Zofia T. Bilinska

Warsaw, MZ, Poland

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 73 publications

Cardiovascular involvement and outcomes in Marfan syndrome: new observations on evolving aortic risk associations in a single-center cohort from Poland.

Cardiovascular involvement and outcomes in Marfan syndrome: new observations on evolving aortic risk associations in a single-center cohort from Poland.

Journal: Polish archives of internal medicine

Published: July 09, 2026

Genetic architecture of dilated cardiomyopathy in Poland: variant distribution, clinical characteristics, and prognosis.

Genetic architecture of dilated cardiomyopathy in Poland: variant distribution, clinical characteristics, and prognosis.

Journal: Polish archives of internal medicine

Published: August 12, 2025

Multiparametric Approach to Arrhythmic Mitral Valve Prolapse: Novel and Recognized Markers of Increased Sudden Cardiac Arrest Risk.

Multiparametric Approach to Arrhythmic Mitral Valve Prolapse: Novel and Recognized Markers of Increased Sudden Cardiac Arrest Risk.

Journal: Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography

Published: May 23, 2025

PRKAG2 Syndrome: Clinical Features, Imaging Findings and Cardiac Events.

PRKAG2 Syndrome: Clinical Features, Imaging Findings and Cardiac Events.

Journal: Biomedicines

Published: February 24, 2025

Expanding the phenotype of myosin heavy chain 11-related thoracic aortic disease: a case of mitral annular disjunction in a family.

Expanding the phenotype of myosin heavy chain 11-related thoracic aortic disease: a case of mitral annular disjunction in a family.

Journal: Polish archives of internal medicine

Published: February 10, 2025

Rare transthyretin gene variants (p.Ala45Thr, p.Val91Ala, p.Phe53Cys, p.Ala101Val, p.Glu109Lys, and p.Phe53Leu): diagnostic pitfalls and clinical characteristics of Polish patients with transthyretin cardiac amyloidosis.

Rare transthyretin gene variants (p.Ala45Thr, p.Val91Ala, p.Phe53Cys, p.Ala101Val, p.Glu109Lys, and p.Phe53Leu): diagnostic pitfalls and clinical characteristics of Polish patients with transthyretin cardiac amyloidosis.

Journal: Polish archives of internal medicine

Published: October 29, 2024

Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Journal: European heart journal

Published: September 18, 2024

Mitral valve prolapse in sudden cardiac arrest survivors: Coincidence or causal relationship?

Mitral valve prolapse in sudden cardiac arrest survivors: Coincidence or causal relationship?

Journal: Heart rhythm

Published: July 26, 2024

Coexistence of Marfan syndrome and fibromuscular dysplasia.

Coexistence of Marfan syndrome and fibromuscular dysplasia.

Journal: Polish archives of internal medicine

Published: July 10, 2024

Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities.

Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities.

Journal: Kardiologia polska

Published: April 29, 2024

ERRATUM: Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities.

ERRATUM: Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities.

Journal: Kardiologia polska

Published: April 29, 2024

Troponin T Assessment Allows for Identification of Mutation Carriers among Young Relatives of Patients with LMNA-Related Dilated Cardiomyopathy.

Troponin T Assessment Allows for Identification of Mutation Carriers among Young Relatives of Patients with LMNA-Related Dilated Cardiomyopathy.

Journal: Journal of clinical medicine

Published: April 25, 2024

Showing 1-12 of 73

Last Updated: 09/26/2026