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

Effectiveness of caplacizumab in the first-line treatment for acquired thrombotic thrombocytopenic purpura: single center experience

卡普拉西珠单抗一线治疗获得性血栓性血小板减少性紫癜的疗效:单中心经验

Belakova, Kristina Maria; Pizurova, Renata; Simurda, Tomas; Plamenova, Ivana; Holly, Pavol; Skornova, Ingrid; Agouba, Sohaib Mukhtar; Drotarova, Miroslava; Brunclikova, Monika; Stryckova, Alena; Jusko, Richard; Stasko, Jan; Sokol, Juraj; Jezikova, Alena

Selected PEAR1 and MRVI1 Gene Polymorphisms in Patients with Migraine and Sticky Platelet Syndrome

偏头痛和血小板粘性综合征患者的PEAR1和MRVI1基因多态性分析

Simurda, Tomas; Belakova, Kristina Maria; Stasko, Jan; Skerenova, Maria; Ivankova, Jela; Drotarova, Miroslava; Brunclikova, Monika; Stanciakova, Lucia; Skornova, Ingrid; Sokol, Juraj

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

A Functional Assay for the Determination of Heparin-Induced Thrombocytopenia via Flow Cytometry

利用流式细胞术测定肝素诱导的血小板减少症的功能性检测

Skornova, Ingrid; Simurda, Tomas; Stanciakova, Lucia; Lauko, Viliam; Holly, Pavol; Samos, Matej; Bolek, Tomas; Schnierer, Martin; Drotarova, Miroslava; Belakova, Kristina Maria; Sokol, Juraj; Stasko, Jan; Mokan, Marian; Gumulec, Jaroslav; Chrastinova, Leona

Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing

使用高通量靶向测序检测抗凝血酶、蛋白 C 和蛋白 S 缺乏症中的未知和罕见致病变异

Petr Vrtel, Ludek Slavik, Radek Vodicka, Julia Stellmachova, Martin Prochazka, Jana Prochazkova, Jana Ulehlova, Peter Rohon, Tomas Simurda, Jan Stasko, Ivana Martinkova, Radek Vrtel

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

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

Association of Genetic Variability in Selected Genes in Patients With Deep Vein Thrombosis and Platelet Hyperaggregability

深静脉血栓形成和血小板高聚集性患者特定基因遗传变异的相关性

Sokol, Juraj; Skerenova, Maria; Ivankova, Jela; Simurda, Tomas; Stasko, Jan