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Journal Abstract Search

265 related items for PubMed ID: 9027857

  • 41. Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12.
    Jung D, Leturcq F, Sunada Y, Duclos F, Tomé FM, Moomaw C, Merlini L, Azibi K, Chaouch M, Slaughter C, Fardeau M, Kaplan JC, Campbell KP.
    FEBS Lett; 1996 Feb 26; 381(1-2):15-20. PubMed ID: 8641426
    [Abstract] [Full Text] [Related]

  • 42. 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
    [Abstract] [Full Text] [Related]

  • 43. Abnormal expression of laminin beta 1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy.
    Li M, Dickson DW, Spiro AJ.
    Arch Neurol; 1997 Dec 12; 54(12):1457-61. PubMed ID: 9400354
    [Abstract] [Full Text] [Related]

  • 44. [Gene analysis in patients with muscular dystrophy: alpha-sarcoglycan (adhalin) gene mutations in patients with malignant limb-girdle muscular dystrophy].
    Akaike M, Kawai H.
    Rinsho Byori; 1997 Feb 12; 45(2):136-40. PubMed ID: 9120997
    [Abstract] [Full Text] [Related]

  • 45. Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice.
    Duclos F, Straub V, Moore SA, Venzke DP, Hrstka RF, Crosbie RH, Durbeej M, Lebakken CS, Ettinger AJ, van der Meulen J, Holt KH, Lim LE, Sanes JR, Davidson BL, Faulkner JA, Williamson R, Campbell KP.
    J Cell Biol; 1998 Sep 21; 142(6):1461-71. PubMed ID: 9744877
    [Abstract] [Full Text] [Related]

  • 46. Muscle degeneration without mechanical injury in sarcoglycan deficiency.
    Hack AA, Cordier L, Shoturma DI, Lam MY, Sweeney HL, McNally EM.
    Proc Natl Acad Sci U S A; 1999 Sep 14; 96(19):10723-8. PubMed ID: 10485893
    [Abstract] [Full Text] [Related]

  • 47. The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
    Vainzof M, Passos-Bueno MR, Canovas M, Moreira ES, Pavanello RC, Marie SK, Anderson LV, Bonnemann CG, McNally EM, Nigro V, Kunkel LM, Zatz M.
    Hum Mol Genet; 1996 Dec 14; 5(12):1963-9. PubMed ID: 8968750
    [Abstract] [Full Text] [Related]

  • 48. Sarcolemmal defect and subsarcolemmal lesion in a patient with gamma-sarcoglycan deficiency.
    Li M, Dickson DW, Spiro AJ.
    Neurology; 1998 Mar 14; 50(3):807-9. PubMed ID: 9521284
    [Abstract] [Full Text] [Related]

  • 49. Sarcoglycan complex: a muscular supporter of dystroglycan-dystrophin interplay?
    Matsumura K, Saito F, Yamada H, Hase A, Sunada Y, Shimizu T.
    Cell Mol Biol (Noisy-le-grand); 1999 Sep 14; 45(6):751-62. PubMed ID: 10541473
    [Abstract] [Full Text] [Related]

  • 50. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population.
    Vainzof M, Passos-Bueno MR, Pavanello RC, Marie SK, Oliveira AS, Zatz M.
    J Neurol Sci; 1999 Mar 15; 164(1):44-9. PubMed ID: 10385046
    [Abstract] [Full Text] [Related]

  • 51. Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy.
    Ginjaar HB, van der Kooi AJ, Ceelie H, Kneppers AL, van Meegen M, Barth PG, Busch HF, Wokke JH, Anderson LV, Bönnemann CG, Jeanpierre M, Bolhuis PA, Moorman AF, de Visser M, Bakker E, Ommen GJ.
    J Neurol; 2000 Jul 15; 247(7):524-9. PubMed ID: 10993494
    [Abstract] [Full Text] [Related]

  • 52. 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 15; 59(5):1040-7. PubMed ID: 8900232
    [Abstract] [Full Text] [Related]

  • 53. Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.
    Eymard B, Romero NB, Leturcq F, Piccolo F, Carrié A, Jeanpierre M, Collin H, Deburgrave N, Azibi K, Chaouch M, Merlini L, Thémar-Noël C, Penisson I, Mayer M, Tanguy O, Campbell KP, Kaplan JC, Tomé FM, Fardeau M.
    Neurology; 1997 May 15; 48(5):1227-34. PubMed ID: 9153448
    [Abstract] [Full Text] [Related]

  • 54. Limb girdle muscular dystrophy: a pathological and immunohistochemical reevaluation.
    van der Kooi AJ, Ginjaar HB, Busch HF, Wokke JH, Barth PG, de Visser M.
    Muscle Nerve; 1998 May 15; 21(5):584-90. PubMed ID: 9572237
    [Abstract] [Full Text] [Related]

  • 55. Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy.
    Matsumura K, Tomé FM, Collin H, Azibi K, Chaouch M, Kaplan JC, Fardeau M, Campbell KP.
    Nature; 1992 Sep 24; 359(6393):320-2. PubMed ID: 1406935
    [Abstract] [Full Text] [Related]

  • 56. New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency.
    Higuchi I, Iwaki H, Kawai H, Endo T, Kunishige M, Fukunaga H, Nakagawa M, Arimura K, Osame M.
    J Neurol Sci; 1997 Dec 09; 153(1):100-5. PubMed ID: 9455986
    [Abstract] [Full Text] [Related]

  • 57. Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene.
    McNally EM, Ly CT, Kunkel LM.
    FEBS Lett; 1998 Jan 23; 422(1):27-32. PubMed ID: 9475163
    [Abstract] [Full Text] [Related]

  • 58. Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.
    Durbeej M, Cohn RD, Hrstka RF, Moore SA, Allamand V, Davidson BL, Williamson RA, Campbell KP.
    Mol Cell; 2000 Jan 23; 5(1):141-51. PubMed ID: 10678176
    [Abstract] [Full Text] [Related]

  • 59. Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate.
    Duclos F, Broux O, Bourg N, Straub V, Feldman GL, Sunada Y, Lim LE, Piccolo F, Cutshall S, Gary F, Quetier F, Kaplan JC, Jackson CE, Beckmann JS, Campbell KP.
    Neuromuscul Disord; 1998 Feb 23; 8(1):30-8. PubMed ID: 9565988
    [Abstract] [Full Text] [Related]

  • 60. Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family.
    Vainzof M, Moreira ES, Canovas M, Anderson LV, Pavanello RC, Passos-Bueno MR, Zatz M.
    Muscle Nerve; 2000 Jun 23; 23(6):984-8. PubMed ID: 10842281
    [Abstract] [Full Text] [Related]

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