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Journal Abstract Search

823 related items for PubMed ID: 23035061

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  • 3. Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.
    Hong JS, Ki CS, Kim JW, Suh YL, Kim JS, Baek KK, Kim BJ, Ahn KJ, Kim DK.
    J Korean Med Sci; 2005 Apr; 20(2):283-90. PubMed ID: 15832002
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  • 6. Reliability and accuracy of skeletal muscle imaging in limb-girdle muscular dystrophies. Author response.
    ten Dam L, van der Kooi AJ, van Wattingen M, de Haan RJ, de Visser M.
    Neurology; 2013 Jun 11; 80(24):2275-6. PubMed ID: 23905173
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  • 7. Reliability and accuracy of skeletal muscle imaging in limb-girdle muscular dystrophies. Author response.
    ten Dam L, van der Kooi AJ, van Wattingen M, de Haan RJ, de Visser M.
    Neurology; 2013 Jun 11; 80(24):2276-7. PubMed ID: 23905175
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  • 8. Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures.
    Mercuri E, Bushby K, Ricci E, Birchall D, Pane M, Kinali M, Allsop J, Nigro V, Sáenz A, Nascimbeni A, Fulizio L, Angelini C, Muntoni F.
    Neuromuscul Disord; 2005 Feb 11; 15(2):164-71. PubMed ID: 15694138
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  • 9. Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex.
    Xie Z, Xie Z, Yu M, Zheng Y, Sun C, Liu Y, Ling C, Zhu Y, Zhang W, Xiao J, Wang Z, Yuan Y.
    Orphanet J Rare Dis; 2019 Nov 12; 14(1):250. PubMed ID: 31747956
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  • 10. 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
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  • 11. Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5.
    Penttilä S, Palmio J, Suominen T, Raheem O, Evilä A, Muelas Gomez N, Tasca G, Waddell LB, Clarke NF, Barboi A, Hackman P, Udd B.
    Neurology; 2012 Mar 20; 78(12):897-903. PubMed ID: 22402862
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  • 12. Perturbation of muscle metabolism in patients with muscular dystrophy in early or acute phase of disease: In vitro, high resolution NMR spectroscopy based analysis.
    Srivastava NK, Yadav R, Mukherjee S, Sinha N.
    Clin Chim Acta; 2018 Mar 20; 478():171-181. PubMed ID: 29278724
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  • 13. The trefoil with single fruit sign in muscle magnetic resonance imaging is highly specific for dystrophinopathies.
    Zheng Y, Li W, Du J, Jin S, Li S, Zhao Y, Xu C, Wang Z, Lv H, Zhang W, Xiao J, Yuan Y.
    Eur J Radiol; 2015 Oct 20; 84(10):1992-8. PubMed ID: 26119801
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  • 14. Reliability and accuracy of skeletal muscle imaging in limb-girdle muscular dystrophies.
    Morrow JM, Reilly MM, Hanna MG.
    Neurology; 2013 Jun 11; 80(24):2276. PubMed ID: 23905174
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  • 15. Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophies.
    Ten Dam L, van der Kooi AJ, Rövekamp F, Linssen WH, de Visser M.
    Neuromuscul Disord; 2014 Dec 11; 24(12):1097-102. PubMed ID: 25176504
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  • 16. Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients.
    Lin F, Yang K, Lin X, Jin M, Chen L, Zheng FZ, Qiu LL, Ye ZX, Chen HZ, Lin MT, Wang N, Wang ZQ.
    Orphanet J Rare Dis; 2023 Nov 16; 18(1):356. PubMed ID: 37974208
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  • 17. Abnormal lipid metabolism in skeletal muscle tissue of patients with muscular dystrophy: In vitro, high-resolution NMR spectroscopy based observation in early phase of the disease.
    Srivastava NK, Yadav R, Mukherjee S, Pal L, Sinha N.
    Magn Reson Imaging; 2017 May 16; 38():163-173. PubMed ID: 28069416
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  • 18. Cardiac involvement in patients with limb-girdle muscular dystrophy type 2 and Becker muscular dystrophy.
    Sveen ML, Thune JJ, Køber L, Vissing J.
    Arch Neurol; 2008 Sep 16; 65(9):1196-201. PubMed ID: 18779423
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  • 19. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
    Park YE, Hayashi YK, Goto K, Komaki H, Hayashi Y, Inuzuka T, Noguchi S, Nonaka I, Nishino I.
    Neuromuscul Disord; 2009 Jan 16; 19(1):29-36. PubMed ID: 19070492
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  • 20. LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies.
    Løkken N, Born AP, Duno M, Vissing J.
    Muscle Nerve; 2015 Oct 16; 52(4):547-53. PubMed ID: 25663498
    [Abstract] [Full Text] [Related]

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