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Journal ArticleDOI

Recommended diagnostic criteria for multiple sclerosis: Guidelines from the International Panel on the Diagnosis of Multiple Sclerosis

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TLDR
The revised criteria facilitate the diagnosis of MS in patients with a variety of presentations, including “monosymptomatic” disease suggestive of MS, disease with a typical relapsing‐remitting course, and disease with insidious progression, without clear attacks and remissions.
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Elevated white matter myo-inositol in clinically isolated syndromes suggestive of multiple sclerosis.

TL;DR: The concentration of Ins was elevated in CIS NAWM and the early increase may reflect a process of pathogenic importance in multiple sclerosis NAWM, and follow-up studies will investigate whether the increase is of prognostic importance for future relapses and disability.
Journal ArticleDOI

High nationwide prevalence of multiple sclerosis in Sweden

TL;DR: In Sweden, the risk of MS increases with increasing north latitude for both men and women, and the MS prevalence of 188.9/100,000 in Sweden is among the highest nationwide prevalence estimates in the world.
Journal ArticleDOI

Pivotal Advance: HMGB1 expression in active lesions of human and experimental multiple sclerosis

TL;DR: It is demonstrated that high mobility group box chromosomal protein 1 (HMGB1), a DNA‐binding protein with proinflammatory properties, is evident in active lesions of MS and experimental autoimmune encephalomyelitis (EAE) and that HMGB1 levels correlate with active inflammation.
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Antibody to aquaporin 4 in the diagnosis of neuromyelitis optica.

TL;DR: In the largest series reported so far to the authors' knowledge, AQP4 antibodies in patients with NMO versus various other diseases are quantified, and it is shown that the aquaporin 4 water channel is a target antigen in a majority of patients withNMO.
References
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Journal ArticleDOI

The clinical course of neuromyelitis optica (Devic's syndrome)

TL;DR: Clinical, laboratory, and imaging features generally distinguish neuromyelitis optica from MS, and patients with relapsing optic neuritis and myelitis may have neuromyeliitis opticas rather than MS.
Journal ArticleDOI

Comparison of MRI criteria at first presentation to predict conversion to clinically definite multiple sclerosis.

TL;DR: It is concluded that a four-parameter dichotomized MRI model including gadolinium-enhancement, juxtacortical, infratentorial and periventricular lesions best predicts conversion to clinically definite multiple sclerosis.
Journal ArticleDOI

MRI in the diagnosis of MS A prospective study with comparison of clinical evaluation, evoked potentials, oligoclonal banding, and CT

TL;DR: MRI was the best method for demonstrating dissemination in space and laboratory-supported definite MS (LSDMS) could be diagnosed in 85 patients of the total 200, and MRI predicted that diagnosis in 18/19 (95%).
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