Výsledky vyhledávání - "Martina Divoka"

Akademický článek

Characterization of iron metabolism and erythropoiesis in erythrocyte membrane defects and thalassemia traits

Autor: Lucie Sulovska, Dusan Holub, Zuzana Zidova, Martina Divoka, Marian Hajduch, Vladimir Mihal, Jana Vrbkova, Monika Horvathova, Dagmar Pospisilova

Publikováno v: Biomedical Papers, Vol 160, Iss 2, Pp 231-237 (2016)

Background and Aims: Erythropoiesis is closely related to iron metabolism in a balanced homeostasis. Analyses of diverse erythroid and iron metabolism disorders have shown that disrupted erythropoiesis negatively affects iron homeostasis and vice ver

Externí odkaz: https://doaj.org/article/6fdb986ad67d428c95aaf258675681f8

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Akademický článek

Interferon-α Revisited: Individualized Treatment Management Eased the Selective Pressure of Tyrosine Kinase Inhibitors on BCR-ABL1 Mutations Resulting in a Molecular Response in High-Risk CML Patients.

Autor: Vaclava Polivkova, Peter Rohon, Hana Klamova, Olga Cerna, Martina Divoka, Nikola Curik, Jan Zach, Martin Novak, Iuri Marinov, Simona Soverini, Edgar Faber, Katerina Machova Polakova

Publikováno v: PLoS ONE, Vol 11, Iss 5, p e0155959 (2016)

Bone marrow transplantation or ponatinib treatment are currently recommended strategies for management of patients with chronic myeloid leukemia (CML) harboring the T315I mutation and compound or polyclonal mutations. However, in some individual case

Externí odkaz: https://doaj.org/article/eec7181a37d04b6a995c86b77927b702

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Characterization of iron metabolism and erythropoiesis in erythrocyte membrane defects and thalassemia traits

Autor: Marian Hajduch, Zuzana Zidova, Jana Vrbkova, Lucie Sulovska, Monika Horvathova, Dusan Holub, Dagmar Pospisilova, Vladimír Mihál, Martina Divoka

Publikováno v: Biomedical Papers, Vol 160, Iss 2, Pp 231-237 (2016)

Background and Aims. Erythropoiesis is closely related to iron metabolism in a balanced homeostasis. Analyses of diverse erythroid and iron metabolism disorders have shown that disrupted erythropoiesis negatively affects iron homeostasis and vice ver

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6dd5c53a30ceb6eff742ce7b40f2bc1
https://biomed.papers.upol.cz/artkey/bio-201602-0008_Characterization_of_iron_metabolism_and_erythropoiesis_in_erythrocyte_membrane_defects_and_thalassemia_traits.php

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Effect of CALR and JAK2 mutations on the clinical and hematological phenotypes of the disease in patients with myelofibrosis - long-term experience from a single center

Autor: Tomáš Szotkowski, Hlusi A, J Navratilova, Karel Indrak, Palova M, Tomas Papajik, Martina Divoka

Publikováno v: Neoplasma. 65(2)

Primary myelofibrosis (PMF) is a chronic clonal myeloid disorder. Together with essential thrombocythemia (ET) and polycythemia vera (PV), it belongs to a group of Philadelphia chromosome-negative myeloproliferative neoplasms. An integral part of lab

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6fbd942af0b597d38ff2531a464c425
https://pubmed.ncbi.nlm.nih.gov/29534592

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Thrombin Generation Testing in Patients with Myelofibrosis

Autor: M Palova, Luděk Slavík, T Szotkowski, J Navratilova, Martina Divoka, Tomas Papajik, Antonin Hlusi, Jana Ulehlova

Publikováno v: Clinical Laboratory. 64

Background Primary myelofibrosis (PMF) is a chronic clonal myeloid disorder. Together with essential thrombocythemia (ET) and polycythemia vera (PV), it belongs to a group of Philadelphia chromosome-negative myeloproliferative neoplasms. Thrombotic e

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::838782d11968f4fbae2ab4b9b5527381
https://doi.org/10.7754/clin.lab.2018.180204

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Acute promyelocytic leukemia successfully treated also in elderly patients with significant comorbidities: a 20-year single-center experienc

Autor: Edgar Faber, Hubácek J, Karel Indrak, Tomáš Szotkowski, Z. Pikalová, J Vrbkova, Adam Kuba, Tomas Papajik, Martina Divoka, Marie Jarošová, Peter Rohon, Luděk Raida, Milena Holzerova

Publikováno v: Neoplasma. 62:146-151

UNLABELLED Acute promyelocytic leukemia is a unique entity among acute leukemias. Introduction of all-trans retinoic acid and, subsequently, arsenic trioxide in its treatment has markedly improved treatment outcomes for this once frequently fatal dis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2af8a447c867b492187b698e518152fd
https://doi.org/10.4149/neo_2015_019

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