Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Joanna, Dziaczkowska"'
Autor:
Karolina Chromik, Agata Wieczorkiewicz-Kabut, Krzysztof Woźniczka, Anna Koclęga, Dariusz Kata, Katarzyna Wiśniewska-Piąty, Joanna Dziaczkowska-Suszek, Iwona Grygoruk-Wiśniowska, Patrycja Zielinska, Grzegorz Helbig
Publikováno v:
Acta Haematologica Polonica. 51:88-94
BackgroundMyelodysplastic syndromes (MDSs) are a heterogeneous group of clonal myeloid neoplasms. Allogeneic stem cell transplantation (allo-SCT) remains the curative method for MDS treatment. Little is known about the monitoring of minimal residual
Autor:
Grzegorz Helbig, Agata Wieczorkiewicz, Joanna Dziaczkowska-Suszek, Miroslaw Majewski, Slawomira Kyrcz-Krzemien
Publikováno v:
Haematologica, Vol 94, Iss 9 (2009)
Background A T-cell clone, thought to be the source of eosinophilopoietic cytokines, identified by clonal rearrangement of the T-cell receptor and by the presence of aberrant T-cell immunophenotype in peripheral blood defines lymphocytic variant of h
Externí odkaz:
https://doaj.org/article/ae22440bca444a2c9d2fe6ef193e461e
Autor:
Joanna Dziaczkowska-Suszek, Karolina Chromik, Anna Kopińska, Grzegorz Helbig, Krzysztof Woźniczka, Slawomira Kyrcz-Krzemien
Publikováno v:
Acta Haematologica Polonica. 48:364-368
Systemic mastocytosis (SM) includes a wide spectrum of clonal disorders characterized by an abnormal growth and accumulation of mast cells. SM may be associated with other hematological neoplasms (SM-AHN) among them the myeloproliferative neoplasms a
Autor:
Mirosław Markiewicz, Kinga Gwóźdź, Monika Dzierzak-Mietla, Agnieszka Karolczyk, Joanna Dziaczkowska-Suszek, Małgorzata Stachowicz, Ewa Rzenno
Publikováno v:
Medycyna Rodzinna. 21
Introduction. The broad indications for allogenic transplantation of hematopoietic stem cells (allo-HSCT) and the use of immunosuppression after transplantation pose a risk of frequent occurrence of viral infections. Aim. The subject of the work is t
Autor:
Katarzyna Bieszczad, Krystyna Jagoda, Joanna Dziaczkowska-Suszek, Anna Kopińska, Malgorzata Krawczyk-Kulis, Slawomira Kyrcz-Krzemien
Publikováno v:
Hematological Oncology. 35:225-231
Introduction Autologous hematopoietic stem cell transplantation (AHSCT) remains the treatment of choice in multiple myeloma (MM) patients (pts). In earlier research it has been suggested that the expression of dipeptidyl peptidase-4 (DPP4, CD26) infl
Autor:
Joanna Dziaczkowska-Suszek, Slawomira Kyrcz-Krzemien, Anna Kopińska, Małgorzata Krawczyk-Kuliś, Katarzyna Bieszczad, Krystyna Jagoda
Publikováno v:
Acta Haematologica Polonica. 45:264-268
Dipeptidyl peptidase IV is a membrane enzyme involved in intracellular interactions governing processes. Proven its effects on engraftment the transplanted allogeneic hematopoietic cells. The aim of this study was to analyze the expression of CD26 in
Autor:
Slawomira Kyrcz-Krzemien, Andrzej Frankiewicz, Katarzyna Wiśniewska-Piąty, Joanna Dziaczkowska-Suszek, Grzegorz Helbig, Krzysztof Woźniczka
Publikováno v:
Acta Haematologica Polonica. 44:409-412
Richter's Syndrome (RS) is a transformation from chronic lymphocytic leukemia (CLL) into more aggressive lymphoma. RS occurs in about 5% of patients with CLL and its clinical outcome is poor. Extranodal involvements of RS may be present in up to 40%
Autor:
Katarzyna Wiśniewska-Piąty, Grzegorz Helbig, Slawomira Kyrcz-Krzemien, Joanna Dziaczkowska-Suszek, Tomasz Francuz
Publikováno v:
Leukemia & Lymphoma. 54:807-811
Idiopathic hypereosinophilic syndrome (IHES) is characterized by blood hypereosinophilia with no underlying cause and eosinophilia-associated organ dysfunction. Thirty-three patients, 20 female (61%) and 13 male (29%), with a median age of 56 years a
Autor:
Aleksandra Bartkowska-Chrobok, Joanna Dziaczkowska-Suszek, Małgorzata Krawczyk-Kuliś, Slawomira Kyrcz-Krzemien
Publikováno v:
Acta Haematologica Polonica. 43:271-276
STRESZCZENIE Przewlekla bialaczka limfocytowa (PBL) jest klonalną chorobą limfoproliferacyjną charakteryzującą sie namnazaniem i nagromadzeniem w krwi, szpiku oraz innych tkankach malych limfocytow B z koekspresją antygenu CD5. O rozpoznaniu PB
Autor:
Małgorzata Krawczyk-Kuliś, Joanna Dziaczkowska-Suszek, Slawomira Kyrcz-Krzemien, Anna Kopińska
Publikováno v:
American Journal of Case Reports, The. 12:145-149