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Maintenance treatment of glutaryl-CoA dehydrogenase deficiency

  • Published:2004-11 Issue:6 Volume:27 Page:885-892
  • ISSN:0141-8955
  • Container-title:Journal of Inherited Metabolic Disease
  • language:en
  • Short-container-title:J Inherit Metab Dis

Author:

Mühlhausen C.1,Hoffmann G. F.2,Strauss K. A.3,KÖlker S.2,Okun J. G.2,Greenberg C. R.4,Naughten E. R.5,Ullrich K.1

Affiliation:

1. ; Departments of Paediatrics, Metabolic Service; University Medical Centers; Hamburg Germany

2. Departments of Paediatrics, Metabolic Service; University Medical Centers; Heidelberg Germany

3. ; Clinic for Special Children; Strasburg Pennsylvania USA

4. ; Departments of Biochemistry and Medical Genetics; University of Manitoba; Winnipeg, Manitoba Canada

5. ; Children's Hospital; Dublin Ireland

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. Glutaric aciduria type I: clinical heterogeneity and neuroradiologic features;Amir;Neurology,1987

2. NADH-CoQ reductase deficient myopathy: successful treatment with riboflavin;Arts;Lancet,1983

3. Nuclear magnetic resonance spectroscopy in glutaryl-CoA dehydrogenase deficiency;Bodamer;JInheritMetabDis,2004

4. Treatment of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria);Brandt;JPeiatr,1979

5. On the mechanisms of neuroprotection by creatine and phosphocreatine;Brustovetsky;J Neurochem,2001
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