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searching for Metabolic myopathy 10 found (36 total)

ENO3 (1,215 words) [view diff] exact match in snippet view article find links to article

deficiency (glycogen storage disease type XIII) is a rare inherited metabolic myopathy caused by a defect in the enzyme's active site, thus disrupting its

Aldolase A deficiency (1,616 words) [view diff] case mismatch in snippet view article find links to article

Schachenmayr W, Schiegel K, Lampert F (1996). "Brief Report: Inherited Metabolic Myopathy and Hemolysis Due to a Mutation in Aldolase A". The New England Journal

Enolase deficiency (673 words) [view diff] exact match in snippet view article find links to article

Scarlato G, Bresolin N (August 2001). "Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis". Annals of Neurology. 50 (2): 202–7. doi:10

AMP deaminase (1,060 words) [view diff] exact match in snippet view article find links to article

of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. A research report shows that the widely prescribed diabetes

Calpainopathy (957 words) [view diff] exact match in snippet view article find links to article

LGMD2, facioscapulohumeral muscular dystrophy, dystrophinopathy, Metabolic myopathy Management Physical therapy, bracing, orthopedic surgery Frequency

Phosphoglycerate mutase (1,574 words) [view diff] exact match in snippet view article find links to article

managed with changes in lifestyle.[citation needed] This presents as a metabolic myopathy and is one of the many forms of syndromes formerly referred to as

Mitochondrial complex II deficiency (866 words) [view diff] exact match in snippet view article find links to article

Müller, R.; Ringqvist, T.; Sörnäs, R. (October 1964). "Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis1". Journal

Noncompaction cardiomyopathy (2,386 words) [view diff] exact match in snippet view article find links to article

Becker's muscular dystrophy Mitochondrial myopathy Polyneuropathy and metabolic myopathy Genetic related Emery–Dreifuss muscular dystrophy Myotubular cardiomyopathy

ISCU (1,761 words) [view diff] exact match in snippet view article find links to article

Linderholm H, Müller R, Ringqvist T, Sörnäs R (October 1964). "Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis1". Journal

Carnitine palmitoyltransferase II deficiency (3,163 words) [view diff] exact match in snippet view article find links to article

or infection (especially febrile illness) can also provoke this metabolic myopathy. In a minority of cases, disease severity can be exacerbated by three