Pediatrics Medical News about mitochondrial diseases

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Clinical characteristics of patients with non-specific and non-categorized mitochondrial diseases
Acta Pediatrica, 08/04/09

Kim JT et al. – Mitochondrial respiratory chain complex I defect was the most common finding in this study. Though neuromuscular symptoms predominated, with presence of numerous extraneurological findings, authors could not find any novel symptoms that might be unique to this category of mitochondrial disease. But, comparatively, more patients presented with unremarkable birth histories and normal brain MRI findings.

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Protein-misfolding in neurodegenerative disease
The Internet Journal of Neurology, 11/04/09 Relevance Score: 66%

Mitochondrial DNA Damage Is Induced by 7-Ketocholesterol in Human Retinal Pigment Epithelial Cells In Vitro
Investigative Ophthalmology and Visual Science, 11/05/09 Relevance Score: 65%

Cardiomyopathy and Kidney Disease in a Patient with Maternally Inherited Diabetes and Deafness Caused by the 3243A>G Mutation of Mitochondrial DNA
Cardiology, 10/28/09 Relevance Score: 65%

Leigh's Disease Associated With a Dorsal Midbrain Syndrome
Journal of Pediatric Ophthalmology & Strabismus, 10/08/09 Relevance Score: 65%

Cerebral oxygen and glucose metabolism in patients with mitochondrial m.3243A>G mutation
Brain, 11/03/09 Relevance Score: 64%