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Journal Abstract Search

182 related items for PubMed ID: 34819192

  • 21.
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  • 22. Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern.
    Deconinck N, Dion E, Ben Yaou R, Ferreiro A, Eymard B, Briñas L, Payan C, Voit T, Guicheney P, Richard P, Allamand V, Bonne G, Stojkovic T.
    Neuromuscul Disord; 2010 Aug; 20(8):517-23. PubMed ID: 20576434
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. Emery-Dreifuss muscular dystrophy - a 40 year retrospective.
    Emery AE.
    Neuromuscul Disord; 2000 Jun; 10(4-5):228-32. PubMed ID: 10838246
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  • 27. Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy.
    Raharjo WH, Enarson P, Sullivan T, Stewart CL, Burke B.
    J Cell Sci; 2001 Dec; 114(Pt 24):4447-57. PubMed ID: 11792810
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  • 28.
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  • 29. Emery dreifuss muscular dystrophy: a clinico-pathological study.
    Gayathri N, Taly AB, Sinha S, Suresh TG, Gorai D.
    Neurol India; 2006 Jun; 54(2):197-9. PubMed ID: 16804269
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  • 32. Novel LMNA mutation in a Taiwanese family with autosomal dominant Emery-Dreifuss muscular dystrophy.
    Liang WC, Yuo CY, Liu CY, Lee CS, Goto K, Hayashi YK, Jong YJ.
    J Formos Med Assoc; 2007 Feb; 106(2 Suppl):S27-31. PubMed ID: 17493893
    [Abstract] [Full Text] [Related]

  • 33. 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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  • 34.
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  • 35. Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy.
    Sabatelli P, Lattanzi G, Ognibene A, Columbaro M, Capanni C, Merlini L, Maraldi NM, Squarzoni S.
    Muscle Nerve; 2001 Jun; 24(6):826-9. PubMed ID: 11360268
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  • 36.
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  • 37. Three novel FHL1 variants cause a mild phenotype of Emery-Dreifuss muscular dystrophy.
    Borch JDS, Krag T, Holm-Yildiz SD, Cetin H, Solheim TA, Fornander F, Straub V, Duno M, Vissing J.
    Hum Mutat; 2022 Sep; 43(9):1234-1238. PubMed ID: 35607917
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  • 38.
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  • 39. A mutation in the X-linked Emery-Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy.
    Vohanka S, Vytopil M, Bednarik J, Lukas Z, Kadanka Z, Schildberger J, Ricotti R, Bione S, Toniolo D.
    Neuromuscul Disord; 2001 May; 11(4):411-3. PubMed ID: 11369194
    [Abstract] [Full Text] [Related]

  • 40. Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.
    Muntoni F, Bonne G, Goldfarb LG, Mercuri E, Piercy RJ, Burke M, Yaou RB, Richard P, Récan D, Shatunov A, Sewry CA, Brown SC.
    Brain; 2006 May; 129(Pt 5):1260-8. PubMed ID: 16585054
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