日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemia

纤维蛋白原γ链基因中一种新的致病变异p.Glu275Lys会导致先天性低纤维蛋白原血症

Drotarova, Miroslava; Asselta, Rosanna; Caccia, Sonia; Skornova, Ingrid; Zolkova, Jana; Kolkova, Zuzana; Loderer, Dusan; Podusel, Vladimir; Stasko, Jan; Simurda, Tomas

Diagnostic value of clot formation parameters determined by rotational thromboelastometry in 63 patients with congenital dysfibrinogenemia

旋转血栓弹力图测定的凝块形成参数在63例先天性纤维蛋白原异常血症患者中的诊断价值

Simurda, Tomas; Marchi, Rita; Casini, Alessandro; Neerman-Arbez, Marguerite; Drotarova, Miroslava; Skornova, Ingrid; Zolkova, Jana; Kolkova, Zuzana; Loderer, Dusan; Brunclikova, Monika; Belakova, Kristina Maria; Stasko, Jan

How can Secondary Thromboprophylaxis in High-Risk Pregnant Patients be Improved?

如何改进高危妊娠患者的二级血栓预防?

Stanciakova, Lucia; Dobrotova, Miroslava; Holly, Pavol; Zolkova, Jana; Vadelova, Lubica; Skornova, Ingrid; Ivankova, Jela; Samos, Matej; Bolek, Tomas; Grendar, Marian; Danko, Jan; Kubisz, Peter; Stasko, Jan

Multimer Analysis of Von Willebrand Factor in Von Willebrand Disease with a Hydrasys Semi-Automatic Analyzer-Single-Center Experience

利用Hydrasys半自动分析仪对血管性血友病中的血管性血友病因子进行多聚体分析——单中心经验

Skornova, Ingrid; Simurda, Tomas; Stasko, Jan; Zolkova, Jana; Sokol, Juraj; Holly, Pavol; Dobrotova, Miroslava; Plamenova, Ivana; Hudecek, Jan; Brunclikova, Monika; Stryckova, Alena; Kubisz, Peter

How Can Rotational Thromboelastometry as a Point-of-Care Method Be Useful for the Management of Secondary Thromboprophylaxis in High-Risk Pregnant Patients?

旋转血栓弹力图作为一种床旁检测方法,如何能用于高危妊娠患者的二级血栓预防管理?

Stanciakova, Lucia; Dobrotova, Miroslava; Holly, Pavol; Zolkova, Jana; Vadelova, Lubica; Skornova, Ingrid; Ivankova, Jela; Bolek, Tomas; Samos, Matej; Grendar, Marian; Danko, Jan; Kubisz, Peter; Stasko, Jan

Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management

先天性无纤维蛋白原血症和低纤维蛋白原血症:罕见出血性疾病的实验室和基因检测及其危及生命的临床表现和棘手的治疗难题

Simurda, Tomas; Asselta, Rosanna; Zolkova, Jana; Brunclikova, Monika; Dobrotova, Miroslava; Kolkova, Zuzana; Loderer, Dusan; Skornova, Ingrid; Hudecek, Jan; Lasabova, Zora; Stasko, Jan; Kubisz, Peter

A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype

纤维蛋白原β链中FGB基因(c.1421G>A;p.Trp474Ter)的新型无义突变导致低纤维蛋白原血症伴出血表型

Simurda, Tomas; Vilar, Rui; Zolkova, Jana; Ceznerova, Eliska; Kolkova, Zuzana; Loderer, Dusan; Neerman-Arbez, Marguerite; Casini, Alessandro; Brunclikova, Monika; Skornova, Ingrid; Dobrotova, Miroslava; Grendar, Marian; Stasko, Jan; Kubisz, Peter

Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation

依度沙班对凝血酶依赖性血小板聚集的影响

Juraj Sokol, Frantisek Nehaj, Jela Ivankova, Michal Mokan, Lenka Lisa, Jana Zolkova, Lubica Vadelova, Marian Mokan, Jan Stasko

Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders

在两个患有定量纤维蛋白原紊乱的斯洛伐克家族中鉴定出两种新的纤维蛋白原Bβ链突变

Simurda, Tomas; Zolkova, Jana; Snahnicanova, Zuzana; Loderer, Dusan; Skornova, Ingrid; Sokol, Juraj; Hudecek, Jan; Stasko, Jan; Lasabova, Zora; Kubisz, Peter