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Journal Abstract Search

124 related items for PubMed ID: 18277035

  • 1. Asymptomatic sporadic dysferlinopathy presenting with elevation of serum creatine kinase. Typical distribution of muscle involvement shown by MRI but not by CT.
    Okahashi S, Ogawa G, Suzuki M, Ogata K, Nishino I, Kawai M.
    Intern Med; 2008; 47(4):305-7. PubMed ID: 18277035
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  • 2. Heterogeneous characteristics of Korean patients with dysferlinopathy.
    Park HJ, Hong JM, Suh GI, Shin HY, Kim SM, Sunwoo IN, Suh BC, Choi YC.
    J Korean Med Sci; 2012 Apr; 27(4):423-9. PubMed ID: 22468107
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  • 3. Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes.
    Nguyen K, Bassez G, Krahn M, Bernard R, Laforêt P, Labelle V, Urtizberea JA, Figarella-Branger D, Romero N, Attarian S, Leturcq F, Pouget J, Lévy N, Eymard B.
    Arch Neurol; 2007 Aug; 64(8):1176-82. PubMed ID: 17698709
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  • 4. Diagnosis of dysferlinopathy masked by a superimposed hypothyroid myopathy.
    Benn KW, Bhalala OG, Day TJ, French CR.
    BMJ Case Rep; 2024 Aug 16; 17(8):. PubMed ID: 39153757
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  • 8. [Dysferlin expression in limb-girdle muscular dystrophy and Miyoshi myopathy: analysis of 45 cases].
    Ren SC, Yan CZ, Li MX, Liu SP, Wu JL, Zhao YY, Li W, Li DN.
    Zhonghua Yi Xue Za Zhi; 2007 Jun 05; 87(21):1486-90. PubMed ID: 17785089
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  • 10. Dysferlinopathy presenting as rhabdomyolysis and acute renal failure.
    Moody S, Mancias P.
    J Child Neurol; 2013 Apr 05; 28(4):502-5. PubMed ID: 22550092
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  • 11. Toward an objective measure of functional disability in dysferlinopathy.
    Woudt L, Di Capua GA, Krahn M, Castiglioni C, Hughes R, Campero M, Trangulao A, González-Hormazábal P, Godoy-Herrera R, Lévy N, Urtizberea JA, Jara L, Bevilacqua JA.
    Muscle Nerve; 2016 Jan 05; 53(1):49-57. PubMed ID: 25900324
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  • 13. The same answer using a simpler method: diagnosis in dysferlin muscle disease.
    Wicklund MP.
    Muscle Nerve; 2014 Sep 05; 50(3):313-4. PubMed ID: 25042040
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  • 16. Serum exosomes can restore cellular function in vitro and be used for diagnosis in dysferlinopathy.
    Dong X, Gao X, Dai Y, Ran N, Yin H.
    Theranostics; 2018 Sep 05; 8(5):1243-1255. PubMed ID: 29507617
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  • 18. Diagnosis by protein analysis of dysferlinopathy in two patients mistaken as polymyositis.
    Angelini C, Grisold W, Nigro V.
    Acta Myol; 2011 Dec 05; 30(3):185-7. PubMed ID: 22616201
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  • 19. A case of dysferlinopathy presenting choreic movements.
    Takahashi T, Aoki M, Imai T, Yoshioka M, Konno H, Higano S, Onodera Y, Saito H, Kimura I, Itoyama Y.
    Mov Disord; 2006 Sep 05; 21(9):1513-5. PubMed ID: 16817213
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  • 20. Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype.
    Berciano J, Gallardo E, Domínguez-Perles R, Gallardo E, García A, García-Barredo R, Combarros O, Infante J, Illa I.
    J Neurol Neurosurg Psychiatry; 2008 Feb 05; 79(2):205-8. PubMed ID: 17698502
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