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Journal ArticleDOI

New diagnostic criteria for multiple sclerosis: guidelines for research protocols.

TLDR
Today there is a need for more exact criteria than existed earlier in order to conduct therapeutic trials in multicenter programs, to compare epidemiological surveys, to evaluate new diagnostic procedures, and to estimate the activity of the disease process in MS.
Abstract
Several schemes for the diagnosis and clinical classification of multiple sclerosis (MS) have been advanced [l}. The best known is that published by Schumacher et alC31. The criteria for this scheme were established in order to select patients for participation in therapeutic trials, and pertain only to what might be called definite MS. No provision was made for incorporating supportive laboratory data into the diagnostic criteria. As no reliable specific laboratory test for the diagnosis of MS has been discovered, the diagnosis remains a clinical one, and there is still a need for clinical diagnostic criteria. However, several laboratory and clinical procedures have been developed within the last decade which aid greatly in demonstrating neurological dysfunction attributable to lesions, and even the lesions themselves. One problem with the various published diagnostic classifications is their discrepant terminology: what is considered “probable” in one is called “definite” in another. Another problem is that all the proposed schemes require much subjective judgment, a difficulty which cannot be completely overcome but can be diminished by adding to the clinical evaluation the results of laboratory, neuroimaging, neuropsychological, and neurophysiological procedures. Today there is a need for more exact criteria than existed earlier in order to conduct therapeutic trials in multicenter programs, to compare epidemiological surveys, to evaluate new diagnostic procedures, and to estimate the activity of the disease process in MS. Method and Procedure

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Citations
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Journal ArticleDOI

Diagnosis of multiple sclerosis: 2017 revisions of the McDonald criteria

TL;DR: The 2017 McDonald criteria continue to apply primarily to patients experiencing a typical clinically isolated syndrome, define what is needed to fulfil dissemination in time and space of lesions in the CNS, and stress the need for no better explanation for the presentation.
Journal ArticleDOI

Heterogeneity of multiple sclerosis lesions: implications for the pathogenesis of demyelination.

TL;DR: At a given time point of the disease, the patterns of demyelination were heterogeneous between patients, but were homogenous within multiple active lesions from the same patient, suggesting that MS may be a disease with heterogeneous pathogenetic mechanisms.
Journal ArticleDOI

A serum autoantibody marker of neuromyelitis optica : distinction from multiple sclerosis

TL;DR: NMO-IgG is a specific marker autoantibody of neuromyelitis optica and binds at or near the blood-brain barrier that distinguishes neuromyleitis opticas from multiple sclerosis.
References
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Journal ArticleDOI

The design of clinical studies to assess therapeutic efficacy in multiple sclerosis.

TL;DR: The diagnosis, clinical course, and definitions of the stages of MS are discussed as they relate to trials of therapy, and specific strategies and design considerations be applied to preliminary, pilot, and full trials.
Book

The Diagnosis of multiple sclerosis

TL;DR: The Diagnosis of multiple sclerosis is described in detail in the book “Diagnosis of Multiple Sclerosis: A Beginner’s Guide” (2003).
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