Nuclear magnetic resonance spectroscopy in glutaryl-CoA dehydrogenase deficiency

Journal of Inherited Metabolic Disease

Volumn 27, Issue 6, 2004, Pages 877-883

  Bodamer, Olaf A ^a   Gruber, S ^b   Stockler Ipsiroglu S ^a  

^a ST ANNA CHILDREN S HOSPITAL   (Austria)

^b UNIVERSITY OF VIENNA   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL COMPOUND; CHOLINE; CREATINE PHOSPHATE; CREATININE; GLUCOSE; GLUTARYL COENZYME A DEHYDROGENASE; LACTIC ACID; MYELIN; N ACETYLASPARTIC ACID; NEUROTRANSMITTER;

ADOLESCENT; ARTICLE; BASAL GANGLION; BRAIN LEVEL; BRAIN REGION; CASE REPORT; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; ENZYME DEFICIENCY; GLUCOSE METABOLISM; HUMAN; IN VIVO STUDY; MALE; NEUROLOGIC DISEASE; NON INVASIVE MEASUREMENT; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PATHOPHYSIOLOGY; QUANTITATIVE ANALYSIS; SAFETY; WHITE MATTER;

ADOLESCENT; AMINO ACID METABOLISM, INBORN ERRORS; ASPARTIC ACID; BRAIN CHEMISTRY; CHOLINE; DNA; DNA MUTATIONAL ANALYSIS; GLUTARYL-COA DEHYDROGENASE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; OXIDOREDUCTASES ACTING ON CH-CH GROUP DONORS;

EID: 7244234275     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:BOLI.0000045772.09776.e0     Document Type: Article

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