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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

166 related items for PubMed ID: 10428430

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  • 3. Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy.
    Muntoni F, Lichtarowicz-Krynska EJ, Sewry CA, Manilal S, Recan D, Llense S, Taylor J, Morris GE, Dubowitz V.
    Neuromuscul Disord; 1998 Apr; 8(2):72-6. PubMed ID: 9608559
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  • 5. Changes at P183 of emerin weaken its protein-protein interactions resulting in X-linked Emery-Dreifuss muscular dystrophy.
    Ellis JA, Yates JR, Kendrick-Jones J, Brown CA.
    Hum Genet; 1999 Mar; 104(3):262-8. PubMed ID: 10323252
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  • 7. Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophy.
    Wulff K, Parrish JE, Herrmann FH, Wehnert M.
    Hum Mutat; 1997 Mar; 9(6):526-30. PubMed ID: 9195226
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  • 9. Cardiac involvement in Emery Dreifuss muscular dystrophy: a case series.
    Buckley AE, Dean J, Mahy IR.
    Heart; 1999 Jul; 82(1):105-8. PubMed ID: 10377322
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  • 10. Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy.
    Bione S, Maestrini E, Rivella S, Mancini M, Regis S, Romeo G, Toniolo D.
    Nat Genet; 1994 Dec; 8(4):323-7. PubMed ID: 7894480
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  • 14. Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophy.
    Talkop UA, Talvik I, Sõnajalg M, Sibul H, Kolk A, Piirsoo A, Warzok R, Wulff K, Wehnert MS, Talvik T.
    Neuromuscul Disord; 2002 Nov; 12(9):878-81. PubMed ID: 12398842
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  • 15. Emerin and cardiomyopathy in Emery-Dreifuss muscular dystrophy.
    Funakoshi M, Tsuchiya Y, Arahata K.
    Neuromuscul Disord; 1999 Mar; 9(2):108-14. PubMed ID: 10220866
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  • 18. A protein truncation test for Emery-Dreifuss muscular dystrophy (EMD): detection of N-terminal truncating mutations.
    de Koning Gans PA, Ginjaar I, Bakker E, Yates JR, den Dunnen JT.
    Neuromuscul Disord; 1999 Jun; 9(4):247-50. PubMed ID: 10399752
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