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2. Diagnosis of multiple sclerosis - Wikipedia

   en.wikipedia.org/.../Diagnosis_of_multiple_sclerosis

   Unusual types of MS have been described; these include Devic's disease, Balo concentric sclerosis, Schilder's diffuse sclerosis, and Marburg multiple sclerosis. There is debate on whether they are MS variants or different diseases. [31] Multiple sclerosis behaves differently in children, taking more time to reach the progressive stage. [5]

3. Multiple sclerosis - Wikipedia

   en.wikipedia.org/wiki/Multiple_sclerosis

   Multiple sclerosis. Multiple sclerosis is an autoimmune disease, primarily mediated by T-cells. [15] The three main characteristics of MS are the formation of lesions in the central nervous system (also called plaques), inflammation, and the destruction of myelin sheaths of neurons.

4. Pathophysiology of multiple sclerosis - Wikipedia

   en.wikipedia.org/wiki/Pathophysiology_of...

   Currently it is unknown what the primary cause of MS is; if MS is a heterogeneous disease, the lesion development process would not be unique. In particular, some PPMS patients having a special clinical course named rapidly progressive multiple sclerosis could have a special genetic cause [47] and a different development process.

5. How Do Doctors Diagnose Multiple Sclerosis? - AOL

   www.aol.com/lifestyle/doctors-diagnose-multiple...

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6. Signs of multiple sclerosis can be detected in blood 5 years ...

   www.aol.com/lifestyle/signs-multiple-sclerosis...

   “Multiple sclerosis is a complex autoimmune disease that is difficult to diagnose,” Colin Zamecnik, a researcher at UC San Francisco and lead author on the paper, tells Yahoo Life. “We ...

7. Biomarkers of multiple sclerosis - Wikipedia

   en.wikipedia.org/wiki/Biomarkers_of_multiple...

   The autoimmune disease-associated transcription factors EOMES and TBX21 are dysregulated in multiple sclerosis and define a molecular subtype of disease. [67] The importance of this discovery is that the expression of these genes appears in blood and can be measured by a simple blood analysis. NR1H3 Mutation.