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Journal Abstract Search

143 related items for PubMed ID: 2859691

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. The histochemical characterization of the coupling state of skeletal muscle mitochondria.
    Meijer AE, Vloedman AH.
    Histochemistry; 1980; 69(3):217-32. PubMed ID: 6449494
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  • 23.
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  • 24. [Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)].
    Pongratz D, Hübner G, Deufel T, Wieland O, Pongratz E, Liphardt R.
    Klin Wochenschr; 1979 Sep 17; 57(18):927-36. PubMed ID: 502358
    [Abstract] [Full Text] [Related]

  • 25. Fatal infantile mitochondrial myopathy due to cytochrome c oxidase deficiency.
    Minchom PE, Dormer RL, Hughes IA, Stansbie D, Cross AR, Hendry GA, Jones OT, Johnson MA, Sherratt HS, Turnbull DM.
    J Neurol Sci; 1983 Sep 17; 60(3):453-63. PubMed ID: 6313867
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  • 26. Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case.
    Engel AG, Banker BQ, Eiben RM.
    J Neurol Neurosurg Psychiatry; 1977 Apr 17; 40(4):313-22. PubMed ID: 874508
    [Abstract] [Full Text] [Related]

  • 27. [A case of myopathy with carnitine deficiency].
    Martin P, Carrier H, Renaud JF, Kullmann B, Delpont E, Romey G, Cartier B, Bedoucha P.
    Rev Neurol (Paris); 1986 Apr 17; 142(6-7):625-34. PubMed ID: 3797933
    [Abstract] [Full Text] [Related]

  • 28. A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
    Morgan-Hughes JA, Darveniza P, Kahn SN, Landon DN, Sherratt RM, Land JM, Clark JB.
    Brain; 1977 Dec 17; 100(4):617-40. PubMed ID: 608115
    [No Abstract] [Full Text] [Related]

  • 29. [Myopathy with carnitine deficiency and lactic acidosis. A contribution to differential diagnosis of carnitine deficiency myopathies and mitochondrial myopathies].
    Cammann R, Dunker H, Schumacher H, Ruitenbeek W, Sperner J.
    Z Arztl Fortbild (Jena); 1992 Jul 10; 86(13):667-71. PubMed ID: 1642019
    [No Abstract] [Full Text] [Related]

  • 30.
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  • 31. A case of lipid storage myopathy with carnitine deficiency. Biochemical and electromyographic correlations.
    Scarlato G, Albizzati MG, Bassi S, Cerri C, Frattola L.
    Eur Neurol; 1977 Jul 10; 16(1-6):222-9. PubMed ID: 615713
    [Abstract] [Full Text] [Related]

  • 32. Respiratory failure revealing mitochondrial myopathy in adults.
    Cros D, Palliyath S, DiMauro S, Ramirez C, Shamsnia M, Wizer B.
    Chest; 1992 Mar 10; 101(3):824-8. PubMed ID: 1541151
    [Abstract] [Full Text] [Related]

  • 33. Fatal cases of lipid storage myopathy with carnitine deficiency.
    Cornelio F, Di Donato S, Peluchetti D, Bizze A, Bertagnolio B, D'Angelo A, Wiesmann U.
    J Neurol Neurosurg Psychiatry; 1977 Feb 10; 40(2):170-8. PubMed ID: 194020
    [Abstract] [Full Text] [Related]

  • 34. Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency.
    DiMauro S, Mendell JR, Sahenk Z, Bachman D, Scarpa A, Scofield RM, Reiner C.
    Neurology; 1980 Aug 10; 30(8):795-804. PubMed ID: 6251406
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells.
    Scholte HR, Busch HF, Luyt-Houwen IE, Vaandrager-Verduin MH, Przyrembel H, Arts WF.
    J Inherit Metab Dis; 1987 Aug 10; 10 Suppl 1():81-97. PubMed ID: 2824921
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  • 37.
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  • 40. Histochemical and ultrastructural analysis of the mitochondrial changes in a familial mitochondrial myopathy.
    Tassin S, Walter GF, Brucher JM, Rousseau JJ.
    Neuropathol Appl Neurobiol; 1980 Aug 10; 6(5):337-47. PubMed ID: 6161318
    [Abstract] [Full Text] [Related]

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