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Journal Abstract Search

626 related items for PubMed ID: 15832002

  • 1. 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]

  • 2. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
    Park YE, Hayashi YK, Goto K, Komaki H, Hayashi Y, Inuzuka T, Noguchi S, Nonaka I, Nishino I.
    Neuromuscul Disord; 2009 Jan; 19(1):29-36. PubMed ID: 19070492
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  • 3. [The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene].
    Onishi Y, Higuchi J, Ogawa T, Namekawa A, Hayashi H, Odakura H, Goto K, Hayashi YK.
    Rinsho Shinkeigaku; 2002 Feb; 42(2):140-4. PubMed ID: 12424964
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  • 4. Emery-Dreifuss muscular dystrophy.
    Zacharias AS, Wagener ME, Warren ST, Hopkins LC.
    Semin Neurol; 1999 Feb; 19(1):67-79. PubMed ID: 10711990
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  • 5. 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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  • 6. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
    Bonne G, Mercuri E, Muchir A, Urtizberea A, Bécane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F.
    Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
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  • 7. Identification of lamin A/C ( LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy 1B.
    Ki CS, Hong JS, Jeong GY, Ahn KJ, Choi KM, Kim DK, Kim JW.
    J Hum Genet; 2002 Aug; 47(5):225-8. PubMed ID: 12032588
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  • 8. X-linked Emery-Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures.
    Brisset M, Ben Yaou R, Carlier RY, Chanut A, Nicolas G, Romero NB, Wahbi K, Decrocq C, Leturcq F, Laforêt P, Malfatti E.
    Neuromuscul Disord; 2019 Sep; 29(9):678-683. PubMed ID: 31474437
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  • 10. [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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  • 12. Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes.
    Bernasconi P, Carboni N, Ricci G, Siciliano G, Politano L, Maggi L, Mongini T, Vercelli L, Rodolico C, Biagini E, Boriani G, Ruggiero L, Santoro L, Schena E, Prencipe S, Evangelisti C, Pegoraro E, Morandi L, Columbaro M, Lanzuolo C, Sabatelli P, Cavalcante P, Cappelletti C, Bonne G, Muchir A, Lattanzi G.
    Nucleus; 2018 Jan 01; 9(1):292-304. PubMed ID: 29693488
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  • 13. Cardiomyopathy and atrioventricular block in Emery-Dreifuss muscular dystrophy--a case report.
    Kanada M, Demirtaş M, Güzel R, San M, Tuncer I.
    Angiology; 2002 Jan 01; 53(1):109-12. PubMed ID: 11863303
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  • 14. Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy.
    Menezes MP, Waddell LB, Evesson FJ, Cooper S, Webster R, Jones K, Mowat D, Kiernan MC, Johnston HM, Corbett A, Harbord M, North KN, Clarke NF.
    Neurology; 2012 Apr 17; 78(16):1258-63. PubMed ID: 22491857
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  • 15. Emery-Dreifuss humeroperoneal muscular dystrophy: cardiac manifestations.
    Parmar MS, Parmar KS.
    Can J Cardiol; 2012 Apr 17; 28(4):516.e1-3. PubMed ID: 22480903
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