Seuraa
Umberto Aguglia
Umberto Aguglia
Full professor of Neurology, Catanzaro University, Italy
Vahvistettu sähköpostiosoite verkkotunnuksessa unicz.it
Nimike
Viittaukset
Viittaukset
Vuosi
Mutations in Col4a1 Cause Perinatal Cerebral Hemorrhage and Porencephaly
DB Gould, FC Phalan, GJ Breedveld, SE Van Mil, RS Smith, JC Schimenti, ...
Science 308 (5725), 1167-1171, 2005
6242005
Disease‐modifying therapies and coronavirus disease 2019 severity in multiple sclerosis
MP Sormani, N De Rossi, I Schiavetti, L Carmisciano, C Cordioli, L Moiola, ...
Annals of neurology 89 (4), 780-789, 2021
5102021
MR Imaging Index for Differentiation of Progressive Supranuclear Palsy from Parkinson Disease and the Parkinson Variant of Multiple System Atrophy1
A Quattrone, G Nicoletti, D Messina, F Fera, F Condino, P Pugliese, ...
Radiology 246 (1), 214-221, 2008
4662008
Autologous hematopoietic stem cell transplantation in multiple sclerosis: a phase II trial
GL Mancardi, MP Sormani, F Gualandi, A Saiz, E Carreras, E Merelli, ...
Neurology 84 (10), 981-988, 2015
2772015
The long‐term effect of vagus nerve stimulation on quality of life in patients with pharmacoresistant focal epilepsy: The PuLsE (Open P rospective Randomized L ong‐term E …
P Ryvlin, FG Gilliam, DK Nguyen, G Colicchio, A Iudice, P Tinuper, ...
Epilepsia 55 (6), 893-900, 2014
2102014
Neuroanatomic correlates of psychogenic nonepileptic seizures: a cortical thickness and VBM study
A Labate, A Cerasa, M Mula, L Mumoli, MC Gioia, U Aguglia, A Quattrone, ...
Epilepsia 53 (2), 377-385, 2012
2092012
GABA (B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy
A Gambardella, I Manna, A Labate, R Chifari, A La Russa, P Serra, ...
Neurology 60 (4), 560-563, 2003
1972003
Randomized trial comparing two different high doses of methylprednisolone in MS A clinical and MRI study
RL Oliveri, P Valentino, C Russo, G Sibilia, U Aguglia, F Bono, F Fera, ...
Neurology 50 (6), 1833-1836, 1998
1961998
Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6
T Arsov, KR Smith, J Damiano, S Franceschetti, L Canafoglia, ...
The American Journal of Human Genetics 88 (5), 566-573, 2011
1922011
Epilepsy in cerebrovascular diseases: review of experimental and clinical data with meta‐analysis of risk factors
E Ferlazzo, S Gasparini, E Beghi, C Sueri, E Russo, A Leo, A Labate, ...
Epilepsia 57 (8), 1205-1214, 2016
1832016
Prolactin secretion in man: a useful tool to evaluate the activity of drugs on central 5‐hydroxytryptaminergic neurones. Studies with fenfluramine.
A Quattrone, G Tedeschi, U Aguglia, F Scopacasa, GF Direnzo, ...
British journal of clinical pharmacology 16 (5), 471-475, 1983
1801983
Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD
RL Oliveri, G Annesi, M Zappia, D Civitelli, R Montesanti, D Branca, ...
Neurology 53 (7), 1425-1425, 1999
1551999
Autosornal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family
A Quattrone, A Gambardella, F Bono, U Aguglia, A Bolino, AC Bruni, ...
Neurology 46 (5), 1318-1318, 1996
1461996
Hyperhomocysteinemia in epileptic patients on new antiepileptic drugs
V Belcastro, P Striano, G Gorgone, C Costa, C Ciampa, D Caccamo, ...
Epilepsia 51 (2), 274-279, 2010
1382010
Deep learning representation from electroencephalography of early-stage Creutzfeldt-Jakob disease and features for differentiation from rapidly progressive dementia
FC Morabito, M Campolo, N Mammone, M Versaci, S Franceschetti, ...
International journal of neural systems 27 (02), 1650039, 2017
1372017
DMTs and Covid‐19 severity in MS: a pooled analysis from Italy and France
MP Sormani, M Salvetti, P Labauge, I Schiavetti, H Zephir, L Carmisciano, ...
Annals of Clinical and Translational Neurology 8 (8), 1738-1744, 2021
1202021
Hippocampal and thalamic atrophy in mild temporal lobe epilepsy: a VBM study
A Labate, A Cerasa, A Gambardella, U Aguglia, A Quattrone
Neurology 71 (14), 1094-1101, 2008
1172008
MRI evidence of mesial temporal sclerosis in sporadic “benign” temporal lobe epilepsy
A Labate, P Ventura, A Gambardella, E Le Piane, E Colosimo, U Leggio, ...
Neurology 66 (4), 562-565, 2006
1152006
The spectrum of Notch3 mutations in 28 Italian CADASIL families
MT Dotti, A Federico, R Mazzei, S Bianchi, O Scali, FL Conforti, ...
Journal of Medical Genetics 42 (6), 478-478, 2005
1152005
Benign mesial temporal lobe epilepsy
A Labate, A Gambardella, E Andermann, U Aguglia, F Cendes, ...
Nature Reviews Neurology 7 (4), 237-240, 2011
1112011
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Artikkelit 1–20