Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Katerina Zdrahalova"'
Autor:
Ester Mejstrikova, Jana Volejnikova, Eva Fronkova, Katerina Zdrahalova, Tomas Kalina, Jaroslav Sterba, Yahia Jabali, Vladimir Mihal, Bohumir Blazek, Zdena Cerna, Daniela Prochazkova, Jiri Hak, Zuzana Zemanova, Marie Jarosova, Alexandra Oltova, Petr Sedlacek, Jiri Schwarz, Jan Zuna, Jan Trka, Jan Stary, Ondrej Hrusak
Publikováno v:
Haematologica, Vol 95, Iss 6 (2010)
Background Mixed phenotype acute leukemia (MPAL) represents a diagnostic and therapeutic dilemma. The European Group for the Immunological Classification of Leukemias (EGIL) scoring system unambiguously defines MPAL expressing aberrant lineage marker
Externí odkaz:
https://doaj.org/article/00e3c2b1f9cb4fb2adcf9b49b33ebc86
Autor:
Ondrej Hrusak, Katerina Zdrahalova, Jan Trka, Ester Mejstrikova, Jan Stary, Eva Fronkova, Y. Jabali, Barbora Vakrmanova, Iveta Janotova, Leona Reznickova, Jan Zuna
Publikováno v:
Leukemialymphoma. 62(3)
Early treatment response is a widely accepted herald of curability of acute lymphoblastic leukemia (ALL) in children [1]. While complete remission is expected to be achieved by the end of induction...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9f6de937370811a2e47b52d61cee773
https://pubmed.ncbi.nlm.nih.gov/33118409
https://pubmed.ncbi.nlm.nih.gov/33118409
Autor:
Tomas Honzik, Marta Korbasova, Radka Kremlikova Pourova, Lubica Dudakova, Eva Jadvidzakova, Petra Liskova, Jana Moravikova, Katerina Zdrahalova
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 24:352.e1-352.e5
Background Hereditary hyperferritinemia-cataract syndrome (HHCS) is an autosomal dominant disorder manifesting with high serum ferritin levels and the formation of early-onset cataracts, with numerous small opacities, predominantly in the lens cortex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b448af9066440b6ceca8b3307d55f5a
https://doi.org/10.1016/j.jaapos.2020.07.014
https://doi.org/10.1016/j.jaapos.2020.07.014
Autor:
Jana Volejnikova, Bohumir Blazek, Jan Stary, Petr Sedlacek, Jaroslav Sterba, Jiri Hak, Vladimír Mihál, Jan Zuna, Y. Jabali, Jiri Schwarz, Ondrej Hrusak, Tomas Kalina, Jan Trka, Katerina Zdrahalova, Zuzana Zemanova, Zdena Cerna, Daniela Prochazkova, Marie Jarošová, Ester Mejstrikova, Alexandra Oltová, Eva Fronkova
Publikováno v:
Haematologica. 95:928-935
Background Mixed phenotype acute leukemia (MPAL) represents a diagnostic and therapeutic dilemma. The European Group for the Immunological Classification of Leukemias (EGIL) scoring system unambiguously defines MPAL expressing aberrant lineage marker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a67a2e5f80653dbcf10a3fa644e0544
https://doi.org/10.3324/haematol.2009.014506
https://doi.org/10.3324/haematol.2009.014506
Autor:
Martin Kovac, Ester Mejstrikova, Jan Trka, Jan Stary, Ondrej Hrusak, Karolina Skvarova Kramarzova, Katerina Zdrahalova
Publikováno v:
Blood. 112:2512-2512
ProB ALL is considered an unfavorable subset of ALL both in children and adults. It is currently defined as B precursor ALL with no expression of CD10. MLL/AF4pos cases, who are almost never express CD10, contribute to the poorer prognosis of proB AL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88cf695822fb6c398d890b012c8d1f23
https://doi.org/10.1182/blood.v112.11.2512.2512
https://doi.org/10.1182/blood.v112.11.2512.2512
Autor:
Martin Kovac, Leona Reznickova, Katerina Zdrahalova, Elena Vodickova, Tomas Kalina, Ester Mejstrikova, Zuzana Zemanova, Jan Trka, Martina Vaskova, Jan Stary, Eva Fronkova, Andrea Poloučková, Jana Volejnikova, Ondrej Hrusak, Jan Zuna
Publikováno v:
ResearcherID
Three types of diagnostic findings fulfill the definition of acute hybrid/biphenotypic leukemias (AHL): coexpression of multiple myeloid/lymphoid markers on lymphoid/myeloid population, coexistence of two or more distinct populations from different l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2f87026c9972e6fa30cca6914be08f1
https://doi.org/10.1182/blood.v110.11.4247.4247
https://doi.org/10.1182/blood.v110.11.4247.4247
Autor:
Jan Stary, Klara Dubravčić, Katerina Zdrahalova, Flóra Kiss, Shai Izraeli, János Kappelmayer, Ester Mejstrikova, Jan Trka, Martina Vaskova, Drago Batinić, Batia Stark, Eva Fronkova, Tomas Kalina, Ondrej Hrusak, Margaret H.L. Ng, Alice Suk Hang Cheng, Drorit Luria, Yonna Leung
Publikováno v:
Blood. 108:1842-1842
Several studies showed a good correlation between minimal residual disease (MRD) obtained by flow cytometry (FC) and by PCR (Ig/TCR rearrangements). However, before FC is widely applied for therapeutic decisions we need exact and standardized criteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0e924cc592ba2328e388499b1d3da81
https://doi.org/10.1182/blood.v108.11.1842.1842
https://doi.org/10.1182/blood.v108.11.1842.1842
Autor:
Leona Reznickova, Ki Wai Chik, Luis Castillo, Ondrej Hrusak, Shai Izraeli, Manor Sigal, Katerina Zdrahalova, Martin Schrappe, Chi Kong Li, Jan Stary, Ester Mejstrikova, Eva Fronkova, Batia Stark, Valentino Conter, Smadar Avigad, Jan Trka, Tatana Skocovska
Publikováno v:
Blood. 108:2271-2271
More than 800 children with acute lymphoblastic leukaemia (ALL) are treated every year according to ALL IC-BFM 2002 protocol, which was designed by the International-BFM Group as a parallel to MRD-based ALL/AIEOP BFM 2000 study. The ALL-IC BFM 2002 r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1186f9c9983c008f649fa5da22bdd46b
https://doi.org/10.1182/blood.v108.11.2271.2271
https://doi.org/10.1182/blood.v108.11.2271.2271
Autor:
Ester Mejstrikova, Katerina Zdrahalova, Renata Formankova, Petr Sedlacek, Tomas Kalina, H. Zizkova, A. Sediva, J. Bartunkova, A. Janda, O. Hrusak, J. Stary, D. Blazek
Publikováno v:
Biology of Blood and Marrow Transplantation. 12:127
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c93e4e4b951dc44773d684fda33f9ea3
https://doi.org/10.1016/j.bbmt.2005.11.390
https://doi.org/10.1016/j.bbmt.2005.11.390
Autor:
Jan Stary, Jirina Bartunkova, Hana Zizkova, Katerina Zdrahalova, Petra Keslova, Petr Sedlacek, Ondrej Hrusak, Karel Dlask, Renata Formankova, Ester Mejstrikova, Tomas Kalina, Anna Sediva
Publikováno v:
Blood. 106:5438-5438
Complete DiGeorge syndrome (DGS) is a congenital disorder characterized by developmental defects of the heart, parathyroid glands and thymus associated with T-cell deficiency. Peripheral expansion of mature donor T cells thus represents a rational th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94f01873a22c28c51a42c8ca5a1be775
https://doi.org/10.1182/blood.v106.11.5438.5438
https://doi.org/10.1182/blood.v106.11.5438.5438