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Journal Abstract Search

264 related items for PubMed ID: 7366606

  • 1. 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; 3(2):176-80. PubMed ID: 7366606
    [Abstract] [Full Text] [Related]

  • 2.
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  • 3. Autosomal recessive generalized myotonia.
    Sun SF, Streib EW.
    Muscle Nerve; 1983 Feb; 6(2):143-8. PubMed ID: 6855798
    [Abstract] [Full Text] [Related]

  • 4. [Becker's myotonia in Peru].
    Torres L, Vélez M, Cosentino C.
    Rev Neurol; 1983 Feb; 30(11):1033-6. PubMed ID: 10904948
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  • 6. Myotonia levior: contribution to the nosography.
    Siciliano G, Risaliti R, Vignocchi G, Rossi B.
    Riv Neurol; 1988 Feb; 58(5):204-9. PubMed ID: 3231989
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  • 8. [Cardiological studies on patients with autosomal dominant and autosomal recessive hereditary myotonia congenital and myotonia dystrophica].
    Bodem R, Boikhan MS, Kuhn E.
    Verh Dtsch Ges Inn Med; 1971 Feb; 77():1289-90. PubMed ID: 5156008
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. [Regional clinico-genetic features of myotonias].
    Khannanova FK.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1986 Feb; 86(3):342-6. PubMed ID: 2939672
    [Abstract] [Full Text] [Related]

  • 11. Clinical consequences of heterozygosity for autosomal-recessive diseases.
    Vogel F.
    Clin Genet; 1984 May; 25(5):381-415. PubMed ID: 6373070
    [Abstract] [Full Text] [Related]

  • 12. [2 patients with autosomal recessive generalized myotonia].
    Frijns CJ, Wouda EJ, Linssen WH, Snijders CJ.
    Ned Tijdschr Geneeskd; 1994 Apr 02; 138(14):726-8. PubMed ID: 8152515
    [Abstract] [Full Text] [Related]

  • 13. The myotonias: their diagnosis and treatment.
    Moxley RT.
    Compr Ther; 1996 Jan 02; 22(1):8-21. PubMed ID: 8654027
    [No Abstract] [Full Text] [Related]

  • 14. A family with autosomal recessive generalised myotonia with Herculean appearance.
    Sinha MK, Chaurasia RN, Verma R.
    J Assoc Physicians India; 2011 Feb 02; 59():120-2. PubMed ID: 21751653
    [Abstract] [Full Text] [Related]

  • 15. Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita.
    Lyons MJ, Duron R, Molinero I, Sangiuolo F, Holden KR.
    Pediatr Neurol; 2010 May 02; 42(5):365-8. PubMed ID: 20399394
    [Abstract] [Full Text] [Related]

  • 16. Myotonia congenita in a large consanguineous Arab family: insight into the clinical spectrum of carriers and double heterozygotes of a novel mutation in the chloride channel CLCN1 gene.
    Shalata A, Furman H, Adir V, Adir N, Hujeirat Y, Shalev SA, Borochowitz ZU.
    Muscle Nerve; 2010 Apr 02; 41(4):464-9. PubMed ID: 19697366
    [Abstract] [Full Text] [Related]

  • 17. Autosomal dominant monosymptomatic myotonia permanens.
    Colding-Jørgensen E, Duno M, Vissing J.
    Neurology; 2006 Jul 11; 67(1):153-5. PubMed ID: 16832098
    [Abstract] [Full Text] [Related]

  • 18. Myotonia congenita.
    Gutmann L, Phillips LH.
    Semin Neurol; 1991 Sep 11; 11(3):244-8. PubMed ID: 1947487
    [Abstract] [Full Text] [Related]

  • 19. Phenotypic variability of autosomal dominant myotonia congenita in a Taiwanese family with muscle chloride channel (CLCN1) mutation.
    Chang TY, Kuo HC, Hsiao KM, Huang CC.
    Acta Neurol Taiwan; 2007 Dec 11; 16(4):214-20. PubMed ID: 18220014
    [Abstract] [Full Text] [Related]

  • 20. [Case history contribution and findings in Thomsen's myotonia congenita].
    Hauschild G, Schäfer A.
    Arch Kinderheilkd; 1966 Aug 11; 174(3):365-79. PubMed ID: 5994000
    [No Abstract] [Full Text] [Related]

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