URGENCES NEONATALES EN RAPPORT AVEC UNE MALADIE HEREDITAIRE DU METABOLISME DES ACIDES AMINES ET DES HYDRATES DE CARBONESAUDUBRAY JM; CHARPENTIER C; COUDE FX et al.1978; REV. PEDIATR.; FRA; DA. 1978; VOL. 14; NO 10; PP. 611-619; ABS. ENGArticle

EFFECT OF PROPIONATE AND PYRUVATE ON CITRULLINE SYNTHESIS AND ATP CONTENT IN RAT LIVER MITOCHONDRIACATHELINEAU L; PETIT FP; COUDE FX et al.1979; BIOCHEM. BIOPHYS. RES. COMMUNIC.; USA; DA. 1979; VOL. 90; NO 1; PP. 327-332; BIBL. 19 REF.Article

N-ACETYL GLUTAMATE SYNTHETASE IN HUMAN LIVER: REGULATION OF ACTIVITY BY L-ARGININE AND N-ACETYLGLUTAMATECOUDE FX; GRIMBER G; PARVY P et al.1981; BIOCHEM. BIOPHYS. RES. COMMUN.; ISSN 0006-291X; USA; DA. 1981; VOL. 102; NO 3; PP. 1016-1020; BIBL. 10 REF.Article

CORRELATION BETWEEN BLOOD AMMONIA CONCENTRATION AND ORGANIC ACID ACCUMULATION IN ISOVALERIC AND PROPIONIC ACIDEMIACOUDE FX; OGIER H; GRIMBER G et al.1982; PEDIATRICS (EVANSTON); ISSN 0031-4005; USA; DA. 1982; VOL. 69; NO 1; PP. 115-117; BIBL. 10 REF.Article

OXIDATION OF FATTY ACIDS IN CULTURED FIBROBLASTS: A MODEL SYSTEM FOR THE DETECTION AND STUDY OF DEFECTS IN OXIDATIONSAUDUBRAY JM; COUDE FX; DEMAUGRE F et al.1982; PEDIATRIC RESEARCH; ISSN 0031-3998; USA; DA. 1982; VOL. 16; NO 10; PP. 877-881; BIBL. 37 REF.Article

L'INTOLERANCE AUX PROTEINES AVEC LYSINURIE: UNE HYPERAMMONIEMIE SEVERE PAR CARENCE EN L-ARGININECOUDE FX; OGIER H; CHARPENTIER C et al.1981; ARCH. FR. PEDIATR.; ISSN 0003-9764; FRA; DA. 1981; VOL. 38; SUPPL. NO 1; PP. 829-835; ABS. ENG; BIBL. 46 REF.Article

DEVELOPMENTAL CHANGES OF CITRULLINOGENESIS, MITOCHONDRIAL N-ACETYLGLUTAMATE CONTENT AND N-ACETYLGLUTAMATE SYNTHETASE IN FETAL AND NEONATAL RATSRABIER D; BRIAND P; COUDE FX et al.1983; BIOCHIMIE; ISSN 0300-9084; FRA; DA. 1983; VOL. 65; NO 1; PP. 1-6; ABS. FRE; BIBL. 39 REF.Article

DEFECTIVE INSULIN RESPONSE TO INTRAVENOUS GLUCOSE IN CONGENITAL LACTIC ACIDOSISCOUDE FX; OGIER H; MUNNICH A et al.1981; PEDIATR. RES.; ISSN 0031-3998; USA; DA. 1981; VOL. 16; NO 1; PP. 85; BIBL. 7 REF.Article

VARIATION IN PLASMA KETONE BODIES DURING A 24-HOUR FAST IN NORMAL AND IN HYPOGLYCEMIC CHILDREN: RELATIONSHIP TO AGESAUDUBRAY JM; MARSAC C; LIMAL JM et al.1981; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1981; VOL. 98; NO 6; PP. 904-908; BIBL. 20 REF.Article

AMINO ACID PROFILE IN PYRUVATE CARBOXYLASE DEFICIENCY: COMPARISON WITH SOME OTHER METABOLIC DISORDERSCHARPENTIER C; TETAU JM; OGIER H et al.1982; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; SUPPL. 1; PP. 11-12; BIBL. 4 REF.Article

OCCURRENCE OF HYPERAMMONEMIA IN THE COURSE OF 17 CASES OF METHYLMALONIC ACIDEMIACATHELINEAU L; BRIAND P; OGIER H et al.1981; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1981; VOL. 99; NO 2; PP. 279-280; BIBL. 10 REF.Article

BIOTIN-RESPONSIVE IMMUNOREGULATORY DYSFUNCTION IN MULTIPLE CARBOXYLASE DEFICIENCYFISCHER A; MUNNICH A; SAUDUBRAY JM et al.1982; J. CLIN. IMMUNOL.; ISSN 503894; USA; DA. 1982; VOL. 2; NO 1; PP. 35-38; BIBL. 10 REF.Article

TRAITEMENT D'URGENCE DES AMINOACIDOPATHIES A REVELATION NEONATALESAUDUBRAY JM; AMEDEE MANESME O; LAVAUD J et al.1979; ARCH. FR. PEDIATR.; FRA; DA. 1979; VOL. 36; NO 10; PP. 969-980; ABS. ENG; BIBL. 26 REF.Article

CONGENITAL LACTIC ACIDOSIS ALPHA -KETOGLUTARIC ACIDURIA AND VARIANT FORM OF MAPLE SYRUP URINE DISEASE DUE TO A SINGLE ENZYME DEFECT: DIHYDROLIPOYL DEHYDROGENASE DEFICIENCYMUNNICH A; SAUDUBRAY JM; TAYLOR J et al.1982; ACTA PAEDIATR. SCAND.; ISSN 0001-656X; SWE; DA. 1982; VOL. 71; NO 1; PP. 167-171; BIBL. 12 REF.Article