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Journal of Neurology, Neurosurgery, and Psychiatry|April 27, 2016
Multicentre comparison of a diagnostic assay: aquaporin-4 antibodies in neuromyelitis opticaPatrick Waters, Markus Reindl, Albert Saiz, et al.Journal of Neurology|November 17, 2022
Clinical pitfalls and serological diagnostics of MuSK myasthenia gravisYoung Nam Kwon, Mark Woodhall, Jung-Joon Sung, et al.Journal of Neurology|February 2, 2020
The clinical profile of NMOSD in Australia and New ZealandWajih Bukhari, Laura Clarke, Cullen O'Gorman, et al.Frontiers in Neurology|September 27, 2021
MRI Patterns Distinguish AQP4 Antibody Positive Neuromyelitis Optica Spectrum Disorder From Multiple SclerosisLaura Clarke, Simon Arnett, Wajih Bukhari, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 28, 2017
Incidence and prevalence of NMOSD in Australia and New ZealandWajih Bukhari, Kerri M Prain, Patrick Waters, et al.Frontiers in Neurology|July 3, 2020
Relapse Patterns in NMOSD: Evidence for Earlier Occurrence of Optic Neuritis and Possible Seasonal VariationElham Khalilidehkordi, Laura Clarke, Simon Arnett, et al.Pageof 7