Found: 14
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Diagnostika poruch hemostázy.
- Published in:
- Internal Medicine / Vnitrni Lekarstvi, 2018, v. 64, n. 5, p. 537
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- Article
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?
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- Biomedical Papers of the Medical Faculty of Palacky University in Olomouc, 2014, v. 158, n. 2, p. 238, doi. 10.5507/bp.2012.070
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- Article
Diagnosing Czech Patients with Inherited Platelet Disorders.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 22, p. 14386, doi. 10.3390/ijms232214386
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- Article
Correction to: Molecular basis and outcomes of a typical haemolytic uraemic syndrome in Czech children.
- Published in:
- 2022
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- Publication type:
- Correction Notice
Molecular basis and outcomes of atypical haemolytic uraemic syndrome in Czech children.
- Published in:
- European Journal of Pediatrics, 2020, v. 179, n. 11, p. 1739, doi. 10.1007/s00431-020-03666-9
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- Article
Interaction of P-selectin and PSGL-1 generates microparticles that correct hemostasis in a mouse model of hemophilia A.
- Published in:
- Nature Medicine, 2003, v. 9, n. 8, p. 1020, doi. 10.1038/nm899
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- Publication type:
- Article
The Homozygous Type II Antithrombin Deficient Pregnant Woman Monitored by Thrombin Generation Assay.
- Published in:
- Clinical Laboratory, 2023, v. 69, n. 10, p. 2171, doi. 10.7754/Clin.Lab.2023.230435
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- Article
Extracorporeal membrane oxygenation seems to induce impairment of primary hemostasis pathology as measured by a Multiplate analyzer: An observational retrospective study.
- Published in:
- Artificial Organs, 2022, v. 46, n. 5, p. 899, doi. 10.1111/aor.14142
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- Publication type:
- Article
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.
- Published in:
- European Journal of Haematology, 2009, v. 82, n. 2, p. 148, doi. 10.1111/j.1600-0609.2008.01175.x
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- Publication type:
- Article
Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP.
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- Pediatric Nephrology, 2012, v. 27, n. 1, p. 73, doi. 10.1007/s00467-011-1943-5
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- Publication type:
- Article
Fibrinogen Šumperk II: Dysfibrinogenemia in an individual with two coding mutations.
- Published in:
- American Journal of Hematology, 2012, v. 87, n. 5, p. 555, doi. 10.1002/ajh.23162
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- Publication type:
- Article
Two novel fibrinogen variants in the C-terminus of the Bβ-chain: fibrinogen Rokycany and fibrinogen Znojmo.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2010, v. 30, n. 3, p. 311, doi. 10.1007/s11239-010-0505-1
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- Publication type:
- Article
Identifying risk factors and optimizing standard of care for patients with acquired haemophilia A: Results from a Czech patient cohort.
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- Haemophilia, 2020, v. 26, n. 4, p. 643, doi. 10.1111/hae.14084
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- Publication type:
- Article
Thrombin Generation Decrease After LMWH Administration in an Antithrombin-Deficient Pregnant Woman With a Homozygous HBS II Mutation.
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- Clinical & Applied Thrombosis/Hemostasis, 2023, v. 29, p. 1, doi. 10.1177/10760296231197174
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- Publication type:
- Article