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Results: 1-11 |
Results: 11
LONG-TERM TREATMENT OF PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY WITH DIAZOXIDE - A RETROSPECTIVE REVIEW OF 77 CASES AND ANALYSISOF EFFICACY-PREDICTING CRITERIA
Authors: TOUATI G POGGITRAVERT F DEBAULNY HO RAHIER J BRUNELLE F NIHOULFEKETE C CZERNICHOW P SAUDUBRAY JM
Citation: G. Touati et al., LONG-TERM TREATMENT OF PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY WITH DIAZOXIDE - A RETROSPECTIVE REVIEW OF 77 CASES AND ANALYSISOF EFFICACY-PREDICTING CRITERIA, European journal of pediatrics, 157(8), 1998, pp. 628-633
REMETHYLATION DEFECTS - GUIDELINES FOR CLINICAL-DIAGNOSIS AND TREATMENT
Authors: DEBAULNY HO GERARD M SAUDUBRAY JM ZITTOUN J
Citation: Ho. Debaulny et al., REMETHYLATION DEFECTS - GUIDELINES FOR CLINICAL-DIAGNOSIS AND TREATMENT, European journal of pediatrics, 157, 1998, pp. 77-83
IN-VIVO FUNCTIONAL INVESTIGATIONS OF LACTIC-ACID IN PATIENTS WITH RESPIRATORY-CHAIN DISORDERS
Authors: TOUATI G RIGAL O LOMBES A FRACHON P GIRAUD M DEBAULNY HO
Citation: G. Touati et al., IN-VIVO FUNCTIONAL INVESTIGATIONS OF LACTIC-ACID IN PATIENTS WITH RESPIRATORY-CHAIN DISORDERS, Archives of Disease in Childhood, 76(1), 1997, pp. 16-21
LYSINURIC PROTEIN INTOLERANCE WITH CHARAC TERISTIC BONE-MARROW ABNORMALITIES
Authors: DOIREAU V FENNETEAU O DUVAL M PERELMAN S VILMER E TOUATI G SCHLEGEL N DEBAULNY HO
Citation: V. Doireau et al., LYSINURIC PROTEIN INTOLERANCE WITH CHARAC TERISTIC BONE-MARROW ABNORMALITIES, Archives de pediatrie, 3(9), 1996, pp. 877-880
PREGNANCY AND INFANT OF MOTHER WITH HYPER PHENYLALANINEMIA
Authors: ABADIE V DEPONDT E FARRIAUX JP LEPERCQ J LYONNET S MAURIN N DEBAULNY HO VIDAILHET M
Citation: V. Abadie et al., PREGNANCY AND INFANT OF MOTHER WITH HYPER PHENYLALANINEMIA, Archives de pediatrie, 3(5), 1996, pp. 489-496
MORPHOLOGICAL-STUDIES OF SKELETAL-MUSCLE IN LACTIC-ACIDOSIS
Authors: ROMERO NB LOMBES A TOUATI G RIGAL O FRACHON P CHEVAL MA GIRAUD M POSSEKEL S FARDEAU M DEBAULNY HO
Citation: Nb. Romero et al., MORPHOLOGICAL-STUDIES OF SKELETAL-MUSCLE IN LACTIC-ACIDOSIS, Journal of inherited metabolic disease, 19(4), 1996, pp. 528-534
CLINICAL AND MOLECULAR HETEROGENEITY OF CYTOCHROME-C-OXIDASE DEFICIENCY IN THE NEWBORN
Authors: LOMBES A ROMERO NB TOUATI G FRACHON P CHEVAL MA GIRAUD M SIMON D DEBAULNY HO
Citation: A. Lombes et al., CLINICAL AND MOLECULAR HETEROGENEITY OF CYTOCHROME-C-OXIDASE DEFICIENCY IN THE NEWBORN, Journal of inherited metabolic disease, 19(3), 1996, pp. 286-295
IMMUNOHISTOCHEMICAL ANALYSIS OF MUSCLE CYTOCHROME-C-OXIDASE DEFICIENCY IN CHILDREN
Authors: POSSEKEL S LOMBES A DEBAULNY HO CHEVAL MA FARDEAU M KADENBACH B ROMERO NB
Citation: S. Possekel et al., IMMUNOHISTOCHEMICAL ANALYSIS OF MUSCLE CYTOCHROME-C-OXIDASE DEFICIENCY IN CHILDREN, HISTOCHEM C, 103(1), 1995, pp. 59-68
ATYPICAL HEMOLYTIC-UREMIC SYNDROME DUE TO AN INTRACELLULAR ABNORMALITY IN VITAMIN-B12 METABOLISM
Authors: LOIRAT C DEBAULNY HO BAUDOUIN V PEUCHMAUR M
Citation: C. Loirat et al., ATYPICAL HEMOLYTIC-UREMIC SYNDROME DUE TO AN INTRACELLULAR ABNORMALITY IN VITAMIN-B12 METABOLISM, Annales de pediatrie, 42(10), 1995, pp. 625-634
NEONATAL HYPERAMMONEMIA CAUSED BY A DEFECT OF CARNITINE-ACYLCARNITINETRANSLOCASE
Authors: DEBAULNY HO SLAMA A TOUATI G TURNBULL DM POURFARZAM M BRIVET M
Citation: Ho. Debaulny et al., NEONATAL HYPERAMMONEMIA CAUSED BY A DEFECT OF CARNITINE-ACYLCARNITINETRANSLOCASE, The Journal of pediatrics, 127(5), 1995, pp. 723-728
INTERMITTENT SUBACUTE HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS WITH CHRONICHEMOLYSIS IS A CONSTANT AND CHARACTERISTIC FEATURE OF LYSINURIC
Authors: DUVAL M FENNETEAU O DOIREAU V ROHRLICH P YOTNDA P DRAPIER JC EMILIE D STERKERS G SCHLEGEL N DEBAULNY HO VILMER E
Citation: M. Duval et al., INTERMITTENT SUBACUTE HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS WITH CHRONICHEMOLYSIS IS A CONSTANT AND CHARACTERISTIC FEATURE OF LYSINURIC, Blood, 86(10), 1995, pp. 1999-1999
Risultati: 1-11 |