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

The diversity of peritoneal dialysis care trajectories: A study based on the REIN registry and SNDS database

腹膜透析治疗路径的多样性:一项基于REIN注册库和SNDS数据库的研究

Legendre, Bruno; Lobbedez, Thierry; Couchoud, Cécile; Lanot, Antoine; Kolko, Anne; Courivaud, Cécile; Boyer, Annabel; Béchade, Clémence

Complete genome sequence data of Xylella fastidiosa subspecies multiplex ST88 and ST89 indicate distinct introductions in France

快速木霉菌亚种多重亚种ST88和ST89的完整基因组序列数据表明,它们在法国是不同的引入种。

Cunty, Amandine; Dittmer, Jessica; Merda, Déborah; Legendre, Bruno; Remenant, Benoit; Blanchard, Yannick; Cesbron, Sophie; Jacques, Marie-Agnès; Gentit, Pascal; Boutigny, Anne-Laure

Modifiable Factors Associated with Prolonged Dialysis Recovery Time and Fatigue in Hemodialysis Patients

血液透析患者透析恢复时间延长和疲劳相关的可控因素

Aoun, Mabel; Laruelle, Eric; Duneau, Gabrielle; Duquennoy, Simon; Legendre, Bruno; Baluta, Simona; Maroun, Thérèse; Lamri, Aldjia; Gosselin, Morgane; Chemouny, Jonathan; Champtiaux-Dechamps, Béatrice; Baleynaud, Juliette; Le Mouellic, Lionel; Bellier, Céline; Gritti, Marion; Cain, Claire; Hervé, Juliette; Colin, Pauline; Fleury, Sandrine; Floch, Christel; Jousset, Philippe; Dolley-Hitze, Thibault

Suspicions of two bridgehead invasions of Xylella fastidiosa subsp. multiplex in France

法国疑似发生两起多形木霉菌(Xylella fastidiosa subsp. multiplex)桥头堡入侵事件

Dupas, Enora; Durand, Karine; Rieux, Adrien; Briand, Martial; Pruvost, Olivier; Cunty, Amandine; Denancé, Nicolas; Donnadieu, Cécile; Legendre, Bruno; Lopez-Roques, Céline; Cesbron, Sophie; Ravigné, Virginie; Jacques, Marie-Agnès

New Coffee Plant-Infecting Xylella fastidiosa Variants Derived via Homologous Recombination.

通过同源重组产生的新型咖啡树感染快速木霉菌变种

Jacques Marie-Agnès, Denancé Nicolas, Legendre Bruno, Morel Emmanuelle, Briand Martial, Mississipi Stelly, Durand Karine, Olivier Valérie, Portier Perrine, Poliakoff Françoise, Crouzillat Dominique

Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects

RSPH1 的功能丧失突变导致原发性纤毛运动障碍,伴有中枢复合体和放射状辐条缺陷

Esther Kott, Marie Legendre, Bruno Copin, Jean-François Papon, Florence Dastot-Le Moal, Guy Montantin, Philippe Duquesnoy, William Piterboth, Daniel Amram, Laurence Bassinet, Julie Beucher, Nicole Beydon, Eric Deneuville, Véronique Houdouin, Hubert Journel, Jocelyne Just, Nadia Nathan, Aline Tamalet