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PUBMED FOR HANDHELDS

Journal Abstract Search


247 related items for PubMed ID: 4577474

  • 21. Carrier detection in X-linked muscular dystrophy.
    Walton JN.
    J Genet Hum; 1969 Oct; 17(3):497-510. PubMed ID: 5387424
    [No Abstract] [Full Text] [Related]

  • 22. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.
    Jackson CE, Strehler DA.
    Pediatrics; 1968 Feb; 41(2):495-502. PubMed ID: 5637795
    [No Abstract] [Full Text] [Related]

  • 23. Electromyographic characteristics of congenital and early onset motor unit diseases.
    Fowler WM, Taylor RG, Munsat TL.
    Arch Phys Med Rehabil; 1971 Aug; 52(8):343-61. PubMed ID: 5284447
    [No Abstract] [Full Text] [Related]

  • 24. [Frequency analysis in clinical electromyography. Study in normal and myopathic subjects].
    Cosi V, Mazzella GL.
    Riv Neurobiol; 1969 Aug; 15(3):422-70. PubMed ID: 5386490
    [No Abstract] [Full Text] [Related]

  • 25. Observations on the electrocardiogram in Duchenne's progressive muscular dystrophy.
    Durnin RE, Ziska JH, Zellweger H.
    Helv Paediatr Acta; 1971 Aug; 26(3):331-9. PubMed ID: 5116168
    [No Abstract] [Full Text] [Related]

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  • 30. Needle biopsy of skeletal muscle: a phase and electron microscopic evaluation of its usefulness in the study of muscle dsease.
    Porro RS, Webster HF, Tobin W.
    J Neuropathol Exp Neurol; 1969 Apr; 28(2):229-42. PubMed ID: 4892052
    [No Abstract] [Full Text] [Related]

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  • 32. [Possibilities and limitations of ultrastructural investigations in muscle diseases (author's transl)].
    Ketelsen UP.
    Beitr Pathol; 1974 Jan; 151(1):1-29. PubMed ID: 4817522
    [No Abstract] [Full Text] [Related]

  • 33. [Case of polymyositis resembling progressive muscular dystrophy].
    Miyoshi S.
    Naika; 1970 Sep; 26(3):581-4. PubMed ID: 5473967
    [No Abstract] [Full Text] [Related]

  • 34. The molecular genetics of neurological disease. Recent advances.
    Rosenberg RN.
    Neurologia; 1993 May; 8(5):116-23. PubMed ID: 8507504
    [No Abstract] [Full Text] [Related]

  • 35. [Various features of muscle tissue metabolism in various muscular and neuromuscular diseases of a hereditary nature (clinico-histochemical study)].
    Anosov NN, Saĭkova LA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982 May; 82(3):22-5. PubMed ID: 6952668
    [Abstract] [Full Text] [Related]

  • 36. [Progressive muscular diseases--clinical picture, pathophysiology, and differential diagnosis].
    Heyck H.
    Dtsch Med J; 1971 Jun; 22(12):389-99. PubMed ID: 5087609
    [No Abstract] [Full Text] [Related]

  • 37. [Histochemical aspects of primary and secondary myopathies (author's transl)].
    Bundschu HD, Suchenwirth R.
    Fortschr Neurol Psychiatr Grenzgeb; 1973 Aug; 41(8):419-49. PubMed ID: 4147575
    [No Abstract] [Full Text] [Related]

  • 38. [Distal myopathies: critical study and report on one case (author's transl)].
    Serratrice G, Pellissier JF, Pouget J.
    Ann Med Interne (Paris); 1982 Aug; 133(3):192-9. PubMed ID: 7103305
    [Abstract] [Full Text] [Related]

  • 39. The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome.
    Ricker K, Mertens HG.
    Eur Neurol; 1968 Aug; 1(5):275-307. PubMed ID: 5696602
    [No Abstract] [Full Text] [Related]

  • 40. Diagnostic criteria for Duchenne and Becker muscular dystrophy and myotonic dystrophy.
    Jennekens FG, ten Kate LP, de Visser M, Wintzen AR.
    Neuromuscul Disord; 1991 Aug; 1(6):389-91. PubMed ID: 1822350
    [No Abstract] [Full Text] [Related]


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