tallózása szerző szerint "Rutkowski S"

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  • A very rare cancer in Down syndrome: medulloblastoma. Epidemiological data from 13 countries 
    Satgé D; Stiller CA; Rutkowski S; von Bueren AO; Lacour B; Sommelet D; Nishi M; Massimino M; Garré ML; Moreno F; Hasle H; Jakab, Zsuzsanna; Greenberg M; von der Weid N; Kuehni C; Zurriaga O; Vicente M-L; Peris-Bonet R; Benesch M; Vekemans M; Sullivan SG; Rickert C (2013)
    Persons with Down syndrome (DS) uniquely have an increased frequency of leukemias but a decreased total frequency of solid tumors. The distribution and frequency of specific types of brain tumors have never been studied ...
  • Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma 
    Northcott PA; Lee C; Zichner T; Stutz AM; Erkek S; Kawauchi D; Shih DJ; Hovestadt V; Zapatka M; Sturm D; Jones DT; Kool M; Remke M; Cavalli FM; Zuyderduyn S; Bader GD; VandenBerg S; Esparza LA; Ryzhova M; Wang W; Wittmann A; Stark S; Sieber L; Seker-Cin H; Linke L; Kratochwil F; Jager N; Buchhalter I; Imbusch CD; Zipprich G; Raeder B; Schmidt S; Diessl N; Wolf S; Wiemann S; Brors B; Lawerenz C; Eils J; Warnatz HJ; Risch T; Yaspo ML; Weber UD; Bartholomae CC; von Kalle C; Turányi, Eszter; Hauser, Péter; Sanden E; Darabi A; Siesjo P; Sterba J; Zitterbart K; Sumerauer D; van Sluis P; Versteeg R; Volckmann R; Koster J; Schuhmann MU; Ebinger M; Grimes HL; Robinson GW; Gajjar A; Mynarek M; von Hoff K; Rutkowski S; Pietsch T; Scheurlen W; Felsberg J; Reifenberger G; Kulozik AE; von Deimling A; Witt O; Eils R; Gilbertson RJ; Korshunov A; Taylor MD; Lichter P; Korbel JO; Wechsler-Reya RJ; Pfister SM (2014)
    Medulloblastoma is a highly malignant paediatric brain tumour currently treated with a combination of surgery, radiation and chemotherapy, posing a considerable burden of toxicity to the developing child. Genomics has ...
  • Evaluation of age-dependent treatment strategies for children and young adults with pineoblastoma 
    Mynarek M; Pizer B; Dufour C; van Vuurden D; Garami, Miklós; Massimino M; Fangusaro J; Davidson T; Gil-da-Costa MJ; Sterba J; Benesch M; Gerber N; Juhnke BO; Kwiecien R; Pietsch T; Kool M; Clifford S; Ellison DW; Giangaspero F; Wesseling P; Gilles F; Gottardo N; Finlay JL; Rutkowski S; von Hoff K (2017)
  • Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis 
    Torchia J; Picard D; Lafay-Cousin L; Hawkins C E; Kim S -K; Letourneau; Ra Y -S; Ho K C; Chan T S Y; Sin-Chan P; Dunham C; Yip S; Ng H -K; Lu J -Q; Albrecht S; Pimentel J; Chan J A; Somers G R; Zielenska M; Faria C C; Roque L; Baskin B; Birks D; Foreman N; Strother D; Klekner, Álmos; Garami, Miklós; Hauser, Péter; Hortobágyi, Tibor; Bognár L; Wilson B; Hukin J; Carret A -S; Van Meter T E; Nakamura H; Toledano H; Fried I; Fults D; Wataya T; Fryer C; Eisenstat D D; Scheineman K; Johnston D; Michaud J; Zelcer S; Hammond R; Ramsay D A; Fleming A J; Lulla R R; Fangusaro J R; Sirachainan N; Larbcharoensub N; Hongeng S; Barakzai M A; Montpetit A; Stephens D; Grundy R G; Schüller U; Nicolaides T; Tihan T; Phillips J; Taylor M D; Rutka J T; Dirks P; Bader G D; Warmuth-Metz M; Rutkowski S; Pietsch T; Judkins A R; Jabado N; Bouffet E; Huang A (2015)
    BACKGROUND: Rhabdoid brain tumours, also called atypical teratoid rhabdoid tumours, are lethal childhood cancers with characteristic genetic alterations of SMARCB1/hSNF5. Lack of biological understanding of the substantial ...