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Journal Abstract Search

559 related items for PubMed ID: 10904948

  • 1. [Becker's myotonia in Peru].
    Torres L, Vélez M, Cosentino C.
    Rev Neurol; ; 30(11):1033-6. PubMed ID: 10904948
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  • 2. [The spectrum of CLCN1 gene mutations in patients with nondystrophic Thomsen's and Becker's myotonias].
    Ivanova EA, Dadali EL, Fedotov VP, Kurbatov SA, Rudenskaia GE, Proskokova TN, Poliakov AV.
    Genetika; 2012 Sep; 48(9):1113-23. PubMed ID: 23113340
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  • 3. A family with autosomal recessive generalised myotonia with Herculean appearance.
    Sinha MK, Chaurasia RN, Verma R.
    J Assoc Physicians India; 2011 Feb; 59():120-2. PubMed ID: 21751653
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  • 4. Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita.
    Lyons MJ, Duron R, Molinero I, Sangiuolo F, Holden KR.
    Pediatr Neurol; 2010 May; 42(5):365-8. PubMed ID: 20399394
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  • 8. Autosomal recessive generalized myotonia.
    Zellweger H, Pavone L, Biondi A, Cimino V, Gullotta F, Hart M, Ionasescu V, Mollica F, Schieken R.
    Muscle Nerve; 1980 May; 3(2):176-80. PubMed ID: 7366606
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  • 9. Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia.
    Sun C, Tranebjaerg L, Torbergsen T, Holmgren G, Van Ghelue M.
    Eur J Hum Genet; 2001 Dec; 9(12):903-9. PubMed ID: 11840191
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  • 10. [Muscle weakness or rigidity due to hereditary ion channel diseases].
    Links TP, van der Hoeven JH.
    Ned Tijdschr Geneeskd; 2001 Feb 10; 145(6):249-51. PubMed ID: 11236369
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  • 12. Identification of two mutations and a polymorphism in the chloride channel CLCN-1 in patients with Becker's generalized myotonia.
    Esteban J, Neumeyer AM, McKenna-Yasek D, Brown RH.
    Neurogenetics; 1998 Mar 10; 1(3):185-8. PubMed ID: 10737121
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  • 15. A novel muscle sodium channel mutation causes painful congenital myotonia.
    Rosenfeld J, Sloan-Brown K, George AL.
    Ann Neurol; 1997 Nov 10; 42(5):811-4. PubMed ID: 9392583
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