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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.
Citations
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Journal ArticleDOI

Oropharyngeal dysphagia in multiple sclerosis.

TL;DR: The results emphasize the importance of assessment and management of swallowing function in MS patients, particularly in patients with a high EDSS score; more sever cerebellar dysfunction, and long disease duration.
Journal ArticleDOI

Frequency of blood CX3CR1-positive natural killer cells correlates with disease activity in multiple sclerosis patients.

TL;DR: An RNA screen in peripheral mononuclear cells from relapsing‐remitting and primary progressive MS patients compared with healthy donors (HD) indicated a role for the chemokine receptor CX3CR1 as a diagnostic marker, and found a correlation between disease activity and frequency of CX 3CR1‐positive NK cells in RRMS patients.
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Inflammatory multiple-sclerosis plaques generate characteristic metabolic profiles in cerebrospinal fluid.

TL;DR: CSF metabolic profiles suggest a close link between MS plaque activity in CIS patients on the one hand and organic-acid metabolism on the other, and increased BHIB levels points to a hitherto unsuspected role for this compound in MS with active plaques.
Journal ArticleDOI

Distinct cognitive impairments in different disease courses of multiple sclerosis-A systematic review and meta-analysis.

TL;DR: Results imply that, previously under‐recognized, PPMS patients display severe degrees of CI and need more specialized disease management than RRMS patients.
Journal ArticleDOI

Acute disseminated encephalomyelitis: a review of 18 cases in childhood.

TL;DR: The present study was initiated to report on the various modes of presentation and raise the awareness of the diagnosis of ADEM among general paediatricians.
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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