Antonio Gambardella
Antonio Gambardella
Verified email at unicz.it
TitleCited byYear
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
7242012
Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results
A Palmini, A Gambardella, F Andermann, F Dubeau, JC da Costa, ...
Annals of neurology 37 (4), 476-487, 1995
7101995
Dose-dependent risk of malformations with antiepileptic drugs: an analysis of data from the EURAP epilepsy and pregnancy registry
T Tomson, D Battino, E Bonizzoni, J Craig, D Lindhout, A Sabers, ...
The Lancet Neurology 10 (7), 609-617, 2011
5972011
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
A Bolino, M Muglia, FL Conforti, E LeGuern, MAM Salih, DM Georgiou, ...
Nature genetics 25 (1), 17, 2000
4752000
The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy
M De Fusco, A Becchetti, A Patrignani, G Annesi, A Gambardella, ...
Nature genetics 26 (3), 275, 2000
4742000
Seizure control and treatment in pregnancy: observations from the EURAP epilepsy pregnancy registry
EURAP Study Group
Neurology 66 (3), 354-360, 2006
3132006
Benign familial neonatal‐infantile seizures: characterization of a new sodium channelopathy
SF Berkovic, SE Heron, L Giordano, C Marini, R Guerrini, RE Kaplan, ...
Annals of neurology 55 (4), 550-557, 2004
2882004
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ...
Nature neuroscience 17 (5), 664, 2014
2572014
Operative strategies for patients with cortical dysplastic lesions and intractable epilepsy
A Palmini, A Gambardella, F Andermann, F Dubeau, JC Cos, A Olivi, ...
Epilepsia 35, S57-S71, 1994
2221994
Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsy
F Cendes, F Andermann, P Gloor, A Gambardella, I Lopes-Cendes, ...
Brain 117 (4), 739-746, 1994
1901994
Usefulness of focal rhythmic discharges on scalp EEG of patients with focal cortical dysplasia and intractable epilepsy
A Gambardella, A Palmini, F Andermann, F Dubeau, JC Da Costa, ...
Electroencephalography and clinical neurophysiology 98 (4), 243-249, 1996
1841996
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study
M Zappia, G Annesi, G Nicoletti, G Arabia, F Annesi, D Messina, ...
Archives of neurology 62 (4), 601-605, 2005
1832005
Seizure control and treatment changes in pregnancy: observations from the EURAP epilepsy pregnancy registry
D Battino, T Tomson, E Bonizzoni, J Craig, D Lindhout, A Sabers, ...
Epilepsia 54 (9), 1621-1627, 2013
1732013
Identification of an Nav1. 1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures
M Mantegazza, A Gambardella, R Rusconi, E Schiavon, F Annesi, ...
Proceedings of the National Academy of Sciences 102 (50), 18177-18182, 2005
1712005
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
A Chi˛, G Borghero, G Restagno, G Mora, C Drepper, BJ Traynor, ...
Brain 135 (3), 784-793, 2012
1632012
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
1522003
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
1511998
Alteration of the in vivo nicotinic receptor density in ADNFLE patients: a PET study
F Picard, D Bruel, D Servent, W Saba, C Fruchart-Gaillard, ...
Brain 129 (8), 2047-2060, 2006
1462006
Relationship between adverse effects of antiepileptic drugs, number of coprescribed drugs, and drug load in a large cohort of consecutive patients with drug‐refractory epilepsy
MP Canevini, G De Sarro, CA Galimberti, G Gatti, L Licchetta, A Malerba, ...
Epilepsia 51 (5), 797-804, 2010
1362010
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
M Muona, SF Berkovic, LM Dibbens, KL Oliver, S Maljevic, MA Bayly, ...
Nature genetics 47 (1), 39, 2015
1352015
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