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List of works by Ingrid Hrachovinová

A common origin of the 4143insA ADAMTS13 mutation

scientific article

A novel Kunitz protein with proposed dual function from Eudiplozoon nipponicum (Monogenea) impairs haemostasis and action of complement in vitro

scientific article published on 20 February 2019

Clinical manifestation and molecular genetic characterization of MYH9 disorders

scientific article

Congenital dysfibrinogenemia Aα Gly13Glu associated with bleeding during pregnancy

scientific article published on 26 November 2010

Fibrinogen Šumperk II: Dysfibrinogenemia in an individual with two coding mutations

scientific article published on March 9, 2012

High-resolution melting analysis for detection of MYH9 mutations

scientific article

Identifying risk factors and optimizing standard of care for patients with acquired haemophilia A: Results from a Czech patient cohort

scientific article published on 26 June 2020

Interaction of P-selectin and PSGL-1 generates microparticles that correct hemostasis in a mouse model of hemophilia A.

scientific article published on 13 July 2003

Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP.

scientific article

Molecular basis and outcomes of atypical haemolytic uraemic syndrome in Czech children

scientific article published on 18 May 2020

Patients with acute coronary syndromes have low tissue factor activity and microparticle count, but normal concentration of tissue factor antigen in platelet free plasma: a pilot study

scientific article published on 06 November 2008

Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population

scientific article published on 02 March 2020

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at enrolment until 2017

scientific article published on 21 February 2019

Two novel fibrinogen variants in the C-terminus of the Bβ-chain: fibrinogen Rokycany and fibrinogen Znojmo

scientific article published on 01 October 2010