Transfusion and Haematology Today - Issue Ahead of Print/2024
Review/Educational Papers
1
Disorders induced by deposits of monoclonal immunoglobulin IgM and free light Chain in Waldenström’s macroglobulinaemia – case report and review of literature
P. Flodr, Z. Adam, M. Navratilova, D. Holub, P. Džubák, L. Křen, J. Dobrovolný, P. Malíková, O. Pollaková, M. Šenkyřík, L. Zdražilová Dubská, Z. Řehák, R. Koukalová, M. Krejčí, L. Pour, Z. Král, I. Svobodová
VEXAS syndrome – newly described autoinflammatory disease with haematologic symptoms. Case report and review of the literature
Z. Adam, J. Mayer, D. Frič, J. Kissová, M. Jarošová, M. Beličková, L. Kratochvílová, T. Freiberger, L. Červinek, P. Komínková, Z. Řehák, Z. Král
VEXAS syndrome – a diagnosis at the interface of rheumatology and haematology
M. Vostrý, B. Stibůrková, H. Mann, V. Balajková, H. Ciferská, J. Soukupová Maaloufová, C. Šálek, M. Beličková
Case Reports
1
Rare granulomatous processes
J. Kufa, J. Novotná, M. Lukášová, V. Látal, V. Hanáčková, T. Tichý, D. Skanderová, N. Rušarová, P. Jakubec
Original Papers
1
Splanchnic vein thrombosis: aetiology, therapy, and results – a retrospective analysis
T. Kriegler, P. Ďulíček, T. Dušek
A family study of MNS system antigen polymorphism
P. Papoušek, M. Kracík, I. Dolinová, L. Řehořová, R. Procházková
Transfusion and Haematology Today
2024 Issue Ahead of Print
Most read in this issue
- VEXAS syndrome – newly described autoinflammatory disease with haematologic symptoms. Case report and review of the literature
- VEXAS syndrome – a diagnosis at the interface of rheumatology and haematology
- Rare granulomatous processes
- A family study of MNS system antigen polymorphism