Folyóiratcikkek tallózása szerző szerint "SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika"

A találatok rendezése: Rendezés: Találatok:

  • Xu H; Han Y; Lou J; Zhang H; Zhao Y; Győrffy, Balázs; Li R (2017)
    To explore the key genes associated with both PCOS and breast cancer, we overlapped the synchronously differently expressed genes in two obese insulin-resistant GEO datasets in muscle tissue and genes exert essential roles ...
  • Hegyi, Márta; Arany, Ádám; Semsei, Ágnes F; Csordas, Katalin; Eipel, Olivér; Gézsi, András; Kutszegi, Nóra; Csóka, Monika; Müller, Judit; Erdélyi, Dániel; Antal, Péter; Szalai, Csaba; Kovács, Gábor (2017)
    Inter-individual differences in toxic symptoms and pharmacokinetics of high-dose methotrexate (MTX) treatment may be caused by genetic variants in the MTX pathway. Correlations between polymorphisms and pharmacokinetic ...
  • C. Sági, Judit; Kutszegi N; Kelemen A; Fodor LE; Gézsi, András; Kovács, Gábor; Erdélyi, Dániel; Szalai, Csaba; Semsei, Ágnes F (2016)
    Anthracyclines constitute a fundamental part of the chemotherapy regimens utilized to treat a number of different malignancies both in pediatric and adult patients. These drugs are one of the most efficacious anticancer ...
  • C. Sági, Judit; Gézsi, András; Egyed, Bálint; Jakab, Zsuzsanna; Benedek, Noémi; Attarbaschi, Andishe; Köhrer, Stefan; Sipek, Jakub; Winkowska, Lucie; Zaliova, Marketa; Anastasopoulou, Stavroula; Wolthers, Benjamin Ole; Ranta, Susanna; Szalai, Csaba; Kovács, Gábor; Semsei, Ágnes F; Erdélyi, Dániel (2021)
  • Hennermann, Julia B; Arash-Kaps, Laila; Fekete, György; Schaaf, Andreas; Busch, Andreas; Frischmuth, Thomas (2019)
    Moss-aGalactosidase A (moss-aGal) is a moss-derived version of human α-galactosidase developed for enzyme replacement therapy in patients with Fabry disease. It exhibits a homogenous N-glycosylation profile with >90% ...
  • Szőke D; Molnár, Béla; Solymosi, Norbert; Rácz, Károly; Gergics, Péter; Blaskó, Bernadett; Vásárhelyi, Barna; Vannay, Ádám; Mándy Y; Klausz, Gergely; Gyulai, Zsófia; Udvardyné Galamb, Orsolya; Spisák, Sándor; Hutkai B; Somogyi, Anikó; Berta K; Szabó, András; Tulassay, Tivadar; Tulassay, Zsolt (2009)
    Genetic polymorphisms of the genes involved in angiogenesis, the inflammatory cascade or apoptosis control can influence the chronic complications of diabetic patients. Parallel evaluation of multiple genetic polymorphisms ...
  • Hasselblatt M; Thomas C; Hovestadt V; Schrimpf D; Johann P; Johann P; Bens S; Oyen F; Peetz-Dienhart S; Crede Y; Wefers A; Vogel H; Riemenschneider MJ; Antonelli M; Giangaspero F; Bernardo MC; Giannini C; Ud Din N; Perry A; Keyvani K; van Landeghem F; Sumerauer D; Hauser, Péter; Capper D; Korshunov A; Jones DT; Pfister SM; Schneppenheim R; Siebert R; Fruhwald MC; Kool M (2016)
  • Stréhn Anita,; Szőnyi, László; Kriván, Gergely; Kovács, Lajos; Reusz, György; Szabó, Attila; Rényi, Imre; Kovács, Gábor; Dezsőfi, Antal (2014)
    Bevezetés: A poszttranszplantációs lymphoproliferativ betegség a leggyakoribb szolid szerv- vagy allogén vérképző őssejt-transzplantációt követően kialakuló malignitás gyermekkorban. E széles spektrumú betegség immunszuppresszió ...
  • Luczay, Andrea; Török, Dóra; Ferenczi A; Majnik Judit, Zsuzsanna; Sólyom, János; Fekete, György (2006)
    OBJECTIVE: Congenital adrenal hyperplasia (CAH) shows a range of severity which is explained in part by the different mutations of the CYP21 gene. To better understand the incomplete concordance between genotype and phenotype ...
  • Han Y; Lian S; Cui X; Meng K; Győrffy, Balázs; Jin T; Huang D (2016)
  • Jiang T; Shi W; Wali VB; Pongor, Lőrinc; Li C; Lau R; Győrffy, Balázs; Lifton RP; Symmans WF; Pusztai L; Hatzis C (2016)
    Background: Triple negative breast cancer (TNBC) is a highly heterogeneous and aggressive disease, and although no effective targeted therapies are available to date, about one-third of patients with TNBC achieve pathologic ...
  • Váncsa, Andrea; Ponyi, Andrea; Constantin, Tamás; Zeher, Margit; Dankó, Katalin (2007)
    The aim of our study was to assess the prevalence and outcome of pregnancy in idiopathic inflammatory myopathy patients who became pregnant after the onset of the disease. Female idiopathic inflammatory myopathy patients ...
  • Theodoropoulou M; Barta, Csaba; Szoke M; Guttman, András; Staub M; Niederland T; Sólyom, János; Fekete, György; Sasvári-Székely, Mária (2001)
  • Al-Halabi H; Nantel A; Klekner, Álmos; Guiot MC; Albrecht S; Hauser, Péter; Garami, Miklós; Bognár, László; Kavan P; Gerges N; Shirinian M; Roberge D; Muanza T; Jabado N (2011)
  • Rényi, Imre; Bárdi, Edit; Udvardi E; Kovács, Gábor; Bartyik K; Kajtár P; Masát P; Nagy K; Galántai I; Kiss, Csongor (2007)
  • Balogh, Petra; Bánusz, Rita; Csóka, Monika; Váradi, Zsófia; Varga, Edit; Sápi, Zoltán (2016)
    BACKGROUND: Rhabdomyosarcoma (RMS) is a malignant tumor of mesenchymal origin and comprises the largest category of soft-tissue sarcomas both in children and adolescents. From a pediatric oncology point of view, RMS has ...
  • Szilágyi, Ágnes; Varga, Lilian; Prohászka, Zoltán; Dérfalvi, Beáta (2014)
  • Branchi, V; García, SA; Radhakrishnan, P; Győrffy, Balázs; Hissa, B; Schneider, M; Reißfelder, C; Schölch, S (2019)
    DLG7 (disc large homolog 7) is a microtubule-associated protein encoded by DLGAP5 (DLG associated protein 5) gene and has an important role during spindle assembly. Spindle assembly deregulation is a well-known cause of ...
  • Thompson, EM; Hielscher, T; Bouffet, E; Remke, M; Luu, B; Gururangan, S; McLendon, RE; Bigner, DD; Lipp, ES; Perreault, S; Cho, YJ; Grant, G; Kim, SK; Lee, JY; Rao, AA; Giannini, C; Li, KK; Ng, HK; Yao, Y; Kumabe, T; Tominaga, T; Grajkowska, WA; Perek-Polnik, M; Low, DC; Seow, WT; Chang, KT; Mora, J; Pollack, IF; Hamilton, RL; Leary, S; Moore, AS; Ingram, WJ; Hallahan, AR; Jouvet, A; Fevre-Montange, M; Vasiljevic, A; Faure-Conter, C;; Shofuda, T; Kagawa, N; Hashimoto, N; Jabado, N; Weil, AG; Gayden, T; Wataya, T; Shalaby, T; Grotzer, M; Zitterbart, K; Sterba, J; Kren, L; Hortobágyi, Tibor; Klekner, Álmos; Laszlo, B; Pócza, Tímea; Hauser, Péter; Schuller, U; Jung, S; Jang, WY; French, PJ; Kros, JM; van Veelen, MC; Massimi, L; Leonard, JR; Rubin, JB; Vibhakar, R; Chambless, LB; Cooper, MK; Thompson, RC; Faria, CC; Carvalho, A; Nunes, S; Pimentel, J; Fan, X; Muraszko, KM; Lopez-Aguilar, E; Lyden, D; Garzia, L; Shih, DJ; Kijima, N; Schneider, C; Adamski, J; Northcott, PA; Kool, M; Jones, DT; Chan, JA; Nikolic, A; Garre, ML; Van, Meir EG; Osuka, S; Olson, JJ; Jahangiri, A; Castro, BA; Gupta, N; Weiss, WA; Moxon-Emre, I; Mabbott, DJ; Lassaletta, A; Hawkins, CE; Tabori, U; Drake, J; Kulkarni, A; Dirks, P; Rutka, JT; Korshunov, A; Pfister, SM; Packer, RJ; Ramaswamy, V; Taylor, MD (2016)
    BACKGROUND: Patients with incomplete surgical resection of medulloblastoma are controversially regarded as having a marker of high-risk disease, which leads to patients undergoing aggressive surgical resections, so-called ...
  • Zhu CJ; Ma XL; Ling WW; Xiao Y; Győrffy, Balázs (2016)
    Therapeutic effectiveness of treatments for ovarian cancer is not optimal. PDCD-1 and CTLA-4 offers the potential as a prognostic marker in addition to being a target for therapy. To assess the prognostic roles of PDCD-1 ...