Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism

Journal of Inherited Metabolic Disease

Volumn 26, Issue 2-3, 2003, Pages 299-308

  Stromberger, C ^a,b   Bodamer, O A ^a   Stockler Ipsiroglu S ^a  

^a UNIVERSITY OF VIENNA   (Austria)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR BLOCKING AGENT; ANTICONVULSIVE AGENT; CREATINE; GLYCINE AMIDINOTRANSFERASE; GUANIDINOACETIC ACID; METHYLTRANSFERASE; ORNITHINE;

ARTICLE; BIOCHEMISTRY; BODY FLUID; BRAIN CORTEX LESION; CLINICAL FEATURE; CONCENTRATION (PARAMETERS); CREATINE DEFICIENCY SYNDROME; DIAGNOSTIC TEST; DIET SUPPLEMENTATION; DRUG EFFICACY; DYSTONIA; ENZYME DEFICIENCY; EPILEPSY; GRAY MATTER; HUMAN; HYPERKINESIA; IN VIVO STUDY; INBORN ERROR OF METABOLISM; MENTAL DEFICIENCY; MOTOR DYSFUNCTION; NONHUMAN; PHENOTYPE; PHENOTYPIC VARIATION; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 0038497516     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1024453704800     Document Type: Article

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