Výsledky vyhledávání - "Joanna Rupa‐Matysek"

Akademický článek

Autoimmune hemolytic anemia: current knowledge and perspectives

Autor: Sylwia Sulimiera Michalak, Anna Olewicz-Gawlik, Joanna Rupa-Matysek, Edyta Wolny-Rokicka, Elżbieta Nowakowska, Lidia Gil

Publikováno v: Immunity & Ageing, Vol 17, Iss 1, Pp 1-16 (2020)

Abstract Autoimmune hemolytic anemia (AIHA) is an acquired, heterogeneous group of diseases which includes warm AIHA, cold agglutinin disease (CAD), mixed AIHA, paroxysmal cold hemoglobinuria and atypical AIHA. Currently CAD is defined as a chronic,

Externí odkaz: https://doaj.org/article/0c09385451254e63bfd2e32f8a70e58d

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Akademický článek

Evaluation of the ThroLy score for the prediction of venous thromboembolism in newly diagnosed patients treated for lymphoid malignancies in clinical practice

Autor: Joanna Rupa‐Matysek, Katarzyna Brzeźniakiewicz‐Janus, Lidia Gil, Zbigniew Krasiński, Mieczysław Komarnicki

Publikováno v: Cancer Medicine, Vol 7, Iss 7, Pp 2868-2875 (2018)

Abstract The utility in clinical practice of a recently developed and validated predictive model for venous thromboembolism (VTE) events in lymphoma patients, known as the thrombosis lymphoma (ThroLy) score, is unknown. We evaluated the association o

Externí odkaz: https://doaj.org/article/ae3e886617cd42e497b6c5ad4c9e994f

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Akademický článek

Risk Factors for Catheter-Related Thrombosis in Multiple Myeloma Patients Undergoing Autologous Stem Cell Transplantation

Autor: Anna Hoppe, Joanna Rupa-Matysek, Bartosz Małecki, Dominik Dytfeld, Krzysztof Hoppe, Lidia Gil

Publikováno v: Medicina, Vol 57, Iss 10, p 1020 (2021)

Background and Objectives: Cancer associated thrombosis (CAT) is a common complication of neoplasms. Multiple myeloma (MM) carries one of the highest risks of CAT, especially in the early phases of treatment. Autologous stem cell transplantation (ASC

Externí odkaz: https://doaj.org/article/1bc64089010141dbb6f73178fd6a8857

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Akademický článek

Successful treatment of pulmonary candidiasis and aspergillosis in patient with refractory Hodgkin lymphoma using micafungin – case study and brief literature review

Autor: Marta Barańska, Renata Kroll-Balcerzak, Lidia Gil, Joanna Rupa-Matysek, Mieczysław Komarnicki

Publikováno v: Central European Journal of Immunology, Vol 42, Iss 1, Pp 111-115 (2017)

The number of patients with hematological malignancies who develop invasive fungal disease (IFD) has increased dramatically in recent decades. This increase is attributed to impairment of the host immune system due to intensive cytotoxic chemotherapi

Externí odkaz: https://doaj.org/article/d49c1e451f29442ca7797c2545e1c4b8

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Akademický článek

Dangers resulting from DNA profiling of biological materials derived from patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT) with regard to forensic genetic analysis

Autor: Renata Jacewicz, Krzysztof Lewandowski, Joanna Rupa-Matysek, Maciej Jędrzejczyk, Jarosław Berent

Publikováno v: Archives of Forensic Medicine and Criminology, Vol 65, Iss 4, Pp 225-247 (2016)

The study documents the risk that comes with DNA analysis of materials derived from patients after allogeneic hematopoietic stem cell transplantation (allo-HSCT) in forensic genetics. DNA chimerism was studied in 30 patients after allo-HSCT, based on

Externí odkaz: https://doaj.org/article/195e05bd82664b42b86afa4cd8c985cf

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Clinical challenge of managing patients with multiple myeloma and acquired hemophilia A with risk of both thrombosis and bleeding: a narrative review

Autor: Anna Hoppe, Joanna Rupa-Matysek, Lidia Gil

Publikováno v: Acta Haematologica Polonica. 53:303-315

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d2dde68a8b6eff09b70c73cb3ddb5dff
https://doi.org/10.5603/ahp.a2022.2041

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Emicizumab: a novel drug in hemophilia A prophylaxis – a narrative review

Autor: Łukasz Mazurkiewicz, Krystian Czernikiewicz, Joanna Rupa-Matysek, Lidia Gil

Publikováno v: Expert Review of Hematology. 15:933-942

Hemophilia A is a genetically conditioned disease leading to hemostatic disorders due to factor VIII (FVIII) deficiency. The treatment of hemophilia has evolved throughout the past years and has significantly changed. One of the newest drugs for prop

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::156b09acb9e307b76773d6369732b2ee
https://doi.org/10.1080/17474086.2022.2131526

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