Part I Hereditary Primary Myopathies in Laboratory Animals: HEREDITARY MOUSE MUSCULAR DYSTROPHY WITH PARTICULAR EMPHASIS ON PATHOGENESIS AND ATTEMPTS AT THERAPY*
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1966.tb41150.x/fullpdf
Reference37 articles.
1. Studies on the pentose phosphate pathway in hereditary muscular dystrophy in mice;Canal;Med. Exp,1962
2. Studies on the acetoacetate-like compound found in dystrophic mouse muscle homogenates;Coleman;Arch. Biochem. Biophys,1965a
3. Accumulation of triose phosphates in dystrophic mouse muscle homogenates;Coleman;Arch. Biochem. Biophys,1965b
4. Influence of diet on transamidinase activity in dystrophic mice;Coleman;Amer. J. Physiol,1960
5. Effects of nutrition on growth, lifespan, and histopathology of mice with hereditary muscular dystrophy;Coleman;J. Nutr.,1961
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1. Two successful double-blind trials with coenzyme Q10 (vitamin Q10) on muscular dystrophies and neurogenic atrophies;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;1995-05
2. Increased viability and differentiation of normal and dystrophic striated muscle in vitro;In Vitro Cellular & Developmental Biology;1986-09
3. Biochemical rationale and the cardiac response of patients with muscle disease to therapy with coenzyme Q10.;Proceedings of the National Academy of Sciences;1985-07-01
4. Changes in muscle esterases in genetically dystrophic and control littermate mice;Muscle & Nerve;1982-07
5. Parenteral branched-chain amino acid treatment and avian dystrophy;Muscle & Nerve;1982-07
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