Branched-chain organic acidurias

Seminars in Neonatology

Volumn 7, Issue 1, 2002, Pages 65-74

  Ogier De Baulny, H ^a   Saudubray, J M ^b  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

3 methylcrotonyl glycinuria; Hyperammonaemia; Isovaleric acidaemia; Ketoacidosis; Malonic aciduria; Maple syrup urine disease; Methylmalonic aciduria; Organic acidurias; Propionic acidaemia

Indexed keywords

ACYLCARNITINE; BRANCHED CHAIN AMINO ACID; CARBOXYLIC ACID; ISOLEUCINE; LEUCINE; MALONIC ACID; VALINE;

ACIDURIA; AMINO ACID METABOLISM; ARTICLE; DEHYDRATION; ENZYME SPECIFICITY; HUMAN; HYPERAMMONEMIA; INBORN ERROR OF METABOLISM; KETOACIDOSIS; MAPLE SYRUP URINE DISEASE; PROPIONIC ACIDEMIA; SEPSIS; TANDEM MASS SPECTROMETRY;

EID: 0036304671     PISSN: 10842756     EISSN: None     Source Type: Journal    
DOI: 10.1053/siny.2001.0087     Document Type: Article

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