Effect of high-dose vitamins, coenzyme Q and high-fat diet in paediatric patients with mitochondrial diseases

By Panetta J.   Smith L.   Boneh A.  

Journal of Inherited Metabolic Disease, Vol. 27, Iss. 4, 2004-07 ,pp. : 487-498

Springer Publishing Company

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Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency

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Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I

By Budde S. M. S.   van den Heuvel L. P. W. J.   Smeets R. J. P.   Skladal D.   Mayr J. A.   Boelen C.   Petruzzella V.   Papa S.   Smeitink J. A. M.  

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Glutathione deficiency in patients with mitochondrial disease: Implications for pathogenesis and treatment

By Hargreaves I.   Sheena Y.   Land J.   Heales S.  

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Complex I deficiency in association with structural abnormalities of the diaphragm and brain

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