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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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CSF and serum levels of soluble fractalkine (CX3CL1) in inflammatory diseases of the nervous system.

TL;DR: Fractalkine CSF/serum ratios in diseases without CSF pleocytosis and a lack of correlation between fractalkine levels and CSF leukocyte counts suggested that soluble fractalkin is not a major chemokine in the CSF.
Journal ArticleDOI

Quantitative assessment of upper limb motor function in Multiple Sclerosis using an instrumented Action Research Arm Test

TL;DR: The present study showed that the proposed ARAT method is able to discriminate between control and MS groups and to reveal subtle arm alterations not detectable from ARAT score, suggesting that instrumented ARAT could be a valid quick and easy-to-use method for a sensitive quantification of arm function in MS.
Journal ArticleDOI

Patient characteristics and determinants of quality of life in an international population with multiple sclerosis: assessment using the MusiQoL and SF-36 questionnaires.

TL;DR: Sociodemographic and clinical factors are linked to HRQoL in patients with MS in a large international study using the MS International QoL (MusiZoL) questionnaire.
Journal ArticleDOI

Multiple sclerosis in Jordan: a clinical and epidemiological study

TL;DR: Young age of onset, shorter duration of illness, a relapsing remitting pattern, and use of interferon were identified as statistically significant predictors of less disability.
Journal ArticleDOI

Higher sensitivity in the detection of inflammatory brain lesions in patients with clinically isolated syndromes suggestive of multiple sclerosis using high field MRI: an intraindividual comparison of 1.5 T with 3.0 T.

TL;DR: High-field MRI at 3.0 T provides a significantly higher detection rate of inflammatory brain lesions especially in the infratentorial, juxtacortical and periventricular anatomic region.
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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