Umberto Aguglia
Umberto Aguglia
Full professor of Neurology, Catanzaro University, Italy
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Cited by
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
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
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
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
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
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
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
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
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
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
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
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 Eá…
P Ryvlin, FG Gilliam, DK Nguyen, G Colicchio, A Iudice, P Tinuper, ...
Epilepsia 55 (6), 893-900, 2014
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
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
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
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1
A Gambardella, G Annesi, M De Fusco, A Patrignani, U Aguglia, F Annesi, ...
Neurology 55 (10), 1467-1471, 2000
Startle‐induced epileptic seizures
U Aguglia, P Tinuper, H Gastaut
Epilepsia 25 (6), 712-720, 1984
Snoring as a risk factor for cardiac and circulatory problems: an epidemiological study
S Mondini
Sleep/wake disorders: natural history, epidemiology, and long-term evolution, 1983
Benign mesial temporal lobe epilepsy
A Labate, A Gambardella, E Andermann, U Aguglia, F Cendes, ...
Nature Reviews Neurology 7 (4), 237, 2011
Silent celiac disease in patients with childhood localization‐related epilepsies
A Labate, A Gambardella, D Messina, S Tammaro, E Le Piane, D Pirritano, ...
Epilepsia 42 (9), 1153-1155, 2001
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