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Journal Abstract Search

262 related items for PubMed ID: 14755494

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  • 3. Type 2 myotonic dystrophy can be predicted by the combination of type 2 muscle fiber central nucleation and scattered atrophy.
    Bassez G, Chapoy E, Bastuji-Garin S, Radvanyi-Hoffman H, Authier FJ, Pellissier JF, Eymard B, Gherardi RK.
    J Neuropathol Exp Neurol; 2008 Apr; 67(4):319-25. PubMed ID: 18379436
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  • 6. Musculoskeletal pain in patients with myotonic dystrophy type 2.
    George A, Schneider-Gold C, Zier S, Reiners K, Sommer C.
    Arch Neurol; 2004 Dec; 61(12):1938-42. PubMed ID: 15596616
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  • 7. Congenital myotonic dystrophy: variability in muscle involvement and histopathological process.
    Kuo HC, Huang CC, Chu CC, Wai YY, Hsiao KM, Chu NS.
    Acta Neurol Taiwan; 2006 Mar; 15(1):13-20. PubMed ID: 16599279
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  • 8. Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2.
    Vihola A, Bassez G, Meola G, Zhang S, Haapasalo H, Paetau A, Mancinelli E, Rouche A, Hogrel JY, Laforêt P, Maisonobe T, Pellissier JF, Krahe R, Eymard B, Udd B.
    Neurology; 2003 Jun 10; 60(11):1854-7. PubMed ID: 12796551
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  • 9. Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1.
    Thornell LE, Lindstöm M, Renault V, Klein A, Mouly V, Ansved T, Butler-Browne G, Furling D.
    Neuropathol Appl Neurobiol; 2009 Dec 10; 35(6):603-13. PubMed ID: 19207265
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  • 10. [A case of myotonic dystrophy showing proximal dominant muscle involvement but not myotonia].
    Mihori A, Miyauchi H, Kaneda K, Nakayama M, Ono S, Shimizu N.
    Rinsho Shinkeigaku; 1999 Apr 10; 39(4):461-4. PubMed ID: 10391974
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  • 11. Proximal myotonic myopathy: clinical, neuropathologic, and molecular genetic features.
    Eisenschenk S, Triggs WJ, Pearl GS, Rojiani AM.
    Ann Clin Lab Sci; 2001 Apr 10; 31(2):140-6. PubMed ID: 11337902
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  • 12. Predominant fiber atrophy and fiber type disproportion in early ullrich disease.
    Schessl J, Goemans NM, Magold AI, Zou Y, Hu Y, Kirschner J, Sciot R, Bönnemann CG.
    Muscle Nerve; 2008 Sep 10; 38(3):1184-91. PubMed ID: 18720506
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  • 13. Unusual clinical, laboratory, and muscle histopathological findings in a family with myotonic dystrophy type 2.
    Toth C, Dunham C, Suchowersky O, Parboosingh J, Brownell K.
    Muscle Nerve; 2007 Feb 10; 35(2):259-64. PubMed ID: 17068784
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  • 15. Muscle histopathology in myotonic dystrophy in relation to age and muscular weakness.
    Tohgi H, Kawamorita A, Utsugisawa K, Yamagata M, Sano M.
    Muscle Nerve; 1994 Sep 10; 17(9):1037-43. PubMed ID: 8065390
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  • 16. Cardiac and skeletal muscle involvement in myotonic dystrophy type 2 (DM2): a quantitative 31P-MRS and MRI study.
    Schneider-Gold C, Beer M, Köstler H, Buchner S, Sandstede J, Hahn D, Toyka KV.
    Muscle Nerve; 2004 Nov 10; 30(5):636-44. PubMed ID: 15452841
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  • 17. Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2.
    Merlini L, Sabatelli P, Columbaro M, Bonifazi E, Pisani V, Massa R, Novelli G.
    Muscle Nerve; 2005 Jun 10; 31(6):764-7. PubMed ID: 15704146
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  • 19. Winged scapula in patients with myotonic dystrophy type 1.
    Hamano T, Mutoh T, Hirayama M, Uematsu H, Higuchi I, Koga H, Umehara F, Komai K, Kuriyama M.
    Neuromuscul Disord; 2012 Aug 10; 22(8):755-8. PubMed ID: 22683376
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