Zobrazeno 1 - 10 of 64 pro vyhledávání: '"Jacek, Treliński"'
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Assessment of megakaryocytes’ size and morphology in selected myeloproliferative neoplasms
Autor: Emilia Krzemińska, Marta Robak, Jacek Treliński, Krzysztof Chojnowski
Publikováno v: Diagnostyka Laboratoryjna. 57:188-194
Introduction: Contemporary technological development make the cytological analysis of megakaryocytes (MKs) a valuable tool for supporting differential diagnosis of myeloproliferative neoplasms’ (MPNs) early stages. Aim: The aim of the study was to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5696499e639aea510c33540e71767061
https://doi.org/10.5604/01.3001.0016.0258
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Antithrombin Deficiency Is Associated with Prothrombotic Plasma Fibrin Clot Phenotype
Autor: Joanna Natorska, Javier Corral, Maria Eugenia de la Morena-Barrio, Carlos Bravo-Pérez, Zsuzsa Bagoly, Zsuzsanna Bereczky, Jacek Treliński, Michał Witkowski, Adrianna Klajmon, Anetta Undas, Michał Ząbczyk
Publikováno v: Thrombosis and Haemostasis.
Background Deficiency of antithrombin increases risk of venous thromboembolism. We hypothesized that antithrombin deficiency affects fibrin clot structure and function. Methods We evaluated 148 patients (age: 38 [32–50] years; 70% women) with genet
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa30336efcea024fc5c1206177bc4e72
https://doi.org/10.1055/s-0043-1768712
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7
Emicizumab (Hemlibra®) in hemophilia A patients with inhibitors against factor VIII — guidelines of the Group for Haemostasis of the Polish Society of Haematology and Transfusion Medicine
Autor: Wojciech Młynarski, Jerzy Windyga, Paweł Łaguna, Tomasz Urasiński, Jacek Musiał, Andrzej Mital, Anna Klukowska, Magdalena Łętowska, Krzysztof Chojnowski, Jacek Treliński, Joanna Zdziarska, Anetta Undas, Maria Podolak-Dawidziak
Publikováno v: Journal of Transfusion Medicine. 13:165-175
In this document, the Group for Haemostasis of the Polish Society of Haematology and Transfusion Medicine presents the guidelines for the use of emicizumab. Emicizumab (Hemlibra®, F. Hoffmann — La Roche, Basel, Switzerland) has been licensed for u
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08cbcf03739096b67eb37fc3d76039f8
https://doi.org/10.5603/jtm.2020.0006
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Six molecular patterns leading to hemophilia A phenotype in 18 females from Poland
Autor: Walentyna Balwierz, Jacek Treliński, Teresa Iwaniec, Andrzej Kołtan, Iwona Rurańska, Izabela Jatczak-Pawlik, Karolina Janczar, Edyta Odnoczko, Joanna Zdziarska, Szymon Janczar, Anna Klukowska, Danuta Pietrys, Pawel Laguna, Katarzyna Babol-Pokora, Jerzy Windyga, Michał Jamrozik, Wojciech Młynarski, Tomasz Szczepański, Joanna Taha
Publikováno v: Thrombosis Research. 193:9-14
Introduction Female hemophilia is an intriguing rare disorder and few larger reports on its genetic etiology are available. While historically the diagnosis was satisfactorily reached by factor VIII activity assays, the clinical and potentially thera
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08de5c1d08b102937532a42fa3a948f8
https://doi.org/10.1016/j.thromres.2020.05.041
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Management of inherited thrombocytopenia. Recommendations of the Group on Hemostasis of the Polish Society of Hematology and Transfusion Medicine, 2019
Autor: Maria Podolak-Dawidziak, Wojciech Młynarski, Krystyna Zawilska, Krzysztof Chojnowski, Anna Klukowska, Magdalena Łętowska, Jacek Treliński, Joanna Zdziarska, Anetta Undas, Tomasz Urasiński, Jacek Musiał, Andrzej Mital, Jerzy Windyga
Publikováno v: Journal of Transfusion Medicine. 13:16-28
Inherited thrombocytopenias (IT) comprise a highly heterogeneous group of rare haemostatic disorders which vary in terms of degree of thrombocytopenia, platelet size, pattern of inheritance and clinical course. Due to difficult diagnosis and frequent
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfec969b8739fb99d3a73b7d54f2a25f
https://doi.org/10.5603/jtm.2020.0001
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