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Drug Treatment of Clinically Isolated Syndrome

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F19%3A73598991" target="_blank" >RIV/61989592:15110/19:73598991 - isvavai.cz</a>

  • Result on the web

    <a href="https://link.springer.com/article/10.1007%2Fs40263-019-00647-x" target="_blank" >https://link.springer.com/article/10.1007%2Fs40263-019-00647-x</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s40263-019-00647-x" target="_blank" >10.1007/s40263-019-00647-x</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Drug Treatment of Clinically Isolated Syndrome

  • Original language description

    Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS) that leads to inflammation, demyelination and ultimately axonal degeneration. In most cases, it is preceded by its precursor, clinically isolated syndrome (CIS) with conversion rates to clinically definite MS (CDMS) of roughly 20–75%. Neurologists are therefore faced with the challenge of initiating a disease-modifying therapy (DMT) as early as possible to favorably influence the course of the disease. During the past 20 years, a multitude of drugs have been incorporated into our therapeutic armamentarium for MS and CIS. Choosing the right drug for an individual patient is complex and should be based not only on the drug’s overall efficacy to prevent disease progression but also its specific adverse reaction profile, the severity of individual disease courses and, finally, patient compliance in order to adequately weigh associated risks and benefits. Here, we review the available data on the efficacy, safety and tolerability of DMTs tested for CIS and discuss their value regarding a delay of progression to CDMS.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30210 - Clinical neurology

Result continuities

  • Project

  • Continuities

    N - Vyzkumna aktivita podporovana z neverejnych zdroju

Others

  • Publication year

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    CNS DRUGS

  • ISSN

    1172-7047

  • e-ISSN

  • Volume of the periodical

    2019

  • Issue of the periodical within the volume

    33

  • Country of publishing house

    NZ - NEW ZEALAND

  • Number of pages

    18

  • Pages from-to

    659-676

  • UT code for WoS article

    000475573400004

  • EID of the result in the Scopus database

    2-s2.0-85068829171