Lista de obras -

12-month patterns of serum markers of collagen synthesis, transforming growth factor and connective tissue growth factor are similar in new-onset and chronic dilated cardiomyopathy in patients both with and without cardiac fibrosis.

artículo científico publicado en 2017

A missense mutation G109R in the PROC gene associated with type I protein C deficiency in a young Polish man with acute myocardial infarction

artículo científico publicado en 2013

A prothrombotic state and denser clot formation in patients following acute limb ischemia of unknown cause

artículo científico publicado en 2020

Adiponectin, leptin, and resistin in patients with aortic stenosis without concomitant atherosclerotic vascular disease

scientific article published on 01 October 2011

Alpha-2-antiplasmin Arg407Lys polymorphism and cryptogenic ischemic cerebrovascular events: Association with neurological deficit

artículo científico publicado en 2017

Altered plasma fibrin clot properties in hypertensive patients with obstructive sleep apnoea are improved by continuous positive airway pressure treatment

artículo científico publicado en 2017

Association of Interleukin-10 promoter polymorphisms with neurosyphilis

artículo científico publicado en 2015

Association of the C-Reactive Protein Gene (CRP) rs1205 C>T Polymorphism with Aortic Valve Calcification in Patients with Aortic Stenosis

artículo científico publicado en 2015

Biomechanical strain regulates TNFR2 but not TNFR1 in TMJ cells

artículo científico publicado en 2006

Bleeding predictors in patients following venous thromboembolism treated with vitamin K antagonists: Association with increased number of single nucleotide polymorphisms

artículo científico publicado en 2018

CYP2C9 Polymorphism and Unstable Anticoagulation with Warfarin in Patients Within the First 3 Months Following Heart Valve Replacement

artículo científico publicado en 2015

Detection and a functional characterization of the novel FBN1 intronic mutation underlying Marfan syndrome: case presentation

artículo científico publicado en 2017

Determinants of elevated factor VIII in patients screened for thrombophilia

artículo científico publicado en 2020

Does Diabetes Accelerate the Progression of Aortic Stenosis through Enhanced Inflammatory Response within Aortic valves? ⬇️

artículo científico publicado el 1 de junio de 2012

Dynamic biophysical strain modulates proinflammatory gene induction in meniscal fibrochondrocytes

artículo científico publicado en 2006

Effect of the E-selectin gene polymorphism (S149R) on platelet activation and adverse events after coronary artery surgery.

artículo científico publicado en 2011

Effects of rivaroxaban and dabigatran on local expression of coagulation and inflammatory factors within human aortic stenotic valves

artículo científico publicado en 2020

Exercise stress testing enhances blood coagulation and impairs fibrinolysis in asymptomatic aortic valve stenosis

scientific article published on 26 August 2014

Factor XIII Val34Leu polymorphism and ischaemic stroke in patients with patent foramen ovale

artículo científico publicado en 2009

Factor XIII Val34Leu polymorphism as a modulator of fibrin clot permeability and resistance to lysis in patients with severe coronary artery disease.

artículo científico publicado en 2009

Factor XIII expression within aortic valves and its plasma activity in patients with aortic stenosis: association with severity of disease.

artículo científico publicado en 2012

False-positive lupus anticoagulant in patients receiving rivaroxaban: 24 h since the last dose are needed to exclude antiphospholipid syndrome

artículo científico publicado en 2015

Fibrinogen beta-chain -C148T polymorphism is associated with increased fibrinogen, C-reactive protein, and interleukin-6 in patients undergoing coronary artery bypass grafting

artículo científico publicado en 2012

Fibrinogen β chain and FXIII polymorphisms affect fibrin clot properties in acute pulmonary embolism

artículo científico publicado en 2021

Fibrosis of extracellular matrix is related to the duration of the disease but is unrelated to the dynamics of collagen metabolism in dilated cardiomyopathy.

artículo científico publicado en 2016

First report of a large PROS1 deletion from exon 1 through 12 detected in Polish patients with deep-vein thrombosis

artículo científico publicado en 2013

First report of the genetic background of Marfan syndrome in Polish patients.

artículo científico publicado en 2013

Genetic characterization of antithrombin, protein C, and protein S deficiencies in Polish patients.

artículo científico publicado en 2017

Genetic determinants of acenocoumarol and warfarin maintenance dose requirements in Slavic population: a potential role of CYP4F2 and GGCX polymorphisms.

artículo científico publicado en 2014

High levels of latent antithrombin in plasma from patients with antithrombin deficiency.

artículo científico publicado en 2017

ID: 228

scholarly article by Agnieszka Irena Mazur-Bialy et al published November 2015 in Cytokine

Identification of a New Mechanism of Antithrombin Deficiency Hardly Detected by Current Methods: Duplication of SERPINC1 Exon 6.

artículo científico publicado en 2018

IgA Antiphospholipid Antibodies and Anti-Domain 1 of Beta 2 Glycoprotein 1 Antibodies are Associated with Livedo Reticularis and Heart Valve Disease in Antiphospholipid Syndrome

artículo científico publicado en 2014

Impaired Fibrinolysis in Patients with Isolated Aortic Stenosis is Associated with Enhanced Oxidative Stress

artículo científico publicado en 2020

Increased levels of bone remodeling biomarkers (osteoprotegerin and osteopontin) in hypertensive individuals

artículo científico publicado en 2011

Interaction between functional polymorphisms in FCER1A and TLR2 and the severity of atopic dermatitis

artículo científico publicado en 2020

Interleukin-6 receptor Asp358Ala gene polymorphism is associated with plasma C-reactive protein levels and severity of aortic valve stenosis

artículo científico publicado en 2014

Iron deficiency: a novel risk factor of recurrence in patients after unprovoked venous thromboembolism

scientific article published on 04 March 2016

Left ventricular reverse remodeling is not related to biopsy-detected extracellular matrix fibrosis and serum markers of fibrosis in dilated cardiomyopathy, regardless of the definition used for LVRR

artículo científico publicado en 2016

Lymphocyte and monocyte subpopulations in severe aortic stenosis at the time of surgical intervention

artículo científico publicado en 2018

MPI-CDG with transient hypoglycosylation and antithrombin deficiency

scholarly article by María Eugenia de la Morena-Barrio et al published February 2019 in Haematologica

Mast cells are responsible for the lack of anti-inflammatory effects of morphine in CBA mice

artículo científico publicado en 2004

Mechanical signals control SOX-9, VEGF, and c-Myc expression and cell proliferation during inflammation via integrin-linked kinase, B-Raf, and ERK1/2-dependent signaling in articular chondrocytes

artículo científico publicado en 2010

Morphine-modulated mast cell migration and proliferation during early stages of zymosan-induced peritonitis in CBA mice

artículo científico publicado en 2011

Non-classical and intermediate monocytes in patients following venous thromboembolism: Links with inflammation

artículo científico publicado en 2019

Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism

artículo científico publicado en 2014

Protein C and protein S deficiency - practical diagnostic issues

artículo científico publicado en 2013

Protein S deficiency and Heerlen polymorphism in a Polish patient with acute myocardial infarction and previous venous thromboembolism.

artículo científico publicado en 2013

Quantification of airborne birch (Betula sp.) pollen grains and allergens in Krakow.

artículo científico publicado en 2005

Reduced plasma fibrin clot permeability and susceptibility to fibrinolysis are associated with increased intima-media thickness in patients with primary antiphospholipid syndrome

artículo científico publicado en 2014

Regulation of RANKL by biomechanical loading in fibrochondrocytes of meniscus

artículo científico publicado en 2005

Relations between circulating microRNAs (miR-21, miR-26, miR-29, miR-30 and miR-133a), extracellular matrix fibrosis and serum markers of fibrosis in dilated cardiomyopathy.

artículo científico publicado en 2016

Repeated bleeding complications during therapy with vitamin K antagonists in a patient with the VKORC12A and the CYP2C93/*3 alleles: genetic testing to support switching to new oral anticoagulants

artículo científico publicado en 2012

Residual iliofemoral thrombosis in a 31-year-old woman on oral contraceptives possessing heterozygous factor V Leiden, factor XIII Val34Leu allele and alpha-fibrinogen Thr312Ala allele: case report

artículo científico publicado en 2009

Right ventricular morphology and function is not related with microRNAs and fibrosis markers in dilated cardiomyopathy.

artículo científico publicado en 2017

Shorter preoperative fibrin clot lysis time predisposes to higher chest tube drainage in patients undergoing elective coronary artery bypass grafting surgery

artículo científico publicado en 2010

Similar prevalence of platelet factor 4/heparin immunoglobulin G antibodies in patients following cardiac surgery and other patients suspected of heparin-induced thrombocytopaenia

artículo científico publicado en 2018

Stenotic Bicuspid and Tricuspid Aortic Valves　- Micro-Computed Tomography and Biological Indices of Calcification

artículo científico publicado en 2017

The New *G29A and G1222A of HCRTR1, 5-HTTLPR of SLC6A4 Polymorphisms and Hypocretin-1, Serotonin Concentrations in Migraine Patients.

artículo científico publicado en 2018

Toll-like receptors expression and NF-κB activation in peritoneal leukocytes in morphine-mediated impairment of zymosan-induced peritonitis in swiss mice

artículo científico publicado en 2012

Vascular Ehlers-Danlos syndrome in 2 Polish patients: identification of 2 novel COL3A1 gene mutations

scientific article published on 01 October 2019

Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review

artículo científico publicado en 2017

Warfarin Metabolites in Patients Following Cardiac Valve Implantation: A Contribution of Clinical and Genetic Factors

artículo científico publicado en 2015

Lista de obras de

12-month patterns of serum markers of collagen synthesis, transforming growth factor and connective tissue growth factor are similar in new-onset and chronic dilated cardiomyopathy in patients both with and without cardiac fibrosis.

A missense mutation G109R in the PROC gene associated with type I protein C deficiency in a young Polish man with acute myocardial infarction

A prothrombotic state and denser clot formation in patients following acute limb ischemia of unknown cause

Adiponectin, leptin, and resistin in patients with aortic stenosis without concomitant atherosclerotic vascular disease

Alpha-2-antiplasmin Arg407Lys polymorphism and cryptogenic ischemic cerebrovascular events: Association with neurological deficit

Altered plasma fibrin clot properties in hypertensive patients with obstructive sleep apnoea are improved by continuous positive airway pressure treatment

Association of Interleukin-10 promoter polymorphisms with neurosyphilis

Association of the C-Reactive Protein Gene (CRP) rs1205 C>T Polymorphism with Aortic Valve Calcification in Patients with Aortic Stenosis

Biomechanical strain regulates TNFR2 but not TNFR1 in TMJ cells

Bleeding predictors in patients following venous thromboembolism treated with vitamin K antagonists: Association with increased number of single nucleotide polymorphisms

CYP2C9 Polymorphism and Unstable Anticoagulation with Warfarin in Patients Within the First 3 Months Following Heart Valve Replacement

Detection and a functional characterization of the novel FBN1 intronic mutation underlying Marfan syndrome: case presentation

Determinants of elevated factor VIII in patients screened for thrombophilia

Does Diabetes Accelerate the Progression of Aortic Stenosis through Enhanced Inflammatory Response within Aortic valves? ⬇️

Dynamic biophysical strain modulates proinflammatory gene induction in meniscal fibrochondrocytes

Effect of the E-selectin gene polymorphism (S149R) on platelet activation and adverse events after coronary artery surgery.

Effects of rivaroxaban and dabigatran on local expression of coagulation and inflammatory factors within human aortic stenotic valves

Exercise stress testing enhances blood coagulation and impairs fibrinolysis in asymptomatic aortic valve stenosis

Factor XIII Val34Leu polymorphism and ischaemic stroke in patients with patent foramen ovale

Factor XIII Val34Leu polymorphism as a modulator of fibrin clot permeability and resistance to lysis in patients with severe coronary artery disease.

Factor XIII expression within aortic valves and its plasma activity in patients with aortic stenosis: association with severity of disease.

False-positive lupus anticoagulant in patients receiving rivaroxaban: 24 h since the last dose are needed to exclude antiphospholipid syndrome

Fibrinogen beta-chain -C148T polymorphism is associated with increased fibrinogen, C-reactive protein, and interleukin-6 in patients undergoing coronary artery bypass grafting

Fibrinogen β chain and FXIII polymorphisms affect fibrin clot properties in acute pulmonary embolism

Fibrosis of extracellular matrix is related to the duration of the disease but is unrelated to the dynamics of collagen metabolism in dilated cardiomyopathy.

First report of a large PROS1 deletion from exon 1 through 12 detected in Polish patients with deep-vein thrombosis

First report of the genetic background of Marfan syndrome in Polish patients.

Genetic characterization of antithrombin, protein C, and protein S deficiencies in Polish patients.

Genetic determinants of acenocoumarol and warfarin maintenance dose requirements in Slavic population: a potential role of CYP4F2 and GGCX polymorphisms.

High levels of latent antithrombin in plasma from patients with antithrombin deficiency.

ID: 228

Identification of a New Mechanism of Antithrombin Deficiency Hardly Detected by Current Methods: Duplication of SERPINC1 Exon 6.

IgA Antiphospholipid Antibodies and Anti-Domain 1 of Beta 2 Glycoprotein 1 Antibodies are Associated with Livedo Reticularis and Heart Valve Disease in Antiphospholipid Syndrome

Impaired Fibrinolysis in Patients with Isolated Aortic Stenosis is Associated with Enhanced Oxidative Stress

Increased levels of bone remodeling biomarkers (osteoprotegerin and osteopontin) in hypertensive individuals

Interaction between functional polymorphisms in FCER1A and TLR2 and the severity of atopic dermatitis

Interleukin-6 receptor Asp358Ala gene polymorphism is associated with plasma C-reactive protein levels and severity of aortic valve stenosis

Iron deficiency: a novel risk factor of recurrence in patients after unprovoked venous thromboembolism

Left ventricular reverse remodeling is not related to biopsy-detected extracellular matrix fibrosis and serum markers of fibrosis in dilated cardiomyopathy, regardless of the definition used for LVRR

Lymphocyte and monocyte subpopulations in severe aortic stenosis at the time of surgical intervention

MPI-CDG with transient hypoglycosylation and antithrombin deficiency

Mast cells are responsible for the lack of anti-inflammatory effects of morphine in CBA mice

Mechanical signals control SOX-9, VEGF, and c-Myc expression and cell proliferation during inflammation via integrin-linked kinase, B-Raf, and ERK1/2-dependent signaling in articular chondrocytes

Morphine-modulated mast cell migration and proliferation during early stages of zymosan-induced peritonitis in CBA mice

Non-classical and intermediate monocytes in patients following venous thromboembolism: Links with inflammation

Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism

Protein C and protein S deficiency - practical diagnostic issues

Protein S deficiency and Heerlen polymorphism in a Polish patient with acute myocardial infarction and previous venous thromboembolism.

Quantification of airborne birch (Betula sp.) pollen grains and allergens in Krakow.

Reduced plasma fibrin clot permeability and susceptibility to fibrinolysis are associated with increased intima-media thickness in patients with primary antiphospholipid syndrome

Regulation of RANKL by biomechanical loading in fibrochondrocytes of meniscus

Relations between circulating microRNAs (miR-21, miR-26, miR-29, miR-30 and miR-133a), extracellular matrix fibrosis and serum markers of fibrosis in dilated cardiomyopathy.

Repeated bleeding complications during therapy with vitamin K antagonists in a patient with the VKORC1*2A and the CYP2C9*3/*3 alleles: genetic testing to support switching to new oral anticoagulants

Residual iliofemoral thrombosis in a 31-year-old woman on oral contraceptives possessing heterozygous factor V Leiden, factor XIII Val34Leu allele and alpha-fibrinogen Thr312Ala allele: case report

Right ventricular morphology and function is not related with microRNAs and fibrosis markers in dilated cardiomyopathy.

Shorter preoperative fibrin clot lysis time predisposes to higher chest tube drainage in patients undergoing elective coronary artery bypass grafting surgery

Similar prevalence of platelet factor 4/heparin immunoglobulin G antibodies in patients following cardiac surgery and other patients suspected of heparin-induced thrombocytopaenia

Stenotic Bicuspid and Tricuspid Aortic Valves - Micro-Computed Tomography and Biological Indices of Calcification

The New *G29A and G1222A of HCRTR1, 5-HTTLPR of SLC6A4 Polymorphisms and Hypocretin-1, Serotonin Concentrations in Migraine Patients.

Toll-like receptors expression and NF-κB activation in peritoneal leukocytes in morphine-mediated impairment of zymosan-induced peritonitis in swiss mice

Vascular Ehlers-Danlos syndrome in 2 Polish patients: identification of 2 novel COL3A1 gene mutations

Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review

Warfarin Metabolites in Patients Following Cardiac Valve Implantation: A Contribution of Clinical and Genetic Factors

Repeated bleeding complications during therapy with vitamin K antagonists in a patient with the VKORC12A and the CYP2C93/*3 alleles: genetic testing to support switching to new oral anticoagulants

Stenotic Bicuspid and Tricuspid Aortic Valves　- Micro-Computed Tomography and Biological Indices of Calcification