Zsofia Polai

Publication Activity (10 Years)

Years Active: 2023-2023
Publications (10 Years): 6

Top Topics

Replacement Therapy

Molecular Dynamics

Venous Thromboembolism

Top Venues

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Steven Philip Grover, Tomohiro Kawano, Jun Wan, Pansakorn Tanratana, Zsofia Polai, Young Jun Shim, Omri Snir, Sigrid Kufaas Brækkan, Sophia Dhrolia, Rohan Raj Kasthuri, Pavan K Bendapudi, Keith R McCrae, Alisa S Wolberg, John-Bjarne Hansen, Henriette Farkas, Nigel Mackman
C1 inhibitor deficiency enhances contact pathway mediated activation of coagulation and venous thrombosis. Blood (2023)
Steven Philip Grover, Tomohiro Kawano, Jun Wan, Pansakorn Tanratana, Zsofia Polai, Young Jun Shim, Omri Snir, Sigrid Kufaas Brækkan, Sophia Dhrolia, Rohan Raj Kasthuri, Pavan K Bendapudi, Keith R McCrae, Alisa S Wolberg, John-Bjarne Hansen, Henriette Farkas, Nigel Mackman
C1 inhibitor deficiency enhances contact pathway mediated activation of coagulation and venous thrombosis. Blood (2023)
Zsofia Polai, Erika Kajdacsi, Laszlo Cervenak, Zsuzsanna Balla, Szabolcs Benedek, Lilian Varga, Henriette Farkas
C1-inhibitor/C1-inhibitor antibody complexes in acquired angioedema due to C1-inhibitor deficiency. Orphanet journal of rare diseases 18 (1) (2023)
Zsofia Polai, Erika Kajdacsi, Laszlo Cervenak, Zsuzsanna Balla, Szabolcs Benedek, Lilian Varga, Henriette Farkas
C1-inhibitor/C1-inhibitor antibody complexes in acquired angioedema due to C1-inhibitor deficiency. Orphanet journal of rare diseases 18 (1) (2023)
Zsofia Polai, Erika Kajdacsi, Laszlo Cervenak, Zsuzsanna Balla, Szabolcs Benedek, Lilian Varga, Henriette Farkas
C1-inhibitor/C1-inhibitor antibody complexes in acquired angioedema due to C1-inhibitor deficiency. Orphanet journal of rare diseases 18 (1) (2023)
Zsofia Polai, Erika Kajdacsi, Laszlo Cervenak, Zsuzsanna Balla, Szabolcs Benedek, Lilian Varga, Henriette Farkas
C1-inhibitor/C1-inhibitor antibody complexes in acquired angioedema due to C1-inhibitor deficiency. Orphanet journal of rare diseases 18 (1) (2023)