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Results: 1-25/29
Authors:
TRIOCHE P
LABRUNE P
ODIEVRE M
HEDCHOUEL M
DELEUZE JF
Citation: P. Trioche et al., NOVEL MUTATION (G188R) IN THE G6PASE GENE OF A PATIENT WITH GLYCOGEN-STORAGE-DISEASE TYPE 1A, Human mutation, 1998, pp. 323-324
Authors:
TRIOCHE P
CHALAS J
FRANCOUAL J
CAPEL L
BERNARD O
ODIEVRE M
HADCHOUEL M
LABRUNE P
Citation: P. Trioche et al., APPLICATIONS OF MOLECULAR-BIOLOGY IN GLYCOGEN-STORAGE-DISEASE TYPE 1A, INCLUDING 2 PRENATAL-DIAGNOSIS, European journal of human genetics, 6, 1998, pp. 5019-5019
Authors:
ODIEVRE M
Citation: M. Odievre, ASTHMA-TREATMENT WITH DRUG INHALERS - REP LY, Archives de pediatrie, 5(5), 1998, pp. 580-580
Authors:
ODIEVRE M
GROSDESORMEAUX A
JOUANNAULT S
TISON M
Citation: M. Odievre et al., HEADACHE, AN UNKNOWN RISK FOR INFANTS GIV EN RIBAVIRIN, Archives de pediatrie, 5(3), 1998, pp. 347-347
Authors:
DAVID L
ODIEVRE M
Citation: L. David et M. Odievre, A NEW SECTION - DAILY PEDIATRICS, Archives de pediatrie, 5(1), 1998, pp. 1-2
Authors:
TRIOCHE P
FRANCOUAL J
AUDIBERT F
CHALAS J
LINDENBAUM A
ODIEVRE M
LABRUNE P
Citation: P. Trioche et al., PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE IA BY RESTRICTIONENZYME DIGESTION, Prenatal diagnosis, 18(6), 1998, pp. 629-631
Authors:
ODIEVRE M
DAVID L
Citation: M. Odievre et L. David, VAE SOLI, Archives de pediatrie, 4(10), 1997, pp. 935-936
Authors:
LABRUNE P
TRIOCHE P
DUVALTIER I
CHEVALIER P
ODIEVRE M
Citation: P. Labrune et al., HEPATOCELLULAR ADENOMAS IN GLYCOGEN-STORAGE-DISEASE TYPE-I AND TYPE-III - A SERIES OF 43 PATIENTS AND REVIEW OF THE LITERATURE, Journal of pediatric gastroenterology and nutrition, 24(3), 1997, pp. 276-279
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:
TRIOCHE P
SAMUEL D
ODIEVRE M
LABRUNE P
Citation: P. Trioche et al., ONDANSETRON FOR PRURITUS IN CHILD WITH CHRONIC CHOLESTASIS, European journal of pediatrics, 155(11), 1996, pp. 990-990
Authors:
VANDERVEERE CN
SINAASAPPEL M
MCDONAGH AF
ROSENTHAL P
LABRUNE P
ODIEVRE M
FEVERY J
OTTE JB
MCCLEAN P
BURK G
MASAKOWSKI V
SPERL W
MOWAT AP
VERGANI CM
HELLER K
WILSON JP
SHEPHERD R
JANSEN PLM
Citation: Cn. Vanderveere et al., CURRENT THERAPY FOR CRIGLER-NAJJAR SYNDROME TYPE-1 - REPORT OF A WORLD REGISTRY, Hepatology, 24(2), 1996, pp. 311-315
Authors:
JEHENSON P
DUBOC D
LABRUNE P
FARDEAU M
ODIEVRE M
SYROTA A
Citation: P. Jehenson et al., DIAGNOSTIC-VALUE OF THE EVALUATION OF THE GLYCOGEN-CONTENT IN MUSCLE DISEASES BY CARBON-13 NUCLEAR-MAGNETIC-RESONANCE, Journal de chimie physique et de physico-chimie biologique, 92(10), 1995, pp. 1797-1800
Authors:
HENDRICKX J
COUCKE P
DAMS E
LEE P
ODIEVRE M
CORBEEL L
FERNANDES JF
WILLEMS PJ
Citation: J. Hendrickx et al., MUTATIONS IN THE PHOSPHORYLASE-KINASE GENE PHKA2 ARE RESPONSIBLE FOR X-LINKED LIVER-GLYCOGEN STORAGE DISEASE, Human molecular genetics, 4(1), 1995, pp. 77-83
Authors:
ZEGHOUD F
DELAVEYNE R
REHEL P
CHALAS J
GARABEDIAN M
ODIEVRE M
Citation: F. Zeghoud et al., VITAMIN-D AND PUBERTAL MATURATION - INTER EST AND TOLERANCE OF VITAMIN-D SUPPLEMENTATION DURING THE WINTER, Archives de pediatrie, 2(3), 1995, pp. 221-226
Authors:
DUVALTIER I
SITBON O
DELAVEAUCOUPET J
RAIN B
ODIEVRE M
Citation: I. Duvaltier et al., ACUTE LIPID PNEUMONIA, Archives de pediatrie, 2(1), 1995, pp. 39-42
Authors:
GUIBERT M
CHAHIME H
PETIT J
ODIEVRE M
LABRUNE P
Citation: M. Guibert et al., FAILURE OF CEFOTAXIME TREATMENT IN 2 CHILDREN WITH MENINGITIS CAUSED BY HIGHLY PENICILLIN-RESISTANT STREPTOCOCCUS-PNEUMONIAE, Acta paediatrica, 84(7), 1995, pp. 831-833
Authors:
ODIEVRE M
Citation: M. Odievre, BREAST-FEEDING AND VITAMIN-D SUPPLEMENTAT ION - COMMENTS, Archives de pediatrie, 1(6), 1994, pp. 615-616
Authors:
DOMMERGUES JP
GUBLER MC
HABIB R
HADCHOUEL M
ODIEVRE M
BERNARD O
ALAGILLE D
Citation: Jp. Dommergues et al., CONSTITUTIONAL HEPATORENAL DISEASES - INV OLVEMENT IN ALAGILLES SYNDROME, Archives de pediatrie, 1(4), 1994, pp. 411-413
Authors:
ODIEVRE M
DAVID L
Citation: M. Odievre et L. David, A JOURNAL FOR FRENCH-SPEAKING PEDIATRICIA NS, Archives de pediatrie, 1(1), 1994, pp. 3-4
Authors:
SEDEL D
HUGUET P
LEBBE C
DONADIEU J
ODIEVRE M
LABRUNE P
Citation: D. Sedel et al., SWEET SYNDROME AS THE PRESENTING MANIFESTATION OF CHRONIC GRANULOMATOUS-DISEASE IN AN INFANT, Pediatric dermatology, 11(3), 1994, pp. 237-240
Authors:
LABRUNE P
MYARA A
HADCHOUEL M
RONCHI F
BERNARD O
TRIVIN F
CHOWDHURY NR
CHOWDHURY JR
MUNNICH A
ODIEVRE M
Citation: P. Labrune et al., GENETIC-HETEROGENEITY OF CRIGLER-NAJJAR-SYNDROME TYPE-I - A STUDY OF 14 CASES, Human genetics, 94(6), 1994, pp. 693-697
Authors:
LABRUNE P
BENATTAR C
AMMOURY N
CHALAS J
LINDENBAUM A
ODIEVRE M
Citation: P. Labrune et al., SERUM CONCENTRATIONS OF ALBUMIN, C-REACTIVE PROTEIN, ALPHA(2)-MACROGLOBULIN, PREALBUMIN, FIBRONECTIN, FIBRINOGEN, TRANSFERRIN, AND RETINOL-BINDING PROTEIN IN 55 PATIENTS WITH HEPATIC GLYCOGEN-STORAGE DISEASES, Journal of pediatric gastroenterology and nutrition, 18(1), 1994, pp. 41-44
Authors:
LABRUNE P
MISRAHI M
HADCHOUEL M
BERNARD O
MILGROM E
ODIEVRE M
Citation: P. Labrune et al., MOLECULAR DIAGNOSIS OF PRESYMPTOMATIC WILSONS-DISEASE, Pediatric research, 35(2), 1994, pp. 267-267
Authors:
LABRUNE P
MYARA A
HADCHOUEL M
RONCHI F
BERNARD O
TRIVIN F
MUNNICH A
CHOWDHURY NR
CHOWDHURY JR
ODIEVRE M
Citation: P. Labrune et al., GENETIC-HETEROGENEITY OF CRIGLER-NAJJAR SYNDROME TYPE-I - A STUDY OF 14 CASES, Hepatology, 18(4), 1993, pp. 10000126-10000126
Authors:
LABRUNE P
PONS JC
KHALIL M
MIRLESSE V
IMBERT MC
ODIEVRE M
DAFFOS F
TCHERNIA G
FRYDMAN R
Citation: P. Labrune et al., ANTENATAL THROMBOCYTOPENIA IN 3 PATIENTS WITH TAR (THROMBOCYTOPENIA WITH ABSENT RADII) SYNDROME, Prenatal diagnosis, 13(6), 1993, pp. 463-466