Neuromyelitis optica
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
https://www.nature.com/articles/s41572-020-0214-9.pdf
Reference375 articles.
1. Jarius, S. & Wildemann, B. The history of neuromyelitis optica. J. Neuroinflammation 10, 8 (2013).
2. Jarius, S. & Wildemann, B. The history of neuromyelitis optica. Part 2: ‘spinal amaurosis’, or how it all began. J. Neuroinflammation 16, 280 (2019).
3. Jarius, S. & Wildemann, B. Devic’s index case: a critical reappraisal – AQP4-IgG-mediated neuromyelitis optica spectrum disorder, or rather MOG encephalomyelitis? J. Neurol. Sci. 407, 116396 (2019).
4. Jarius, S. & Wildemann, B. Aquaporin-4 antibodies (NMO-IgG) as a serological marker of neuromyelitis optica: a critical review of the literature. Brain Pathol. 23, 661–683 (2013).
5. Lennon, V. A. et al. A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis. Lancet 364, 2106–2112 (2004). First report on anti-astrocytic autoantibodies (later identified as antibodies to AQP4) in NMO.
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1. Inhibition of repulsive guidance molecule-a ameliorates compromised blood–spinal cord barrier integrity associated with neuromyelitis optica in rats;Journal of Neuroimmunology;2024-03
2. Therapeutic plasma exchange for neuromyelitis optica attacks: Evidence and challenges from a real-world cohort from Brazil;Journal of Neuroimmunology;2024-03
3. Altered immune co-inhibitory receptor expression and correlation of LAG-3 expression to disease severity in NMOSD;Journal of Neuroimmunology;2024-03
4. Clinical features and prognosis of Tibetan patients with neuromyelitis optica spectrum disorder are different from those of Han Chinese patients;Journal of Neuroimmunology;2024-03
5. Chimeric AQP4-based immunosorbent for highly-specific removal of AQP4-IgG from blood;Journal of Chromatography A;2024-02
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