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Pediatric Neurology
Volume 34, Issue 2
, Pages 127-131
, February 2006
Peripheral Neuropathy in Genetic Mitochondrial Diseases
References
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- A double mutation (A8296G and G8353A) in the mitochondrial DNA tRNALys gene associated with myoclonus epilepsy with ragged-red fibers . Neurology . 1999;52:377–382
- . Ekbom’s syndrome (Lipomas, ataxia, and neuropathy with MEERF) . Muscle Nerve . 1994;17:943–945
- A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNA . Neuromuscul Disord . 2001;11:470–476
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- . Haem oxygenase 1 gene induction by glucose deprivation is mediated by reactive oxygen species via the mitochondrial electron transport chain . Biochem J . 2003;371:877–885
- . Neuropathy associated with mitochondrial disorders . Brain Pathol . 1993;3:177–190
- . Nerve conduction and biopsy correlation in over 100 consecutive patients with suspected polyneuropathy . Muscle Nerve . 1994;17:1010–1020
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Oxidative stress and nitration in neurodegeneration
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PII: S0887-8994(05)00464-9
doi: 10.1016/j.pediatrneurol.2005.08.006
© 2006 Elsevier Inc. All rights reserved.
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Pediatric Neurology
Volume 34, Issue 2
, Pages 127-131
, February 2006
