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Journal Abstract Search

157 related items for PubMed ID: 8866424

  • 21.
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  • 23. 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; 34(12):973-7. PubMed ID: 9429136
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  • 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; 24(2):262-72. PubMed ID: 11180210
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  • 29. A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy.
    van der Kooi AJ, de Visser M, van Meegen M, Ginjaar HB, van Essen AJ, Jennekens FG, Jongen PJ, Leschot NJ, Bolhuis PA.
    Neuromuscul Disord; 1998 Jun; 8(5):305-8. PubMed ID: 9673983
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  • 30. epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D.
    Ettinger AJ, Feng G, Sanes JR.
    J Biol Chem; 1997 Dec 19; 272(51):32534-8. PubMed ID: 9405466
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  • 31. Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.
    Crosbie RH, Barresi R, Campbell KP.
    FASEB J; 2002 Nov 19; 16(13):1786-91. PubMed ID: 12409321
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  • 32. [Adhalin(alpha-sarcoglycan) gene mutations in patients with malignant limb-girdle muscular dystrophy (MLGMD) (Miyoshi)].
    Endo T, Kawai H.
    Nihon Rinsho; 1997 Dec 19; 55(12):3159-64. PubMed ID: 9436428
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  • 33. 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 19; 39(11):770-4. PubMed ID: 9393893
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  • 35. Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.
    Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, Collin H, Dovico SA, Stolle CA, Fardeau M, Tomé FM, Campbell KP.
    Hum Mol Genet; 2000 Aug 12; 9(13):2019-27. PubMed ID: 10942431
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  • 37. Concomitant deficiency of beta- and gamma-sarcoglycans in 20 alpha-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspects.
    Barresi R, Confalonieri V, Lanfossi M, Di Blasi C, Torchiana E, Mantegazza R, Jarre L, Nardocci N, Boffi P, Tezzon F, Pini A, Cornelio F, Mora M, Morandi L.
    Acta Neuropathol; 1997 Jul 12; 94(1):28-35. PubMed ID: 9224527
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  • 38. 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
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  • 39. 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 13; 92(4):369-77. PubMed ID: 8891069
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  • 40. Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.
    McNally EM, Passos-Bueno MR, Bönnemann CG, Vainzof M, de Sá Moreira E, Lidov HG, Othmane KB, Denton PH, Vance JM, Zatz M, Kunkel LM.
    Am J Hum Genet; 1996 Nov 13; 59(5):1040-7. PubMed ID: 8900232
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