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Journal Abstract Search

122 related items for PubMed ID: 5647944

  • 41. Familial myopathy with abnormal muscle mitochondria.
    D'Agostino AN, Ziter FA, Rallison ML, Bray PF.
    Arch Neurol; 1968 Apr; 18(4):388-401. PubMed ID: 5638542
    [No Abstract] [Full Text] [Related]

  • 42. Hypotrophic type I muscle fibres with central nuclei, and central myofibrillar lysis preferentially involving type II fibres.
    Radu H, Ionescu V, Radu A, Paler V, Roşu AM, Marian A.
    Eur Neurol; 1974 Apr; 11(2):108-27. PubMed ID: 4275778
    [No Abstract] [Full Text] [Related]

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  • 46. The myopathy of hyperkalemic periodic paralysis. An electron microscopic study.
    Macdonald RD, Rewcastle NB, Humphrey JG.
    Arch Neurol; 1968 Sep; 19(3):274-83. PubMed ID: 5698042
    [No Abstract] [Full Text] [Related]

  • 47. [Relation between the size of muscle fibers, motor endplates nd nerve fibers during hypertrophy and atrophy].
    Granbacher N.
    Z Anat Entwicklungsgesch; 1971 Sep; 135(1):76-87. PubMed ID: 5117467
    [No Abstract] [Full Text] [Related]

  • 48. Myopathy of hypokalemic periodic paralysis. An electron microscopic study.
    Macdonald RD, Rewcastle NB, Humphrey JG.
    Arch Neurol; 1969 Jun; 20(6):565-85. PubMed ID: 5769838
    [No Abstract] [Full Text] [Related]

  • 49. Recent contributions of electron microscopy to the study of normal and pathological muscle.
    Pellegrino C, Franzini-Armstrong C.
    Int Rev Exp Pathol; 1969 Jun; 7():139-226. PubMed ID: 4237232
    [No Abstract] [Full Text] [Related]

  • 50. [Congenital non-progressive myopathy with central axis (central core disease)].
    Jean R, Bonnet H, Pages A, Cadilhac J, Baldet P, Dumas R.
    Arch Fr Pediatr; 1971 Jan; 28(1):65-82. PubMed ID: 5545870
    [No Abstract] [Full Text] [Related]

  • 51. [Ultrastructural aspect of the degeneration of ischemic striated muscle].
    Reznik M.
    Ann Anat Pathol (Paris); 1967 Jan; 12(3):209-22. PubMed ID: 6079368
    [No Abstract] [Full Text] [Related]

  • 52. [Hreditary myopathies].
    Kuhn E.
    Ergeb Inn Med Kinderheilkd; 1969 Jan; 28():188-290. PubMed ID: 4897097
    [No Abstract] [Full Text] [Related]

  • 53. A neuromuscular syndrome of scapuloperoneal distribution.
    Feigenbaum JA, Munsat TL.
    Bull Los Angeles Neurol Soc; 1970 Apr; 35(2):47-57. PubMed ID: 4314731
    [No Abstract] [Full Text] [Related]

  • 54. Fingerprint body myopathy, a newly recognized congenital muscle disease.
    Engel AG, Angelini C, Gomez MR.
    Mayo Clin Proc; 1972 Jun; 47(6):377-88. PubMed ID: 4339422
    [No Abstract] [Full Text] [Related]

  • 55. Myotubular myopathy.
    Kinoshita M, Cadman TE.
    Arch Neurol; 1968 Mar; 18(3):265-71. PubMed ID: 4296080
    [No Abstract] [Full Text] [Related]

  • 56. Nemaline myopathy: report of a fatal case, with histochemical and electron microscopic studies.
    Shafiq SA, Dubowitz V, Peterson Hde C, Milhorat AT.
    Brain; 1967 Dec; 90(4):817-28. PubMed ID: 4169453
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  • 58. Congenital myopathies with "diagnostic" pathological features.
    Korényi-Both A, Korényi-Both I.
    J Med; 1987 Dec; 18(2):93-107. PubMed ID: 3323392
    [Abstract] [Full Text] [Related]

  • 59. [Rod myopathy. A fatal neonatal case].
    Netter JC, Laurent-Pellegrin M, Bildstein G, Chateauneuf R, Petrus M.
    Arch Fr Pediatr; 1986 May; 43(5):327-9. PubMed ID: 3778091
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