Search Results - "CERNA, Zdenka"

Autoimmune disease, familial clustering and thyroid carcinoma coexistent with autoimmune thyroiditis in children and adolescence: A cross-sectional study from the Czech Republic by Pomahacova, Renata, Zamboryova, Jana, Paterova, Petra, Fiklik, Karel, Cerna, Zdenka, Lad, Vaclav, Skalicka, Eva, Huml, Michal, Sykora, Josef

“…Background: The prevalence of autoimmune thyroiditis (AIT), as the most common autoimmune disease (AD) and papillary thyroid cancer (PTC) is steadily rising in…”
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Minimal residual disease in peripheral blood at day 15 identifies a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with superior prognosis by VOLEJNIKOVA, Jana, MEJSTRIKOVA, Ester, HAK, Jiri, CERNA, Zdenka, HRUSAK, Ondrej, STARY, Jan, TRKA, Jan, FRONKOVA, Eva, VALOVA, Tatana, REZNICKOVA, Leona, HODONSKA, Ladislava, MIHAL, Vladimir, STERBA, Jaroslav, JABALI, Yahia, PROCHAZKOVA, Daniela, BLAZEK, Bohumir

“…Most minimal residual disease-directed treatment interventions in current treatment protocols for acute lymphoblastic leukemia are based on bone marrow…”
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Changes of Serum Thymidine Kinase in Children with Acute Leukemia by TOMAS VOTAVA, ONDREJ TOPOLCAN, LUBOS HOLUBEC, Jr, ZDENKA CERNA, LUMIR SASEK, JINDRICH FINEK, STANISLAV KORMUNDA

“…Background: Thymidine kinase (TK) is involved in nucleic acid synthesis and is therefore considered to be an important proliferation tumor marker. Our main…”
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Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome by Nováková, Michaela, Žaliová, Markéta, Suková, Martina, Wlodarski, Marcin, Janda, Aleš, Froňková, Eva, Campr, Vít, Lejhancová, Kateřina, Zapletal, Ondřej, Pospíšilová, Dagmar, Černá, Zdeňka, Kuhn, Tomáš, Švec, Peter, Pelková, Vendula, Zemanová, Zuzana, Kerndrup, Gitte, van den Heuvel-Eibrink, Marry, van der Velden, Vincent, Niemeyer, Charlotte, Kalina, Tomáš, Trka, Jan, Starý, Jan, Hrušák, Ondřej, Mejstříková, Ester

“…GATA-2 deficiency was recently described as common cause of overlapping syndromes of immunodeficiency, lymphedema, familiar myelodysplastic syndrome or acute…”
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The Frequency and Characteristics of the Ribosomal Protein L5 (RPL5) and Ribosomal Protein L11 (RPL11) Gene Mutations in Patients with Diamond-Blackfan Anemia in the Czech National Registry by Pospisilova, Dagmar, Cmejla, Radek, Cmejlova, Jana, Handrkova, Helena, Stary, Jan, Cerna, Zdenka

“…Introduction: Diamond-Blackfan anemia (DBA) is a congenital red cell aplasia that is usually diagnosed during early infancy. Apart from defects in red cell…”
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First 2 cases with thiamine‐responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene—intron 1 mutation c.204+2T>G by Pomahačová, Renata, Zamboryová, Jana, Sýkora, Josef, Paterová, Petra, Fiklík, Karel, Votava, Tomáš, Černá, Zdeňka, Jehlička, Petr, Lád, Václav, Šubrt, Ivan, Dort, Jiří, Dortová, Eva

“…Thiamine‐responsive megaloblastic anemia (TRMA) is a rare autosomal recessive disorder caused by mutations in the SLC19A2 gene. To date at least 43 mutations…”
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Prognostic Impact of Peripheral Blood Involvement during Early Time Points of Childhood ALL Treatment by Volejnikova, Jana, Fronkova, Eva, Mejstrikova, Ester, Muzikova, Katerina, Reznickova, Leona, Pospisilova, Dagmar, Sterba, Jaroslav, Jabali, Yahia, Prochazkova, Daniela, Blazek, Bohumir, Hak, Jiri, Cerna, Zdenka, Stary, Jan, Trka, Jan

“…Minimal residual disease (MRD) testing performed on bone marrow (BM) samples has become a part of the risk group stratification procedure in several of the…”
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Composition of Cellular Subsets by Flow Cytometry Identifies Differences Between MDS Subtypes and Aplastic Anemia but No Differences Are Identified Between Cases with and without Monosomy 7 by Mejstrikova, Ester, Pelkova, Vendula, Reiterová, Michaela, Sukova, Martina, Zemanova, Zuzana, Vodickova, Elena, Campr, Vit, Michalova, Kyra, Jarosova, Marie, Formankova, Renata, Smisek, Petr, Sedlacek, Petr, Pospisilova, Dagmar, Mihal, Vladimir, Hak, Jiri, Jabali, Yahia, Sterba, Jaroslav, Blatny, Jan, Zapletal, Ondrej, Cerna, Zdenka, Votava, Tomas, Prochazkova, Daniela, Trka, Jan, Stary, Jan, Hrusak, Ondrej

“…Abstract 3802 Poster Board III-738 Monosomy 7 or del(7q) are frequent cytogenetic abnormalities in children with myelodysplastic syndrome (MDS) and associates…”
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First 2 cases with thiamine-responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene-intron 1 mutation c.204+2T>G: POMAHAČOVÁ et al by Pomahačová, Renata, Zamboryová, Jana, Sýkora, Josef, Paterová, Petra, Fiklík, Karel, Votava, Tomáš, Černá, Zdeňka, Jehlička, Petr, Lád, Václav, Šubrt, Ivan, Dort, Jiří, Dortová, Eva

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First 2 cases with thiamine-responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene-intron 1 mutation c.204+2T>G by Pomahačová, Renata, Zamboryová, Jana, Sýkora, Josef, Paterová, Petra, Fiklík, Karel, Votava, Tomáš, Černá, Zdeňka, Jehlička, Petr, Lád, Václav, Šubrt, Ivan, Dort, Jiří, Dortová, Eva

“…Thiamine-responsive megaloblastic anemia (TRMA) is a rare autosomal recessive disorder caused by mutations in the SLC19A2 gene. To date at least 43 mutations…”
Get full text