AAAAAA
Results:
1-13
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Results: 13
Authors:
GAREL C
BAUMANN C
BESNARD M
OGIER H
JAEKEN J
HASSAN M
Citation: C. Garel et al., CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I - A NEW CAUSE OF DYSOSTOSIS MULTIPLEX, Skeletal radiology, 27(1), 1998, pp. 43-45
Authors:
VANDERMEER SB
POGGI F
SPADA M
BONNEFONT JP
OGIER H
HUBERT P
DEPONDT E
RAPOPORT D
RABIER D
CHARPENTIER C
PARVY P
BARDET J
KAMOUN P
SAUDUBRAY JM
Citation: Sb. Vandermeer et al., CLINICAL OUTCOME AND LONG-TERM MANAGEMENT OF 17 PATIENTS WITH PROPIONIC ACIDEMIA, European journal of pediatrics, 155(3), 1996, pp. 205-210
Authors:
GIBSON KM
JAKOBS C
OGIER H
HAGENFELDT L
EEGOLOFSSON KE
EEGOLOFSSON O
AKSU F
WEBER HP
ROSSIER E
VOLLMER B
LEHNERT W
Citation: Km. Gibson et al., VIGABATRIN THERAPY IN 6 PATIENTS WITH SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY, Journal of inherited metabolic disease, 18(2), 1995, pp. 143-146
Authors:
NETTER JC
COSSARIZZA G
NARCY C
HUBERT P
OGIER H
REVILLON Y
RABIER D
SAUDUBRAY JM
Citation: Jc. Netter et al., MIDTERM OUTCOME OF 2 CASES OF MAPLE-SYRUP -URINE-DISEASE - EFFECT OF LIVER-TRANSPLANTATION, Archives de pediatrie, 1(8), 1994, pp. 730-734
Authors:
GIBSON KM
BAUMANN C
OGIER H
ROSSIER E
VOLLMER B
JAKOBS C
Citation: Km. Gibson et al., PRENATAL AND POSTNATAL DIAGNOSIS OF SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY USING ENZYME AND METABOLITE ASSAYS, Journal of inherited metabolic disease, 17(6), 1994, pp. 732-737
Authors:
BRIVET M
SLAMA A
OGIER H
BOUTRON A
DEMAUGRE F
SAUDUBRAY JM
LEMONNIER A
Citation: M. Brivet et al., DIAGNOSIS OF CARNITINE ACYLCARNITINE TRANSLOCASE DEFICIENCY BY COMPLEMENTATION ANALYSIS, Journal of inherited metabolic disease, 17(3), 1994, pp. 271-274
Authors:
VANDERMEER SB
POGGI F
SPADA M
BONNEFONT JP
OGIER H
HUBERT P
DEPONDT E
RAPOPORT D
RABIER D
CHARPENTIER C
PARVY P
BARDET J
KAMOUN P
SAUDUBRAY JM
Citation: Sb. Vandermeer et al., CLINICAL OUTCOME OF LONG-TERM MANAGEMENT OF PATIENTS WITH VITAMIN-B-12-UNRESPONSIVE METHYLMALONIC ACIDEMIA, The Journal of pediatrics, 125(6), 1994, pp. 903-908
Authors:
CORMIERDAIRE V
BONNEFONT JP
RUSTIN P
MAURAGE C
OGIER H
SCHMITZ J
RICOUR C
SAUDUBRAY JM
MUNNICH A
ROTIG A
Citation: V. Cormierdaire et al., MITOCHONDRIAL-DNA REARRANGEMENTS WITH ONSET AS CHRONIC DIARRHEA WITH VILLOUS ATROPHY, The Journal of pediatrics, 124(1), 1994, pp. 63-70
Authors:
LARGILLIERE C
OGIER H
Citation: C. Largilliere et H. Ogier, REYES-SYNDROME - REALITY OR FICTION, Gastroenterologie clinique et biologique, 17(4), 1993, pp. 306-307
Authors:
CHAMBLISS KL
LEE CF
OGIER H
RABIER D
JAKOBS C
GIBSON KM
Citation: Kl. Chambliss et al., ENZYMATIC AND IMMUNOLOGICAL DEMONSTRATION OF NORMAL AND DEFECTIVE SUCCINIC SEMIALDEHYDE DEHYDROGENASE-ACTIVITY IN FETAL BRAIN, LIVER AND KIDNEY, Journal of inherited metabolic disease, 16(3), 1993, pp. 523-526
Authors:
CHENEL C
WOOD C
GOURRIER E
ZITTOUN J
CASADEVALL I
OGIER H
Citation: C. Chenel et al., NEONATAL HEMOLYTIC-UREMIC SYNDROME, METHY LMALONIC ACIDURIA AND HOMOCYSTINURIA DUE TO A CONGENITAL DEFECT IN INTRACELLULAR COBALAMIN METABOLISM, Archives francaises de pediatrie, 50(9), 1993, pp. 749-754
Authors:
CHENEL C
WOOD C
GOURRIER E
ZITTOUN J
CASADEVALL I
OGIER H
Citation: C. Chenel et al., NEONATAL HEMOLYTIC-UREMIC SYNDROME, METHY LMALONIC ACIDURIA AND HOMOCYSTINURIA DUE TO A CONGENITAL DEFECT IN INTRACELLULAR COBALAMIN METABOLISM, Archives francaises de pediatrie, 50(9), 1993, pp. 749-754
Authors:
MORIN C
MITCHELL G
LAROCHELLE J
LAMBERT M
OGIER H
ROBINSON BH
DEBRAEKELEER M
Citation: C. Morin et al., CLINICAL, METABOLIC, AND GENETIC-ASPECTS OF CYTOCHROME-C-OXIDASE DEFICIENCY IN SAGUENAY-LAC-SAINT-JEAN, American journal of human genetics, 53(2), 1993, pp. 488-496
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