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PUBMED FOR HANDHELDS

Journal Abstract Search


58 related items for PubMed ID: 1080861

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  • 3. [Myotonic dystrophy: genetic aspects; cytochemical findings].
    LO Curto F, Nappi G, Poloni M, Castello A.
    Riv Neurol; 1977; 47(6):664-7. PubMed ID: 564079
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  • 4. [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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  • 9. [Myotonic dystrophy with a variable symptomatology and favorable clinical prognosis in a large family].
    Marcoz JP, Klein D.
    Rev Med Suisse Romande; 1978 Aug 27; 98(8):431-41. PubMed ID: 694299
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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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  • 12. Myotonic disorders.
    Harper PS.
    Practitioner; 1982 Jun 27; 226(1368):1065-71. PubMed ID: 7111139
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  • 14. Myotonic dystrophy with no trinucleotide repeat expansion.
    Thornton CA, Griggs RC, Moxley RT.
    Ann Neurol; 1994 Mar 27; 35(3):269-72. PubMed ID: 8122879
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  • 18. Direct diagnosis of myotonic dystrophy with a disease-specific DNA marker.
    Shelbourne P, Davies J, Buxton J, Anvret M, Blennow E, Bonduelle M, Schmedding E, Glass I, Lindenbaum R, Lane R.
    N Engl J Med; 1993 Feb 18; 328(7):471-5. PubMed ID: 8421476
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