Ján Staško

ORCID: 0000-0003-3305-0269
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About
Contact & Profiles
Research Areas
  • Venous Thromboembolism Diagnosis and Management
  • Atrial Fibrillation Management and Outcomes
  • Platelet Disorders and Treatments
  • Antiplatelet Therapy and Cardiovascular Diseases
  • Blood Coagulation and Thrombosis Mechanisms
  • Blood properties and coagulation
  • Acute Myocardial Infarction Research
  • Cardiac Arrhythmias and Treatments
  • Hemophilia Treatment and Research
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Trauma, Hemostasis, Coagulopathy, Resuscitation
  • Animal Nutrition and Physiology
  • Heparin-Induced Thrombocytopenia and Thrombosis
  • Pregnancy and preeclampsia studies
  • Blood groups and transfusion
  • Coronary Interventions and Diagnostics
  • Heart Rate Variability and Autonomic Control
  • Peripheral Artery Disease Management
  • Hemostasis and retained surgical items
  • Hemoglobinopathies and Related Disorders
  • Erythrocyte Function and Pathophysiology
  • Angiogenesis and VEGF in Cancer
  • Genetic and phenotypic traits in livestock
  • Lipoproteins and Cardiovascular Health
  • Cardiac electrophysiology and arrhythmias

Comenius University Bratislava
2016-2025

Martin University Hospital
2015-2024

University of Tehran
2023

Rotunda Hospital
2023

Mater Misericordiae University Hospital
2023

Weatherford College
2021-2022

National Blood Transfusion Service
2018

Martin University
2018

Creative Commons
2017

University Library in Bratislava
2017

Venous thromboembolism (VTE) represents one of the leading causes death during pregnancy. The greatest risk for it is presence medical or family history VTE, stillbirth, cesarean section and selected thrombophilia. Appropriate thromboprophylaxis has potential to decrease VTE in at-risk pregnant patients by 60–70%. Based on this, authors reviewed PubMed, Web Science Scopus databases identify possibilities with a high VTE. Moreover, they summarized its management specific situations, such as...

10.3390/ph17060773 article EN cc-by Pharmaceuticals 2024-06-13

Background: Impaired endothelial function has been associated with vascular complications in type 2 diabetes (T2D), but its role T2D-related heart failure (HF) remains indeterminate. The aim of this study was to assess selected markers T2D patients acute decompensated HF. Methods: A pilot prospective on HF requiring in-hospital admission carried out. growth factor (VEGF), intercellular adhesion molecule 1 (ICAM-1), and cell (VCAM-1) were assessed at after decongestion. Subsequently,...

10.3390/metabo15020091 article EN cc-by Metabolites 2025-02-03

Single-nucleotide variants (SNVs) of ABCB1 gene encoding glycoprotein P might be connected with increased or decreased levels direct oral anticoagulants (DOAC), and therefore DOAC-related adverse bleeding embolism. The aim this study was to perform a targeted exome sequencing (TES) in DOAC-treated patients atrial fibrillation, who experienced event (AE) during the therapy. Targeted next generation employed examine SNVs gene, which served as basis for haplotype analysis. enrolled 33 an AE (13...

10.1097/fjc.0000000000001695 article EN Journal of Cardiovascular Pharmacology 2025-03-28

Proton pump inhibition (PPI) administrated together with dabigatran reduces the risk of gastrointestinal hemorrhage. However, there is a discussion regarding possible PPI-dabigatran interaction that may reduce efficacy this therapy.To determine impact concomitant PPI on plasma levels in patients nonvalvular atrial fibrillation (NV-AF).A pilot prospective study NV-AF therapy was performed; 31 were enrolled. either omeprazole or pantoprazole 19 patients.Blood samples taken for assessment...

10.1097/mjt.0000000000000599 article EN American Journal of Therapeutics 2017-04-27

Congenital hypofibrinogenemia is a rare bleeding disorder characterized by proportional decrease of functional and antigenic fibrinogen levels. Hypofibrinogenemia can be considered the phenotypic expression heterozygous loss function mutations occurring within one three genes (FGA, FGB, FGG). Clinical manifestations are highly variable; most patients usually asymptomatic, but may appear with mild to severe or thrombotic complications. We have sequenced all exons FGA, FGG using DNA isolated...

10.3390/biomedicines8120605 article EN cc-by Biomedicines 2020-12-13

Disturbances of coagulation and fibrinolysis in type 2 diabetes mellitus (DM2) contribute to increased rates macrovascular complications such as myocardial infarction ischemic stroke. The aim the study was investigate relationship among plasminogen activator inhibitor 1 (PAI-1), thrombin-activable (TAFI), tissue (t-PA), prothrombin fragments + (F1 2), glycemic control, hypertension, sex body mass index (BMI) DM2 patients with normoalbuminuria microalbuminuria. Forty-two normoalbuminuric...

10.1097/mbc.0b013e328346f8ca article EN Blood Coagulation & Fibrinolysis 2011-04-26

The purpose of this study was to examine plasma levels fibronectin and plasminogen inhibitor type 1 (PAI-1), alterations in uterine artery (UtA) waveforms throughout normotensive preeclamptic pregnancies analyze its predictive value for the detection preeclampsia within second trimester pregnancy.Blood samples were collected from 102 healthy, nulliparous women between 24th 26th gestational week. Preeclampsia developed 13 patients; 89 control subjects matched same cohort. Plasma assayed PAI-1...

10.3233/dma-2011-0772 article EN DOAJ (DOAJ: Directory of Open Access Journals) 2011-01-01

Objective : The purpose of this study was to examine plasma levels fibronectin and plasminogen inhibitor type 1 (PAI-1), alterations in uterine artery (UtA) waveforms throughout normotensive preeclamptic pregnancies analyze its predictive value for the detection preeclampsia within second trimester pregnancy. Material methods Blood samples were collected from 102 healthy, nulliparous women between 24th 26th gestational week. Preeclampsia developed 13 patients; 89 control subjects matched...

10.1155/2011/219350 article EN Disease Markers 2011-01-01
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