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Results: 26-50/101
BAND HETEROTOPIA OR DOUBLE CORTEX IN A MALE - BRIDGING STRUCTURES SUGGEST ABNORMALITY OF THE RADIAL GLIAL GUIDE SYSTEM
Authors: ONO J MANO T ANDERMANN E HARADA K SAKURAI K IKEDA T YOSHIHARA N SHIMIZU K OKADA S ANDERMANN F
Citation: J. Ono et al., BAND HETEROTOPIA OR DOUBLE CORTEX IN A MALE - BRIDGING STRUCTURES SUGGEST ABNORMALITY OF THE RADIAL GLIAL GUIDE SYSTEM, Neurology, 48(6), 1997, pp. 1701-1703
GENETIC AND EPIDEMIOLOGIC STUDIES OF EPILEPSY ON LA GRAZIOSA
Authors: ANDERMANN E ANDERMANN AAJ DUBEAU P ROULEAU G DIAZOBREGON C
Citation: E. Andermann et al., GENETIC AND EPIDEMIOLOGIC STUDIES OF EPILEPSY ON LA GRAZIOSA, Neurology, 48(3), 1997, pp. 1062-1062
FREQUENCY AND MOLECULAR CHARACTERISTICS OF THE SPINOCEREBELLAR ATAXIATYPE-2 MUTATION
Authors: LOPESCENDES I ANDERMANN E NECHIPORUK A ATTIG E BOSH S WAGNER M ANDERMANN F GERSTENBRAND F BOTEZ MI TEIVE H JAIN S PULST SM ROULEAU GA
Citation: I. Lopescendes et al., FREQUENCY AND MOLECULAR CHARACTERISTICS OF THE SPINOCEREBELLAR ATAXIATYPE-2 MUTATION, Neurology, 48(3), 1997, pp. 3077-3077
PEDIGREE ANALYSIS OF LEBERS HEREDITARY OPTIC NEUROPATHY FAMILIES WITHTHE T14484C MTDNA MUTATION
Authors: MACMILLAN C KIRKHAM T FU K ALLISON V ANDERMANN E BABUL R FORTIER D GANS M HARE H QUERCIA N ZACKON D SHOUBRIDGE EA
Citation: C. Macmillan et al., PEDIGREE ANALYSIS OF LEBERS HEREDITARY OPTIC NEUROPATHY FAMILIES WITHTHE T14484C MTDNA MUTATION, Neurology, 48(3), 1997, pp. 4078-4078
INVESTIGATION OF SPINOCEREBELLAR ATAXIA TYPE-6 (SCA6) IN A GROUP OF SPINOCEREBELLAR ATAXIA PATIENTS - FREQUENCY, ALLELE DISTRIBUTION, AND CLINICAL-FEATURES
Authors: HAYES S LOPESCENDES I ANDERMANN E GASPAR C ROULEAU GA
Citation: S. Hayes et al., INVESTIGATION OF SPINOCEREBELLAR ATAXIA TYPE-6 (SCA6) IN A GROUP OF SPINOCEREBELLAR ATAXIA PATIENTS - FREQUENCY, ALLELE DISTRIBUTION, AND CLINICAL-FEATURES, American journal of human genetics, 61(4), 1997, pp. 1812-1812
MOLECULAR ANALYSIS OF PATIENTS WITH FRIEDREICH ATAXIA PHENOTYPE NOT HOMOZYGOUS FOR THE GAA TRIPLET REPEAT EXPANSION
Authors: LABUDA M MONTERMINI L POIRIER J RICHTER A ANDERMANN E KISH S GESCHWIND D PANDOLFO M
Citation: M. Labuda et al., MOLECULAR ANALYSIS OF PATIENTS WITH FRIEDREICH ATAXIA PHENOTYPE NOT HOMOZYGOUS FOR THE GAA TRIPLET REPEAT EXPANSION, American journal of human genetics, 61(4), 1997, pp. 1825-1825
ISOLATION AND CHARACTERIZATION OF GT335, A NOVEL HUMAN GENE CONSERVEDIN ESCHERICHIA-COLI AND MAPPING TO 21Q22.3
Authors: LAFRENIERE RG ROCHEFORT DL KIBAR Z FON EA HAN FY COCHIUS J KANG X BAIRD S KORNELUK RG ANDERMANN E ROMMENS JM ROULEAU GA
Citation: Rg. Lafreniere et al., ISOLATION AND CHARACTERIZATION OF GT335, A NOVEL HUMAN GENE CONSERVEDIN ESCHERICHIA-COLI AND MAPPING TO 21Q22.3, Genomics, 38(3), 1996, pp. 264-272
EVIDENCE OF A 3RD LOCUS FOR BENIGN FAMILIAL CONVULSIONS
Authors: LEWIS TB SHEVELL MI ANDERMANN E RYAN SG LEACH RJ
Citation: Tb. Lewis et al., EVIDENCE OF A 3RD LOCUS FOR BENIGN FAMILIAL CONVULSIONS, Journal of child neurology, 11(3), 1996, pp. 211-214
EXQUISITE SENSITIVITY OF PAROXYSMAL KINESIGENIC CHOREOATHETOSIS TO CARBAMAZEPINE
Authors: WEIN T ANDERMANN F SILVER K DUBEAU F ANDERMANN E ROURKEFREW F KEENE D
Citation: T. Wein et al., EXQUISITE SENSITIVITY OF PAROXYSMAL KINESIGENIC CHOREOATHETOSIS TO CARBAMAZEPINE, Neurology, 47(4), 1996, pp. 1104-1106
X-LINKED MALFORMATIONS OF NEURONAL MIGRATION
Authors: DOBYNS WB ANDERMANN E ANDERMANN F CZAPANSKYBEILMAN D DUBEAU F DULAC O GUERRINI R HIRSCH B LEDBETTER DH LEE NS MOTTE J PINARD JM RADTKE RA ROSS ME TAMPIERI D WALSH CA TRUWIT CL
Citation: Wb. Dobyns et al., X-LINKED MALFORMATIONS OF NEURONAL MIGRATION, Neurology, 47(2), 1996, pp. 331-339
FOCAL SUPPRESSION-BURST
Authors: CENDES F ANDERMANN E ANDERMANN F
Citation: F. Cendes et al., FOCAL SUPPRESSION-BURST, Neurology, 47(2), 1996, pp. 613-613
GENETIC-MAPPING OF THE SPINOCEREBELLAR ATAXIA TYPE-2 GENE ON HUMAN-CHROMOSOME-12
Authors: NECHIPORUK A LOPESCENDES I NECHIPORUK T STARKMAN S ANDERMANN E ROULEAU GA WEISSENBACH JS KORT E PULST SM
Citation: A. Nechiporuk et al., GENETIC-MAPPING OF THE SPINOCEREBELLAR ATAXIA TYPE-2 GENE ON HUMAN-CHROMOSOME-12, Neurology, 46(6), 1996, pp. 1731-1735
PHYSIOLOGICAL-STUDIES OF SPINAL INHIBITORY PATHWAYS IN PATIENTS WITH HEREDITARY HYPEREKPLEXIA
Authors: FLOETER MK ANDERMANN F ANDERMANN E NIGRO M HALLETT M
Citation: Mk. Floeter et al., PHYSIOLOGICAL-STUDIES OF SPINAL INHIBITORY PATHWAYS IN PATIENTS WITH HEREDITARY HYPEREKPLEXIA, Neurology, 46(3), 1996, pp. 766-772
COLLABORATIVE INTERNATIONAL PROSPECTIVE-STUDY ON CONGENITAL-MALFORMATIONS IN CHILDREN OF MOTHERS WITH EPILEPSY
Authors: ANDERMANN E KANEKO S BATTINO D GOTO M
Citation: E. Andermann et al., COLLABORATIVE INTERNATIONAL PROSPECTIVE-STUDY ON CONGENITAL-MALFORMATIONS IN CHILDREN OF MOTHERS WITH EPILEPSY, Neurology, 46(2), 1996, pp. 1001-1001
COGNITIVE OUTCOME IN SCHOOL-AGE OFFSPRING OF EPILEPTIC MOTHERS EXPOSED TO ANTICONVULSANT THERAPY DURING PREGNANCY
Authors: LEONARD G PTITO A SENI MH VINETTE M SCHOPFLOCHER C DAIGNAULT S LOPESCENDES I SILVER K ANDERMANN E
Citation: G. Leonard et al., COGNITIVE OUTCOME IN SCHOOL-AGE OFFSPRING OF EPILEPTIC MOTHERS EXPOSED TO ANTICONVULSANT THERAPY DURING PREGNANCY, Neurology, 46(2), 1996, pp. 1126-1126
PROGRESSIVE MYOCLONUS EPILEPSY DUE TO EARLY-ONSET ALZHEIMERS-DISEASE
Authors: NALBANTOGLU J MELANSON M BERKOVIC SF MELMED C ANDERMANN E CARPENTER S ANDERMANN F
Citation: J. Nalbantoglu et al., PROGRESSIVE MYOCLONUS EPILEPSY DUE TO EARLY-ONSET ALZHEIMERS-DISEASE, Neurology, 46(2), 1996, pp. 4062-4062
THE GENE RESPONSIBLE FOR ANDERMANN SYNDROME MAPS TO CHROMOSOME 15Q
Authors: MELANSON M CASAUBON L LOPESCENDES I MARINEAU C ANDERMANN E ANDERMANN F WEISSENBACH J MATHIEU J BOUCHARD JP PREVOST C ROULEAU GA
Citation: M. Melanson et al., THE GENE RESPONSIBLE FOR ANDERMANN SYNDROME MAPS TO CHROMOSOME 15Q, Neurology, 46(2), 1996, pp. 21005-21005
EFFICACY AND SAFETY OF ADD-ON DIVALPROEX SODIUM IN THE TREATMENT OF COMPLEX PARTIAL SEIZURES
Authors: WILLMORE LJ SHU V WALLIN B ABOUKHALIL B ANDERMANN E BERGEN D BOELLNER SW BOUREGEOIS B EHLE AL GRAEBNER RW HANSON MR HOROWITZ SL HWANG PA IYER V KING J LAI CW LEROY R LOCKE GE MARTINEZ WC MASSEY A MCPHERSON SL OOMMEN K ROSENFIELD W ROWAN AJ SCHEUER M SO E SPITZ M SUNDER TR
Citation: Lj. Willmore et al., EFFICACY AND SAFETY OF ADD-ON DIVALPROEX SODIUM IN THE TREATMENT OF COMPLEX PARTIAL SEIZURES, Neurology, 46(1), 1996, pp. 49-53
FREQUENCY OF SPINOCEREBELLAR ATAXIA TYPE-1, DENTATORUBROPALLIDOLUYSIAN ATROPHY, AND MACHADO-JOSEPH DISEASE MUTATIONS IN A LARGE GROUP OF SPINOCEREBELLAR ATAXIA PATIENTS
Authors: SILVEIRA I LOPESCENDES I KISH S MACIEL P GASPAR C COUTINHO P BOTEZ MI TEIVE H ARRUDA W STEINER CE PINTOJUNIOR W MACIEL JA JAIN S SACK G ANDERMANN E SUDARSKY L ROSENBERG R MACLEOD P CHITAYAT D BABUL R SEQUEIROS J ROULEAU GA
Citation: I. Silveira et al., FREQUENCY OF SPINOCEREBELLAR ATAXIA TYPE-1, DENTATORUBROPALLIDOLUYSIAN ATROPHY, AND MACHADO-JOSEPH DISEASE MUTATIONS IN A LARGE GROUP OF SPINOCEREBELLAR ATAXIA PATIENTS, Neurology, 46(1), 1996, pp. 214-218
USEFULNESS OF FOCAL RHYTHMIC DISCHARGES ON SCALP EEG OF PATIENTS WITHFOCAL CORTICAL DYSPLASIA AND INTRACTABLE EPILEPSY
Authors: GAMBARDELLA A PALMINI A ANDERMANN F DUBEAU F DACOSTA JC QUESNEY LF ANDERMANN E OLIVIER A
Citation: A. Gambardella et al., USEFULNESS OF FOCAL RHYTHMIC DISCHARGES ON SCALP EEG OF PATIENTS WITHFOCAL CORTICAL DYSPLASIA AND INTRACTABLE EPILEPSY, Electroencephalography and clinical neurophysiology, 98(4), 1996, pp. 243-249
THE GENE RESPONSIBLE FOR A SEVERE FORM OF PERIPHERAL NEUROPATHY AND AGENESIS OF THE CORPUS-CALLOSUM MAPS TO CHROMOSOME 15Q
Authors: CASAUBON LK MELANSON M LOPESCENDES I MARINEAU C ANDERMANN E ANDERMANN F WEISSENBACH J PREVOST C BOUCHARD JP MATHIEU J ROULEAU GA
Citation: Lk. Casaubon et al., THE GENE RESPONSIBLE FOR A SEVERE FORM OF PERIPHERAL NEUROPATHY AND AGENESIS OF THE CORPUS-CALLOSUM MAPS TO CHROMOSOME 15Q, American journal of human genetics, 58(1), 1996, pp. 28-34
GENETIC-LINKAGE STUDIES IN FAMILIAL FRONTAL EPILEPSY - EXCLUSION OF THE HUMAN-CHROMOSOME REGIONS HOMOLOGOUS TO THE EL-1 MOUSE LOCUS
Authors: LOPESCENDES I PHILLIPS HA SCHEFFER IE MULLEY JC DESBIENS R ANDERMANN E CENDES F VERRET S ANDERMANN F BERKOVIC SF ROULEAU GA
Citation: I. Lopescendes et al., GENETIC-LINKAGE STUDIES IN FAMILIAL FRONTAL EPILEPSY - EXCLUSION OF THE HUMAN-CHROMOSOME REGIONS HOMOLOGOUS TO THE EL-1 MOUSE LOCUS, Epilepsy research, 22(3), 1995, pp. 227-233
INTRINSIC EPILEPTOGENICITY OF HUMAN DYSPLASTIC CORTEX AS SUGGESTED BYCORTICOGRAPHY AND SURGICAL RESULTS
Authors: PALMINI A GAMBARDELLA A ANDERMANN F DUBEAU F DACOSTA JC OLIVIER A TAMPIERI D GLOOR P QUESNEY F ANDERMANN E PAGLIOLI E PAGLIOLINETO E COUTINHO L LEBLANC R KIM HI
Citation: A. Palmini et al., INTRINSIC EPILEPTOGENICITY OF HUMAN DYSPLASTIC CORTEX AS SUGGESTED BYCORTICOGRAPHY AND SURGICAL RESULTS, Annals of neurology, 37(4), 1995, pp. 476-487
ARE WE ALL OF ONE MIND - CLINICIAN AND PATIENTS OPINIONS REGARDING THE DEVELOPMENT OF A SERVICE PROTOCOL FOR PREDICTIVE TESTING FOR HUNTINGTON-DISEASE
Authors: COPLEY TT WIGGINS S DUFRASNE S BLOCH M ADAM S MCKELLIN W HAYDEN MR IVES E WELCH JP FULLER A MILLER S ANDERMANN E ROY M MCLEOD P HUNTER A MESCHINO W WHELAN D EISENBERG D SOLTAN H KANE J GREENBERG CR KNIGHT J THOMPSON LP SHOKEIR MHK BAMFORTH S GROVER S SUCHOWERSKY O KLIMEK M
Citation: Tt. Copley et al., ARE WE ALL OF ONE MIND - CLINICIAN AND PATIENTS OPINIONS REGARDING THE DEVELOPMENT OF A SERVICE PROTOCOL FOR PREDICTIVE TESTING FOR HUNTINGTON-DISEASE, American journal of medical genetics, 58(1), 1995, pp. 59-69
REFINED LOCALIZATION OF THE BATTEN-DISEASE GENE (CLN3) BY HAPLOTYPE AND LINKAGE DISEQUILIBRIUM MAPPING TO D16S288-D16S383 AND EXCLUSION FROM THIS REGION OF A VARIANT FORM OF BATTEN-DISEASE WITH GRANULAR OSMIOPHILIC DEPOSITS
Authors: MITCHISON HM ORAWE AM LERNER TJ TASCHNER PEM SCHLUMPF K DARIGO K DEVOS N GORMALLY E PHILLIPS HA THOMPSON AD HAINES JL HART YM ANDERMANN E CALLEN DF BREUNING MH GARDINER RM MOLE SE
Citation: Hm. Mitchison et al., REFINED LOCALIZATION OF THE BATTEN-DISEASE GENE (CLN3) BY HAPLOTYPE AND LINKAGE DISEQUILIBRIUM MAPPING TO D16S288-D16S383 AND EXCLUSION FROM THIS REGION OF A VARIANT FORM OF BATTEN-DISEASE WITH GRANULAR OSMIOPHILIC DEPOSITS, American journal of medical genetics, 57(2), 1995, pp. 312-315
Risultati: 1-25 | 26-50 | 51-75 | 76-100 | >>