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Results: 1-21 |
Results: 21
NEW FORM OF AUTOSOMAL-RECESSIVE AXONAL HEREDITARY SENSORY-MOTOR NEUROPATHY
Authors: ECKHARDT SME HICKS EM HERRON B MORRISON PJ AICARDI J
Citation: Sme. Eckhardt et al., NEW FORM OF AUTOSOMAL-RECESSIVE AXONAL HEREDITARY SENSORY-MOTOR NEUROPATHY, Pediatric neurology, 19(3), 1998, pp. 234-235
EPILEPSY IN RETT-SYNDROME - A BRIEF OVERVIEW
Authors: AICARDI J
Citation: J. Aicardi, EPILEPSY IN RETT-SYNDROME - A BRIEF OVERVIEW, European child & adolescent psychiatry, 6, 1997, pp. 40-40
BILATERAL TONIC-CLONIC EPILEPTIC SEIZURES IN NON-BENIGN FAMILIAL NEONATAL CONVULSIONS
Authors: ALFONSO I HAHN JS PAPAZIAN O MARTINEZ YL REYES MA AICARDI J
Citation: I. Alfonso et al., BILATERAL TONIC-CLONIC EPILEPTIC SEIZURES IN NON-BENIGN FAMILIAL NEONATAL CONVULSIONS, Pediatric neurology, 16(3), 1997, pp. 249-251
LEUKOENCEPHALOPATHY, MEGALENCEPHALY, AND MILD CLINICAL COURSE - A RECENTLY INDIVIDUALIZED FAMILIAL LEUKODYSTROPHY - REPORT ON 5 NEW CASES
Authors: GOUTIERES F BOULLOCHE J BOURGEOIS M AICARDI J
Citation: F. Goutieres et al., LEUKOENCEPHALOPATHY, MEGALENCEPHALY, AND MILD CLINICAL COURSE - A RECENTLY INDIVIDUALIZED FAMILIAL LEUKODYSTROPHY - REPORT ON 5 NEW CASES, Journal of child neurology, 11(6), 1996, pp. 439-444
NONFAMILIAL GENERALIZED TONIC-CLONIC EPILEPTIC SEIZURES IN NEONATES
Authors: HAHN JS ALFONSO I PAPAZIAN O REYES MA AICARDI J
Citation: Js. Hahn et al., NONFAMILIAL GENERALIZED TONIC-CLONIC EPILEPTIC SEIZURES IN NEONATES, Neurology, 46(2), 1996, pp. 1124-1124
VIGABATRIN AS INITIAL THERAPY FOR INFANTILE SPASMS - A EUROPEAN RETROSPECTIVE SURVEY
Authors: AICARDI J HAUSER E STEINBOCK H SZYPER M HOLSTEEN V OSTERGAARD J PEDERSEN SA TAUDORF K BARTHEZCARPENTIER MA BADINANDHUBERT N BERQUIN P BOULLOCHE J BOURGEOIS M CARRIERE JP CHABROL B CHIRON C CLARIS O ECHENNE B GAUTHIERMOREL D LIVET MO LOPEZ N MANCINI J NETTER JC QUILLEROU D RICHELME CH ROUSSELLE C DESTMARTIN A DESWARTE M AUERSWALD G BRANDL U KURLEMANN G SIEMES H SPOHR HL AARTS WFM BEGEER JH HEERSMA DJ LAAN LAEM PETERS ACB CAVAZZUTTI GB CURATOLO P FOIS A FRANZONI E GOBBI G INCORPORA G VIGEVANO F CAMPISTOL J CAMPOS J CASAS C HERRANZ JL NIETO M PRATS JM AMARK P BLENNOW G THEORELL K TONNBY B HAENGGELI CA WEISSERT M APPLETON UKR ROBINSON R DESOUSA C THOMAS N ANDERMANN F APPLETON R",ARZIMANOGLOU,"BOYD S BRANDT W BUTI D DULAC O FARRELL K MOSHE S MOTTE J PLOUIN P SHIELDS WD MUMFORD JP DUMAS C WOOD S
Citation: J. Aicardi et al., VIGABATRIN AS INITIAL THERAPY FOR INFANTILE SPASMS - A EUROPEAN RETROSPECTIVE SURVEY, Epilepsia, 37(7), 1996, pp. 638-642
EXECUTIVE BOARD MEETING, OCTOBER 2, 1994 - PRESIDENTS REPORT
Authors: AICARDI J
Citation: J. Aicardi, EXECUTIVE BOARD MEETING, OCTOBER 2, 1994 - PRESIDENTS REPORT, Pediatric neurology, 13(1), 1995, pp. 88-88
WHAT IS CHILD NEUROLOGY
Authors: AICARDI J
Citation: J. Aicardi, WHAT IS CHILD NEUROLOGY, Brain & development, 17, 1995, pp. 17-19
REVERSIBLE DEMENTIA AND APPARENT BRAIN ATROPHY DURING VALPROATE THERAPY
Authors: PAPAZIAN O CANIZALES E ALFONSO I ARCHILA R DUCHOWNY M AICARDI J
Citation: O. Papazian et al., REVERSIBLE DEMENTIA AND APPARENT BRAIN ATROPHY DURING VALPROATE THERAPY, Annals of neurology, 38(4), 1995, pp. 687-691
SIMPLE MANEUVER TO PROVOKE BENIGN NEONATAL SLEEP MYOCLONUS
Authors: ALFONSO I PAPAZIAN O AICARDI J JEFFRIES HE
Citation: I. Alfonso et al., SIMPLE MANEUVER TO PROVOKE BENIGN NEONATAL SLEEP MYOCLONUS, Pediatrics, 96(6), 1995, pp. 1161-1163
EXTENSIVE MACROGYRI OR NO VISIBLE GYRI - DISTINCT CLINICAL, ELECTROENCEPHALOGRAPHIC, AND GENETIC FEATURES ACCORDING TO DIFFERENT IMAGING PATTERNS
Authors: SEBIRE G GOUTIERES F TARDIEU M LANDRIEU P AICARDI J
Citation: G. Sebire et al., EXTENSIVE MACROGYRI OR NO VISIBLE GYRI - DISTINCT CLINICAL, ELECTROENCEPHALOGRAPHIC, AND GENETIC FEATURES ACCORDING TO DIFFERENT IMAGING PATTERNS, Neurology, 45(6), 1995, pp. 1105-1111
VIGABATRIN (VGB) AS FIRST-LINE MONOTHERAPY IN IN INFANTILE SPASMS (IS)
Authors: AICARDI J
Citation: J. Aicardi, VIGABATRIN (VGB) AS FIRST-LINE MONOTHERAPY IN IN INFANTILE SPASMS (IS), Epilepsia, 36, 1995, pp. 3-3
CLINICAL-FEATURES AND SYNDROMES - INFANTS
Authors: AICARDI J
Citation: J. Aicardi, CLINICAL-FEATURES AND SYNDROMES - INFANTS, Epilepsia, 36, 1995, pp. 99-99
EUROPEAN EXPERIENCE WITH USE OF VIGABATRIN AS 1ST-LINE MONOTHERAPY ININFANTILE SPASMS
Authors: AICARDI J
Citation: J. Aicardi, EUROPEAN EXPERIENCE WITH USE OF VIGABATRIN AS 1ST-LINE MONOTHERAPY ININFANTILE SPASMS, Epilepsia, 36, 1995, pp. 102-102
EPILEPSY IN RETT-SYNDROME
Authors: ARZIMANOGLOU AA BOURGEOIS M GOUTIERES F SALEFRANQUE F AICARDI J
Citation: Aa. Arzimanoglou et al., EPILEPSY IN RETT-SYNDROME, Epilepsia, 36, 1995, pp. 238-239
THE PLACE OF NEURONAL MIGRATION ABNORMALITIES IN CHILD NEUROLOGY
Authors: AICARDI J
Citation: J. Aicardi, THE PLACE OF NEURONAL MIGRATION ABNORMALITIES IN CHILD NEUROLOGY, Canadian journal of neurological sciences, 21(3), 1994, pp. 185-193
GM2-GANGLIOSIDOSIS VARIANT B1 - A FAMILY WITH LATE JUVENILE-ONSET
Authors: LECOZ P ASSOULINE E VANIER MT GOUTIERES F MIKOL J WOIMANT F PINARD JM AICARDI J HAGUENAU M
Citation: P. Lecoz et al., GM2-GANGLIOSIDOSIS VARIANT B1 - A FAMILY WITH LATE JUVENILE-ONSET, Revue neurologique, 150(1), 1994, pp. 61-66
THE EPILEPTIC SPECTRUM IN THE CONGENITAL BILATERAL PERISYLVIAN SYNDROME
Authors: KUZNIECKY R ANDERMANN F GUERRINI R KUZNIECKY R ANDERMANN F GUERRINI R TAMPIERI D ANDERMANN E PALMINI A OLIVIER A MELANSON D LEONARD G ROSENBLATT B SHEVELL M FUSCO L VIGEVANO F GRAFFRADFORD N CHRISTIE S HUMPHREYS P WHITING S AICARDI J AMBROSETTO G TASSINARI CA DALLABERNARDINA B COLAMARIA V FAUGHT E MORAWETZ R DRAVET C
Citation: R. Kuzniecky et al., THE EPILEPTIC SPECTRUM IN THE CONGENITAL BILATERAL PERISYLVIAN SYNDROME, Neurology, 44(3), 1994, pp. 379-385
GENETIC HOMOGENEITY OF PELIZAEUS-MERZBACHER-DISEASE - TIGHT LINKAGE TO THE PROTEOLIPOPROTEIN LOCUS IN 16 AFFECTED FAMILIES
Authors: BOESPFLUGTANGUY O MIMAULT C MELKI J CAVAGNA A GIRAUD G DINH DP DASTUGUE B DAUTIGNY A AICARDI J GOUTTIERES F BAUMANN N BERTINI E DAVID A HENOCQ A LANDRIEU P TARDIEU M LEBERRE C LEMAREC B LYON G MAYER M PINARD JM PONSOT G MATHIEU M SAINTIVE JP SAURA R VALLEE L
Citation: O. Boespflugtanguy et al., GENETIC HOMOGENEITY OF PELIZAEUS-MERZBACHER-DISEASE - TIGHT LINKAGE TO THE PROTEOLIPOPROTEIN LOCUS IN 16 AFFECTED FAMILIES, American journal of human genetics, 55(3), 1994, pp. 461-467
THE INHERITED LEUKODYSTROPHIES - A CLINICAL OVERVIEW
Authors: AICARDI J
Citation: J. Aicardi, THE INHERITED LEUKODYSTROPHIES - A CLINICAL OVERVIEW, Journal of inherited metabolic disease, 16(4), 1993, pp. 733-743
ALTERNATING HEMIPLEGIA OF CHILDHOOD
Authors: BOURGEOIS M AICARDI J GOUTIERES F
Citation: M. Bourgeois et al., ALTERNATING HEMIPLEGIA OF CHILDHOOD, The Journal of pediatrics, 122(5), 1993, pp. 673-679
Risultati: 1-21 |