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Results: 1-14 |
Results: 14
4 FAMILIES WITH AN AUTOSOMAL-DOMINANT PARTIAL EPILEPSY SYNDROME WITH FRONTAL OR TEMPORAL FOCI
Authors: PANDOLFO M LABUDA M XIONG L STHILAIRE JM BERKOVIC S SCHEFFER I DESBIENS R VERRET S LANGEVIN P PATRY G ANDERMANN F ANDERMANN E
Citation: M. Pandolfo et al., 4 FAMILIES WITH AN AUTOSOMAL-DOMINANT PARTIAL EPILEPSY SYNDROME WITH FRONTAL OR TEMPORAL FOCI, Annals of neurology, 44(3), 1998, pp. 103-103
DOUBLECORTIN, A BRAIN-SPECIFIC GENE MUTATED IN HUMAN X-LINKED LISSENCEPHALY AND DOUBLE CORTEX SYNDROME, ENCODES A PUTATIVE SIGNALING PROTEIN
Authors: GLEESON JG ALLEN KM FOX JW LAMPERTI ED BERKOVIC S SCHEFFER I COOPER EC DOBYNS WB MINNERATH SR ROSS ME WALSH CA
Citation: Jg. Gleeson et al., DOUBLECORTIN, A BRAIN-SPECIFIC GENE MUTATED IN HUMAN X-LINKED LISSENCEPHALY AND DOUBLE CORTEX SYNDROME, ENCODES A PUTATIVE SIGNALING PROTEIN, Cell, 92(1), 1998, pp. 63-72
HYPERSPHERICAL APPROACH TO THE CALCULATION OF FEW-BODY ATOMIC RESONANCES
Authors: BERKOVIC S KRIVEC R MANDELZWEIG V STOTLAND L
Citation: S. Berkovic et al., HYPERSPHERICAL APPROACH TO THE CALCULATION OF FEW-BODY ATOMIC RESONANCES, Physical review. A, 55(2), 1997, pp. 988-993
LINKAGE AND PHYSICAL MAPPING OF X-LINKED LISSENCEPHALY SBH (XLIS) - AGENE CAUSING NEURONAL MIGRATION DEFECTS IN HUMAN BRAIN/
Authors: ROSS ME ALLEN KM SRIVASTAVA AK FEATHERSTONE T GLEESON JG HIRSCH B HARDING BN ANDERMANN E ABDULLAH R BERG M CZAPANSKYBIELMAN D FLANDERS DJ GUERRINI R MOTTE J MIRA AP SCHEFFER I BERKOVIC S SCARAVILLI F KING RA LEDBETTER DH SCHLESSINGER D DOBYNS WB WALSH CA
Citation: Me. Ross et al., LINKAGE AND PHYSICAL MAPPING OF X-LINKED LISSENCEPHALY SBH (XLIS) - AGENE CAUSING NEURONAL MIGRATION DEFECTS IN HUMAN BRAIN/, Human molecular genetics, 6(4), 1997, pp. 555-562
FOR GENERALIZED SEIZURES ASSOCIATED WITH THE LENNOX-GASTAUT-SYNDROME
Authors: MOTTE J TREVATHAN E ARVIDSSON JFV BARRERA MN MULLENS EL MANASCO P DULAC O MAI J BILLARD C VALLEE L OBERARZTIN F RIED S CHRISTE W RATING D VIGEVANO F TASSINARI C BERNARDINA BD MAJOIE H WEBER A LAEGREID L EEGOLOFSSON O BERMEJO M MARTINEZ A CASTELLO JC SERRA MTI KIRKHAM F NORONHA M WALLACE S BLACK A BERKOVIC S PEDESPAN J ECHENNE B PINSARD N PARAIN D PENIELLO M CARRIERE J CHAUVEL P BERQUIN P GARREL S SCHAFF J TALVIK T DOUCHOWNY M GILMAN J PELLOCK J CHENG R CRUMRINE P LYNCH B HAHN J GRIESEMER D WANNAMAKER B LAXER K BLUESTONE D BEBIN E
Citation: J. Motte et al., FOR GENERALIZED SEIZURES ASSOCIATED WITH THE LENNOX-GASTAUT-SYNDROME, The New England journal of medicine, 337(25), 1997, pp. 1807-1812
PROGRESSIVE MYOCLONUS EPILEPSY IN YOUNG-ADULTS WITH NEUROPATHOLOGIC FEATURES OF ALZHEIMERS-DISEASE
Authors: MELANSON M NALBANTOGLU J BERKOVIC S MELMED C ANDERMANN E ROBERTS LJ CARPENTER S SNIPES GJ ANDERMANN F
Citation: M. Melanson et al., PROGRESSIVE MYOCLONUS EPILEPSY IN YOUNG-ADULTS WITH NEUROPATHOLOGIC FEATURES OF ALZHEIMERS-DISEASE, Neurology, 49(6), 1997, pp. 1732-1733
COMPARISON OF FMRI AND TRANSCRANIAL MAGNETIC STIMULATION BN THE LOCALIZATION OF MOTOR CORTEX
Authors: MACDONELL R JACKSON G BERKOVIC S
Citation: R. Macdonell et al., COMPARISON OF FMRI AND TRANSCRANIAL MAGNETIC STIMULATION BN THE LOCALIZATION OF MOTOR CORTEX, Neurology, 48(3), 1997, pp. 2050-2050
CHRONIC ENCEPHALITIS AND EPILEPSY IN ADULTS AND ADOLESCENTS - A VARIANT OF RASMUSSENS SYNDROME
Authors: HART YM ANDERMANN F FISH DR DUBEAU F ROBITAILLE Y RASMUSSEN T BERKOVIC S MARINO R YAKOUBIAN EM SPILLANE K SCARAVILLI F
Citation: Ym. Hart et al., CHRONIC ENCEPHALITIS AND EPILEPSY IN ADULTS AND ADOLESCENTS - A VARIANT OF RASMUSSENS SYNDROME, Neurology, 48(2), 1997, pp. 418-424
MYOCLONUS AND EPILEPSY IN CHILDHOOD
Authors: DULAC O DRAVET C PLOUIN P SHEWMON A ANDERMANN F APPLETON R BATHIEN N ARI B MENACHEM EB BERKOVIC S BIRABEN A CATALA M CHIRON C BERNARDINA BD DONAT J DREIFUSS F FARRELL K FEJERMAN N GENTON P GOETZ C GUERRINI R HOLTHAUSEN H MARESCAUX C MAUGUIERE F MICHELUCCI R MIZRAHI E RATING D ROBAIN O ROTHWELL J SHIBASAKI H SCHMIDT D TASSINARI A ULDALL P VIGEVANO F VIRI P WALLACE S WATANABE K
Citation: O. Dulac et al., MYOCLONUS AND EPILEPSY IN CHILDHOOD, Epilepsia, 38(11), 1997, pp. 1251-1254
LINKAGE ANALYSIS OF DOUBLE CORTEX X-LINKED LISSENCEPHALY/
Authors: GLEESON J ALLEN K DOBYNS WB ROSS ME SCHEFFER I BERKOVIC S BERG M MOTTE J WALSH C
Citation: J. Gleeson et al., LINKAGE ANALYSIS OF DOUBLE CORTEX X-LINKED LISSENCEPHALY/, Annals of neurology, 40(2), 1996, pp. 19-19
X-LINKED NEURONAL MIGRATION DISORDERS (NMD) - A HITHERTO-UNRECOGNIZEDCAUSE OF FAMILIAL EPILEPSY
Authors: ANDERMANN E DOBYNS WB WALSH C PINARD JM DULAC O PALMINI A SCHEFFER I BERKOVIC S DUBEAU F TAMPIERI D LEE N ANDERMANN F
Citation: E. Andermann et al., X-LINKED NEURONAL MIGRATION DISORDERS (NMD) - A HITHERTO-UNRECOGNIZEDCAUSE OF FAMILIAL EPILEPSY, Neurology, 45(4), 1995, pp. 243-243
AUTOSOMAL-DOMINANT FRONTAL EPILEPSY MISDIAGNOSED AS SLEEP DISORDER
Authors: SCHEFFER IE BHATIA KP LOPESCENDES I FISH DR MARSDEN CD ANDERMANN F ANDERMANN E DESBIENS R CENDES F MANSON JI BERKOVIC S
Citation: Ie. Scheffer et al., AUTOSOMAL-DOMINANT FRONTAL EPILEPSY MISDIAGNOSED AS SLEEP DISORDER, Lancet, 343(8896), 1994, pp. 515-517
GABAPENTIN (NEURONTIN) AS ADD-ON THERAPY IN PATIENTS WITH PARTIAL SEIZURES - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY
Authors: ANHUT H ASHMAN P FEUERSTEIN TJ SAUERMANN W SAUNDERS M SCHMIDT B BAUER G DEISENHAMMER E KLINGLER D MAMOLI B GRAF M DANTA G BERKOVIC S VAJDA F BUCHANAN N SCHAPEL G BLACK A BAJADA S DEBARSY T LATERRE C VANZANDIJCKE M MCLACHLAN RS PURVES SJ LEE MA BRUNI J GAWEL M HOLTLARSEN B WERDELIN L DALBY MA IIVANAINEN MV GIROUD M LECLERCQ E REMY C SALLOU C RICHENS A BILL PLA
Citation: H. Anhut et al., GABAPENTIN (NEURONTIN) AS ADD-ON THERAPY IN PATIENTS WITH PARTIAL SEIZURES - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY, Epilepsia, 35(4), 1994, pp. 795-801
AUTOSOMAL-DOMINANT PROGRESSIVE MYOCLONIC EPILEPSY (PME) - EVIDENCE FOR GENETIC-HETEROGENEITY IN KUFS-DISEASE
Authors: ANDERMANN F ANDERMANN E LEONBERG S CARPENTER S SALASPUIG F FERRER J LOPESCENDES I COCHIUS JI BERKOVIC S ROULEAU GA
Citation: F. Andermann et al., AUTOSOMAL-DOMINANT PROGRESSIVE MYOCLONIC EPILEPSY (PME) - EVIDENCE FOR GENETIC-HETEROGENEITY IN KUFS-DISEASE, American journal of human genetics, 53(3), 1993, pp. 1536-1536
Risultati: 1-14 |