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Journal Abstract Search

114 related items for PubMed ID: 2260862

  • 1. Normal dystrophin in McLeod myopathy.
    Danek A, Witt TN, Stockmann HB, Weiss BJ, Schotland DL, Fischbeck KH.
    Ann Neurol; 1990 Nov; 28(5):720-2. PubMed ID: 2260862
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  • 2. Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy.
    Kimura S, Sugino S, Ohtani Y, Matsukura M, Nishino I, Ikezawa M, Sakata A, Kondo Y, Yoshioka K, Huard J, Nonaka I, Miike T.
    Ann Neurol; 1998 Dec; 44(6):967-71. PubMed ID: 9851444
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  • 3. Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome).
    Carter ND, Morgan JE, Monaco AP, Schwartz MS, Jeffery S.
    J Med Genet; 1990 Jun; 27(6):345-7. PubMed ID: 2193159
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  • 4. [Quadriceps myopathy as dystrophin-associated myopathy].
    von Mitzlaff HC, Liechti-Gallati S, Rösler KM, Burgunder JM.
    Schweiz Med Wochenschr; 1993 Oct 09; 123(40):1865-9. PubMed ID: 8211039
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  • 5. Quadriceps myopathy: forme fruste of Becker muscular dystrophy.
    Sunohara N, Arahata K, Hoffman EP, Yamada H, Nishimiya J, Arikawa E, Kaido M, Nonaka I, Sugita H.
    Ann Neurol; 1990 Nov 09; 28(5):634-9. PubMed ID: 2260849
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  • 6. Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophy.
    Swash M, Schwartz MS, Carter ND, Heath R, Leak M, Rogers KL.
    Brain; 1983 Sep 09; 106 (Pt 3)():717-33. PubMed ID: 6685553
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  • 9. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
    Miranda AF, Francke U, Bonilla E, Martucci G, Schmidt B, Salviati G, Rubin M.
    Am J Med Genet; 1989 Feb 09; 32(2):268-73. PubMed ID: 2648829
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  • 10. [Specificity of the dystrophin immunohistochemical technique in muscular dystrophy].
    Colomer Oferil J, Vila Torres J, Huezo Montoya C.
    Neurologia; 1993 May 09; 8(5):112-5. PubMed ID: 8507503
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  • 13. [Therapy of Duchenne muscular dystrophy with umbilical cord blood stem cell transplantation].
    Zhang C, Feng HY, Huang SL, Fang JP, Xiao LL, Yao XL, Chen C, Ye X, Zeng Y, Lu XL, Wen JM, Zhang WX, Li Z, Feng SW, Xu HG, Huang K, Zhou DH, Chen W, Xie YM, Xi J, Zhang M, Li Y, Liu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug 09; 22(4):399-405. PubMed ID: 16086277
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  • 14. Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family.
    Wilton SD, Chandler DC, Kakulas BA, Laing NG.
    Hum Mutat; 1994 Aug 09; 3(2):133-40. PubMed ID: 8199594
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  • 15. Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy.
    Marini M, Salmi AA, Watihayati MS, SMardziah MD, Zahri MK, Hoh BP, Ankathil R, Lai PS, Zilfalil BA.
    Med J Malaysia; 2008 Mar 09; 63(1):31-4. PubMed ID: 18935728
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  • 18. Deletion of exon 16 of the dystrophin gene is not associated with disease.
    Schwartz M, Dunø M, Palle AL, Krag T, Vissing J.
    Hum Mutat; 2007 Feb 09; 28(2):205. PubMed ID: 17226814
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  • 20. Localization and characterization of dystrophin in muscle biopsy specimens from Duchenne muscular dystrophy and various neuromuscular disorders.
    Uchino M, Araki S, Miike T, Teramoto H, Nakamura T, Yasutake T.
    Muscle Nerve; 1989 Dec 09; 12(12):1009-16. PubMed ID: 2695839
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