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

A találatok rendezése: Rendezés: Találatok:

  • Complement activating antibodies against the human 60 kDa heat shock protein as a new independent family risk factor of coronary heart disease 
    Veres, Amarilla; Szamosi, Tamás; Ablonczy, Mária; Szamosi, Tamás; Singh M; Karádi, István; Romics, László; Füst, György; Prohászka, Zoltán (2002)
    Background: Several groups have reported high levels of antibodies against 60 kDa heat shock proteins (hsp) associated with coronary heart disease. Methods and results: Complement activating (CA) antihsp60 autoantibodies ...
  • Complex X chromosome rearrangement associated with multiorgan autoimmunity 
    Haltrich, Irén; Piko, Henriett; Pamjav H; Somogyi, Anikó; Volgyi A; David D; Beke, Artúr; Garamvölgyi, Zoltán; Kiss, Eszter; Karcagi V; Fekete, György (2015)
    BACKGROUND: Turner syndrome, a congenital condition that affects 1/2,500 births, results from absence or structural alteration of the second sex chromosome. Turner syndrome is usually associated with short stature, gonadal ...
  • Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia 
    Kure S; Kato K; Dinopoulos A; Gail C; DeGrauw TJ; Christodoulou J; Bzduch V; Kálmánchey, Rozália; Fekete, György; Trojovsky A; Plecko B; Breningstall G; Tohyama J; Aoki Y; Matsubara Y (2006)
    Nonketotic hyperglycinemia (NKH) is an inborn error of metabolism characterized by accumulation of glycine in body fluids and various neurological symptoms. NKH is caused by deficiency of the glycine cleavage multi-enzyme ...
  • Comprehensive outline of whole exome sequencing data analysis tools available in clinical oncology 
    Bartha, Á; Győrffy, Balázs (2019)
    Whole exome sequencing (WES) enables the analysis of all protein coding sequences in the human genome. This technology enables the investigation of cancer-related genetic aberrations that are predominantly located in the ...
  • Comprehensive profiling of disease-relevant copy number aberrations for advanced clinical diagnostics of pediatric acute lymphoblastic leukemia 
    Kiss, Richárd; Gángó, Ambrus; Benard-Slagter, Anne; Egyed, Bálint; Haltrich, Irén; Hegyi, Lajos; de Groot, Karel; Király, Péter Attila; Krizsán, Szilvia; Kajtár, Béla; Pikó, Henriett; Pajor, László; Vojcek, Ágnes; Matolcsy, András; Kovács, Gábor; Szuhai, Károly; Savola, Suvi; Bödör, Csaba; Alpár, Donát (2019)
  • Consensus-based recommendations for the management of juvenile dermatomyositis 
    Enders FB; Bader-Meunier B; Baildam E; Constantin, Tamás; Dolezalova P; Feldman BM; Lahdenne P; Magnusson B; Nistala K; Ozen S; Pilkington C; Ravelli A; Russo R; Uziel Y; van Brussel M; van der Net J; Vastert S; Wedderburn LR; Wulffraat N; McCann LJ; van Royen-Kerkhof A (2017)
    BACKGROUND: In 2012, a European initiative called Single Hub and Access point for pediatric Rheumatology in Europe (SHARE) was launched to optimise and disseminate diagnostic and management regimens in Europe for children ...
  • Consensus-based recommendations for the management of juvenile localised scleroderma 
    Zulian, Francesco; Culpo, Roberta; Sperotto, Francesca; Anton, Jordi; Avcin, Tadej; Baildam, Eileen M; Boros, Christina; Chaitow, Jeffrey; Constantin, Tamàs; Kasapcopur, Ozgur; Knupp Feitosa de Oliveira, Sheila; Pilkington, Clarissa A; Russo, Ricardo; Toplak, Natasa; van Royen, Annet; Saad Magalhães, Claudia; Vastert, Sebastiaan J; Wulffraat, Nico M; Foeldvari, Ivan (2019)
    In 2012, a European initiative called Single Hub and Access point for paediatric Rheumatology in Europe (SHARE) was launched to optimise and disseminate diagnostic and management regimens in Europe for children and young ...
  • Correlations of differentially expressed gap junction connexins cx26, cx30, cx32, cx43 and cx46 with breast cancer progression and prognosis. 
    Teleki Ivett; Szász Attila Marcell; Maros Előd Máté; Györffy Balázs; Kulka Janina; Meggyesházi Nóra; Kiszner Gergő; Balla Péter; Samu Aliz; Krenács Tibor (2014)
    BACKGROUND AND AIMS: Connexins and their cell membrane channels contribute to the control of cell proliferation and compartmental functions in breast glands and their deregulation is linked to breast carcinogenesis. Our ...
  • Cribriform neuroepithelial tumor: Molecular characterization of a SMARCB1-deficient non-rhabdoid tumor with favorable long-term outcome. 
    Johann PD; Hovestadt V; Thomas C; Jeibmann A; Hess K; Bens S; Oyen F; Hawkins C; Pierson CR; Aldape K; Kim SP; Widing E; Sumerauer D; Hauser, Péter; van Landeghem F; Ryzhova M; Korshunov A; Capper D; Jones DT; Pfister SM; Schneppenheim R; Siebert R; Paulus W; Fruhwald MC; Kool M; Hasselblatt M (2017)
    Rhabdoid phenotype and loss of SMARCB1 expression in a brain tumor are characteristic features of atypical teratoid/rhabdoid tumors (ATRT). Rare non-rhabdoid brain tumors showing cribriform growth pattern and SMARCB1 loss ...
  • Crohn-beteg gyermekek infliximabkezelésének kezdeti tapasztalatai hazánkban [Analysis of infliximab treated pediatric patients with Crohn disease in Hungary] 
    Veres, Gábor; Szabó, Dolóresz; Herczegné Várkonyi, Ágnes; Tari B; Polgar M; B Kovacs J; Horvath A; Tomsits, Erika; Tokodi I; Bodánszky, Hedvig; Dezsőfi, Antal; Szakos E; Vass, Noémi; Ruszinko V; Kovács, Márta; Müller, Katalin Eszter; Arató, András (2010)
    Infliximab, the chimeric antibody to tumor necrosis factor-alpha, is indicated for medically refractory pediatric Crohn disease. Aim of our study was to examine the efficacy and side effects of infliximab therapy in Hungarian ...
  • Cross-validation of survival associated biomarkers in gastric cancer using transcriptomic data of 1,065 patients 
    Szász, A Marcell; Lánczky A; Nagy, Ádám; Förster S; Hark K; Green JE; Boussioutas A; Busuttil R; Szabó, András; Győrffy, Balázs (2016)
    INTRODUCTION: Multiple gene expression based prognostic biomarkers have been repeatedly identified in gastric carcinoma. However, without confirmation in an independent validation study, their clinical utility is limited. ...
  • Currently favored sampling practices for tumor sequencing can produce optimal results in the clinical setting 
    Pongor, Lőrinc; Munkácsy, Gyöngyi; Vereczkey, I; Pete, Imre; Győrffy, Balázs (2020)
    Tumor heterogeneity is a consequence of clonal evolution, resulting in a fractal-like architecture with spatially separated main clones, sub-clones and single-cells. As sequencing an entire tumor is not feasible, we ask ...
  • Cytogenetic Prognostication Within Medulloblastoma Subgroups 
    Shih, DJ; Northcott, PA; Remke, M; Korshunov, A; Ramaswamy, V; Kool, M; Luu, B; Yao, Y; Wang, X; Dubuc, AM; Garzia, L; Peacock, J; Mack, SC; Wu, X; Rolider, A; Morrissy, AS; Cavalli, FM; Jones, DT; Zitterbart, K; Faria, CC; Schuller, U; Kren, L; Kumabe, T; Tominaga, T; Shin, Ra Y; Garami, Miklós; Hauser, Péter; Chan, JA; Robinson, S; Bognár, László; Klekner, Álmos; Saad, AG; Liau, LM; Albrecht, S; Fontebasso, A; Cinalli, G; De Antonellis, P; Zollo, M; Cooper, MK; Thompson, RC; Bailey, S; Lindsey, JC; Di Rocco, C; Massimi, L; Michiels, EM; Scherer, SW; Phillips, JJ; Gupta, N; Fan, X; Muraszko, KM; Vibhakar, R; Eberhart, CG; Fouladi, M; Lach, B; Jung, S; Wechsler-Reya, RJ; Fevre-Montange, M; Jouvet, A; Jabado, N; Pollack, IF; Weiss, WA; Lee, JY; Cho, BK; Kim, SK; Wang, KC; Leonard, JR; Rubin, JB; de Torres, C; Lavarino, C; Mora, J; Cho, YJD; Tabori, U; Olson, JM; Gajjar, A; Packer, RJ; Rutkowski, S; Pomeroy, SL; French, PJ; Kloosterhof, NK; Kros, JM; Van, Meir EG; Clifford, SC; Bourdeaut, F; Delattre, O; Doz, FF; Hawkins, CE; Malkin, D; Grajkowska, WA; Perek-Polnik, M; Bouffet, E; Rutka, JT; Pfister, SM; Taylor, M (2014)
    PURPOSE: Medulloblastoma comprises four distinct molecular subgroups: WNT, SHH, Group 3, and Group 4. Current medulloblastoma protocols stratify patients based on clinical features: patient age, metastatic stage, extent ...
  • Deciphering and Targeting Oncogenic Mutations and Pathways in Breast Cancer 
    Santarpia L; Bottai G; Kelly CM; Győrffy, Balázs; Székely, Borbála; Pusztai L (2016)
    : Advances in DNA and RNA sequencing revealed substantially greater genomic complexity in breast cancer than simple models of a few driver mutations would suggest. Only very few, recurrent mutations or copy-number variations ...
  • Decreased hormone content of immune cells in children during acute lymphocytic leukemia (ALL) - effect of treatment. 
    Pállinger, Éva; Horváth, Zsuzsanna; Csóka, Monika; Kovács, Gábor; Csaba, György (2011)
    Histamine, serotonin and triiodothyronine (T3) content of different circulating lymphocyte subsets of leukemic (acute lymphocytic leukemia, ALL) and non-leukemic (control) children were investigated by multicolor flow ...
  • Dehydroepiandrosterone Pretreatment Alters the Ischaemia/Reperfusion-Induced VEGF, IL-1 and IL-6 Gene Expression in Acute Renal Failure 
    Vannay Ádám; Fekete Andrea; Langer Róbert; Tóth Tibor; Sziksz Erna; Vásárhelyi Barna; Szabó Attila J.; Losonczy, György; Ádori Csaba; Gál Anikó; Tulassay Tivadar; Szabó András (2009)
    Background: Beneficial effects of dehydroepiandrosterone (DHEA) pretreatment were reported in ischaemia/reperfusion (I/R)-induced kidney damage. Methods: To investigate the mechanism of DHEA pretreatment during renal I/R ...
  • Development of a consensus core dataset in juvenile dermatomyositis for clinical use to inform research 
    McCann LJ; Pilkington CA; Huber AM; Ravelli A; Appelbe D; Kirkham JJ; Williamson PR; Aggarwal A; Christopher-Stine L; Constantin, Tamás; Feldman BM; Lundberg I; Maillard S; Mathiesen P; Murphy R; Pachman LM; Reed AM; Rider LG; van Royen-Kerkof A; Russo R; Spinty S; Wedderburn LR; Beresford MW (2018)
    Objectives This study aimed to develop consensus on an internationally agreed dataset for juvenile dermatomyositis (JDM), designed for clinical use, to enhance collaborative research and allow integration of data between ...
  • Development of minimum standards of care for juvenile localized scleroderma 
    Constantin, Tamás; Foeldvari, I; Pain, CE; Palinkas, A; Hoger, P; Moll, M; Nemkova, D; Weibel, L; Laczkovszki, M; Clements, P; Torok, KS (2018)
    Juvenile localized scleroderma (jLS), also known as morphea, is an orphan disease. Pediatric guidelines regarding diagnosis, assessment, and management are lacking. Our objective was to develop minimum standards of care ...
  • Development of the SIOPE DIPG network, registry and imaging repository: a collaborative effort to optimize research into a rare and lethal disease 
    van Zanten SE; Baugh J; Chaney B; De Jongh D; Aliaga ES; Barkhof F; Noltes J; De Wolf R; Van Dijk J; Cannarozzo A; Damen-Korbijn CM; Lieverst JA; Colditz N; Hoffmann M; Warmuth-Metz M; Bison B; Jones DT; Sturm D; Gielen GH; Jones C; Hulleman E; Calmon R; Castel D; Varlet P; Giraud G; Slavc I; Van Gool S; Jacobs S; Jadrijevic-Cvrlje F; Sumerauer D; Nysom K; Pentikainen V; Kivivuori SM; Leblond P; Entz-Werle N; von Bueren AO; Kattamis A; Hargrave DR; Hauser P; Garami, Miklós; Thorarinsdottir HK; Pears J; Gandola L; Rutkauskiene G; Janssens GO; Torsvik IK; Perek-Polnik M; Gil-da-Costa MJ; Zheludkova O; Shats L; Deak L; Kitanovski L; Cruz O; La Madrid AM; Holm S; Gerber N; Kebudi R; Grundy R; Lopez-Aguilar E; Zapata-Tarres M; Emmerik J; Hayden T; Bailey S; Biassoni V; Massimino M; Grill J; Vandertop WP; Kaspers GJ; Fouladi M; Kramm CM; van Vuurden DG; members of the SIOPE DIPG Network (2017)
    Diffuse intrinsic pontine glioma (DIPG) is a rare and deadly childhood malignancy. After 40 years of mostly single-center, often non-randomized trials with variable patient inclusions, there has been no improvement in ...
  • Development of treatment and clinical results in childhood acute myeloid leukemias in Hungary 
    Szegedi, István; Jakab, Zsuzsanna; Masát P; Kiss, Csongor; Hungarian Pediatric Hematology-Oncology Group (HPOG) (2013)
    Acute myeloid leukemias (AML) comprising approximately 15 % of pediatric leukemias account for 30 % of all leukemic deaths in children worldwide. The 5-year overall survival (OS) rate now reaches 60-65 % in Western Europe, ...