Biochemical and clinical characteristics of creatine deficiency syndromes

Acta Biochimica Polonica

Volumn 51, Issue 4, 2004, Pages 875-882

  Sykut Cegielska, Jolanta ^a   Gradowska, Wanda ^a   Mercimek Mahmutoglu, Saadet ^b   Stöckler Ipsiroglu, Sylvia ^b,c  

^a CHILDREN'S MEMORIAL HEALTH INSTITUTE   (Poland)

^b UNIVERSITY HOSPITAL INNSBRUCK   (Austria)

^c UNIVERSITY OF VIENNA   (Austria)

Author keywords

Creatine deficiency; Creatine monohydrate; Guanidinoacetate

Indexed keywords

CREATINE; GLYCINE AMIDINOTRANSFERASE; GUANIDINOACETIC ACID; ORNITHINE;

ARGININE GLYCINE AMIDINOTRANSFERASE DEFICIENCY; BODY FLUID; CLINICAL FEATURE; CONCENTRATION (PARAMETERS); CREATINE DEFICIENCY SYNDROME; CREATININE TRANSPORTER DEFICIENCY; CREATININE URINE LEVEL; DIAGNOSTIC PROCEDURE; DIET SUPPLEMENTATION; ENZYMATIC ASSAY; EPILEPSY; GRAY MATTER; GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY; HUMAN; IN VIVO STUDY; INBORN ERROR OF METABOLISM; MEASUREMENT; MENTAL DEFICIENCY; MOLECULAR DYNAMICS; PROTON NUCLEAR MAGNETIC RESONANCE; REVIEW; SEIZURE; SIDE EFFECT; SPEECH DEVELOPMENT;

AMIDINOTRANSFERASES; AMINO ACID METABOLISM, INBORN ERRORS; CREATINE; GUANIDINOACETATE N-METHYLTRANSFERASE; HUMANS; MEMBRANE TRANSPORT PROTEINS; METHYLTRANSFERASES;

EID: 13244259284     PISSN: 0001527X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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