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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

202 related items for PubMed ID: 2685312

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  • 2. Emery-Dreifuss syndrome.
    Tsuchiya Y, Arahata K.
    Curr Opin Neurol; 1997 Oct; 10(5):421-5. PubMed ID: 9330889
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  • 7. [Emery-Dreifuss muscular dystrophy].
    Kubo S, Tsukahara T, Arahata K.
    Nihon Rinsho; 1997 Dec; 55(12):3186-9. PubMed ID: 9436433
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  • 11. Autosomal dominant humeroperoneal myopathy.
    Gilchrist JM, Leshner RT.
    Arch Neurol; 1986 Jul; 43(7):734-5. PubMed ID: 3729752
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  • 13. Emery-Dreifuss muscular dystrophy.
    Rowland LP, Fetell M, Olarte M, Hays A, Singh N, Wanat FE.
    Ann Neurol; 1979 Feb; 5(2):111-7. PubMed ID: 426473
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  • 16. Autosomal dominant Emery-Dreifuss syndrome: evidence of a neurogenic variant of the disease.
    Witt TN, Garner CG, Pongratz D, Baur X.
    Eur Arch Psychiatry Neurol Sci; 1988 Feb; 237(4):230-6. PubMed ID: 3203701
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  • 17. Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriers.
    Sabatelli P, Squarzoni S, Petrini S, Capanni C, Ognibene A, Cartegni L, Cobianchi F, Merlini L, Toniolo D, Maraldi NM.
    Neuromuscul Disord; 1998 Apr; 8(2):67-71. PubMed ID: 9608558
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  • 18. Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.
    Hong JS, Ki CS, Kim JW, Suh YL, Kim JS, Baek KK, Kim BJ, Ahn KJ, Kim DK.
    J Korean Med Sci; 2005 Apr; 20(2):283-90. PubMed ID: 15832002
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  • 19. Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease.
    Bione S, Small K, Aksmanovic VM, D'Urso M, Ciccodicola A, Merlini L, Morandi L, Kress W, Yates JR, Warren ST.
    Hum Mol Genet; 1995 Oct; 4(10):1859-63. PubMed ID: 8595407
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