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Journal Abstract Search

140 related items for PubMed ID: 8272119

  • 1. [An unstable mutation as cause of myotonic dystrophy].
    Brunner HG, Höweler CJ, Smeets HJ, Wieringa B.
    Ned Tijdschr Geneeskd; 1993 Nov 27; 137(48):2468-72. PubMed ID: 8272119
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  • 2. Myotonic dystrophy: some genetic problems.
    Harper PS.
    Birth Defects Orig Artic Ser; 1974 Nov 27; 10(10):120-5. PubMed ID: 4462623
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  • 6. Myotonic disorders.
    Harper PS.
    Practitioner; 1982 Jun 27; 226(1368):1065-71. PubMed ID: 7111139
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  • 7. The myotonias: their diagnosis and treatment.
    Moxley RT.
    Compr Ther; 1996 Jan 27; 22(1):8-21. PubMed ID: 8654027
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  • 8. [Clinical aspects and therapy of muscular dystrophies].
    Beckmann R.
    Internist (Berl); 1972 Mar 27; 13(3):108-17. PubMed ID: 4553893
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  • 10. [Orofacial evaluation with a punctuation scale in patients with myotonic dystrophy (Steinert's disease)].
    Noronha CF, Alves Duro LA.
    Arq Neuropsiquiatr; 1995 Sep 27; 53(3-A):424-31. PubMed ID: 8540816
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  • 11. [Familial atrophic myotonia].
    Neĭmark EZ, Tokar' ZM, Vasil'eva AF, Pecherskaia IE.
    Vrach Delo; 1974 Sep 27; 0(7):99-103. PubMed ID: 4421221
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  • 13. [Genetic epidemiology of myotonic dystrophy in Kagoshima and Okinawa districts in Japan].
    Osame M, Furusho T.
    Rinsho Shinkeigaku; 1983 Dec 27; 23(12):1067-71. PubMed ID: 6677410
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  • 14. New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).
    Sallinen R, Vihola A, Bachinski LL, Huoponen K, Haapasalo H, Hackman P, Zhang S, Sirito M, Kalimo H, Meola G, Horelli-Kuitunen N, Wessman M, Krahe R, Udd B.
    Neuromuscul Disord; 2004 Apr 27; 14(4):274-83. PubMed ID: 15019706
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  • 15. Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions.
    Arsenault ME, Prévost C, Lescault A, Laberge C, Puymirat J, Mathieu J.
    Neurology; 2006 Apr 25; 66(8):1248-50. PubMed ID: 16636244
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  • 16. "Shake hands"; diagnosing a floppy infant--myotonic dystrophy and the congenital subtype: a difficult perinatal diagnosis.
    Verrijn Stuart AA, Huisman M, van Straaten HL, Bakker JC, Arabin B.
    J Perinat Med; 2000 Apr 25; 28(6):497-501. PubMed ID: 11155437
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  • 17. [Expansion and mutation rate in CTG repeats in the myotonic dystrophy gene].
    Khidiiatova IM, Fatkhlislamova RI, Magzhanov RV, Popova SN, Slominskiĭ PA, Limborskaia SA, Khusnutdinova EK.
    Genetika; 2000 Oct 25; 36(10):1410-3. PubMed ID: 11094756
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  • 20. Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.
    Hunter AG, Jacob P, O'Hoy K, MacDonald I, Mettler G, Tsilfidis C, Korneluk RG.
    Am J Med Genet; 1993 Feb 01; 45(3):401-7. PubMed ID: 8434633
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