Systematic evaluation of muscle coenzyme Q10 content in children with mitochondrial respiratory chain enzyme deficiencies-Reference-Cited by-同舟云学术

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Systematic evaluation of muscle coenzyme Q10 content in children with mitochondrial respiratory chain enzyme deficiencies

Published:2008-03 Issue:2 Volume:8 Page:170-180
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Miles Michael V.,Miles Lili,Tang Peter H.,Horn Paul S.,Steele Paul E.,DeGrauw Antonius J.,Wong Brenda L.,Bove Kevin E.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference66 articles.

1. Cerebellar ataxia with coenzyme Q10 deficiency: diagnosis and follow-up after coenzyme Q10 supplementation;Artuch;J. Neurol. Sci.,2006

2. Progression despite replacement of a myopathic form of coenzyme Q10 defect;Aure;Neurology,2004

3. Severe depletion of mitochondrial DNA in spinal muscular atrophy;Berger;Acta Neuropathol. (Berl.),2003

4. Diagnostic criteria for respiratory chain disorders in adults and children;Bernier;Neurology,2002

5. A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency;Boitier;J. Neurol. Sci.,1998

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