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Journal Abstract Search

140 related items for PubMed ID: 8272119

  • 21.
    ; . PubMed ID:
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  • 22. [Genotype-phenotype correlation in myotonic dystrophy and prediction of clinical seriousness].
    García-Gómez T, Maestre J, Garrido ML, Vilches R, Fernández MD, Mínguez A, Serrano P.
    Rev Neurol; ; 29(6):499-502. PubMed ID: 10584260
    [Abstract] [Full Text] [Related]

  • 23. Electrocardiographic findings in myotonic dystrophy.
    Olofsson BO, Forsberg H, Andersson S, Bjerle P, Henriksson A, Wedin I.
    Arctic Med Res; 1988; 47 Suppl 1():420-2. PubMed ID: 3272655
    [No Abstract] [Full Text] [Related]

  • 24. Homozygosity for CCTG mutation in myotonic dystrophy type 2.
    Schoser BG, Kress W, Walter MC, Halliger-Keller B, Lochmüller H, Ricker K.
    Brain; 2004 Aug; 127(Pt 8):1868-77. PubMed ID: 15231584
    [Abstract] [Full Text] [Related]

  • 25. Myotonia dystrophica: unusual features in a Labrador family.
    Webb D, Mathews A, Harris M, Muir I, Hostetter J, Marshall W, Salimonu L, Gray J, Faulkner J, Johnson G.
    Can Med Assoc J; 1978 Mar 04; 118(5):497-500, 552. PubMed ID: 630510
    [Abstract] [Full Text] [Related]

  • 26.
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  • 27.
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  • 28. Survey of patients with early-onset myotonic dystrophy in the San-In district, Japan.
    Takeshita K, Tanaka K, Nakashima T, Kasagi S.
    Jinrui Idengaku Zasshi; 1981 Dec 04; 26(4):295-300. PubMed ID: 7345188
    [No Abstract] [Full Text] [Related]

  • 29.
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  • 30. [Congenital myotonic dystrophy].
    Oliván Gonzalvo G, Alonso Gregorio M, López Moreno MJ, Domínguez Arranz MM, Olivares López JL, Pérez González JM.
    An Esp Pediatr; 1990 May 04; 32(5):460-3. PubMed ID: 2400164
    [No Abstract] [Full Text] [Related]

  • 31.
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  • 32. [Myotonic dystrophia. A report of three patients in Cuba].
    Lozada-Mengana Y, Alvarez-Valiente H, Aguilera-Pacheco O.
    Rev Neurol; 1990 May 04; 33(4):398-400. PubMed ID: 11708269
    [No Abstract] [Full Text] [Related]

  • 33. [A new type of myotonic dystrophy].
    Auvinen S, Vihola A, Krahe R, Kupila J, Hackman P, Hietaharju A, Udd B.
    Duodecim; 2003 May 04; 119(8):707-13. PubMed ID: 12806729
    [No Abstract] [Full Text] [Related]

  • 34. Complex patterns of male germline instability and somatic mosaicism in myotonic dystrophy type 1.
    Martorell L, Monckton DG, Gamez J, Baiget M.
    Eur J Hum Genet; 2000 Jun 04; 8(6):423-30. PubMed ID: 10878662
    [Abstract] [Full Text] [Related]

  • 35. Congenital myotonic dystrophy in Britain. II. Genetic basis.
    Harper PS.
    Arch Dis Child; 1975 Jul 04; 50(7):514-21. PubMed ID: 1167063
    [Abstract] [Full Text] [Related]

  • 36. [Myotonic dystrophy--a clinical and genetic study of 4 families].
    Jiang XS.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1984 Dec 04; 17(6):382-4. PubMed ID: 6543729
    [No Abstract] [Full Text] [Related]

  • 37. [The precocious form of myotonic dystrophy (Steinert's disease)].
    Bamatter F, Grasset E, Klein D, Aguercif M.
    Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1967 Dec 04; 41(2-4):82-6. PubMed ID: 5631508
    [No Abstract] [Full Text] [Related]

  • 38. Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes.
    Thornton CA, Johnson K, Moxley RT.
    Ann Neurol; 1994 Jan 04; 35(1):104-7. PubMed ID: 8285579
    [Abstract] [Full Text] [Related]

  • 39. [Steinert's disease in childhood. Study of a family].
    Franchini F, Galluzzi F, Ciampolini M, Di Maria M.
    Riv Clin Pediatr; 1969 Jan 04; 82():253-8. PubMed ID: 5405479
    [No Abstract] [Full Text] [Related]

  • 40. [Encopresis revealing myotonic dystrophy in 2 children].
    Avez-Couturier J, Michaud L, Cuisset JM, Lamblin MD, Dolhem P, Turck D, Vallée L, Gottrand F.
    Arch Pediatr; 2009 May 04; 16(5):430-4. PubMed ID: 19328663
    [Abstract] [Full Text] [Related]

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