Umberto Aguglia
Umberto Aguglia
Full professor of Neurology, Catanzaro University, Italy
Verified email at unicz.it
Title
Cited by
Cited by
Year
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
4442005
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
2832008
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
1721983
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
1601998
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
1572003
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
1522015
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
1402012
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
1322011
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
1291996
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
1211999
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
1002010
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
992014
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
972008
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
972005
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
952006
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
922000
Startle‐induced epileptic seizures
U Aguglia, P Tinuper, H Gastaut
Epilepsia 25 (6), 712-720, 1984
871984
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
831983
Benign mesial temporal lobe epilepsy
A Labate, A Gambardella, E Andermann, U Aguglia, F Cendes, ...
Nature Reviews Neurology 7 (4), 237, 2011
772011
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
772001
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