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

2,8-Dihydroxyadenine disrupts epithelial integrity and alters kidney cell phenotype in vitro

2,8-二羟基腺嘌呤在体外可破坏上皮完整性并改变肾细胞表型。

Helgudottir, Hildur Run; Palsson, Runolfur; Edvardsson, Vidar Orn; Gudjonsson, Thorarinn

A meta-analysis identifies driver genes and characterizes the molecular epidemiology of colorectal cancer

一项荟萃分析确定了驱动基因并描述了结直肠癌的分子流行病学特征

Olafsson, Sigurgeir; Thorarinsson, Thorri; Gudjonsson, Sigurjon A; Bustamante, Mariana; Gunnarsdottir, Helga S; Knutsdottir, Hildur; Jonsson, Hakon; Magnusson, Magnus I; Soebech, Emilia; Runarsdottir, Hjaltey; Magnusdottir, Droplaug N; le Roux, Louise; Saemundsdottir, Jona; Kristinsdottir, Bjarney S; Agnarson, Bjarni A; Jonsdottir, Erna M; Tryggvason, Thordur; Ulfarsson, Magnus O; Gudbjartsson, Daniel F; Jonasson, Jon G; Magnusson, Olafur; Stefansson, Kari; Rafnar, Thorunn

Grand SLAM study protocol: a prospective randomised multicentre study of shortened versus standard duration adjuvant immune checkpoint inhibition for stage IIB-C, III and IV cutaneous melanoma

Grand SLAM 研究方案:一项前瞻性随机多中心研究,比较缩短疗程与标准疗程辅助免疫检查点抑制剂治疗 IIB-C 期、III 期和 IV 期皮肤黑色素瘤的疗效。

Ejder, Patric; Jespersen, Henrik; Hernberg, Micaela; Ny, Lars; Carneiro, Ana; Ellegård, Sander; Mattila, Kalle; Bagge, Roger Olofsson; Fountoukidis, Georgios; Brandberg, Yvonne; Mandala, Mario; O Carrigan, Brent; Schilling, Bastian; Aranche, Ana; Hamid, Omid; Berglund, Anders; Helgadottir, Hildur; Ullenhag, Gustav

Stereotactic body radiation therapy for oligometastatic melanoma: a real-world study of the ESTRO/EORTC nomenclature

立体定向放射治疗寡转移性黑色素瘤:ESTRO/EORTC命名法的真实世界研究

Heurlin, Ellen; Grozman, Vitali; Egyhazi Brage, Suzanne; Lindberg, Karin; Helgadottir, Hildur

SWE-NEO: Swedish NEO-adjuvant trial comparing anti-PD-1 monotherapy to combined anti-CTLA-4/anti-PD-1 blockade in resectable stage III melanoma: study protocol for a phase III open-label multi-centre trial

SWE-NEO:瑞典NEO辅助治疗试验,比较抗PD-1单药治疗与抗CTLA-4/抗PD-1联合阻断治疗在可切除III期黑色素瘤中的疗效:一项III期开放标签多中心试验的研究方案

Helgadottir, Hildur; Carneiro, Ana; Portelli, Francesca; Papadakis, Konstantinos; Björkström, Karl; Yang, Muyi; Johansson, Iva; Skogvall Svensson, Ingela; Jazrawi, Allan; Hallgren, Amanda; Harbst, Katja; Bark, Rusana; Egyhazi Brage, Suzanne; Berglund, Anders; Isaksson, Karolin; Wickström, Stina; Nilsson, Jonas; Ny, Lars; Jönsson, Göran; Olofsson Bagge, Roger

Eribulin-induced resolution of high-risk basal cell carcinoma: implications for microtubule-targeting agents in BCC management: a case report

艾立布林诱导高危基底细胞癌消退:对微管靶向药物在基底细胞癌治疗中的启示:病例报告

Lapins, Jan; Radros, Niki; Schultz, Karina; Vassilaki, Ismini; Linder Stragliotto, Christina; Helgadottir, Hildur

Survival and Quality of Life After Isolated Hepatic Perfusion With Melphalan as a Treatment for Uveal Melanoma Liver Metastases: Final Results From the Phase III Randomized Controlled Trial SCANDIUM

采用美法仑进行孤立性肝灌注治疗葡萄膜黑色素瘤肝转移后患者的生存率和生活质量:SCANDIUM III期随机对照试验的最终结果

Olofsson Bagge, Roger; Nelson, Axel; Shafazand, Amir; All-Eriksson, Charlotta; Cahlin, Christian; Elander, Nils; Gustavsson, Anders; Helgadottir, Hildur; Kiilgaard, Jens Folke; Kinhult, Sara; Ljuslinder, Ingrid; Mattsson, Jan; Rizell, Magnus; Sternby Eilard, Malin; Ullenhag, Gustav J; Nilsson, Jonas A; Ny, Lars; Lindnér, Per

Germline MC1R Variant Status and Efficacy of Immune Checkpoint Inhibitors in Patients With Advanced Melanoma

晚期黑色素瘤患者中种系MC1R变异状态与免疫检查点抑制剂疗效的关系

Yang, Muyi; Brage, Suzanne Egyhazi; Lapins, Jan; Grozman, Vitali; Svedman, Fernanda Costa; Höiom, Veronica; Helgadottir, Hildur

POT1 genetic testing in melanoma-prone families in Sweden: germline variant prevalence and tumor spectrum in identified carriers

瑞典黑色素瘤易感家族中 POT1 基因检测:已识别携带者的种系变异患病率和肿瘤谱

Papadakis, Konstantinos; Portelli, Francesca; Schultz, Karina; Olsson Sterky, Hedvig; Vassilaki, Ismini; Lapins, Jan; Sargen, Michael R; Obolenski, Sofia; Adams, David J; Yang, Muyi; Höiom, Veronica; Helgadottir, Hildur

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

POPDC2基因的双等位基因变异会导致一种常染色体隐性遗传综合征,其特征为心脏传导缺陷和肥厚型心肌病。

Nicastro, Michele; Vermeer, Alexa M C; Postema, Pieter G; Tadros, Rafik; Bowling, Forrest Z; Aegisdottir, Hildur M; Tragante, Vinicius; Mach, Lukas; Postma, Alex V; Lodder, Elisabeth M; van Duijvenboden, Karel; Zwart, Rob; Beekman, Leander; Wu, Lingshuang; Jurgens, Sean J; van der Zwaag, Paul A; Alders, Mariëlle; Allouba, Mona; Aguib, Yasmine; Santome, J Luis; de Una, David; Monserrat, Lorenzo; Miranda, Antonio M A; Kanemaru, Kazumasa; Cranley, James; van Zeggeren, Ingeborg E; Aronica, Eleonora M A; Ripolone, Michela; Zanotti, Simona; Sveinbjornsson, Gardar; Ivarsdottir, Erna V; Hólm, Hilma; Guðbjartsson, Daníel F; Skúladóttir, Ástrós Th; Stefánsson, Kári; Nadauld, Lincoln; Knowlton, Kirk U; Ostrowski, Sisse Rye; Sørensen, Erik; Vesterager Pedersen, Ole Birger; Ghouse, Jonas; Rand, Søren A; Bundgaard, Henning; Ullum, Henrik; Erikstrup, Christian; Aagaard, Bitten; Bruun, Mie Topholm; Christiansen, Mette; Jensen, Henrik K; Carere, Deanna Alexis; Cummings, Christopher T; Fishler, Kristen; Tørring, Pernille Mathiesen; Brusgaard, Klaus; Juul, Trine Maxel; Saaby, Lotte; Winkel, Bo Gregers; Mogensen, Jens; Fortunato, Francesco; Comi, Giacomo Pietro; Ronchi, Dario; van Tintelen, J Peter; Noseda, Michela; Airola, Michael V; Christiaans, Imke; Wilde, Arthur A M; Wilders, Ronald; Clur, Sally-Ann; Verkerk, Arie O; Bezzina, Connie R; Lahrouchi, Najim