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European principles of inhibitor management in patients with haemophilia

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F18%3A00069286" target="_blank" >RIV/65269705:_____/18:00069286 - isvavai.cz</a>

  • Result on the web

    <a href="https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0800-z" target="_blank" >https://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0800-z</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1186/s13023-018-0800-z" target="_blank" >10.1186/s13023-018-0800-z</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    European principles of inhibitor management in patients with haemophilia

  • Original language description

    Background: In spite of recent major advances in the understanding and treatment of inhibitor development in patients with haemophilia, multidisciplinary management of many of these patients remains suboptimal and highly heterogenous across Europe. Methods: Following a series of multidisciplinary meetings and a review of the literature, the European haemophilia community of health professionals and patients jointly defined practical optimum standards for ensuring and harmonizing treatment and care for patients with an inhibitor. Results: Ten complementary principles for the management of inhibitors in haemophilia have been developed, emphasizing the importance and benefits of a centralized, multidisciplinary, expert and holistic approach. Conclusions: This document will serve as a benchmark to improve the multidisciplinary and practical management of patients with inhibitor. Implementation and adherence to each of these principles should have a major positive impact on the management and outcomes of patients developing an inhibitor.

  • 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

    30101 - Human genetics

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Orphanet Journal of Rare Diseases

  • ISSN

    1750-1172

  • e-ISSN

  • Volume of the periodical

    13

  • Issue of the periodical within the volume

    APR 2018

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    6

  • Pages from-to

    66

  • UT code for WoS article

    000431528600001

  • EID of the result in the Scopus database

    2-s2.0-85046255948