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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

223 related items for PubMed ID: 5889019

  • 1. Hereditary myopathies.
    Emery AE.
    Clin Orthop Relat Res; 1964; 33():164-73. PubMed ID: 5889019
    [No Abstract] [Full Text] [Related]

  • 2. Genetic approaches to the nosology of muscular disease: myotonias and similar diseases.
    Becker PE.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):52-62. PubMed ID: 5293617
    [Abstract] [Full Text] [Related]

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

  • 4. [Clinical polymorphism of X-linked myopathies].
    Grinio LP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974 Feb; 74(3):321-9. PubMed ID: 4466264
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  • 10. Molecular genetics and clinical aspects of inherited disorders of nerve and muscle.
    Harding AE.
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):600-4. PubMed ID: 1392132
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  • 12. Changing patterns of genetic counseling.
    Lubs HA, Lubs ML.
    Adv Pathobiol; 1976 Oct; (3):102-18. PubMed ID: 142422
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  • 13. [Severe autosomal recessive myopathies in children in Tunisia].
    Ben Hamida M.
    Bull Acad Natl Med; 1984 Oct; 168(7-8):937-40. PubMed ID: 6398752
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  • 17. Muscular dystrophy: historical overview and classification in the genetic era.
    Kissel JT, Mendell JR.
    Semin Neurol; 1999 Oct; 19(1):5-7. PubMed ID: 10711984
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  • 19. [Problems associated with female conductors of hereditary X-chromosomal recessive muscular dystrophy (Duchenne type)].
    Gundlach HJ, Pelz L, Ernst K.
    Psychiatr Neurol Med Psychol (Leipz); 1974 Nov; 26(11):693-8. PubMed ID: 4449906
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  • 20. [Myocardiopathies in myopathies].
    Kuhn E.
    Verh Dtsch Ges Inn Med; 1971 Nov; 77():289-301. PubMed ID: 4265147
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