يعرض 1 - 9 نتائج من 9 نتيجة بحث عن '"miositis por cuerpos de inclusión"', وقت الاستعلام: 0.70s تنقيح النتائج
  1. 1
    Academic Journal

    المؤلفون: García-Alfonso, Carolina

    المساهمون: Pontificia Universidad Javeriana. Facultad de Medicina. Departamento de Neurociencias. Neurología, García-Alfonso, Carolina, Millan, Sonia

    وصف الملف: PDF; application/pdf

    Relation: 158; 165; Revista Colombiana de Reumatología; 27; https://login.ezproxy.javeriana.edu.co/login?qurl=https%3a%2f%2fsearch.ebscohost.com%2flogin.aspx%3fdirect%3dtrue%26AuthType%3dip%26db%3dedselp%26AN%3dS0121812320300712%26lang%3des%26site%3deds-live; 0121-8123 / 2027-9000 (Electrónico); http://hdl.handle.net/10554/62419; https://doi.org/10.1016/j.rcreu.2020.05.015; instname:Pontificia Universidad Javeriana; reponame:Repositorio Institucional - Pontificia Universidad Javeriana; repourl:https://repository.javeriana.edu.co

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    المساهمون: Gomez Mazuera, Angela Maria

    المصدر: Balakrishnan, A., Aggarwal, R., Agarwal, V., & Gupta, L. (2020). Inclusion body myositis in the rheumatology clinic. Int J Rheum Dis, 23(9), 1126-1135. doi:10.1111/1756-185x.13902
    Belsh, J. M., & Schiffman, P. L. (1996). The amyotrophic lateral sclerosis (ALS) patient perspective on misdiagnosis and its repercussions. J Neurol Sci, 139 Suppl, 110-116. doi:10.1016/0022-510x(96)00088-3
    Dabby, R., Lange, D. J., Trojaborg, W., Hays, A. P., Lovelace, R. E., Brannagan, T. H., & Rowland, L. P. (2001). Inclusion body myositis mimicking motor neuron disease. Arch Neurol, 58(8), 1253-1256. doi:10.1001/archneur.58.8.1253
    Hannaford, A., Pavey, N., van den Bos, M., Geevasinga, N., Menon, P., Shefner, J. M., . . . Vucic, S. (2021). Diagnostic Utility of Gold Coast Criteria in Amyotrophic Lateral Sclerosis. Ann Neurol, 89(5), 979-986. doi:10.1002/ana.26045
    Hardiman, O., Al-Chalabi, A., Chio, A., Corr, E. M., Logroscino, G., Robberecht, W., . . . van den Berg, L. H. (2017). Amyotrophic lateral sclerosis. Nat Rev Dis Primers, 3, 17071. doi:10.1038/nrdp.2017.71
    Hilton-Jones, D., & Brady, S. (2016). Diagnostic criteria for inclusion body myositis. J Intern Med, 280(1), 52-62. doi:10.1111/joim.12480
    Hulisz, D. (2018). Amyotrophic lateral sclerosis: disease state overview. Am J Manag Care, 24(15 Suppl), S320-s326.
    Joy, J. L., Oh, S. J., & Baysal, A. I. (1990). Electrophysiological spectrum of inclusion body myositis. Muscle Nerve, 13(10), 949-951. doi:10.1002/mus.880131010
    Kiernan, M. C., Vucic, S., Cheah, B. C., Turner, M. R., Eisen, A., Hardiman, O., . . . Zoing, M. C. (2011). Amyotrophic lateral sclerosis. Lancet, 377(9769), 942-955. doi:10.1016/s0140-6736(10)61156-7
    Kwan, J., & Vullaganti, M. (2022). Amyotrophic lateral sclerosis mimics. Muscle Nerve. doi:10.1002/mus.27567
    Lenglet, T., & Camdessanché, J. P. (2017). Amyotrophic lateral sclerosis or not: Keys for the diagnosis. Rev Neurol (Paris), 173(5), 280-287. doi:10.1016/j.neurol.2017.04.003
    Masrori, P., & Van Damme, P. (2020). Amyotrophic lateral sclerosis: a clinical review. European Journal of Neurology, 27. doi:10.1111/ene.14393
    Mastaglia, F. L., & Needham, M. (2015). Inclusion body myositis: a review of clinical and genetic aspects, diagnostic criteria and therapeutic approaches. J Clin Neurosci, 22(1), 6-13. doi:10.1016/j.jocn.2014.09.012
    Rickham, P. P. (1964). HUMAN EXPERIMENTATION. CODE OF ETHICS OF THE WORLD MEDICAL ASSOCIATION. DECLARATION OF HELSINKI. Br Med J, 2(5402), 177. doi:10.1136/bmj.2.5402.177
    Schellenberg, K. L., Johnston, W. S., Kalra, S., Resch, L., & Johnson, E. S. (2010). Inclusion body myositis masquerading as amyotrophic lateral sclerosis. Can J Neurol Sci, 37(5), 687-691. doi:10.1017/s031716710001091x
    Shefner, J. M., Al-Chalabi, A., Baker, M. R., Cui, L. Y., de Carvalho, M., Eisen, A., . . . Kiernan, M. C. (2020). A proposal for new diagnostic criteria for ALS. Clin Neurophysiol, 131(8), 1975-1978. doi:10.1016/j.clinph.2020.04.005
    Shen, D., Yang, X., Wang, Y., He, D., Sun, X., Cai, Z., . . . Cui, L. (2021). The Gold Coast criteria increases the diagnostic sensitivity for amyotrophic lateral sclerosis in a Chinese population. Transl Neurodegener, 10(1), 28. doi:10.1186/s40035-021-00253-2
    Talbott, E. O., Malek, A. M., & Lacomis, D. (2016). The epidemiology of amyotrophic lateral sclerosis. Handb Clin Neurol, 138, 225-238. doi:10.1016/b978-0-12-802973-2.00013-6
    van Es, M. A., Hardiman, O., Chio, A., Al-Chalabi, A., Pasterkamp, R. J., Veldink, J. H., & van den Berg, L. H. (2017). Amyotrophic lateral sclerosis. The Lancet, 390(10107), 2084-2098. doi:10.1016/S0140-6736(17)31287-4
    Repositorio EdocUR-U. Rosario
    Universidad del Rosario
    instacron:Universidad del Rosario

    وصف الملف: 30 pp; application/pdf

  3. 3
    Dissertation/ Thesis
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  5. 5
    Academic Journal
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    Academic Journal
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