日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Improving Registration and Dataflows Between Pediatric Oncology Clinics and the Childhood Cancer Registry of Switzerland: Protocol for SwissPedCancer Quality Assurance Study

改善瑞士儿科肿瘤诊所与瑞士儿童癌症登记处之间的登记和数据流:SwissPedCancer质量保证研究方案

Shoman, Yara; Leuenberger, Lorenz; Sommer, Grit; Bielicki, Julia Anna; Brazzola, Pierluigi; Della Valle, Sophia; Diezi, Manuel; Drozdov, Daniel; Gumy-Pause, Fabienne; Guerreiro Stücklin, Ana; Kuehnel, Ursula M; Scheinemann, Katrin; Schindera, Christina; Schilling, Freimut; Waespe, Nicolas; Spycher, Ben D; Schlapbach, Luregn J; Kuehni, Claudia E; Belle, Fabiën N

Genetic polymorphisms contributing to hearing loss in children treated with platinum agents: a systematic review and meta-analysis protocol

铂类药物治疗儿童听力损失的遗传多态性:系统评价和荟萃分析方案

Chavaz, Lara; Ćavar Pavić, Jakica; Dupanloup, Isabelle; Fresneau, Brice; Cao Van, Hélène; Waespe, Nicolas; Gloor, Yvonne; Ansari, Marc

A Health Service Research Study on a Low-Threshold Hearing Screening Program for Childhood Cancer Survivors in Switzerland: Protocol for the HEAR Study

瑞士一项针对儿童癌症幸存者的低门槛听力筛查项目的健康服务研究:HEAR 研究方案

Jörger, Philippa; Nigg, Carina; Mader, Luzius; Strebel, Sven; Kompis, Martin; Tomášiková, Zuzana; Schindera, Christina; Michel, Gisela; von der Weid, Nicolas Xavier; Ansari, Marc; Waespe, Nicolas; Kuehni, Claudia Elisabeth

Recommendations for surveillance of pulmonary dysfunction among childhood, adolescent, and young adult cancer survivors: a report from the International Late Effects of Childhood Cancer Guideline Harmonization Group

儿童、青少年和青年癌症幸存者肺功能障碍监测建议:国际儿童癌症远期效应指南协调小组的报告

Otth, Maria; Kasteler, Rahel; Mulder, Renée L; Agrusa, Jennifer; Armenian, Saro H; Barnea, Dana; Bergeron, Anne; Bhatt, Neel S; Bourke, Stephen J; Constine, Louis S; Goutaki, Myrofora; Green, Daniel M; Hennewig, Ulrike; Houdouin, Veronique; Hudson, Melissa M; Kremer, Leontien; Latzin, Philipp; Ng, Antony; Oeffinger, Kevin C; Schindera, Christina; Skinner, Roderick; Sommer, Grit; Srinivasan, Saumini; Stokes, Dennis C; Versluys, Birgitta; Waespe, Nicolas; Weiner, Daniel J; Dietz, Andrew C; Kuehni, Claudia E

Subsequent female breast cancer risk associated with anthracycline chemotherapy for childhood cancer

儿童癌症蒽环类化疗与女性后续乳腺癌风险相关

Wang, Yuehan; Ronckers, Cécile M; van Leeuwen, Flora E; Moskowitz, Chaya S; Leisenring, Wendy; Armstrong, Gregory T; de Vathaire, Florent; Hudson, Melissa M; Kuehni, Claudia E; Arnold, Michael A; Demoor-Goldschmidt, Charlotte; Green, Daniel M; Henderson, Tara O; Howell, Rebecca M; Ehrhardt, Matthew J; Neglia, Joseph P; Oeffinger, Kevin C; van der Pal, Helena J H; Robison, Leslie L; Schaapveld, Michael; Turcotte, Lucie M; Waespe, Nicolas; Kremer, Leontien C M; Teepen, Jop C

A novel integrative multi-omics approach to unravel the genetic determinants of rare diseases with application in sinusoidal obstruction syndrome

一种新型的整合多组学方法,用于揭示罕见病的遗传决定因素,并应用于窦状隙阻塞综合征的治疗。

Waespe, Nicolas; Mlakar, Simona Jurkovic; Dupanloup, Isabelle; Rezgui, Mohamed Aziz; Bittencourt, Henrique; Krajinovic, Maja; Kuehni, Claudia E; Nava, Tiago; Ansari, Marc

Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group

172 例携带种系 SUFU 致病性变异患者的癌症风险和肿瘤谱:SIOPE 宿主基因组工作组的合作研究

Guerrini-Rousseau, Léa; Masliah-Planchon, Julien; Waszak, Sebastian M; Alhopuro, Pia; Benusiglio, Patrick R; Bourdeaut, Franck; Brecht, Ines B; Del Baldo, Giada; Dhanda, Sandeep Kumar; Garrè, Maria Luisa; Gidding, Corrie E M; Hirsch, Steffen; Hoarau, Pauline; Jorgensen, Mette; Kratz, Christian; Lafay-Cousin, Lucie; Mastronuzzi, Angela; Pastorino, Lorenza; Pfister, Stefan M; Schroeder, Christopher; Smith, Miriam Jane; Vahteristo, Pia; Vibert, Roseline; Vilain, Catheline; Waespe, Nicolas; Winship, Ingrid M; Evans, D Gareth; Brugieres, Laurence

Association study of candidate DNA-repair gene variants and acute graft versus host disease in pediatric patients receiving allogeneic hematopoietic stem-cell transplantation

候选DNA修复基因变异与接受异基因造血干细胞移植的儿科患者急性移植物抗宿主病的关联研究

C R S Uppugunduri #,P Huezo-Diaz Curtis #,T Nava,M A Rezgui,V Mlakar,S Jurkovic Mlakar,N Waespe,Y Théoret,F Gumy-Pause,F Bernard,Y Chalandon,J J Boelens,R G M Bredius,J H Dalle,C Nath,S Corbacioglu,C Peters,P Bader,P Shaw,H Bittencourt  ,M Krajinovic    ,M Ansari

Correction to: GSTM1 and GSTT1 double null genotypes determining cell fate and proliferation as potential risk factors of relapse in children with hematological malignancies after hematopoietic stem cell transplantation

更正:GSTM1 和 GSTT1 双缺失基因型决定细胞命运和增殖,是造血干细胞移植后血液系统恶性肿瘤患儿复发的潜在危险因素

Jurkovic Mlakar, Simona; Uppugunduri, Satyanarayana Chakradhara Rao; Nava, Tiago; Mlakar, Vid; Golay, Hadrien; Robin, Shannon; Waespe, Nicolas; Rezgui, Mohamed Aziz; Chalandon, Yves; Boelens, Jaap Jan; Bredius, Robert G M; Dalle, Jean-Hugues; Peters, Christina; Corbacioglu, Selim; Bittencourt, Henrique; Krajinovic, Maja; Ansari, Marc

GSTM1 and GSTT1 double null genotypes determining cell fate and proliferation as potential risk factors of relapse in children with hematological malignancies after hematopoietic stem cell transplantation

GSTM1 和 GSTT1 双无效基因型决定细胞命运和增殖作为造血干细胞移植后血液系统恶性肿瘤儿童复发的潜在危险因素

Simona Jurkovic Mlakar, Satyanarayana Chakradhara Rao Uppugunduri, Tiago Nava, Vid Mlakar, Hadrien Golay, Shannon Robin, Nicolas Waespe, Mohamed Aziz Rezgui, Yves Chalandon, Jaap Jan Boelens, Robert G M Bredius, Jean-Hugues Dalle, Christina Peters, Selim Corbacioglu, Henrique Bittencourt, Maja Kraji