Biochemical studies in mitochondrial encephalomyopathy.

Author:

Goda S,Ishimoto S,Goto I,Kuroiwa Y,Koike K,Koike M,Nakagawa M,Reichmann H,DiMauro S

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference24 articles.

1. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: a distinctive clinical syndrome associated with ragged-red fibers;SG, I.Pavlakis; PC, Phillips; S, DiMauro; DC, DeVivo; LP, Rowland;Ann Neurol,1983

2. Biochemical properties of mammalian 2-oxo acid dehydrogenase multienzyme complexes and clinical relevancy with chronic lactic acidosis;Koike, M.; Koike, K.;Ann NY Acad Sci,1982

3. Pyruvate carboxylase and phosphoenolpyruvate carboxykinase activity in leukocytes and fibroblasts from a patient with pyruvate carboxylase deficiency;Atkin, B.M.; Utter, M.F.; Weinberg, M.B.;Pediatr Res,1979

4. Purification and comparative properties of human lactate dehydrogenase isozymes from uterus, uterine myoma and cervical cancer;Okabe, K.; Hayakawa, T.; Hamada, M.; Koike, M.;Biochemistry,1968

5. Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle;Bresolin, N.; Zeviani, M.; Bonilla, E.;Neurology,1985

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