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129 related items for PubMed ID: 12235836

  • 1. [Recent advances in limb-girdle muscular dystrophy research].
    Nonaka I, Minami N, Chae J, Hayashi YK, Nishino I, Arahata K.
    Rinsho Shinkeigaku; 2001 Dec; 41(12):1194-7. PubMed ID: 12235836
    [Abstract] [Full Text] [Related]

  • 2. Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy.
    Fanin M, Pegoraro E, Matsuda-Asada C, Brown RH, Angelini C.
    Neurology; 2001 Mar 13; 56(5):660-5. PubMed ID: 11245721
    [Abstract] [Full Text] [Related]

  • 3. Dysferlin protein analysis in limb-girdle muscular dystrophies.
    Vainzof M, Anderson LV, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RC, Passos-Bueno MR, Zatz M.
    J Mol Neurosci; 2001 Aug 13; 17(1):71-80. PubMed ID: 11665864
    [Abstract] [Full Text] [Related]

  • 4.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Pegoraro E, Hoffman EP.
    ; 1993 Aug 13. PubMed ID: 20301582
    [Abstract] [Full Text] [Related]

  • 5. [The frequency of patients with adhalin deficiency in a muscular dystrophy patient population].
    Hayashi YK, Arahata K.
    Nihon Rinsho; 1997 Dec 13; 55(12):3165-8. PubMed ID: 9436429
    [Abstract] [Full Text] [Related]

  • 6. Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G.
    Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M.
    Am J Med Genet; 1999 Feb 19; 82(5):392-8. PubMed ID: 10069710
    [Abstract] [Full Text] [Related]

  • 7. Making sense of the limb-girdle muscular dystrophies.
    Bushby KM.
    Brain; 1999 Aug 19; 122 ( Pt 8)():1403-20. PubMed ID: 10430828
    [Abstract] [Full Text] [Related]

  • 8. Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies.
    Pogue R, Anderson LV, Pyle A, Sewry C, Pollitt C, Johnson MA, Davison K, Moss JA, Mercuri E, Muntoni F, Bushby KM.
    Neuromuscul Disord; 2001 Jan 19; 11(1):80-7. PubMed ID: 11166169
    [Abstract] [Full Text] [Related]

  • 9. Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).
    Anderson LV, Harrison RM, Pogue R, Vafiadaki E, Pollitt C, Davison K, Moss JA, Keers S, Pyle A, Shaw PJ, Mahjneh I, Argov Z, Greenberg CR, Wrogemann K, Bertorini T, Goebel HH, Beckmann JS, Bashir R, Bushby KM.
    Neuromuscul Disord; 2000 Dec 19; 10(8):553-9. PubMed ID: 11053681
    [Abstract] [Full Text] [Related]

  • 10. Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.
    Richard I, Brenguier L, Dinçer P, Roudaut C, Bady B, Burgunder JM, Chemaly R, Garcia CA, Halaby G, Jackson CE, Kurnit DM, Lefranc G, Legum C, Loiselet J, Merlini L, Nivelon-Chevallier A, Ollagnon-Roman E, Restagno G, Topaloglu H, Beckmann JS.
    Am J Hum Genet; 1997 May 19; 60(5):1128-38. PubMed ID: 9150160
    [Abstract] [Full Text] [Related]

  • 11. Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy.
    Chae J, Minami N, Jin Y, Nakagawa M, Murayama K, Igarashi F, Nonaka I.
    Neuromuscul Disord; 2001 Sep 19; 11(6-7):547-55. PubMed ID: 11525884
    [Abstract] [Full Text] [Related]

  • 12. Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan.
    Minami N, Nishino I, Kobayashi O, Ikezoe K, Goto Y, Nonaka I.
    J Neurol Sci; 1999 Dec 01; 171(1):31-7. PubMed ID: 10567047
    [Abstract] [Full Text] [Related]

  • 13. Limb girdle muscular dystrophy type 2A in India: a study based on semi-quantitative protein analysis, with clinical and histopathological correlation.
    Pathak P, Sharma MC, Sarkar C, Jha P, Suri V, Mohd H, Singh S, Bhatia R, Gulati S.
    Neurol India; 2010 Dec 01; 58(4):549-54. PubMed ID: 20739790
    [Abstract] [Full Text] [Related]

  • 14. Molecular bases of autosomal recessive limb-girdle muscular dystrophies.
    Nigro V.
    Acta Myol; 2003 Sep 01; 22(2):35-42. PubMed ID: 14959561
    [Abstract] [Full Text] [Related]

  • 15. Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain).
    Urtasun M, Sáenz A, Roudaut C, Poza JJ, Urtizberea JA, Cobo AM, Richard I, García Bragado F, Leturcq F, Kaplan JC, Martí Massó JF, Beckmann JS, López de Munain A.
    Brain; 1998 Sep 01; 121 ( Pt 9)():1735-47. PubMed ID: 9762961
    [Abstract] [Full Text] [Related]

  • 16. The limb-girdle muscular dystrophies-multiple genes, multiple mechanisms.
    Bushby KM.
    Hum Mol Genet; 1999 Sep 01; 8(10):1875-82. PubMed ID: 10469840
    [Abstract] [Full Text] [Related]

  • 17. Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes.
    Fanin M, Nascimbeni AC, Aurino S, Tasca E, Pegoraro E, Nigro V, Angelini C.
    Neurology; 2009 Apr 21; 72(16):1432-5. PubMed ID: 19380703
    [Abstract] [Full Text] [Related]

  • 18. 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 21; 21(5):584-90. PubMed ID: 9572237
    [Abstract] [Full Text] [Related]

  • 19. A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey.
    Dinçer P, Leturcq F, Richard I, Piccolo F, Yalnizoglu D, de Toma C, Akçören Z, Broux O, Deburgrave N, Brenguier L, Roudaut C, Urtizberea JA, Jung D, Tan E, Jeanpierre M, Campbell KP, Kaplan JC, Beckmann JS, Topaloglu H.
    Ann Neurol; 1997 Aug 21; 42(2):222-9. PubMed ID: 9266733
    [Abstract] [Full Text] [Related]

  • 20. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.
    Nakamura A, Yoshida K, Ikeda S.
    Clin Neurol Neurosurg; 2004 Mar 21; 106(2):122-8. PubMed ID: 15003303
    [Abstract] [Full Text] [Related]

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