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Authors: ROLLAND MO GUFFON N MANDON G DIVRY P
Citation: Mo. Rolland et al., SUCCINYL-COA - ACETOACETATE TRANSFERASE DEFICIENCY - IDENTIFICATION OF A NEW CASE - PRENATAL EXCLUSION IN 3 FURTHER PREGNANCIES, Journal of inherited metabolic disease, 21(6), 1998, pp. 687-688

Authors: FONTAINE M BRIAND G LARGILLIERE C DEGAND P DIVRY P VIANEYSABAN C MOUSSON B VAMECQ J
Citation: M. Fontaine et al., METABOLIC STUDIES IN A PATIENT WITH SEVERE CARNITINE PALMITOYLTRANSFERASE TYPE-II DEFICIENCY, Clinica chimica acta, 273(2), 1998, pp. 161-170

Authors: VIANEYSABAN C DIVRY P BRIVET M NADA M ZABOT MT MATHIEU M ROE C
Citation: C. Vianeysaban et al., MITOCHONDRIAL VERY-LONG-CHAIN ACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY - CLINICAL CHARACTERISTICS AND DIAGNOSTIC CONSIDERATIONS IN 30 PATIENTS, Clinica chimica acta, 269(1), 1998, pp. 43-62

Authors: ZAPATER N PIE J LLOBERAS J ROLLAND MO LEROUX B VIDAILHET M DIVRY P HEGARDT FG CASALS N
Citation: N. Zapater et al., 2 MISSENSE POINT MUTATIONS IN DIFFERENT ALLELES IN THE 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A LYASE GENE PRODUCE 3-HYDROXY-3-METHYLGLUTARIC ACIDURIA IN A FRENCH PATIENT, Archives of biochemistry and biophysics (Print), 358(2), 1998, pp. 197-203

Authors: DELOLME F VIANEYSABAN C GUFFON N FAVREBONVIN J GUIBAUD P BECCHI M MATHIEU M DIVRY P
Citation: F. Delolme et al., DIAGNOSIS OF INBORN-ERRORS OF METABOLISM BY ACYLCARNITINES PROFILING IN BLOOD USING TANDEM MASS-SPECTROMETRY, Archives de pediatrie, 4(9), 1997, pp. 819-826

Authors: PIE J CASALS N CASALE CH BUESA C MASCARO C BARCELO A ROLLAND MO ZABOT T HARO D EYSKENS F DIVRY P HEGARDT FG
Citation: J. Pie et al., A NONSENSE MUTATION IN THE 3-HYDROXY-3-METHYLGLUTARYL-COA LYASE GENE PRODUCES EXON SKIPPING IN 2 PATIENTS OF DIFFERENT ORIGIN WITH 3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY, Biochemical journal, 323, 1997, pp. 329-335

Authors: VIANEYSABAN C GUFFON N DELOLNE F GUIBAUD P MATHIEU M DIVRY P
Citation: C. Vianeysaban et al., DIAGNOSIS OF INBORN-ERRORS OF METABOLISM BY ACYLCARNITINE PROFILING IN BLOOD USING TANDEM MASS-SPECTROMETRY, Journal of inherited metabolic disease, 20(3), 1997, pp. 411-414

Authors: MARTINEZ G JIMENEZSANCHEZ G DIVRY P VIANEYSABAN C RIUDOR E RODES M BRIONES P RIBES A
Citation: G. Martinez et al., PLASMA-FREE FATTY-ACIDS IN MITOCHONDRIAL FATTY-ACID OXIDATION DEFECTS, Clinica chimica acta, 267(2), 1997, pp. 143-154

Authors: ANDRESEN BS BROSS P VIANEYSABAN C DIVRY P ZABOT MT ROE CR NADA MA BYSKOV A KRUSE TA NEVE S KRISTIANSEN K KNUDSEN I CORYDON MJ GREGERSON N
Citation: Bs. Andresen et al., CLONING AND CHARACTERIZATION OF HUMAN VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE CDNA, CHROMOSOMAL ASSIGNMENT OF THE GENE AND IDENTIFICATION IN4 PATIENTS OF 9 DIFFERENT MUTATIONS WITHIN THE VLCAD GENE (VOL 5, PG 461, 1996), Human molecular genetics, 5(9), 1996, pp. 1390-1390

Authors: ANDRESEN BS BROSS P VIANEYSABAN C DIVRY P ZABOT MT ROE CR NADA MA BYSKOV A KRUSE TA NEVE S KRISTIANSEN K KNUDSEN I CORYDON MJ GREGERSEN N
Citation: Bs. Andresen et al., CLONING AND CHARACTERIZATION OF HUMAN VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE CDNA, CHROMOSOMAL ASSIGNMENT OF THE GENE AND IDENTIFICATION IN4 PATIENTS OF 9 DIFFERENT MUTATIONS WITHIN THE VLCAD GENE, Human molecular genetics, 5(4), 1996, pp. 461-472

Authors: PARNET JM DIVRY P VIANEYSABAN C MATHIEU M
Citation: Jm. Parnet et al., STABLE-ISOTOPE SELECTED-ION MONITORING QUANTIFICATION OF METHYLMALONIC ACID IN DRIED FILTER-PAPER URINE SAMPLES, Journal of inherited metabolic disease, 19(5), 1996, pp. 635-637

Authors: MARTINS E COSTA A SILVA E MEDINA M CARDOSO ML VIANEYSABAN C DIVRY P VILARINHO L
Citation: E. Martins et al., LETHAL DILATED CARDIOMYOPATHY DUE TO LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY, Journal of inherited metabolic disease, 19(3), 1996, pp. 373-374

Authors: ANDRESEN BS VIANEYSABAN C BROSS P DIVRY P ROE CR NADA MA KNUDSEN I GREGERSEN N
Citation: Bs. Andresen et al., THE MUTATIONAL SPECTRUM IN VERY LONG-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY, Journal of inherited metabolic disease, 19(2), 1996, pp. 169-172

Authors: FONTAINE M BRIAND G VALLEE L RICART G DEGAND P DIVRY P VIANEYSABAN C VAMECQ J
Citation: M. Fontaine et al., ACYLCARNITINE REMOVAL IN A PATIENT WITH ACYL-COA BETA-OXIDATION DEFICIENCY DISORDER - EFFECT UF L-CARNITINE THERAPY AND STARVATION, Clinica chimica acta, 252(2), 1996, pp. 109-122

Authors: TOURAINE RL ROLLAND MO DIVRY P MATHIEU M GUIBAUD P BOZON D
Citation: Rl. Touraine et al., A 13-BP DELETION (1952 DEL-13) IN THE METHYLMALONYL COA MUTASE GENE OF AN AFFECTED PATIENT, Human mutation, 5(4), 1995, pp. 354-356

Authors: VIANEYSABAN C STREMLER N PAUT O BUTTIN T DIVRY P ZABOT MT CAMBOULIVES J MATHIEU M MOUSSON B
Citation: C. Vianeysaban et al., INFANTILE FORM OF CARNITINE PALMITOYLTRANSFERASE-II DEFICIENCY IN A GIRL WITH RAPID FATAL ONSET, Journal of inherited metabolic disease, 18(3), 1995, pp. 362-363

Authors: COCHAT P BOZON D ROLLAND MO DUMONTEL C LEPOUTRE I SCHELL M DIVRY P
Citation: P. Cochat et al., MOLECULAR ABNORMALITIES IN TYPE-I PRIMARY HYPEROXALURIA, Annales de pediatrie, 42(10), 1995, pp. 596-602

Authors: VALLEE L FONTAINE M NUYTS JP RICART G KRIVOSIC I DIVRY P VIANEYSABAN C LHERMITTE M VAMECQ J
Citation: L. Vallee et al., STROKE, HEMIPARESIS AND DEFICIENT MITOCHONDRIAL BETA-OXIDATION, European journal of pediatrics, 153(8), 1994, pp. 598-603

Authors: COCHAT P ROLLAND MO BOZON D DUMONTEL C DIVRY P
Citation: P. Cochat et al., MOLECULAR PATHOLOGY OF PRIMARY HYPEROXALU RIA TYPE-1, Nephrologie, 15(6), 1994, pp. 375-380

Authors: CHADEFAUXVEKEMANS B ROLLAND MO LYONNET S RABIER D DIVRY P KAMOUN P
Citation: B. Chadefauxvekemans et al., PRENATAL-DIAGNOSIS OF COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA (COBALAMIN CBLC OR CBLD MUTANT), Prenatal diagnosis, 14(5), 1994, pp. 417-418

Authors: MANCINI J PHILIP N CHABROL B DIVRY P ROLLAND MO PINSARD N
Citation: J. Mancini et al., MEVALONIC ACIDURIA IN 3 SIBLINGS - A NEW RECOGNIZABLE METABOLIC ENCEPHALOPATHY, Pediatric neurology, 9(3), 1993, pp. 243-246

Authors: GUFFON N LOPEZMEDIAVILLA C DUMOULIN R MOUSSON B GODINOT C CARRIER H COLLOMBET JM DIVRY P MATHIEU M GUIBAUD P
Citation: N. Guffon et al., 2-KETOGLUTARATE DEHYDROGENASE-DEFICIENCY, A RARE CAUSE OF PRIMARY HYPERLACTATEMIA - REPORT OF A NEW CASE, Journal of inherited metabolic disease, 16(5), 1993, pp. 821-830

Authors: BENNETT MJ GIBSON KM SHERWOOD WG DIVRY P ROLLAND MO ELPELEG ON RINALDO P JAKOBS C
Citation: Mj. Bennett et al., RELIABLE PRENATAL-DIAGNOSIS OF CANAVAN DISEASE (ASPARTOACYLASE DEFICIENCY) - COMPARISON OF ENZYMATIC AND METABOLITE ANALYSIS, Journal of inherited metabolic disease, 16(5), 1993, pp. 831-836

Authors: DIVRY P JAKOBS C VIANEYSABAN C GIBSON KM MICHELAKAKIS H PAPADIMITRIOU A DIVARI R CHABROL B COURNELLE MA LIVET MO
Citation: P. Divry et al., L-2-HYDROXYGLUTARIC ACIDURIA - 2 FURTHER CASES, Journal of inherited metabolic disease, 16(3), 1993, pp. 505-507

Authors: ROLLAND MO DIVRY P MANDON G THOULON JM FIUMARA A MATHIEU M
Citation: Mo. Rolland et al., 1ST-TRIMESTER PRENATAL-DIAGNOSIS OF CANAVAN DISEASE, Journal of inherited metabolic disease, 16(3), 1993, pp. 581-583
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