Neuromyelitis optica and non organ-specific autoimmunity.
By S. Pittock, V. Lennon, J. de Seze, P. Vermersch, H. Homburger, D. Wingerchuk, C. Lucchinetti, H. Zéphir, K. Moder, B. Weinshenker. Archives of Neurology, 2008
603 citations recorded by the source corpus.
Subfields: Pathology and Forensic Medicine, Rheumatology
View Paper: https://www.semanticscholar.org/paper/918a04360adffc13b047a6a55703f9bae9d2eab0
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In Pathology and Forensic Medicine
In Rheumatology
Citations in the corpus
- Differential diagnosis of suspected multiple sclerosis: a consensus approach (2008, background): “The criteria may require revision pending further investigation into the relationship between symptoms of NMO and systemic autoimmune diseases such as systemic lupus erythematosus [46].”
- EULAR recommendations for the management of systemic lupus erythematosus with neuropsychiatric manifestations: report of a task force of the EULAR standing committee for clinical affairs (2010, background): “Other major NPSLE manifestations are present in one third of cases, with optic neuritis being the most common (21–48%). Contrast-enhanced spinal cord MRI is useful to exclude cord compression and to detect T2-weighted hyperintense lesions (70–93%). The involvement of more than three spinal cord segm”