Search Results - "PROCHAZKOVA, Daniela"

Prognosis of children with mixed phenotype acute leukemia treated on the basis of consistent immunophenotypic criteria by MEJSTRIKOVA, Ester, VOLEJNIKOVA, Jana, PROCHAZKOVA, Daniela, HAK, Jiri, ZEMANOVA, Zuzana, JAROSOVA, Marie, OLTOVA, Alexandra, SEDLACEK, Petr, SCHWARZ, Jiri, ZUNA, Jan, TRKA, Jan, STARY, Jan, FRONKOVA, Eva, HRUSAK, Ondrej, ZDRAHALOVA, Katerina, KALINA, Tomas, STERBA, Jaroslav, JABALI, Yahia, MIHAL, Vladimir, BLAZEK, Bohumir, CERNA, Zdena

“…Mixed phenotype acute leukemia (MPAL) represents a diagnostic and therapeutic dilemma. The European Group for the Immunological Classification of Leukemias…”
Get full text

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…”
Get full text

Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin by Mojzikova, Renata, Koralkova, Pavla, Holub, Dusan, Saxova, Zuzana, Pospisilova, Dagmar, Prochazkova, Daniela, Dzubak, Petr, Horvathova, Monika, Divoky, Vladimir

“…Glucose-6-phosphate isomerase (GPI) deficiency, a genetic disorder responsible for chronic nonspherocytic hemolytic anemia, is the second most common red blood…”
Get full text

Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen‐sensing pathway from primary familial and congenital polycythaemia by Sochorcova, Lucie, Hlusickova Kapralova, Katarina, Fialova Kucerova, Jana, Pospisilova, Dagmar, Prochazkova, Daniela, Jahoda, Ondrej, Kurekova, Simona, Kralova, Barbora, Divoka, Martina, Navratilova, Jana, Manakova, Jirina, Kriegova, Eva, Indrak, Karel, Faber, Edgar, Divoky, Vladimir, Horvathova, Monika

“…Congenital erythrocytoses represent a heterogenous group of rare defects of erythropoiesis characterized by elevated erythrocyte mass. We performed…”
Get full text

Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions by Volejnikova, Jana, Vojta, Petr, Urbankova, Helena, Mojzíkova, Renata, Horvathova, Monika, Hochova, Ivana, Cermak, Jaroslav, Blatny, Jan, Sukova, Martina, Bubanska, Eva, Feketeova, Jaroslava, Prochazkova, Daniela, Horakova, Julia, Hajduch, Marian, Pospisilova, Dagmar

“…Diamond-Blackfan anemia (DBA) is a rare congenital erythroid aplasia, underlied by haploinsufficient mutations in genes coding for ribosomal proteins (RP) in…”
Get full text

Molecular Characterization of β-Thalassemia in the Czech and Slovak Populations: Mediterranean, Asian and Unique Mutations by Divoka, Martina, Partschova, Martina, Kucerova, Jana, Mojzikova, Renata, Cermak, Jaroslav, Pospisilova, Dagmar, Fabryova, Viera, Prochazkova, Daniela, Indrak, Karel, Divoky, Vladimir

“…β-Thalassemia (β-thal) is considered rare in Central Europe. As in other malaria-free regions, the presence of β-thal in Central Europe reflects historical and…”
Get full text

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…”
Get full text

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…”
Get full text

Development of treatment and clinical results in childhood acute myeloid leukemia in the Czech Republic by Sramkova, Lucie, Sterba, Jaroslav, Hrstkova, Hana, Mihal, Vladimir, Blazek, Bohumir, Timr, Pavel, Cerna, Zdena, Prochazkova, Daniela, Hak, Jiri, Sedlacek, Petr, Janotova, Iveta, Vodickova, Elena, Zemanova, Zuzana, Jarosova, Marie, Oltova, Alexandra, Zdrahalova, Katerina, Hrusak, Ondrej, Mejstrikova, Ester, Schwarz, Jiri, Zuna, Jan, Trka, Jan, Stary, Jan

“…Purpose Treatment of childhood acute myeloid leukemia (AML) was unified in the year 1993 according to acute myeloid leukemia-Berlin–Frankfurt–Munster (AML-BFM)…”
Get full text

The prospects for children with acute lymphoblastic leukemia of being cured has increased in the Czech Republic in the 21st century to 90% - outcome of the ALL-IC BFM 2002 trial by Zdráhalová, Kateřina, Štěrba, Jaroslav, Domanský, Jiří, Blažek, Bohumír, Ptoszková, Hana, Mihál, Vladimír, Novák, Zbyněk, Hak, Jiří, Procházková, Daniela, Černá, Zdena, Timr, Pavel, Jabali, Yahia, Sedláček, Petr, Smíšek, Petr, Zemanová, Zuzana, Jarošová, Marie, Houdková, Alena, Mejstříková, Ester, Hrušák, Ondřej, Zuna, Jan, Janotová, Iveta, Trka, Jan, Starý, Jan

“…Acute lymphoblastic leukemia (ALL) is the most frequent childhood malignancy. Treatment has been unified in the middle of 1980 in the Czech Republic. In…”
Get more information