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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

109 related items for PubMed ID: 14375867

  • 21. [Heterogenecity of congenital myotonia].
    BECKER PE.
    Nervenarzt; 1957 Oct 20; 28(10):455-60. PubMed ID: 13517431
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  • 25. Myotonia congenita--a cause of muscle weakness and stiffness.
    Chrestian N, Puymirat J, Bouchard JP, Dupré N.
    Nat Clin Pract Neurol; 2006 Jul 20; 2(7):393-9; quiz following 399. PubMed ID: 16932590
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  • 26. Myotonia congenita with "delayed myotonia".
    DUBOWITZ V, LAWSON D.
    Proc R Soc Med; 1960 Sep 20; 53(9):786-7. PubMed ID: 13724666
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  • 27. [A case of amyotonia congenita characterized by a histological and histochemical anomalie of the neuromuscular junction].
    COERS C, PELC S.
    Acta Neurol Psychiatr Belg; 1954 Feb 20; 54(2):166-73. PubMed ID: 13157970
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  • 28. [Myotonic syndromes].
    Petit H, Warot P.
    Cah Coll Med Hop Paris; 1968 Jun 20; 9(7):633-40. PubMed ID: 5678818
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  • 31. [Observations on certain cases of myotonic syndrome].
    DE LAURENZI V.
    G Med Mil; 1954 Jun 20; 104(2):157-72. PubMed ID: 13183362
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  • 32. Becker's variant of myotonia congenita in two siblings--a clinico-genetic study.
    Bhattacharyya KB, Sengupta P, Basu S, Bhattacharya NP.
    Neurol India; 2004 Sep 20; 52(3):363-4. PubMed ID: 15472428
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  • 33. [Atypical familial myotonic syndrome; clinical & electromyographic studies].
    AMICI R, NEGRI S.
    Sist Nerv; 1958 Sep 20; 10(3):231-8. PubMed ID: 13602931
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  • 35. Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1).
    Moxley RT, Logigian EL, Martens WB, Annis CL, Pandya S, Moxley RT, Barbieri CA, Dilek N, Wiegner AW, Thornton CA.
    Muscle Nerve; 2007 Sep 20; 36(3):320-8. PubMed ID: 17587223
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  • 39. [A girl with hereditary myotonia due to an exceptional sodium channel mutation].
    van den Bergen JC, Verbruggen KT, Ginjaar HB, Kerstjens-Frederikse WS.
    Ned Tijdschr Geneeskd; 2006 Nov 11; 150(45):2501-6. PubMed ID: 17137100
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  • 40. Difference in allelic expression of the CLCN1 gene and the possible influence on the myotonia congenita phenotype.
    Dunø M, Colding-Jørgensen E, Grunnet M, Jespersen T, Vissing J, Schwartz M.
    Eur J Hum Genet; 2004 Sep 11; 12(9):738-43. PubMed ID: 15162127
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