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Changing insights in the diagnosis and classification of autosomal recessive and dominant von Willebrand diseases 1980-2015

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F16%3A00092329" target="_blank" >RIV/00216224:14110/16:00092329 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.5315/wjh.v5.i3.61" target="_blank" >http://dx.doi.org/10.5315/wjh.v5.i3.61</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.5315/wjh.v5.i3.61" target="_blank" >10.5315/wjh.v5.i3.61</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Changing insights in the diagnosis and classification of autosomal recessive and dominant von Willebrand diseases 1980-2015

  • Original language description

    The European Clinical Laboratory and Molecular (ECLM) criteria define 10 distinct Willebrand diseases (VWD): recessive type 3, severe 1, 2C and 2N; dominant VWD type 1 secretion/clearance defect, 2A, 2B, 2E, 2M and 2D; and mild type 1 VWD (usually carriers of recessive VWD). Recessive severe 1 and 2C VWD are characterized by secretion and multimerization defects caused by mutations in the D1-D2 domain. Recessive 2N VWD is a mild hemophilia due to D´-FVlH-von Willebrand factor (VWF) binding site mutations. Dominant 2E VWD caused by heterozygous missense mutations in the D3 domain is featured by a secretion-clearance-multimerization VWF defect. Dominant VWD type 2M due to loss of function mutations in the Al domain is characterized by decreased ristocetin-induced platelet aggregation and VWF:RCo, normal VWF multimers and VWF:CB, a poor response of VWF:RCo and good response of VWF:CB to desmopressin (DDAVP).

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    World Journal of Hematology

  • ISSN

    2218-6204

  • e-ISSN

  • Volume of the periodical

    5

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    14

  • Pages from-to

    61-74

  • UT code for WoS article

  • EID of the result in the Scopus database