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Results: 1-10 |
Results: 10
NOVEL MUTATION (G188R) IN THE G6PASE GENE OF A PATIENT WITH GLYCOGEN-STORAGE-DISEASE TYPE 1A
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
PREVALENCE OF THE C282Y MUTATION IN THE HFE GENE IN 47 PATIENTS WITH HEREDITARY HEMOCHROMATOSIS
Authors: CHALAS J FRANCOUAL J CAPEL L GROOTENBOER S TRIOCHE P LINDENBAUM A LABRUNE P
Citation: J. Chalas et al., PREVALENCE OF THE C282Y MUTATION IN THE HFE GENE IN 47 PATIENTS WITH HEREDITARY HEMOCHROMATOSIS, European journal of human genetics, 6, 1998, pp. 5018-5018
APPLICATIONS OF MOLECULAR-BIOLOGY IN GLYCOGEN-STORAGE-DISEASE TYPE 1A, INCLUDING 2 PRENATAL-DIAGNOSIS
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
GILBERTS-DISEASE IN 1998
Authors: LABRUNE P TRIOCHE P
Citation: P. Labrune et P. Trioche, GILBERTS-DISEASE IN 1998, Archives de pediatrie, 5(7), 1998, pp. 719-721
PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE IA BY RESTRICTIONENZYME DIGESTION
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
PROLONGED NEONATAL JAUNDICE DUE TO UNCONJ UGATED BILIRUBIN
Authors: LABRUNE P TRIOCHE P
Citation: P. Labrune et P. Trioche, PROLONGED NEONATAL JAUNDICE DUE TO UNCONJ UGATED BILIRUBIN, Annales de pediatrie, 45(6), 1998, pp. 440-444
HEPATOCELLULAR ADENOMAS IN GLYCOGEN-STORAGE-DISEASE TYPE-I AND TYPE-III - A SERIES OF 43 PATIENTS AND REVIEW OF THE LITERATURE
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
MOYAMOYA DISEASE IN A CHILD WITH GLYCOGEN-STORAGE-DISEASE TYPE IA
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
SEVERE BRAIN AND LIMB DEFECTS WITH POSSIBLE AUTOSOMAL RECESSIVE INHERITANCE - A SERIES OF 6 CASES AND REVIEW OF THE LITERATURE
Authors: LABRUNE P TRIOCHE P FALLETBIANCO C ROUME J NARCY F LEMERRER M
Citation: P. Labrune et al., SEVERE BRAIN AND LIMB DEFECTS WITH POSSIBLE AUTOSOMAL RECESSIVE INHERITANCE - A SERIES OF 6 CASES AND REVIEW OF THE LITERATURE, American journal of medical genetics, 73(2), 1997, pp. 144-149
ONDANSETRON FOR PRURITUS IN CHILD WITH CHRONIC CHOLESTASIS
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
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