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Titolo Data di pubblicazione Autore(i) File
Partial epilepsy of long duration: changing semiology with age 1996 Tinuper, P; Provini, F; Marini, C; Cerullo, A; Plazzi, G; Avoni, P; Baruzzi, A
Epileptic drop attacks in partial epilepsy: clinical features, evolution, and prognosis 1998 Tinuper, P; Cerullo, A; Marini, C; Avoni, P; Rosati, A; Riva, R; Baruzzi, A; Lugaresi, E
Autonomic and hormonal ictal changes in gelastic seizures from hypothalamic hamartomas 1998 Cerullo, A; Tinuper, P; Provini, F; Contin, M; Rosati, A; Marini, C; Cortelli, P
Clinical and video-polygraphic features of epileptic spasms in adults with cortical migration disorder 1999 Cerullo, A; Marini, C; Carcangiu, R; Baruzzi, A; Tinuper, P
Reading epilepsy in a patient with previous idiopathic focal epilepsy with centrotemporal spikes 1999 Valenti, M P; Tinuper, P; Cerullo, A; Carcangiu, R; Marini, C
Colpocephaly in two siblings: further evidence of a genetic transmission 2000 Cerullo, A; Marini, C; Cevoli, S; Carelli, V; Montagna, P; Tinuper, P
A de novo mutation in sporadic nocturnal frontal lobe epilepsy 2000 Phillips, H A; Marini, C; Scheffer, I E; Sutherland, G R; Mulley, J C; Berkovic, S F
Ictal bradycardia in partial epileptic seizures: Autonomic investigation in three cases and literature review 2001 Tinuper, P; Bisulli, F; Cerullo, A; Carcangiu, R; Marini, C; Pierangeli, G; Cortelli, P
Mutant GABAAreceptor γ2-subunit in childhood absence epilepsy and febrile seizures 2001 Wallace, Robyn H.; Marini, Carla; Petrou, Steven; Harkin, Louise A.; Bowser, David N.; Panchal, Rekha G.; Williams, David A.; Sutherland, Grant R.; Mulley, John C.; Scheffer, Ingrid E.; Berkovic, Samuel F.
Altered kinetics and benzodiazepine sensitivity of a GABAAreceptor subunit mutation [γ2(R43Q)] found in human epilepsy 2002 Bowser, David N.; Wagner, David A.; Czajkowski, Cynthia; Cromer, Brett A.; Parker, Michael W.; Wallace, Robyn H.; Harkin, Louise A.; Mulley, John C.; Marini, Carla; Berkovic, Samuel F.; Williams, David A.; Jones, Mathew V.; Petrou, Steven*
Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation 2003 Marini, Carla; Harkin, Louise A; Wallace, Robyn H; Mulley, John C; Scheffer, Ingrid E; Berkovic, Samuel F
Idiopathic generalised epilepsy of adult onset: clinical syndromes and genetics 2003 Marini, C; King, M A; Archer, J S; Newton, M R; Berkovic, S F
Epilepsy in offspring of whom both parents have idiopathic generalized epilepsy: biparental inheritance 2003 Marini, Carla; Harvey, A Simon; Pelekanos, James T; Berkovic, Samuel F
EEG in adult-onset idiopathic generalized epilepsy 2003 Yenjun, Suthida; Harvey, A Simon; Marini, Carla; Newton, Mark R; King, Mark A; Berkovic, Samuel F
Genetic Architecture of Idiopathic Generalized Epilepsy: Clinical Genetic Analysis of 55 Multiplex Families 2004 Marini, Carla; Scheffer, Ingrid E.; Crossland, Kathryn M.; Grinton, Bronwyn E.; Phillips, Fiona L.; McMahon, Jacinta M.; Turner, Samantha J.; Dean, Joanne T.; Kivity, Sara; Mazarib, Aziz; Neufeld, Miriam Y.; Korczyn, Amos D.; Harkin, Louise A.; Dibbens, Leanne M.; Wallace, Robyn H.; Mulley, John C.; Berkovic, Samuel F.
Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy. 2004 Berkovic SF; Heron SE; Giordano L; Marini C; Guerrini R; Kaplan RE; Gambardella A; Steinlein OK; Grinton BE; Dean JT; Bordo L; Hodgson BL; Yamamoto T; Mulley JC; Zara F; Scheffer IE.
Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: Is there overlap? 2004 Taylor, Isabella; Marini, Carla; Johnson, Michael R.; Turner, Samantha; Berkovic, Samuel F.; Scheffer, Ingrid E.
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations. 2004 Bonanni P; Malcarne M; Moro F; Veggiotti P; Buti D; Ferrari AR; Parrini E; Mei D; Volzone A; Zara F; Heron SE; Bordo L; Marini C; Guerrini R.
Familial clustering of seizure types within the idiopathic generalized epilepsies 2005 Winawer, Melodie R.; Marini, C.; Grinton, B.E.; Rabinowitz, D.; Berkovic, S.F.; Scheffer, I.E.; Ottman, R.
Mosaic SCN1A mutation in familial severe myoclonic epilepsy of infancy. 2006 Marini C; Mei D; Helen Cross J; Guerrini R.
Mostrati risultati da 1 a 20 di 105
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