Detalhe da pesquisa
1.
Annual incidence and severity of acute episodes in hereditary thrombotic thrombocytopenic purpura.
Blood
; 137(25): 3563-3575, 2021 06 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33649760
2.
The Homozygous Type II Antithrombin Deficient Pregnant Woman Monitored by Thrombin Generation Assay.
Clin Lab
; 69(10)2023 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37844053
3.
Extracorporeal membrane oxygenation seems to induce impairment of primary hemostasis pathology as measured by a Multiplate analyzer: An observational retrospective study.
Artif Organs
; 46(5): 899-907, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-34904233
4.
Diagnosing Czech Patients with Inherited Platelet Disorders.
Int J Mol Sci
; 23(22)2022 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36430862
5.
Hereditary antithrombin deficiency in pregnancy - severe thrombophilic disorder as a danger for mother and foetus
Ceska Gynekol
; 86(3): 175-182, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34167310
6.
Identifying risk factors and optimizing standard of care for patients with acquired haemophilia A: Results from a Czech patient cohort.
Haemophilia
; 26(4): 643-651, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32590889
7.
Molecular basis and outcomes of atypical haemolytic uraemic syndrome in Czech children.
Eur J Pediatr
; 179(11): 1739-1750, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32424742
8.
The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: key findings at enrollment until 2017.
Haematologica
; 104(10): 2107-2115, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30792199
9.
Diagnostic strategies in disorders of hemostasis.
Vnitr Lek
; 64(5): 537-544, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30193524
10.
Correction to: Molecular basis and outcomes of a typical haemolytic uraemic syndrome in Czech children.
Eur J Pediatr
; 181(4): 1781, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-35013812
11.
Effects of frozen storage conditions and freezing rate on the stability of coagulation proteins in human plasma.
Blood Coagul Fibrinolysis
; 34(6): 377-384, 2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37577899
12.
Thrombin Generation Decrease After LMWH Administration in an Antithrombin-Deficient Pregnant Woman With a Homozygous HBS II Mutation.
Clin Appl Thromb Hemost
; 29: 10760296231197174, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37670493
13.
The impact of PROS1 mutation position on thrombotic risk in protein S-deficient patients.
Res Pract Thromb Haemost
; 7(4): 100194, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37384225
14.
Fibrinogen Sumperk II: dysfibrinogenemia in an individual with two coding mutations.
Am J Hematol
; 87(5): 555-7, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22407772
15.
Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP.
Pediatr Nephrol
; 27(1): 73-81, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21706448
16.
Hereditary thrombotic thrombocytopenic purpura and COVID-19: Impacts of vaccination and infection in this rare disease.
Res Pract Thromb Haemost
; 6(7): e12814, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36284639
17.
Interaction of P-selectin and PSGL-1 generates microparticles that correct hemostasis in a mouse model of hemophilia A.
Nat Med
; 9(8): 1020-5, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12858167
18.
Two novel fibrinogen variants in the C-terminus of the Bß-chain: fibrinogen Rokycany and fibrinogen Znojmo.
J Thromb Thrombolysis
; 30(3): 311-8, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20640913
19.
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.
Eur J Haematol
; 82(2): 148-53, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19018869
20.
Clinical manifestation and molecular genetic characterization of MYH9 disorders.
Platelets
; 20(5): 289-96, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19557653