Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain Acyl-CoA dehydrogenase deficiency

Pediatric Research

Volumn 67, Issue 3, 2010, Pages 304-308

  Van Maldegem, Bianca T ^a   Duran, Marinus ^b   Wanders, Ronald J A ^b   Waterham, Hans R ^b   Wijburg, Frits A ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BUTYRYL COENZYME A DEHYDROGENASE; FLAVINE ADENINE NUCLEOTIDE; RIBOFLAVIN;

ADOLESCENT; ARTICLE; BUTYRYL COENZYME A DEHYDROGENASE DEFICIENCY; CHILD; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED STUDY; DRUG EFFICACY; DRUG MEGADOSE; ENZYME DEFICIENCY; FEMALE; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; MALE; OPEN STUDY; PRIORITY JOURNAL; TREATMENT OUTCOME;

ADOLESCENT; BIOLOGICAL MARKERS; BUTYRYL-COA DEHYDROGENASE; CARNITINE; CHILD; CHILD, PRESCHOOL; FEMALE; FLAVIN-ADENINE DINUCLEOTIDE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFANT; LIPID METABOLISM, INBORN ERRORS; MALE; MALONATES; MUTATION; PHENOTYPE; PROSPECTIVE STUDIES; RIBOFLAVIN; TREATMENT OUTCOME; VITAMIN B COMPLEX;

EID: 76749083355     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1203/PDR.0b013e3181cbd57b     Document Type: Article

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