tallózása szerző szerint "Andrikovics, Hajnalka"

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Allogén vérképzőőssejt-átültetés Magyarországon

Batai, A; Reményi, Péter; Réti, Marienn Györgyi; Barta, A; Gopcsa, L; Lengyel, L; Torbagyi, E; Csukly, Z; Karaszi, E; Tordai, Attila; Andrikovics, Hajnalka; Balassa, Katalin; Tasnády, Szabolcs; Masszi, Tamás (2017)

INTRODUCTION AND AIM: The publication summarizes the 2548 stem cell transplantations performed in the period of 1993-2015 in Szent Laszlo Hospital, Budapest and provides a detailed discussion of the 425 allogeneic ...
Association of some rare haplotypes and genotype combinations in the MDR1 gene with childhood acute lymphoblastic leukaemia.

Semsei, Ágnes F; Erdélyi, Dániel; Ungvári, Ildikó; Kamory E; Csokay B; Andrikovics, Hajnalka; Csagoly E; Tordai, Attila; Falus, András; Kovács, Gábor; Szalai, Csaba (2008)

To investigate their possible roles in disease susceptibility and some disease characteristics we genotyped C3435T and G2677T/A polymorphisms in multidrug resistance-1 (MDR1) gene with a single base extension method and ...
Distinct clinical characteristics of myeloproliferative neoplasms with calreticulin mutations

Andrikovics, Hajnalka; Krähling, Tünde; Balassa, Katalin; Halm G; Bors, András; Koszarska M; Batai A; Dolgos J; Csomor, Judit; Egyed, Miklós; Sipos A; Remenyi P; Tordai, Attila; Masszi, Tamás (2014)

Somatic insertions/deletions in the calreticulin gene have recently been discovered to be causative alterations in myeloproliferative neoplasms. A combination of qualitative and quantitative allele-specific polymerase chain ...
Komplex molekuláris genetikai vizsgálati algoritmus myeloproliferativ neoplasiák diagnosztikájában

Krähling T; Balassa K; Meggyesi N; Bors, András; Csomor, Judit; Bátai A; Halm G; Egyed M; Fekete S; Reményi P; Masszi, Tamás; Tordai, Attila; Andrikovics, Hajnalka (2014)

Introduction: Mutations in Janus kinase 2, calreticulin and thrombopoietin receptor genes have been identified in the genetic background of Philadelphia chromosome negative, "classic" myeloproliferative neoplasms. Aim: The ...
Mennyit vár ma Magyarországon egy myelomás beteg a diagnózisig?

Varga, Gergely; Mikala, Gábor; Andrikovics, Hajnalka; Masszi, Tamás (2014)

INTRODUCTION: Long delays with the diagnosis of myeloma are common. So far there has not been a comprehensive study on this issue in Hungary. AIM: The aim of the authors was to analyze the waiting time from their first ...
NFKB1 -94ins/delATTG polymorphism is a novel prognostic marker in first line-treated multiple myeloma

Varga, Gergely; Mikala, Gábor; Andrikovics, Hajnalka; Koszarska M; Balassa, Katalin; Adam E; Kozma A; Tordai, Attila; Masszi, Tamás (2015)

Nuclear factor kappa B (NFKB) plays an important role in multiple myeloma (MM), and bortezomib affects this pathway. We retrospectively analysed the effect of the NFKB1 -94ins/delATTG polymorphism on the survival of 295 ...
Proteasome Subunit Beta Type 1 P11A polymorphism is a new prognostic marker in multiple myeloma

Varga, Gergely; Mikala, Gábor; Kiss, Katalin Piroska; Kosóczki, Éva; Szabó, Edit Zsuzsanna; Kövy, Petra; Szombath, Gergely; Tordai, Attila; Andrikovics, Hajnalka; Homolya, László; Masszi, Tamás (2017)
Screening the Expression of ABCB6 in Erythrocytes Reveals an Unexpectedly High Frequency of Lan Mutations in Healthy Individuals

Koszarska M; Kucsma, Nóra; Kiss, Katalin; Várady, György; Gera, Melinda; Antalffy G; Andrikovics, Hajnalka; Tordai, Attila; Studzian M; Strapagiel D; Pulaski L; Tani Y; Sarkadi, Balázs; Szakács, Gergely (2014)

Lan is a high-incidence blood group antigen expressed in more than 99.9% of the population. Identification of the human ABC transporter ABCB6 as the molecular basis of Lan has opened the way for studies assessing the ...
Sex-specific survival difference in association with HLA-DRB1 *04 following allogeneic haematopoietic stem cell transplantation for lymphoid malignancies

Balassa K; Andrikovics, Hajnalka; Reményi, Péter; Batai A; Szilvasi A; Bors, András; Kiss KP; Rajczy K; Inotai, Dóra; Torbagyi E; Lengyel L; Barta A; Gopcsa L; Tordai, Attila; Masszi, Tamás (2018)

The role of HLA system in allogeneic haematopoietic stem cell transplantation (allo-HSCT) outcome is unarguable. In this study we investigated association of HLA-A,-B and-DRB1 alleles with overall survival (OS) in 186 ...
Synergistic interaction of ABCB1 and ABCG2 polymorphisms predicts the prevalence of toxic encephalopathy during anticancer chemotherapy

Erdélyi, Dániel; Kamory E; Csokay B; Andrikovics, Hajnalka; Tordai, Attila; Kiss, Csongor; Semsei, Ágnes F; Janszky I; Zalka A; Fekete, György; Falus, András; Kovács, Gábor; Szalai, Csaba (2008)

Polymorphisms of the ABCB1 (MDR1) and ABCG2 (BCRP) genes were reported to alter the expression and function of these drug transporters. Both proteins are present at the main pharmacokinetic barriers including the blood-brain ...
The density of CD8+ T-cell infiltration and expression of BCL2 predicts outcome of primary diffuse large B-cell lymphoma of bone

Rajnai, Hajnalka; Heyning FH; Koens L; Sebestyén, Anna; Andrikovics, Hajnalka; Hogendoorn PCW; Matolcsy, András; Szepesi, Ágota (2014)
The role of ABC-transporter gene polymorphisms in chemotherapy induced immunosuppression, a retrospective study in childhood acute lymphoblastic leukaemia

Erdélyi, Dániel; Kamory E; Zalka A; Semsei, Ágnes F; Csokay B; Andrikovics, Hajnalka; Tordai, Attila; Borgulya G; Magyarosy E; Galantai I; Fekete, György; Falus, András; Szalai, Csaba; Kovács, Gábor (2006)

We examined the association of functional ABCB1 (MDR1) and ABCG2 (BCRP) polymorphisms with acute side effects of chemotherapy. Analyses were performed on clinical data from 138 patients treated with the ALL-BFM-95 protocol ...
The significance of the hemochromatosis genetic variants in multiple myeloma in comparison to that of myelodysplastic syndrome

Várkonyi, Judit; Demeter, Judit; Tordai, Attila; Andrikovics, Hajnalka (2006)

The clinical experience of the significant difference in iron metabolism between multiple myeloma and myelodysplasia prompted us to analyse patients according to mutation frequency in the hemochromatosis gene (HFE) known ...

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