciences Journal. 34: 40-3
Xiao X, Cali I, Yuan J, et al. (2015) Synthetic Aβ peptides acquire prion-like properties in the brain. Oncotarget. 6: 642-50
Ghoshal N, Perry A, McKeel D, et al. (2015) Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old. Alzheimer Disease and Associated Disorders. 29: 173-6
Puoti G, Lerza MC, Ferretti MG, et al. (2014) 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
Strianese D, Napoli M, Russo C, et al. (2014) Coexistence of cavernous hemangioma and other vascular malformations of the orbit. A report of three cases. The Neuroradiology Journal. 27: 223-31
Puoti G, Elefante A, Saracino D, et al. (2013) New-onset refractory status epilepticus mimicking herpes virus encephalitis. Case Reports in Neurology. 5: 162-7
Xiao X, Cali I, Dong Z, et al. (2013) Protease-sensitive prions with 144-bp insertion mutations. Aging. 5: 155-73
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