These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

213 related items for PubMed ID: 7657792

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. A novel insert mutation in gamma-sarcoglycan gene leads to severe childhood autosomal recessive muscular dystrophy.
    Lin S, Ramelli GP, Moser H, Gallati S, Burgunder JM.
    J Neurol; 2002 Nov; 249(11):1608-11. PubMed ID: 12532930
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. Deficiency of adhalin in a patient with muscular dystrophy and cardiomyopathy.
    McNally EM, Bönnemann CG, Kunkel LM, Bhattacharya SK.
    N Engl J Med; 1996 Jun 13; 334(24):1610-1. PubMed ID: 8628353
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Mouse adhalin: primary structure and expression during late stages of muscle differentiation in vitro.
    Liu L, Vachon PH, Kuang W, Xu H, Wewer UM, Kylsten P, Engvall E.
    Biochem Biophys Res Commun; 1997 Jun 09; 235(1):227-35. PubMed ID: 9196068
    [Abstract] [Full Text] [Related]

  • 28. [Identification of adhalin gene mutation in limb-girdle muscular dystrophy in Chinese].
    Sun G, Wu Y, Zhang K, Zhang X, Jin C, Sun K.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Dec 10; 15(6):351-3. PubMed ID: 9845765
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. [Muscular dystrophy due to a mutation in the gene of alpha-sarcoglycan subunit of dystrophin associated protein complex].
    Urtasun M, Poza JJ, Gallano P, Lasa A, Sáenz A, Cobo AM, Leturcq F, López de Munain A, García-Bragado F.
    Med Clin (Barc); 1998 Apr 25; 110(14):538-42. PubMed ID: 9646269
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.
    Fardeau M, Matsumura K, Tomé FM, Collin H, Leturcq F, Kaplan JC, Campbell KP.
    C R Acad Sci III; 1993 Aug 25; 316(8):799-804. PubMed ID: 8044705
    [Abstract] [Full Text] [Related]

  • 37. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.
    Nakamura A, Yoshida K, Ikeda S.
    Clin Neurol Neurosurg; 2004 Mar 25; 106(2):122-8. PubMed ID: 15003303
    [Abstract] [Full Text] [Related]

  • 38. alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations.
    Duggan DJ, Fanin M, Pegoraro E, Angelini C, Hoffman EP.
    J Neurol Sci; 1996 Sep 01; 140(1-2):30-9. PubMed ID: 8866424
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 11.