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

Evaluating Skellytour for Automated Skeleton Segmentation from Whole-Body CT Images

评估Skellytour在全身CT图像自动骨骼分割中的应用

Mann, Daniel C; Rutherford, Michael W; Farmer, Phillip; Eichhorn, Joshua M; Palot Manzil, Fathima Fijula; Wardell, Christopher P

Biallelic Variants in the DARS2 Gene as a Novel Cause of Axonal Charcot-Marie-Tooth Disease

DARS2基因双等位基因变异是轴突型夏科-马里-图斯病的新病因

Berta Estévez-Arias # ,Siiri Sarv # ,Nathalie Bonello-Palot ,Laura Carrera-García ,Carlos Ortez ,Jesica Expósito-Escudero ,Delia Yubero ,Jordi Muchart ,Emilien Delmont ,Eve Õiglane-Shlik ,Teele Meren ,Sanna Puusepp ,Ülle Murumets ,Gajja S Salomons ,Bjarne Udd ,Liis Väli ,Lara Cantarero ,Carsten G Bönnemann ,Andrés Nascimento ,Santiago Ramón-Maiques ,Katrin Õunap ,Janet Hoenicka # ,Daniel Natera-de Benito # ,Francesc Palau #

Impact of long-term non-invasive ventilation on severe exacerbations and survival in COPD: a French nationwide cohort study using multistate models

长期无创通气对慢性阻塞性肺疾病严重急性加重和生存率的影响:一项采用多状态模型的法国全国性队列研究

Pépin, Jean Louis; Herquelot, Eleonore; Denis, Helene; Josseran, Anne; Lavergne, Florent; Benjafield, Adam; Malhotra, Atul; Raphelson, Janna; Cistulli, Peter; Schmidt, Aurelie; Bailly, Sebastien; Palot, Alain; Prigent, Arnaud

Health Trajectories around Noninvasive Ventilation Initiation for Obesity Hypoventilation Syndrome

肥胖低通气综合征患者开始无创通气治疗前后的健康轨迹

Pépin, Jean-Louis; Herquelot, Eleonore; Denis, Hélène; Josseran, Anne; Lavergne, Florent; Benjafield, Adam V; Malhotra, Atul; Cistulli, Peter A; Schmidt, Aurélie; Bailly, Sébastien; Palot, Alain; Prigent, Arnaud

Weave structures of polyester fabric affect the tensile strength and microplastic fiber emission during the laundry process

聚酯织物的编织结构会影响其拉伸强度和洗涤过程中微塑料纤维的释放。

Juntarasakul, Onchanok; Julapong, Pongsiri; Srichonphaisarn, Palot; Meekoch, Thidarat; Janjaroen, Dao; Tabelin, Carlito Baltazar; Phengsaart, Theerayut

Phenotype-genotype correlation in X-linked Charcot-Marie-Tooth disease: A French cohort study

X连锁夏科-马里-图斯病表型-基因型相关性:一项法国队列研究

Barbat du Closel, Luce; Bonello-Palot, Nathalie; Delmont, Emilien; Péréon, Yann; Echaniz-Laguna, Andoni; Camdessanché, Jean Philippe; Pakleza, Aleksandra Nadaj; Chanson, Jean-Baptiste; Frachet, Simon; Magy, Laurent; Cassereau, Julien; Cintas, Pascal; Choumert, Ariane; Devic, Perrine; Louis, Sarah Léonard; Tard, Céline; Solé, Guilhem; Salort-Campana, Emmanuelle; Bouhour, Françoise; Latour, Philippe; Stojkovic, Tanya; Attarian, Shahram

Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With SH3TC2 Gene-Related Demyelinating Peripheral Neuropathy

全国范围内对103例SH3TC2基因相关脱髓鞘性周围神经病患者进行表型和基因型特征分析

Jaubert, Pauline; Loret, Camille; Stojkovic, Tanya; Attarian, Shahram; Bonello-Palot, Nathalie; Bouhour, Françoise; Camdessanche, Jean-Philippe; Cassereau, Julien; Chanson, Jean-Baptiste; Cintas, Pascal; Creange, Alain; Esselin, Florence; Genestet, Steeve; Giordano, Sophie; Gitiaux, Cyril; Guillaud-Bataille, Marine; Isapof, Arnaud; Kumaran, Deiva; Labeyrie, Céline; Laugel, Vincent; Leonard-Louis, Sarah; Lozeron, Pierre; Magy, Laurent; Mercier, Sandra; Merle, Philippe; Michaud, Maud; Nicolas, Guillaume; Ollagnon, Elisabeth; Pereon, Yann; Puma, Angela; Poinsignon, Vianney; Roy, Susana Quijano; Sole, Guilhem; Tard, Céline; Vidoni, Léo; Lia, Anne-Sophie; Echaniz-Laguna, Andoni

A novel red blood cell deformability biomarker is associated with hemolysis and vaso-occlusive crises in sickle cell disease

一种新型红细胞变形能力生物标志物与镰状细胞病中的溶血和血管阻塞危象相关

Sahun, Maxime; Bernit, Emmanuelle; Atwell, Scott; Hornung, Alexander; Charrier, Anne M; Agouti, Imane; Bonello-Palot, Nathalie; Cerino, Mathieu; Helfer, Emmanuèle; Badens, Catherine; Viallat, Annie

A new unstable haemoglobin, Hb Alger, causes a transfusion-dependent anaemia in early childhood

一种新的不稳定血红蛋白,Hb Alger,会导致幼儿期出现输血依赖性贫血。

Bouazizi, Syrine; Cerino, Mathieu; Lim, Suzy; Desgrouas, Camille; Badens, Catherine; Szepetowski, Sarah; Bonello-Palot, Nathalie

Digenesis in Charcot-Marie-Tooth Disease: Impact of Combined Mutations in the MFN2 and GDAP1 Genes

夏科-马里-图斯病中的双基因突变:MFN2 和 GDAP1 基因联合突变的影响

Shumeri, Endrit; Mandorah, Ebrahem; Martini, Nathalie; Boyer, Amandine; Halbert, Cécile; Puma, Angela; Chaussenot, Annabelle; Delmont, Emilien; N'guyen, Karine; Attarian, Shahram; Bonello-Palot, Nathalie