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Results: 1-13 |
Results: 13

Authors: MIKOL J LAVERGNESLOVE A LECOZ P GOUTIERES F VANIER MT
Citation: J. Mikol et al., B1 VARIANT OF GM2 GANGLIOSIDOSIS - PATHOLOGICAL AND BIOCHEMICAL-STUDYOF A LATE-ONSET FORM, Brain pathology, 7(4), 1997, pp. 1062-1062

Authors: GOUTIERES F BOURGEOIS M TRIOCHE P DEMELIER JF ODIEVRE M LABRUNE P
Citation: F. Goutieres et al., MOYAMOYA DISEASE IN A CHILD WITH GLYCOGEN-STORAGE-DISEASE TYPE IA, Neuropediatrics, 28(2), 1997, pp. 133-134

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

Authors: LABRUNE P LACROIX C GOUTIERES F DELAVEAUCOUPET J CHEVALIER P ZERAH M HUSSON B LANDRIEU P
Citation: P. Labrune et al., EXTENSIVE BRAIN CALCIFICATIONS LEUKODYSTROPHY, AND FORMATION OF PARENCHYMAL CYSTS - A NEW PROGRESSIVE DISORDER DUE TO DIFFUSE CEREBRAL MICROANGIOPATHY, Neurology, 46(5), 1996, pp. 1297-1301

Authors: GOUTIERES F
Citation: F. Goutieres, BOURNEVILLE TUBEROUS SCLEROSIS, Archives de pediatrie, 2, 1995, pp. 82-83

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

Authors: ROTIG A GOUTIERES F NIAUDET P RUSTIN P CHRETIEN D GUEST G MIKOL J GUBLER MC MUNNICH A
Citation: A. Rotig et al., DELETION OF MITOCHONDRIAL-DNA IN PATIENT WITH CHRONIC TUBULOINTERSTITIAL NEPHRITIS, The Journal of pediatrics, 126(4), 1995, pp. 597-601

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

Authors: DOERFLINGER N LINDER C OUAHCHI K GYAPAY G WEISSENBACH J LEPASLIER D RIGAULT P BELAL S BENHAMIDA C HENTATI F BENHAMIDA M PANDOLFO M DIDONATO S SOKOL R KAYDEN H LANDRIEU P DURR A BRICE A GOUTIERES F KOHLSCHUTTER A SABOURAUD P BENOMAR A YAHYAOUI M MANDEL JL KOENIG M
Citation: N. Doerflinger et al., ATAXIA WITH VITAMIN-E-DEFICIENCY - REFINEMENT OF GENETIC LOCALIZATIONAND ANALYSIS OF LINKAGE DISEQUILIBRIUM BY USING NEW MARKERS IN 14 FAMILIES, American journal of human genetics, 56(5), 1995, pp. 1116-1124

Authors: LABRUNE P LYONNET S ZUPAN V IMBERT MC GOUTIERES F HUBERT P LEMERRER M
Citation: P. Labrune et al., 3 NEW CASES OF THE SCHINZEL-GIEDION SYNDROME AND REVIEW OF THE LITERATURE, American journal of medical genetics, 50(1), 1994, pp. 90-93

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

Authors: GOUTIERES F
Citation: F. Goutieres, FAMILIAL ENCEPHALOPATHIES WITH CALCIFICAT IONS OF THE BASAL GANGLIA, La Presse medicale, 22(39), 1993, pp. 1948-1950

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
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