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Journal Abstract Search

169 related items for PubMed ID: 10382910

  • 1. Severe clinical expression in X-linked Emery-Dreifuss muscular dystrophy.
    Hoeltzenbein M, Karow T, Zeller JA, Warzok R, Wulff K, Zschiesche M, Herrmann FH, Grosse-Heitmeyer W, Wehnert MS.
    Neuromuscul Disord; 1999 May; 9(3):166-70. PubMed ID: 10382910
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  • 2. Mutation analysis in Emery-Dreifuss muscular dystrophy.
    Nevo Y, Al-Lozi M, Parsadanian AS, Elliott JL, Connolly AM, Pestronk A.
    Pediatr Neurol; 1999 Jul; 21(1):456-9. 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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  • 4. 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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  • 13. 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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  • 14. Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysis.
    Wulff K, Ebener U, Wehnert CS, Ward PA, Reuner U, Hiebsch W, Herrmann FH, Wehnert M.
    Dis Markers; 1997 Apr; 13(2):77-86. PubMed ID: 9160182
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  • 15. 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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  • 16. A novel emerin mutation in a Japanese patient with Emery-Dreifuss muscular dystrophy.
    Yamada T, Kobayashi T.
    Hum Genet; 1996 May; 97(5):693-4. PubMed ID: 8655156
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  • 17. Diagnosis of X-linked Emery-Dreifuss muscular dystrophy by protein analysis of leucocytes and skin with monoclonal antibodies.
    Manilal S, Sewry CA, Man N, Muntoni F, Morris GE.
    Neuromuscul Disord; 1997 Jan; 7(1):63-6. PubMed ID: 9132142
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  • 18. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.
    Mercuri E, Counsell S, Allsop J, Jungbluth H, Kinali M, Bonne G, Schwartz K, Bydder G, Dubowitz V, Muntoni F.
    Neuropediatrics; 2002 Feb; 33(1):10-4. PubMed ID: 11930270
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  • 19. 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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  • 20. Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletion.
    Fujimoto S, Ishikawa T, Saito M, Wada Y, Wada I, Arahata K, Nonaka I.
    Neuropediatrics; 1999 Jun; 30(3):161-3. PubMed ID: 10480214
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