REFERENCES
- Leonard JV, Schapira AHV. Mitochondrial respiratory chain
disorders I: mitochondrial DNA defects. Lancet 2000;
355:299-304.
- Leonard JV, Schapira AHV. Mitochondrial respiratory chain
disorders II: neurodegenerative disorders and nuclear gene
defects. Lancet 2000; 355:389-94.
- Shoffner JM. Oxidative phosphorylation disease diagnosis.
Ann NY Acad Sci 1999; 893:42-60.
- Shoffner JM. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds.
The metabolic and molecular basis of inherited disease.
Oxidative phosphorylation diseases. McGraw-Hill, Inc. 2001
pp 2367-2423.
- de Lonlay-Debeney P, von Kleist-Retzow JC, Hertz-Pannier L, et al.
Cerebral white matter disease in children may be caused by
mitochondrial respiratory chain deficiency:
J Pediatr 2000;136(2):209-214.
- de Konig TJ, de Vries LS, Groenendaal F, et al.
Pontocerebellar hypoplasia associated with respiratory-chain
defects:.
Neuropediatrics 1999;30:93-95.
- Argov Z, Arnold DL.
MR spectroscopy and imaging in metabolic myopathies.
Neurol Clin 2000;18(1):35-52.
- Wang ZJ, Zimmerman RA.
Proton MR spectroscopy of pediatric brain metabolic disorders
Neuroimaging Clin N Am 1998;8(4):781-807.
- Munoz A, Mateos F, Simon R, et al.
Mitochondrial disease in children: neuroradiological and
clinical features in 17 patients.
Neuroradiology 1999;41(12):820-828
- Valanne L, Ketonen L, Majander A, et al.
Neuroradiologic findings in children with mitochondrial
disorders.
American Journal of Neuroradiology 1998;19(2):369-77
- Barkovich AJ, Good WV, Koch LTK, et al.
Mitochondrial disorders: analysis of their clinical and imaging
characteristics
American Journal of Neuroradiology 1993;14(5):1119-37.
- Smeitink JAM, Sengers RCA, Trijbels FJM, et al.
Nuclear genes and oxidative phosphorylation disorders: a review.
Eur J Pediatr 2000;159:S227-S231.
Acknowledgement
Dave Moyer for the set up of the database and Rob Merritt for the
statistical analysis.
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