يعرض 1 - 2 نتائج من 2 نتيجة بحث عن '"Ф. А. Аббасов"', وقت الاستعلام: 0.30s تنقيح النتائج
  1. 1
    Academic Journal

    المصدر: Neuromuscular Diseases; Том 13, № 2 (2023); 72-82 ; Нервно-мышечные болезни; Том 13, № 2 (2023); 72-82 ; 2413-0443 ; 2222-8721 ; 10.17650/2222-8721-2023-13-2

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    Relation: https://nmb.abvpress.ru/jour/article/view/545/352; Malik A., Hayat G., Kalia J.S. et al. Idiopathic inflammatory myopathies: clinical approach and management. Front Neurol 2016;7:64. DOI:10.3389/fneur.2016.00064; Pinal-Fernandez I., Casal-Dominguez M., Mammen A.L. Immune-mediated necrotizing myopathy. Curr Rheumatol Rep 2018;20(4):21. DOI:10.1007/s11926-018-0732-6; McGrath E.R., Doughty C.T., Amato A.A. Autoimmune myopathies: updates on evaluation and treatment. Neurotherapeutics 2018;15(4):976–94. DOI:10.1007/s13311-018-00676-2; Ghirardello A., Borella E., Beggio M. et al. Myositis autoantibodies and clinical phenotypes. Auto Immun Highlights 2014;5(3):69–75. DOI:10.1007/s13317-014-0060-4; Betteridge Z., McHugh N. Myositis-specific autoantibodies: an important tool to support diagnosis of myositis. J Intern Med 2016;280(1):8–23. DOI:10.1111/joim.12451; Антелава О.А. Полимиозит/дерматомиозит: дифференциаль ная диагностика. Научно-практическая ревматология 2016;54(2):191–8. DOI:10.14412/1995-4484-2016-191-198; Rodríguez-Muguruza S., Lozano-Ramos I., Coll-Canti J. et al. Anti-SRP auto-antibodies are not specific for myositis: report of 8 cases. Joint Bone Spine 2017;84(1):103–5. DOI:10.1016/j.jbspin.2015.12.005; Satoh M., Tanaka S., Ceribelli A. et al. A comprehensive overview on myositis-specific antibodies: new and old biomarkers in idiopathic inflammatory myopathy. Clin Rev Allergy Immunol 2017;52(1):1–19. DOI:10.1007/s12016-015-8510-y; Wang L., Liu L., Hao H. et al. Myopathy with anti-signal recognition particle antibodies: clinical and histopathological features in Chinese patients. Neuromuscul Disord 2014;24(4):335–41. DOI:10.1016/j.nmd.2014.01.002; Suzuki S., Nishikawa A., Kuwana M. et al. Inflammatory myopathy with anti-signal recognition particle antibodies: case series of 100 patients. Orphanet J Rare Dis 2015;10:61. DOI:10.1186/s13023-015-0277-y; Allenbach Y., Mammen A.L., Benveniste O. et al. Immune-Mediated Necrotizing Myopathies Working Group. 224th ENMC International Workshop: Clinico-sero-pathological classification of immune-mediated necrotizing myopathies Zandvoort, The Netherlands, 14–16 October 2016. Neuromuscul Disord 2018;28(1):87–99. DOI:10.1016/j.nmd.2017.09.016; Pinal-Fernandez I., Casal-Dominguez M., Carrino J.A. et al. Thigh muscle MRI in immune-mediated necrotising myopathy: extensive oedema, early muscle damage and role of anti-SRP autoantibodies as a marker of severity. Ann Rheum Dis 2017;76(4):681–87. DOI:10.1136/annrheumdis-2016-210198; Lundberg I.E., Tjärnlund A., Bottai M. et al. International Myositis Classification Criteria Project consortium, The Euromyositis register and The Juvenile Dermatomyositis Cohort Biomarker Study and Repository (JDRG) (UK and Ireland). 2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups. Ann Rheum Dis 2017;76(12):1955–64. DOI:10.1136/annrheumdis-2017-211468; Dimachkie M.M., Barohn R.J., Amato A. Idiopathic inflammatory myopathies. Neurol Clin 2014;32:595–628. DOI:10.1016/j.ncl.2014.04.007; Mammen A. Autoimmune muscle disease. Handbook of clinical neurology. 2016;133:467–84. DOI: 1016/B978-0-444-63432-0.00025-6; Kassardjian C.D, Lennon V.A., Alfugham N.B. et al. Clinical features and treatment outcomes of necrotizing autoimmune myopathy. JAMA Neurol 2015;72:996–1003. DOI:10.1001/jamaneurol.2015.1207; Kim H.I., Chung S.H., Hwang J.E. et al. Dermatomyositis associated with cancer of unknown primary site. J Korean Med Sci 2007;22 Suppl(Suppl):S174–7. DOI:10.3346/jkms.2007.22.S.S174; Zantos D., Zhang Y., Felson D. The overall and temporal association of cancer with polymyositis and dermatomyositis. J Rheumatol 1994;21(10):1855–9.; Hill C.L., Zhang Y., Sigurgeirsson B. et al. Frequency of specific cancer types in dermatomyositis and polymyositis: a population-based study. Lancet 2001;357(9250):96–100. DOI:10.1016/S0140-6736(00)03540-6; Allenbach Y., Keraen J., Bouvier A.M. et al. High risk of cancer in autoimmune necrotizing myopathies: usefulness of myositis specific antibody. Brain 2016;139(Pt 8):2131–5. DOI:10.1093/brain/aww054; Pinal-Fernandez I., Parks C., Werner J.L. et al. Longitudinal course of disease in a large cohort of myositis patients with autoantibodies recognizing the signal recognition particle. Arthritis Care Res (Hoboken) 2017;69(2):263–70. DOI:10.1002/acr.22920; Watanabe Y., Uruha A., Suzuki S. et al. Clinical features and prognosis in anti-SRP and anti-HMGCR necrotising myopathy. J Neurol Neurosur Psychiatry 2016;87:1038–44. DOI:10.1136/jnnp-2016-313166; https://nmb.abvpress.ru/jour/article/view/545

  2. 2
    Academic Journal

    المساهمون: This article has been supported by Servier., Статья спонсируется компанией «Сервье».

    المصدر: Neurology, Neuropsychiatry, Psychosomatics; Vol 14, No 4 (2022); 103-107 ; Неврология, нейропсихиатрия, психосоматика; Vol 14, No 4 (2022); 103-107 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2022-4

    وصف الملف: application/pdf

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Eur J Neurol. 2017 Feb;24(2):404-11. doi:10.1111/ene.13217. Epub 2016 Dec 29.; Pertovaara A, Haapalinna A, Sirvio J, et al. Pharmacological properties, central nervous system effects, and potential therapeutic applications of atipamezole, a selective alpha2-adrenoceptor antagonist. CNS Drug Rev. 2005 Autumn;11(3):273-88. doi:10.1111/j.1527-3458.2005.tb00047.x; Tellez S, Colpaert F, Marien M. Acetylcholine release in the rat prefrontal cortex in vivo: modulation by alpha 2-adrenoceptor agonists and antagonists. J Neurochem. 1997 Feb;68(2):778-85. doi:10.1046/j.1471-4159.1997.68020778.x; Scheinin M, Sallinen J, Haapalinna A. Evaluation of the alpha2C-adrenoceptor as a neuropsychiatric drug target studies in transgenic mouse models. Life Sci. 2001 Apr 6;68(19-20):2277-85. doi:10.1016/s0024-3205(01)01016-5; Rizk P, Salazar J, Raisman-Vozari R, et al. The alpha2-adrenoceptor antagonist dexefaroxan enhances hippocampal neurogenesis by increasing the survival and differentiation of new granule cells. Neuropsychopharmacology. 2006 Jun;31(6):1146-57. doi:10.1038/sj.npp.1300954; Smith L, De Salvia M, Jenner P, et al. An appraisal of the antiparkinsonian activity of piribedil in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated common marmosets. Mov Disord. 1996 Mar;11(2):125-35. doi:10.1002/mds.870110203; Smith LA, Jackson MG, Bonhomme C, et al. Transdermal administration of piribedil reverses MPTP-induced motor deficits in the common marmoset. Clin Neuropharmacol. 2000 May-Jun;23(3):133-42. doi:10.1097/00002826-200005000-00002; Smith LA, Tel BC, Jackson MJ, et al. Repeated administration of piribedil induces less dyskinesia than L-dopa in MPTP-treated common marmosets: a behavioural and biochemical investigation. Mov Disord. 2002 Sep;17(5):887-901. doi:10.1002/mds.10200; Millan MJ, Cussac D, Milligan G, et al. Antiparkinsonian agent piribedil displays antagonist properties at native, rat, and cloned, human alpha(2)-adrenoceptors: cellular and functional characterization. J Pharmacol Exp Ther. 2001 Jun;297(3):876-87.; Turle-Lorenzo N, Maurin B, Puma C, et al. The dopamine agonist piribedil with L-DOPA improves attentional dysfunction: relevance for Parkinson’s disease. J Pharmacol Exp Ther. 2006 Nov;319(2):914-23. doi:10.1124/jpet.106.109207. Epub 2006 Aug 18.; Flynn DD, Mash DC. Characterization of L-[3H]nicotine binding in human cerebral cortex: comparison between Alzheimer’s disease and the normal. J Neurochem. 1986;47:1948-54.; Marighetto A, Valerio S, Philippin JN, et al. Comparative effects of the dopaminergic agonists piribedil and bromocriptine in three different memory paradigms in rodents. J Psychopharmacol. 2008 Jul;22(5):511-21. doi:10.1177/0269881107083836. Epub 2008 Feb 28.; Brocco M, Dekeyne A, Papp M, et al. Antidepressant-like properties of the anti-Parkinson agent, piribedil, in rodents: mediation by dopamine D2 receptors. Behav Pharmacol. 2006 Nov;17(7):559-72. doi:10.1097/01.fbp.0000236267.41806.5b; Thobois S, Lhommee E, Klinger H, et al. Parkinsonian apathy responds to dopaminergic stimulation of D2/D3 receptors with piribedil. Brain. 2013 May;136(Pt 5):1568-77. doi:10.1093/brain/awt067. Epub 2013 Mar 29.; Eggert K, Ohlwein C, Kassubek J, et al. Influence of the nonergot dopamine agonist piribedil on vigilance in patients With Parkinson Disease and excessive daytime sleepiness (PiViCog-PD): an 11-week randomized comparison trial against pramipexole and ropinirole. Clin Neuropharmacol. 2014 JulAug;37(4):116-22. doi:10.1097/WNF.0000000000000041; Peretti CS, Gierski F, Harrois S. Cognitive skill learning in healthy older adults after 2 months of double-blind treatment with piribedil. Psychopharmacology. 2004 Nov;176(2):175-81. doi:10.1007/s00213-004-1869-8. Epub 2004 May 12.; Schuck S, Bentue-Ferrer D, Kleinermans D, et al. Psychomotor and cognitive effects of piribedil, a dopamine agonist, in young healthy volunteers. Fundam Clin Pharmacol. 2002 Feb;16(1):57-65. doi:10.1046/j.1472-8206.2002.00070.x; Straka I, Minar M, Skorvanek M, et al. Adherence to Pharmacotherapy in Patients With Parkinson's Disease Taking Three and More Daily Doses of Medication. Front Neurol. 2019 Jul 31;10:799. doi:10.3389/fneur.2019.00799. eCollection 2019.; Daley DJ, Myint PK, Gray RJ, Deane KH. Systematic review on factors associated with medication non-adherence in Parkinson's disease. Parkinsonism Relat Disord. 2012 Dec;18(10):1053-61. doi:10.1016/j.parkreldis.2012.09.004. Epub 2012 Sep 28.; https://nnp.ima-press.net/nnp/article/view/1869