Ivana Hadacova

Prague, PR 15006, Czech Republic

Last Updated: 09/26/2026

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Found 8 publications

Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress.

Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress.

Journal: Blood cells, molecules & diseases

Published: December 29, 2021

Acute portal vein thrombosis in noncirrhotic patients - different prognoses based on presence of inflammatory markers: a long-term multicenter retrospective analysis.

Acute portal vein thrombosis in noncirrhotic patients - different prognoses based on presence of inflammatory markers: a long-term multicenter retrospective analysis.

Journal: Scandinavian journal of gastroenterology

Published: October 22, 2019

Impact of CYP2C19 Polymorphisms on Clinical Outcomes and Antiplatelet Potency of Clopidogrel in Caucasian Poststroke Survivors.

Impact of CYP2C19 Polymorphisms on Clinical Outcomes and Antiplatelet Potency of Clopidogrel in Caucasian Poststroke Survivors.

Journal: American journal of therapeutics

Published: March 07, 2018

Endogenous Heparinoids May Cause Bleeding in Mucor Infection and can be Detected by Nonactivated Thromboelastometry and Treated by Recombinant Activated Factor VII: A Case Report.

Endogenous Heparinoids May Cause Bleeding in Mucor Infection and can be Detected by Nonactivated Thromboelastometry and Treated by Recombinant Activated Factor VII: A Case Report.

Journal: Medicine

Published: March 04, 2016

Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency.

Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency.

Journal: Haematologica

Published: April 15, 2014

Thrombophilic mutation by women with serious pregnancy complications

Thrombophilic mutation by women with serious pregnancy complications

Journal: Ceska gynekologie

Published: June 19, 2012

Does the asymptomatic carriage of FV Leiden and FII prothrombin in heterozygous configuration represent the increased risk of thrombembolic complications during pregnancy, childbirth and postpartum?

Does the asymptomatic carriage of FV Leiden and FII prothrombin in heterozygous configuration represent the increased risk of thrombembolic complications during pregnancy, childbirth and postpartum?

Journal: Ceska gynekologie

Published: April 28, 2012

Does asymptomatic carriage of FV Leiden and FII prothrombin mutations in heterozygous configuration pose an increased risk of thrombembolic complications in the course of pregnancy, labor and puerperium?

Does asymptomatic carriage of FV Leiden and FII prothrombin mutations in heterozygous configuration pose an increased risk of thrombembolic complications in the course of pregnancy, labor and puerperium?

Journal: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia

Published: January 03, 2012

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Last Updated: 09/26/2026