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Research Database: Myopathy
Research Database
(McNab 2005) Acromegaly as an endocrine form of myopathy
(Baysal 2001) Phenotypic dichotomy in mitochondrial complex II genetic disorders
(Vergani 1999) Riboflavin therapy and biochemical heterogeneity in two adult lipid storage myopathies
(Bernsen 1993) Treatment of complex I deficiency with riboflavin
(Campos 1993) Muscle carnitine deficiency and lipid storage myopathy in mitochondrial myopathy
(Ghirlanda 1993) Evidence of plasma CoQ10-lowering effect by HMG-CoA reductase inhibitors
(Campos 1993) Carnitine insufficiency and L-carnitine therapy in mitochondrial myopathy
(Bach 1992) Myalgia and elevated CK associated with subcutaneous injections of diluent
(Korenke 1990) Isolated and combined complex I deficiencies in muscle of children with mitochondrial myopathies
(DiMauro 1987) Mitochondrial myopathies
(Di Donato 1986) Systemic carnitine deficiency due to lack of electron transfer flavoprotein:ubiquinone oxidoreductase
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