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Journal Abstract Search

265 related items for PubMed ID: 9027857

  • 21. Abnormalities of dystrophin, the sarcoglycans, and laminin alpha2 in the muscular dystrophies.
    Jones KJ, Kim SS, North KN.
    J Med Genet; 1998 May; 35(5):379-86. PubMed ID: 9610800
    [Abstract] [Full Text] [Related]

  • 22. Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex.
    Barresi R, Moore SA, Stolle CA, Mendell JR, Campbell KP.
    J Biol Chem; 2000 Dec 08; 275(49):38554-60. PubMed ID: 10993904
    [Abstract] [Full Text] [Related]

  • 23. Dystrophin-associated protein abnormalities in dystrophin-deficient muscle fibers from symptomatic and asymptomatic Duchenne/Becker muscular dystrophy carriers.
    Di Blasi C, Morandi L, Barresi R, Blasevich F, Cornelio F, Mora M.
    Acta Neuropathol; 1996 Oct 08; 92(4):369-77. PubMed ID: 8891069
    [Abstract] [Full Text] [Related]

  • 24. Confocal analysis of the dystrophin protein complex in muscular dystrophy.
    Draviam R, Billington L, Senchak A, Hoffman EP, Watkins SC.
    Muscle Nerve; 2001 Feb 08; 24(2):262-72. PubMed ID: 11180210
    [Abstract] [Full Text] [Related]

  • 25. Absence of alpha-sarcoglycan and novel missense mutations in the alpha-sarcoglycan gene in a young British girl with muscular dystrophy.
    Quinlivan RM, Robb SA, Sewry C, Dubowitz V, Piccolo F, Kaplan JC.
    Dev Med Child Neurol; 1997 Nov 08; 39(11):770-4. PubMed ID: 9393893
    [Abstract] [Full Text] [Related]

  • 26. [Clinicopathological characteristics and molecular genetics of adhalin deficiency (severe childhood autosomal recessive muscular dystrophy/SCARMD)].
    Matsumura K.
    Nihon Rinsho; 1997 Dec 08; 55(12):3154-8. PubMed ID: 9436427
    [Abstract] [Full Text] [Related]

  • 27. Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).
    Bönnemann CG, Passos-Bueno MR, McNally EM, Vainzof M, de Sá Moreira E, Marie SK, Pavanello RC, Noguchi S, Ozawa E, Zatz M, Kunkel LM.
    Hum Mol Genet; 1996 Dec 08; 5(12):1953-61. PubMed ID: 8968749
    [Abstract] [Full Text] [Related]

  • 28. Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle.
    Mizuno Y, Noguchi S, Yamamoto H, Yoshida M, Suzuki A, Hagiwara Y, Hayashi YK, Arahata K, Nonaka I, Hirai S.
    Biochem Biophys Res Commun; 1994 Sep 15; 203(2):979-83. PubMed ID: 8093083
    [Abstract] [Full Text] [Related]

  • 29. Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations.
    Fanin M, Duggan DJ, Mostacciuolo ML, Martinello F, Freda MP, Sorarù G, Trevisan CP, Hoffman EP, Angelini C.
    J Med Genet; 1997 Dec 15; 34(12):973-7. PubMed ID: 9429136
    [Abstract] [Full Text] [Related]

  • 30. Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy.
    Metzinger L, Blake DJ, Squier MV, Anderson LV, Deconinck AE, Nawrotzki R, Hilton-Jones D, Davies KE.
    Hum Mol Genet; 1997 Jul 15; 6(7):1185-91. PubMed ID: 9215691
    [Abstract] [Full Text] [Related]

  • 31. Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?
    Klinge L, Dekomien G, Aboumousa A, Charlton R, Epplen JT, Barresi R, Bushby K, Straub V.
    Neuromuscul Disord; 2008 Dec 15; 18(12):934-41. PubMed ID: 18996010
    [Abstract] [Full Text] [Related]

  • 32. 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 15; 249(11):1608-11. PubMed ID: 12532930
    [No Abstract] [Full Text] [Related]

  • 33. Sarcoglycan deficiency in a large Italian population of myopathic patients.
    Prelle A, Comi GP, Tancredi L, Rigoletto C, Ciscato P, Fortunato F, Nesti S, Sciacco M, Robotti M, Bazzi P, Felisari G, Moggio M, Scarlato G.
    Acta Neuropathol; 1998 Nov 15; 96(5):509-14. PubMed ID: 9829815
    [Abstract] [Full Text] [Related]

  • 34. Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient mice.
    Sasaoka T, Imamura M, Araishi K, Noguchi S, Mizuno Y, Takagoshi N, Hama H, Wakabayashi-Takai E, Yoshimoto-Matsuda Y, Nonaka I, Kaneko K, Yoshida M, Ozawa E.
    Neuromuscul Disord; 2003 Mar 15; 13(3):193-206. PubMed ID: 12609501
    [Abstract] [Full Text] [Related]

  • 35. Immunohistochemistry of sarcolemmal membrane-associated proteins in formalin-fixed and paraffin-embedded skeletal muscle tissue: a promising tool for the diagnostic evaluation of common muscular dystrophies.
    Suriyonplengsaeng C, Dejthevaporn C, Khongkhatithum C, Sanpapant S, Tubthong N, Pinpradap K, Srinark N, Waisayarat J.
    Diagn Pathol; 2017 Feb 20; 12(1):19. PubMed ID: 28219397
    [Abstract] [Full Text] [Related]

  • 36. A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families.
    Dinçer P, Akçören Z, Demir E, Richard I, Sancak O, Kale G, Ozme S, Karaduman A, Tan E, Urtizberea JA, Beckmann JS, Topaloğlu H.
    J Med Genet; 2000 May 20; 37(5):361-7. PubMed ID: 10807695
    [Abstract] [Full Text] [Related]

  • 37. Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster.
    Straub V, Duclos F, Venzke DP, Lee JC, Cutshall S, Leveille CJ, Campbell KP.
    Am J Pathol; 1998 Nov 20; 153(5):1623-30. PubMed ID: 9811355
    [Abstract] [Full Text] [Related]

  • 38. Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations.
    Barresi R, Di Blasi C, Negri T, Brugnoni R, Vitali A, Felisari G, Salandi A, Daniel S, Cornelio F, Morandi L, Mora M.
    J Med Genet; 2000 Feb 20; 37(2):102-7. PubMed ID: 10662809
    [Abstract] [Full Text] [Related]

  • 39. gamma-sarcoglycan deficiency muscular dystrophy in two adults.
    Lin KL, Wang HS, Chen ST, Ro LS.
    J Formos Med Assoc; 2000 Oct 20; 99(10):789-91. PubMed ID: 11061077
    [Abstract] [Full Text] [Related]

  • 40. Rescue of skeletal muscles of gamma-sarcoglycan-deficient mice with adeno-associated virus-mediated gene transfer.
    Cordier L, Hack AA, Scott MO, Barton-Davis ER, Gao G, Wilson JM, McNally EM, Sweeney HL.
    Mol Ther; 2000 Feb 20; 1(2):119-29. PubMed ID: 10933922
    [Abstract] [Full Text] [Related]

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