Pediatric Mitochondrial Disease: Do We Have the Energy to Make the Diagnosis?
Author:
Affiliation:
1. Departments of Laboratory Medicine and Pathology, University of Washington School of Medicine and Children's Hospital and Regional Medical Center, 4800 Sand Point Way NE, Seattle, WA 98105, USA
Publisher
SAGE Publications
Subject
General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health
Link
http://journals.sagepub.com/doi/pdf/10.1007/s10024-004-5049-y
Reference19 articles.
1. Mitochondrial oxidative phosphorylation system assembly in man: recent achievements
2. Mitochondrial DNA mutations in human disease
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4. Diagnostic criteria for respiratory chain disorders in adults and children
5. Epidemiology and treatment of mitochondrial disorders
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1. Systematic evaluation of muscle coenzyme Q10 content in children with mitochondrial respiratory chain enzyme deficiencies;Mitochondrion;2008-03
2. Focal Segmental Glomerulosclerosis Associated with Mitochondrial Cytopathy: Report of Two Cases with Special Emphasis on Podocytes;Pediatric and Developmental Pathology;2005-11
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