Suchergebnisse - "Dobrotova, Miroslava"

PubPharm (40)

1

Perioperative Monitoring with Rotational Thromboelastometry in a Severe Hemophilia A Patient Undergoing Elective Ankle Surgery

enthalten in: Seminars in thrombosis and hemostasis | 2024

von Simurda, T. | Drotarova, M. | Skornova, I. | +6

2

At-risk Pregnant Woman with Sticky Platelet Syndrome, Previous Recurrent Preeclampsia, and Current Proteinuria - A Rare Experience

enthalten in: Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion | 2023

von Stančiaková, L. | Dobrotová, M. | Ivanková, J. | +8

3

DNA Polymorphisms in Pregnant Women with Sticky Platelet Syndrome

enthalten in: Journal of clinical medicine | 2022

von Stančiaková, L. | Žolková, J. | Vadelová, �. | +15

4

Heterogeneity of Genotype-Phenotype in Congenital Hypofibrinogenemia-A Review of Case Reports Associated with Bleeding and Thrombosis

enthalten in: Journal of clinical medicine | 2022

von Brunclikova, M. | Simurda, T. | Zolkova, J. | +9

5

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

enthalten in: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis | 2022

von Stanciakova, L. | Dobrotova, M. | Holly, P. | +10

6

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

enthalten in: Diagnostics (Basel, Switzerland) | 2021

von Skornova, I. | Simurda, T. | Stasko, J. | +9

7

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

enthalten in: Diagnostics (Basel, Switzerland) | 2021

von Simurda, T. | Asselta, R. | Zolkova, J. | +9

8

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

enthalten in: Diagnostics (Basel, Switzerland) | 2021

von Stanciakova, L. | Dobrotova, M. | Holly, P. | +10

9

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

enthalten in: Biomedicines | 2020

von Simurda, T. | Vilar, R. | Zolkova, J. | +11

10

Genetic Background of von Willebrand Disease : History, Current State, and Future Perspectives

enthalten in: Seminars in thrombosis and hemostasis | 2020

von Zolkova, J. | Sokol, J. | Simurda, T. | +9