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

Multimodal tumor-agnostic ctDNA analysis for minimal residual disease detection and risk stratification in ovarian cancer: results from the MITO16a/MaNGO-OV2 trial

多模式肿瘤非特异性ctDNA分析用于卵巢癌微小残留病灶检测和风险分层:MITO16a/MaNGO-OV2试验结果

Paracchini, L; Velle, A; Di Gennaro, P; Mannarino, L; Ancona, L; Lorusso, D; Cecere, S C; Colombo, N; Beltrame, L; Fagotti, A; Tasca, G; Piemontese, M; Arenare, L; Califano, D; Galdiero, F; Zadro, R; Chiodini, P; Perrone, F; Biagioli, E; D'Incalci, M; Romualdi, C; Pignata, S; Marchini, S

Design and Implementation of an Eyewear-Integrated Infrared Eye-Tracking System

眼镜集成式红外眼动追踪系统的设计与实现

Pezzoli, Carlo; Paracchini, Marco Brando Mario; Crafa, Daniele Maria; Carminati, Marco; Merigo, Luca; Ongarello, Tommaso; Marcon, Marco

Toward an Improved Understanding of Dyslexia: Reflections on a New Consensus Definition and Its Implications

增进对阅读障碍的理解:对新的共识定义及其意义的反思

Morsanyi, Kinga; Paracchini, Silvia; Krishnan, Saloni; Manning, Catherine; Milne, Jennifer; Van Herwegen, Jo; Luciano, Michelle

HR-SC-an academic-developed machine learning framework to classify HRD-positive ovarian cancer patients and predict sensitivity to olaparib

HR-SC 是一个学术界开发的机器学习框架,用于对 HRD 阳性卵巢癌患者进行分类并预测其对奥拉帕尼的敏感性。

Beltrame, L; Mannarino, L; Sergi, A; Velle, A; Treilleux, I; Pignata, S; Paracchini, L; Harter, P; Scambia, G; Perrone, F; González-Martin, A; Berger, R; Arenare, L; Hietanen, S; Califano, D; Derio, S; Van Gorp, T; Dalessandro, M L; Fujiwara, K; Provansal, M; Lorusso, D; Buderath, P; Masseroli, M; Ray-Coquard, I; Pujade-Lauraine, E; Romualdi, C; D'Incalci, M; Marchini, S

Novel (d)PCR assays for influenza A(H5Nx) viruses clade 2.3.4.4b surveillance

新型(d)PCR检测方法用于甲型流感病毒(H5Nx) 2.3.4.4b分支的监测

Buttinger, Gerhard; Petrillo, Mauro; Valastro, Viviana; Marciano, Sabrina; Crimaudo, Marika; D'Amico, Valeria; Leoni, Gabriele; Seigneuric, Renaud; Paracchini, Valentina; Robouch, Piotr; Lambrecht, Bénédicte; Gawlik, Bernd Manfred; Terregino, Calogero; Veneri, Carolina; La Rosa, Giuseppina; Suffredini, Elisabetta; Querci, Maddalena; Panzarin, Valentina; Marchini, Antonio

Unraveling the complexity of HRD assessment in ovarian cancer by combining genomic and functional approaches: translational analyses of MITO16-MaNGO-OV-2 trial

结合基因组学和功能性方法揭示卵巢癌 HRD 评估的复杂性:MITO16-MaNGO-OV-2 试验的转化分析

B Pellegrino, E D Capoluongo, M Bagnoli, L Arenare, D Califano, G Scambia, S C Cecere, E M Silini, G L Scaglione, A Spina, G Tognon, N Campanini, C Pisano, D Russo, A Pettinato, P Scollo, R Iemmolo, L De Cecco, A Musolino, S Marchini, L Beltrame, L Paracchini, F Perrone, D Mezzanzanica, S Pignata6

Mapping the potential of Natural Pest Control services in pan-European landscapes at 50 m resolution

以 50 米分辨率绘制泛欧景观中自然害虫防治服务的潜力图

Catarino, Rui; Klinnert, Ana; Barbosa, Ana Luisa; d'Andrimont, Raphael; Fellmann, Thomas; Koeble, Renate; Paracchini, Maria Luisa; Terres, Jean-Michel; van der Velde, Marijn; Vogt, Peter; Rega, Carlo

Italian multicentre study on the management of pLeural infection and empyema: IMPLE study

意大利多中心胸膜感染和脓胸治疗研究:IMPLE 研究

Gonnelli, F; Bonifazi, M; Iommi, M; Sediari, M; Cirilli, L; DiMarcoBerardino, A; Zuccatosta, L; Fantin, A; Tomassetti, S; Trigiani, M; Marchetti, G; Poletti, V; Ravaglia, C; Sorino, C; Scala, R; Balbo, P E; Paracchini, E; Tamburrini, M; Papi, A; Carpagnano, G E; Intiglietta, P; Pinelli, V; Puppo, G; Balestro, E; Daverio, M; Mondoni, M; Carlucci, P; Lacedonia, D; Vancheri, C; Impellizzeri, P; Carle, F; Gesuita, R; Mei, F

TP53 mutations and survival in ovarian carcinoma patients receiving first-line chemotherapy plus bevacizumab: Results of the MITO16A/MaNGO OV-2 study

TP53突变与接受一线化疗联合贝伐单抗治疗的卵巢癌患者的生存率:MITO16A/MaNGO OV-2研究结果

Bignotti, Eliana; Simeon, Vittorio; Ardighieri, Laura; Kuhn, Elisabetta; Marchini, Sergio; Califano, Daniela; Cecere, Sabrina Chiara; Bugatti, Mattia; Spina, Anna; Scognamiglio, Giosuè; Paracchini, Lara; Russo, Daniela; Arenare, Laura; Tognon, Germana; Lorusso, Domenica; Beltrame, Luca; D'Incalci, Maurizio; Sartori, Enrico; De Censi, Andrea; Odicino, Franco; Perrone, Francesco; Chiodini, Paolo; Pignata, Sandro

Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes

对患有阅读障碍的儿童进行全外显子组测序发现,CLDN3 和离子通道基因中的罕见变异与阅读障碍有关。

Marianski, Krzysztof; Talcott, Joel B; Stein, John; Monaco, Anthony P; Fisher, Simon E; Bishop, Dorothy V M; Newbury, Dianne F; Paracchini, Silvia