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Статті в журналах з теми "Neuromyelitis Optica Spectrum Disorder"
Wingerchuk, Dean M., and Claudia F. Lucchinetti. "Neuromyelitis Optica Spectrum Disorder." New England Journal of Medicine 387, no. 7 (August 18, 2022): 631–39. http://dx.doi.org/10.1056/nejmra1904655.
Повний текст джерелаBeekman, Janine, Aysha Keisler, Omar Pedraza, Masayuki Haramura, Athos Gianella-Borradori, Eliezer Katz, John N. Ratchford, et al. "Neuromyelitis optica spectrum disorder." Neurology - Neuroimmunology Neuroinflammation 6, no. 4 (June 20, 2019): e580. http://dx.doi.org/10.1212/nxi.0000000000000580.
Повний текст джерелаBrody, Judith, Mark A. Hellmann, Romain Marignier, Itay Lotan, and Hadas Stiebel-Kalish. "Neuromyelitis Optica Spectrum Disorder." Journal of Neuro-Ophthalmology 36, no. 4 (December 2016): 356–62. http://dx.doi.org/10.1097/wno.0000000000000403.
Повний текст джерелаKim, Jee-Eun, Sang-Hyun Park, Kyungdo Han, Ho Jin Kim, Dong-Wook Shin, and Sung-Min Kim. "Prevalence and incidence of neuromyelitis optica spectrum disorder and multiple sclerosis in Korea." Multiple Sclerosis Journal 26, no. 14 (November 21, 2019): 1837–44. http://dx.doi.org/10.1177/1352458519888609.
Повний текст джерелаFragoso, Yara Dadalti, Nise Alessandra C. Sousa, Tania Saad, Soniza Vieira Alves-Leon, Maria Lucia V. Pimentel, Marcus Vinicius M. Goncalves, Carla Vieira Stella, et al. "Clinical Characteristics of Patients With Neuromyelitis Optica Spectrum Disorders With Early Onset." Journal of Child Neurology 34, no. 9 (April 23, 2019): 487–90. http://dx.doi.org/10.1177/0883073819842421.
Повний текст джерелаMcCreary, M., MA Mealy, DM Wingerchuk, M. Levy, A. DeSena, and BM Greenberg. "Updated diagnostic criteria for neuromyelitis optica spectrum disorder: Similar outcomes of previously separate cohorts." Multiple Sclerosis Journal - Experimental, Translational and Clinical 4, no. 4 (October 2018): 205521731881592. http://dx.doi.org/10.1177/2055217318815925.
Повний текст джерелаŚciegienna-Zdeb, Grażyna, and Marta Mierzwa-Molenda. "Neuromyelitis optica spectrum disorder – case report." Medical Studies 1 (2016): 45–48. http://dx.doi.org/10.5114/ms.2016.58805.
Повний текст джерелаVerma, Rajesh, and Chetan Kumar. "Tumefactive Demyelination Associated with Bilateral Optic Neuritis in Neuromyelitis Optica Spectrum Disorders." Journal of Neurosciences in Rural Practice 10, no. 04 (October 2019): 693–96. http://dx.doi.org/10.1055/s-0039-3399614.
Повний текст джерелаUzawa, Akiyuki, Masahiro Mori, Saeko Masuda, Kazuhiko Aoe, and Satoshi Kuwabara. "Relapse of Neuromyelitis Optica Spectrum Disorder Associated with Intravenous Lidocaine." Case Reports in Medicine 2011 (2011): 1–3. http://dx.doi.org/10.1155/2011/405837.
Повний текст джерелаNakashima, Ichiro. "II. Neuromyelitis Optica Spectrum Disorder." Nihon Naika Gakkai Zasshi 110, no. 8 (August 10, 2021): 1568–74. http://dx.doi.org/10.2169/naika.110.1568.
Повний текст джерелаДисертації з теми "Neuromyelitis Optica Spectrum Disorder"
Combes, Anna Julie Elise. "Brain and cervical cord myelin water imaging in neuromyelitis optica spectrum disorder." Thesis, King's College London (University of London), 2018. https://kclpure.kcl.ac.uk/portal/en/theses/brain-and-cervical-cord-myelin-water-imaging-in-neuromyelitis-optica-spectrum-disorder(7eddb105-165a-430d-853d-cce4bbb20902).html.
Повний текст джерелаChou, I.-Jun. "Comparative epidemiology and quantitative neuroimaging of neuromyelitis optica spectrum disorder and multiple sclerosis." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/47717/.
Повний текст джерелаChan, Koon-ho, and 陳灌豪. "Clinical features, diagnosis and immunopathogenesis of neuromyelitis optica spectrum disorders." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B48521681.
Повний текст джерелаpublished_or_final_version
Medicine
Doctoral
Doctor of Philosophy
Oertel, Frederike Cosima [Verfasser]. "Afferent visual system changes in patients with Neuromyelitis Optica Spectrum Disorders / Frederike Cosima Oertel." Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2021. http://d-nb.info/122885940X/34.
Повний текст джерелаChien, Claudia [Verfasser]. "Spinal cord atrophy measured from cerebral T1-weighted MRI: applications in clinical investigations of neuromyelitis optica spectrum disorders / Claudia Chien." Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2021. http://d-nb.info/1228860939/34.
Повний текст джерелаLo, Yuk-fai, and 盧育輝. "Comparison between tissue-based indirect immunofluorescence andenzyme-linked immunosorbent assays, two detection methods for anti-aquaporin-4 antibodies in neuromyelitis optica spectrum disorders." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B46579266.
Повний текст джерелаLopes, Catarina Beatriz Pacheco. "Neuromyelitis optica spectrum disorder: contributions for a neuropsychological profile." Master's thesis, 2021. https://hdl.handle.net/10216/134993.
Повний текст джерелаLopes, Catarina Beatriz Pacheco. "Neuromyelitis optica spectrum disorder - contributions for the cognitive profile." Dissertação, 2021. https://hdl.handle.net/10216/134993.
Повний текст джерелаCunha, Ana Carolina Lucas. "Treatment of pediatric neuromyelitis optica spectrum disorders." Master's thesis, 2020. http://hdl.handle.net/10316/97698.
Повний текст джерелаNeuromyelitis optica spectrum disorders (NMOSD) are a group of autoimmune inflammatory and demyelinating disorders of the central nervous system. They are predominantly mediated by an autoantibody targeting the Aquaporin-4 channel (AQP4-IgG). However, some patients are positive for myelin-oligodendrocyte glycoprotein antibodies (MOG-IgG), and others are negative for both antibodies. This is an aggressive disease that follows a relapse-remitting course with a relapse-dependent disability, that can be extremely severe. It may lead to blindness, paraplegia, quadriplegia, and even life-threatening respiratory failure. Characteristic clinical manifestations are optic neuritis, longitudinally extensive transverse myelitis and area postrema syndrome, though others may be present. As few studies have been conducted in children, the diagnostic criteria and the treatment approaches are inferred based on adult experience. Thus, this review aims to analyze and summarize all reports on this subject, so that the management of the patients is more evidence-based.Treatment of relapses is, almost consensually, initiated with intravenous methylprednisolone (IVMP), and, in refractory patients, intravenous immunoglobulin (IVIG) or plasma exchange (PLEX) are tried. Some evidence of IVMP+PLEX as initial therapy is available, with good results. First-line drugs for maintenance treatment are mycophenolate mofetil, rituximab, and azathioprine. There is contradictory evidence on which one should be the first choice. Nevertheless, before resorting to second-line drugs, treatment may be switched between these three drugs. Recently, new drugs have been approved for treatment of NMOSD in adults and may be a promising new line of therapy for children. MOG-IgG positive patients show good results in acute relapse treatment with IVMP+IVIG and maintenance treatment with IVIG. Though it seems that age does not bring significant differences in disease features, this review pointed out that extrapolating adult evidence to children, in terms of therapeutic approaches, might not be as straightforward as it is believed. With this review, we highlight the importance of further research. Since this is a very rare disease, the best way to study its features and treatment efficacy and safety is through multicenter studies. Hence, in order to develop those, an additional effort to share the information of these cases is crucial.
As doenças do espetro da neuromielite óptica (DENMO) são um grupo de doenças autoimunes, inflamatórias e desmielinizantes do sistema nervoso central. São mediadas, predominantemente, por um auto-anticorpo contra o canal da Aquaporina 4 (AQP4-IgG). No entanto, alguns doentes são positivos para o anticorpo contra a glicoproteína oligodendrocítica da mielina (MOG-IgG) e outros são negativos para ambos os anticorpos. Esta é uma doença agressiva, que segue um padrão de surtos e remissões, com consequente incapacidade neurológica dependente dos surtos, a qual pode ser extremamente grave. Pode conduzir a cegueira, paraplegia, tetraplegia e, ainda, falência respiratória potencialmente fatal. As manifestações clínicas características desta doença são a nevrite óptica, a mielite transversa longitudinalmente extensa e a síndrome da área postrema, apesar de outras poderem estar presentes. Tendo em conta o limitado número de estudos realizados em crianças, os critérios de diagnóstico e as estratégias de tratamento são inferidas da experiência adquirida em adultos. Assim, esta revisão visa analisar e sumariar os artigos disponíveis sobre esta matéria, de forma a que o tratamento destes doentes seja baseado na evidência. De um modo quase consensual, o tratamento dos surtos faz-se com metilprednisolona intravenosa (MPIV) e, nos casos refratários, usa-se a imunoglobulina intravenosa (IGIV) ou a plasmaferese. Existe alguma evidência que o uso inicial de MPIV+plasmaferese conduz a bons resultados. Os fármacos utilizados como primeira linha na terapêutica de manutenção são o micofenolato de mofetil, o rituximab e a azatioprina. A decisão de que fármaco utilizar como primeira escolha não é consensual. Contudo, estes três fármacos devem ser experimentados antes de recorrer aos de segunda linha. Foram recentemente aprovados novos fármacos para o tratamento das DENMO em adultos, que podem ser promissores para uso em crianças. Por outro lado, os doentes positivos para MOG-IgG demonstram bons resultados com MPIV+IGIV no controlo dos surtos e com IGIV no tratamento de manutenção. Apesar de não haver uma aparente influência significativa da idade nas características da doença, este trabalho revelou que a extrapolação de dados de adultos para crianças, em termos terapêuticos, pode não ser tão simples quanto seria expectável. Com este trabalho, destaca-se a importância de se realizarem novos estudos. Visto tratar-se de uma doença muito rara, a melhor abordagem para estudar as suas características e a eficácia e segurança da terapêutica seria através de estudos multicêntricos. Portanto, uma divulgação mais alargada destes casos é essencial para que estes possam ser desenvolvidos.
Freitas, Eduardo Manuel Pinto Ferreira Silva. "Neuromyelitis Optica Spectrum Disorders associated with other autoimmune diseases." Master's thesis, 2014. https://repositorio-aberto.up.pt/handle/10216/72977.
Повний текст джерелаКниги з теми "Neuromyelitis Optica Spectrum Disorder"
Wingerchuk, Dean M. Neuromyelitis Optica Spectrum Disorders. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199341016.003.0023.
Повний текст джерелаMiller, Aaron E., and Teresa M. DeAngelis. Neuromyelitis Optica. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199732920.003.0005.
Повний текст джерелаSchreiner, Teri L., and Jeffrey L. Bennett. Neuromyelitis Optica. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0088.
Повний текст джерелаCai, Yu, Yangtai Guan, Wei Qiu, Fu-Dong Shi, and Jodie Burton, eds. Advances in Neuromyelitis Optica Spectrum Disorders (NMOSD). Frontiers Media SA, 2022. http://dx.doi.org/10.3389/978-2-83250-175-7.
Повний текст джерелаCoyle, Patricia K. Immune-mediated Disorders of the Central Nervous System. Edited by Emma Ciafaloni, Cheryl Bushnell, and Loralei L. Thornburg. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190667351.003.0010.
Повний текст джерелаBielekova, Bibiana, Gary Birnbaum, and Robert P. Lisak, eds. Neuroimmunology. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780190050801.001.0001.
Повний текст джерелаFreedman, Mark S., and Mohammad Abdoli. The Importance and Utility of Cerebrospinal Fluid Evaluation in the Diagnosis of Central Demyelinating Diseases. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199341016.003.0008.
Повний текст джерелаMatiello, Marcelo, and Tamara B. Kaplan. A Mother Who Could Not See Her Baby. Edited by Angela O’Neal. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190609917.003.0027.
Повний текст джерелаGraham, Andrew, and Clare Galton. Nervous system. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0018.
Повний текст джерелаЧастини книг з теми "Neuromyelitis Optica Spectrum Disorder"
Saadoun, Samira, Vincent T. W. Chang, and Marios C. Papadopoulos. "Neuromyelitis Optica Spectrum Disorder." In Neuroimmune Diseases, 523–41. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-19515-1_16.
Повний текст джерелаGaletta, Kristin M., and Marcelo Matiello. "Neuromyelitis Optica Spectrum Disorders." In Neurorheumatology, 187–95. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-16928-2_19.
Повний текст джерелаFilippi, Massimo, and Maria A. Rocca. "Neuromyelitis Optica Spectrum Disorders." In White Matter Diseases, 67–94. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38621-4_3.
Повний текст джерелаWingerchuk, Dean M. "Neuromyelitis Optica Spectrum Disorders." In Clinical Neuroimmunology, 219–32. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-60327-860-7_12.
Повний текст джерелаCarroll, William M. "Neuromyelitis optica spectrum disorders." In International Neurology, 365–71. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118777329.ch91.
Повний текст джерелаCahill, Jonathan F. "Neuromyelitis Optica Spectrum Disorders." In Clinical Neuroimmunology, 227–34. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-24436-1_12.
Повний текст джерелаWeis, Serge, Michael Sonnberger, Andreas Dunzinger, Eva Voglmayr, Martin Aichholzer, Raimund Kleiser, and Peter Strasser. "Demyelinating Diseases: Neuromyelitis Optica Spectrum Disorder." In Imaging Brain Diseases, 1097–104. Vienna: Springer Vienna, 2019. http://dx.doi.org/10.1007/978-3-7091-1544-2_42.
Повний текст джерелаWuerfel, Jens, Alex Rovira, Friedemann Paul, and Frederik Barkhof. "Neuromyelitis Optica Spectrum Disorders (NMOSD)." In Clinical Neuroradiology, 1–17. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-61423-6_71-1.
Повний текст джерелаWuerfel, Jens, Àlex Rovira, Friedemann Paul, and Frederik Barkhof. "Neuromyelitis Optica Spectrum Disorders (NMOSD)." In Clinical Neuroradiology, 769–85. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-68536-6_71.
Повний текст джерелаNarula, Sona, and Amy T. Waldman. "Neuromyelitis Optica Spectrum Disorder with Brainstem Presentation." In Pediatric Demyelinating Diseases of the Central Nervous System and Their Mimics, 189–94. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-61407-6_24.
Повний текст джерелаТези доповідей конференцій з теми "Neuromyelitis Optica Spectrum Disorder"
Santos, Artur de Paula, Rafael Fusaro Aguiar Oliveira, and Fabrícia Fonseca Simil. "Neuromyelitis Optica Spectrum Disorder associated with Sjögren's Syndrome." In XXXIX Congresso Brasileiro de Reumatologia. Sociedade Brasileiro de Reumatologia, 2022. http://dx.doi.org/10.47660/cbr.2022.1847.
Повний текст джерелаMoslander, C., M. K. McGraw, P. Yau, and S. A. Ghamande. "Symptomatic Narcolepsy: A Case of Neuromyelitis Optica Spectrum Disorder." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a7628.
Повний текст джерелаEssado Dantas, Aurivan, Camila Gabriela Xavier de Brito, Ana Luisa Bagno de Almeida, Matheus Fonseca Cardoso, Larissa Maria Oliveira Gonzaga, Samara de Quadros Lobê, Victória Carneiro Dal Moro, and Leandro Augusto Tanure. "SJÖGREN'S SYNDROME AND NEUROMYELITIS OPTICA SPECTRUM DISORDER: CASE REPORT." In Congresso Brasileiro de Reumatologia 2020. Sociedade Brasileira de Reumatologia, 2021. http://dx.doi.org/10.47660/cbr.2020.17407.
Повний текст джерелаSjöberg, A., I. Gunnarsson, and E. Svenungsson. "195 Systemic lupus erythematosus and neuromyelitis optica spectrum disorders." In LUPUS 2017 & ACA 2017, (12th International Congress on SLE &, 7th Asian Congress on Autoimmunity). Lupus Foundation of America, 2017. http://dx.doi.org/10.1136/lupus-2017-000215.195.
Повний текст джерелаSilva Koike, Matheus, André Silva Franco, Isabele Parente de Brito Antonelli, Guilherme Guimarães Moreira Balbi, Karina Fernanda Pucha Aguinsaca, Matheus Dalben Fiorentino, Sandra Gofinet Pasoto, Samuel Katsuyuki Shinjo, and Diogo Souza Domiciano. "Aquaporin 4 antibody–negative neuromyelitis optica spectrum disorder (NMOSD) associated with Sjogren's Syndrome." In SBR 2021 Congresso Brasileiro de Reumatologia. Sociedade Brasileira de Reumatologia, 2021. http://dx.doi.org/10.47660/cbr.2021.2060.
Повний текст джерелаLechner, Christian, Matthias Baumann, Eva-Maria Hennes, Kathrin Schanda, Markus Reindl, and Kevin Rostasy. "P 855. Epidemiology of Neuromyelitis Optica Spectrum Disorders in Children and Adolescents." In Abstracts of the 44th Annual Meeting of the Society for Neuropediatrics. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1675982.
Повний текст джерелаLechner, Christian, Eva-Maria Wendel, Markus Breu, Ines El Naggar, Kathrin Schanda, Matthias Baumann, Markus Reindl, and Kevin Rostásy. "Results of the ESPED Study “Neuromyelitis Optica Spectrum Disorders in Children and Adolescents." In Abstracts of the 45th Annual Meeting of the Society for Neuropediatrics. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1698199.
Повний текст джерелаMartin Nares, E., G. Hernández Molina, and H. Fragoso Loyo. "THU0347 Aquaporin-4 immunoglobulin g antibody positive neuromyelitis optica spectrum disorder and systemic autoimmune diseases overlap syndrome: a single centreexperience." In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.6173.
Повний текст джерелаWronski, Miriam, and Justine J. Wang. "104 Overlapping autoimmunity: a case of concomitant aquaporin-4 and myelin oligodendrocyte glycoprotein (MOG) antibody positivity in neuromyelitis optica spectrum disorder." In ANZAN Annual Scientific Meeting 2021 Abstracts. BMJ Publishing Group Ltd, 2021. http://dx.doi.org/10.1136/bmjno-2021-anzan.104.
Повний текст джерелаOliveira, Daniela Gomes Chicre, Isabela Tambelli Pires Cardoso, Carlos Eduardo Garcez Teixeira, Marina Ferreira Simões, Arlete Maria Valente Coimbra, Zoraida Sachetto, and Alisson Pugliesi. "Myelitis with Aquaporin-4 autoantibody in a patient with Sjogren´s syndrome: Neurological Manifestation or coexistence of Neuromyelitis Optica Spectrum Disorder?" In XXXIX Congresso Brasileiro de Reumatologia. Sociedade Brasileiro de Reumatologia, 2022. http://dx.doi.org/10.47660/cbr.2022.1928.
Повний текст джерелаЗвіти організацій з теми "Neuromyelitis Optica Spectrum Disorder"
Wu, Zhihong, Dong Wang, and Lirong Chen. Association between Sjögren’s syndrome and neuromyelitis optica spectrum disorder patients : a systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, July 2022. http://dx.doi.org/10.37766/inplasy2022.7.0080.
Повний текст джерелаYin, Ziqian, Youjia Qiu, Aojie Duan, Ting Fang, Zhouqing Chen, Jiang Wu, Zhong Wang, and Gang Chen. Different monoclonal antibodies and immunosuppressants administration in patients with Neuromyelitis Optica Spectrum Disorder: A Bayesian Network Meta-Analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, December 2022. http://dx.doi.org/10.37766/inplasy2022.12.0018.
Повний текст джерелаSong, Honglu, Yucai Chuai, and Tao Jin. The efficacy and safety of IL-6R inhibitors in treating Neuromyelitis Optica Spectrum Disorders: A protocol for systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, August 2020. http://dx.doi.org/10.37766/inplasy2020.8.0055.
Повний текст джерела