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1Academic Journal
المؤلفون: T. M. Alekseeva, T. R. Stuchevskaya, V. S. Demeshonok, Т. М. Алексеева, Т. Р. Стучевская, В. С. Демешонок
المصدر: Neuromuscular Diseases; Том 8, № 4 (2018); 12-18 ; Нервно-мышечные болезни; Том 8, № 4 (2018); 12-18 ; 2413-0443 ; 2222-8721 ; 10.17650/2222-8721-2018-8-4
مصطلحات موضوعية: маситиниб, amyotrophic lateral sclerosis, pathogenetic therapy, clinical trial, riluzole, edaravone, nuedexta, masitinib, боковой амиотрофический склероз, патогенетическая терапия, клинические исследования, рилузол, эдаравон, нудекста
وصف الملف: application/pdf
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An analysis of extended survival in patients with ALS treated with riluzole. Arch Neurol 1998;55(4):526–8. DOI:10.1001/archneur.55.4.526. PMID: 9561981.; Brooks B.R., Belden D.S., Roelke K. et al. Survival in non-riluzole treated amyotrophic lateral sclerosis (ALS) – motor neuron disease (MND) patients with disease onset before and since 1996 is identical: a clinic-based epidemiological study. Amyotroph Lateral Scler Other Motor Neuron Disord 2001;2(Suppl 2):60–1.; Turner M.R., Bakker M., Sham P. et al. Prognostic modelling of therapeutic interventions in amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 2002;3(1):15–21. DOI:10.1080/146608202317576499. PMID: 12061944.; Al-Chalabi A., Hardiman O. The epidemiology of ALS: a conspiracy of genes, environment and time. Nat Rev Neurol 2013;9(11):617–28. DOI:10.1038/nrneurol.2013.203. PMID: 24126629.; Васенина Е.Е., Левин О.С. Окислительный стресс в патогенезе нейродегенеративных заболеваний: возможности терапии. Современная терапия в психиатрии и неврологии 2013;3(4): 39–46.; King A.E., Woodhouse A., Kirkcaldie M.T., Vickers J.C. Excitotoxicity in ALS: Overstimulation, or overreaction? Exp Neurol 2016;275:162–71. DOI:10.1016/j.expneurol.2015.09.019. PMID: 26584004.; Bräuer S., Zimyanin V., Hermann A. Prion-like properties of disease-relevant proteins in amyotrophic lateral sclerosis. J Neural Transm (Vienna) 2018;125(4):591–613. DOI:10.1007/s00702-018-1851-y. PMID: 29417336.; Ramesh N., Pandey U.B. Autophagy dysregulation in ALS: When protein aggregates get out of hand. Front Mol Neurosci 2017;10:263. DOI:10.3389/fn-mol.2017.00263. PMID: 28878620.; Hooten K.G., Beers D.R., Zhao W., Appel S.H. Protective and toxic neuroinflammation in amyotrophic lateral sclerosis. Neurotherapeutics 2015;12(2):364–75. DOI:10.1007/s13311-014-0329-3. PMID: 25567201.; Ugras S.E., Shorter J. RNA-binding proteins in amyotrophic lateral sclerosis and neurodegeneration. Neurol Res Int 2012;2012:432780. DOI:10.1155/2012/432780. PMID: 22919483.; De Vos K.J., Hafezparast M. Neurobiology of axonal transport defects in motor neuron diseases: Opportunities for translational research? Neurobiol Dis 2017;105:283–99. DOI: 1016/j. nbd.2017.02.004. PMID: 28235672.; Smith E.F., Shaw P.J., De Vos K.J. The role of mitochondria in amyotrophic lateral sclerosis. Neurosci Lett 2017 Jun 30. Available at: https://www.sciencedirect.com/science/article/pii/S030439401730544X?via%3Dihub. DOI:10.1016/j.neulet.2017.06.052. PMID: 28669745.; Al-Chalabi A., Calvo A., Chio A. et al. Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study. Lancet Neurol 2014;13(11):1108–13. DOI:10.1016/S1474-4422(14)70219-4. PMID: 25300936.; Chia R., Chiò A., Traynor B.J. Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications. Lancet Neurol 2018;17(1):94–102. DOI:10.1016/S1474-4422(17)30401-5. PMID: 29154141.; Maurel C., Dangoumau A., Marouillat S. Causative genes in amyotrophic lateral sclerosis and protein degradation pathways: a link to neurodegeneration. Mol Neurobiol 2018;55(8);6480–99. DOI:10.1007/s12035-017-0856-0. PMID: 29322304.; Blokhuis A.M., Groen E.J., Koppers M. et al. Protein aggregation in amyotrophic lateral sclerosis. Acta Neuropathol 2013;125(6):777–94. DOI:10.1007/s00401-013-1125-6. PMID: 23673820.; Liu J., Wang F. Role of neuroinflammation in amyotrophic lateral sclerosis: cellular mechanisms and therapeutic implications. Front Immunol 2017;8:1005. DOI:10.3389/fimmu.2017.01005. PMID: 28871262.; Markiewicz I., Lukomska B. The role of astrocytes in the physiology and pathology of the central nervous system. Acta Neurobiol Exp 2006;66(4):343–58. PMID:17265695; Talbot K., Turner M.R., Mersden R. et al. Motor neuron disease. A practical manual. New York: Oxford University Press, 2009. 214 p. DOI:10.1093/ med/9780199547364.003.02.; Мамчур В.И., Кравченко К.А., Опрышко В.И. Нейрофармакологический профиль действия глутаматергических препаратов (обзор литературы и собственных исследований). Журнал Академии медицинских наук Украины 2009;15(1):50–69.; Miyaji Y., Yoshimura S., Sakai N. et al. Effect of edaravone on favorable outcome in patients with acute cerebral large vessel occlusion: subanalysis of RESCUE-Japan registry. Neurol Med Chir (Tokyo) 2015;55(3):241–7. DOI: 2176/nmc.ra.20140219. PMID: 25739433.; Brooks B.R., Miller R.G., Swash M. et al. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 2000;1(5):293–9. DOI:10.1080/146608200300079536. PMID: 11464847.; Abe K., Aoki M., Tsuji S. et al. Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial. Lancet Neurol 2017;16(7):505–12. 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Adaptive design single center phosphodiesterase type 4 (PDE4) inhibitor – ibudilast (MN-166-ALS-1201) phase 1b/2a clinical trial double-blind (DB) with open label extension (OLE) [NCT02238626] for amyotrophic lateral sclerosis (ALS) patients [1] not requiring non-invasive ventilation (no NIV) up to 5 years (Early Cohort – EC) and [2] requiring non-invasive ventilation (NIV) up to 10 years (advanced NIV cohort – ANC) from disease onset – report of clinical trial DB, OLE and post-treatment cessation epochs – perprotocol (PP) treatment completion associated with improved survival and post treatment cessation loss of muscle strength (P3.127). Neurology 2017;88(16).; Ascherio A., LeWitt P.A., Xu K. et al. Urate as a predictor of the rate of clinical decline in Parkinson disease. Arch Neurol 2009;66(12):1460–8. DOI:10.1001/archneurol.2009.247. PMID: 19822770.; Schwarzschild M.A., Ascherio A., Beal M.F. et al. 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DOI:10.1172/jci.insight.97152. PMID: 29202456.; Cudkowicz M.E., Shefner J.M., Simpson E. et al. Arimoclomol at dosages up to 300 mg/day is well tolerated and safe in amyotrophic lateral sclerosis. MuscleNerve 2008;38(1):837-44. DOI:10.1002/mus.21059. PMID: 18551622.; Barral J.M., Broadley S.A., Schaffar G., Hartl F.U. Roles of molecular chaperones in protein misfolding diseases. Semin Cell Dev Biol 2004;15(1):17–29. DOI:10.1016/j.semcdb.2003.12.010. PMID: 15036203.; Kieran D., Kalmar B., Dick J.R. et al. Treatment with arimoclomol, a coinducer of heat shock proteins, delays disease progression in ALS mice. Nat Med 2004;10(4):402-5. DOI:10.1038/nm1021. PMID: 15034571.; Benatar M.M., Wuu J., Andersen P.M. et al. Randomized, double-blind, placebocontrolled trial of arimoclomol in rapidly progressive SOD1 ALS Neurology 2018;90(7):565-74. DOI:10.1212/WNL.0000000000004960. PMID: 29367439.; Garnock-Jones K.P. Dextromethorphan/ quinidine: in pseudobulbar affect. CNS Drugs 2011;25(5):435-45. DOI:10.2165/11207260-000000000-00000. PMID: 21476614.; Pioro E.P., Brooks B.R., Cummings J. et al. Safety, Tolerability, and Efficacy Results Trial of AVP-923 in PBA Investigators. Dextromethorphan plus ultra low-dose quinidine reduces pseudobulbar affect. Ann Neurol 2010;68(5):693-702. DOI:10.1002/ana.22093. PMID: 20839238.; Smith R., Pioro E., Myers K. et al. Enhanced bulbar function in amyotrophic lateral sclerosis: the nuedexta treatment trial. Neurotherapeutics 2017;14(3):762-72. DOI:10.1007/s13311-016-0508-5. PMID: 28070747.; Trias E., Ibarburu S., Barreto-Núñez R. et al. Evidence for mast cells contributing to neuromuscular pathology in an inherited model of ALS. JCI Insight 2017;2(20):e95934. DOI:10.1172/jci.insight.95934. PMID: 29046475.; RocheJ.C., Rojas-Garcia R., Scott K. M. et al. A proposed staging system for amyotrophic lateral sclerosis. Brain 2012;135(3):847–52. DOI:10.1093/brain/awr351. PMID: 22271664.; https://nmb.abvpress.ru/jour/article/view/300
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المؤلفون: Halushko, O. A., Trischynska, M. A., Vityuk, A. D.
المصدر: Запорожский медицинский журнал; Том 22 № 4 (2020)
Zaporozhye Medical Journal; Vol. 22 No. 4 (2020)مصطلحات موضوعية: нейропротекция, нейропротекція, едаравон, edaravone, эдаравон, neuroprotection, инсульт, women, інсульт, жінки, stroke, женщины
وصف الملف: application/pdf
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3
المؤلفون: Ivanov, D.D.
المصدر: Počki, Vol 8, Iss 3, Pp 136-138 (2019)
KIDNEYS; Том 8, № 3 (2019); 136-138
Почки-Počki; Том 8, № 3 (2019); 136-138
Нирки-Počki; Том 8, № 3 (2019); 136-138مصطلحات موضوعية: contrast-induced nephropathy, hydration, chronic kidney disease, edaravone, контраст-индуцированная нефропатия, гидратация, хроническая болезнь почек, эдаравон, lcsh:Diseases of the genitourinary system. Urology, lcsh:RC870-923, контраст-індукована нефропатія, гідратація, хронічна хвороба нирок, едаравон, female genital diseases and pregnancy complications
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4
المؤلفون: Halushko, O.A.
المصدر: EMERGENCY MEDICINE; № 3.98 (2019); 51-55
МЕДИЦИНА НЕОТЛОЖНЫХ СОСТОЯНИЙ; № 3.98 (2019); 51-55
МЕДИЦИНА НЕВІДКЛАДНИХ СТАНІВ; № 3.98 (2019); 51-55مصطلحات موضوعية: острый ишемический инсульт, нейропротекция, эдаравон, Ксаврон, гострий ішемічний інсульт, нейропротекція, едаравон, acute ischemic stroke, neuroprotection, edaravone, Xavron
وصف الملف: application/pdf
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5Electronic Resource
Additional Titles: Контраст-индуцированная нефропатия: поиск новых решений для предотвращения ее развития
Контраст-індукована нефропатія: пошук нових рішень для запобігання її розвиткуالمصدر: KIDNEYS; Том 8, № 3 (2019); 136-138; Почки - Počki; Нирки - Počki; 2307-1265; 2307-1257
مصطلحات الفهرس: contrast-induced nephropathy, hydration, chronic kidney disease, edaravone, контраст-индуцированная нефропатия, гидратация, хроническая болезнь почек, эдаравон, контраст-індукована нефропатія, гідратація, хронічна хвороба нирок, едаравон, info:eu-repo/semantics/article, info:eu-repo/semantics/publishedVersion