Comparison of clinical and radiological features of Aquaporin4 (AQP-4) antibody positive Neuromyelitis Optica Spectrum Disorder (NMOSD) and Anti Myelin Oligodendrocyte Glycoprotein (Anti-MOG) syndrome-our experience from Northwest India

Author:

Jain RajendraSingh,Jain Deepak,Murarka Sourabh,Vyas Arvind,Sharma Bhawna,Srivastava Trilochan,Kumar Kamlesh,Jain Yavnika,Rao Kavya,Agrawal Jitesh,Tejwani Shankar

Publisher

Medknow

Subject

Neurology (clinical)

Reference29 articles.

1. Failure of natalizumab to prevent relapses in neuromyelitis optica;Kleiter;Arch Neurol,2012

2. Development of extensive brain lesions following fingolimod (fty720) treatment in a patient with neuromyelitis optica spectrum disorder;Min;Mult Scler,2012

3. Update on the diagnosis and treatment of neuromyelitis optica: Recommendations of the neuromyelitis optica study group (nemos) J Neurol;Trebst,2014

4. Neuromyelitis optica spectrum disorders: Comparison of clinical and magnetic resonance imaging characteristics of aqp4-igg versus mog-igg seropositive cases in the netherlands;van;Eur J Neurol,2016

5. Mog antibody disease: A review of mog antibody seropositive neuromyelitis optica spectrum disorder;Narayan;Mult Scler Relat Disord,2018

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