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Abnormalities of Muscle-fibers in Maple Syrup Urine Disease

Bibliographic reference Ferrière, G. ; Decastro, M. ; Rodriguez, J.. Abnormalities of Muscle-fibers in Maple Syrup Urine Disease. In: Acta Neuropathologica, Vol. 63, no. 3, p. 249-254 (1984)
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  1. Adibi AS (1980) Roles of branched-chain amino acids in metabolic regulation. J Lab Clin Med 95:475?484
  2. Barka T, Anderson PJ (1963) In: Histochemistry. Hoeber, New York pp 286?293
  3. Chua B, Siehl DL, Morgan HE (1979) Effect of leucine and metabolites of branced-chain amino acids on protein turnover in heart. J Biol Chem 254:8358
  4. Clara R, Lowenthal A (1966) Familial and congenital lysinecystinuria with benign myopathy and dwarfism. J Neurol Sci 3:433?434
  5. Drews GA, Engel WK (1966) Reversal of ATPase reaction in muscle fibers by EDTA. Nature 212:1551
  6. Engel WR, Cunningham CG (1963) Rapid examination of muscle tissue: an improved trichrome method for fresh-frozen biopsy sections. Neurology (Minneap) 13:919?923
  7. Er�nk� O, Palkama A (1961) Improved localization of phosphorylase by the use of polyvinyl pyrrolidone and high substrate concentration. J Histochem Cytochem 9:585
  8. Estable-Puig JF, Bauer WC, Blumberg JM (1965) Paraphenylenediamine staining of osmium-fixed, plastic-embedded tissue for light and phase microscopy. J Neuropathol Exp Neurol 24:531?535
  9. Ferri�re G, Rodriguez J, Denef J, Guzzetta F (1984) Morphometric studies of normal sural nerve in children (submitted)
  10. Fulks RM, Li JB, Goldberg AL (1975) Effects of insulin, glucose and amino acids on protein turnover in rat diaphragm. J Biol Chem 250:290
  11. Hedden MP, Buse MG (1979) General stimulation of muscle protein synthesis by branched-chain acids in vitro. Proc Soc Exp Biol Med 160:410?415
  12. Hudecki MS, Pallina CM, Heffner RR (1982) Parenteral branched-chain amino acid treatment and avian dystrophy. Muscle Nerve 5:447?457
  13. Hurwitz LJ, Carson N, Allen J, Chopra JS (1969) Congenital ophthalmoplegia, floppy baby syndrome, myopathy and amino-aciduria. J Neurol Neurol Neurosurg Psychiatry 32:495?508
  14. Hurwitz LJ, McCornick D (1970) Paper chromatographic survey of urinary amino acids in muscular dystrophy. Br Med J 3:29?30
  15. Luft JH (1961) Improvements in epoxy-resin embedding methods. J Biophys Biochem Cytol 9:409?414
  16. Monckton G, Marusyk H (1976) Myofibrillary incorporation of3H(G)l-leucine in progressive muscular dystrophy and motor neuron disease. Neurology 26:234?237
  17. Padykula HA, Herman E (1976) The specificity of the histochemical method of adenosine triphosphatase. J Histochem Cytochem 3:170?183
  18. Pearce AG (1961) Intracellular localization of dehydrogenase system using monotetrazolium salts and metal chelation of their formations. J Histochem Cytochem 5:515?527
  19. Reynolds ES (1963) The use of lead citrate at high pH as an electronopaque stain in electron microscopy. J Cell Biol 17:209?212
  20. Slonim AE, Coleman RA, McElligot MA, Najjar J, Hirschhorn K, Labachie GU, Mrak R, Evans OB, Shipp E, Presson R (1983) Improvement of muscle function in acid maltase deficiency by high protein therapy. Neurology (NY) 33:34?38
  21. Stewart PM, Wolser M, Drachman DB (1982) Branched-chain ketoacids reduce muscle protein degradation in Duchenne muscular dystrophy. Muscle Nerve 5:197?201
  22. Trump BF, Smuckler EA, Benditt EP (1961) A method for staining epoxy sections for light microscopy. J Ultratruct Res 5:343?348
  23. Van Hinsbergh VW, Werkamp JH, Engele PJM, Ghijsen WJ (1978) Effect ofl-carnitine on the oxidation of leucine and valine by the rat skeletal muscle. Biochem Med 20:125?127