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

Kappa free light chain index as a diagnostic and prognostic biomarker in multiple sclerosis

κ游离轻链指数作为多发性硬化症的诊断和预后生物标志物

Moreno-Navarro, Luis; Mora-Diaz, Sergio; Ruiz-Escribano-Menchen, Lourdes; Sempere, Angel P

Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlations

对 1236 名已进行基因分型的原发性纤毛运动障碍患者的分析,发现了不同 DNA 变异的区域性聚集以及显著的基因型-表型相关性。

Raidt, Johanna; Riepenhausen, Sarah; Pennekamp, Petra; Olbrich, Heike; Amirav, Israel; Athanazio, Rodrigo A; Aviram, Micha; Balinotti, Juan E; Bar-On, Ophir; Bode, Sebastian F N; Boon, Mieke; Borrelli, Melissa; Carr, Siobhan B; Crowley, Suzanne; Dehlink, Eleonora; Diepenhorst, Sandra; Durdik, Peter; Dworniczak, Bernd; Emiralioğlu, Nagehan; Erdem, Ela; Fonnesu, Rossella; Gracci, Serena; Große-Onnebrink, Jörg; Gwozdziewicz, Karolina; Haarman, Eric G; Hansen, Christine R; Hogg, Claire; Holgersen, Mathias G; Kerem, Eitan; Körner, Robert W; Kötz, Karsten; Kouis, Panayiotis; Loebinger, Michael R; Lorent, Natalie; Lucas, Jane S; Maj, Debora; Mall, Marcus A; Marthin, June K; Martinu, Vendula; Mazurek, Henryk; Mitchison, Hannah M; Nöthe-Menchen, Tabea; Özçelik, Ugur; Pifferi, Massimo; Pogorzelski, Andrzej; Ringshausen, Felix C; Roehmel, Jobst F; Rovira-Amigo, Sandra; Rumman, Nisreen; Schlegtendal, Anne; Shoemark, Amelia; Sperstad Kennelly, Synne; Staar, Ben O; Sutharsan, Sivagurunathan; Thomas, Simon; Ullmann, Nicola; Varghese, Julian; von Hardenberg, Sandra; Walker, Woolf T; Wetzke, Martin; Witt, Michal; Yiallouros, Panayiotis; Zschocke, Anna; Ziętkiewicz, Ewa; Nielsen, Kim G; Omran, Heymut

Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis

隐性遗传的分泌型WFDC2(HE4)缺乏症会导致鼻息肉和支气管扩张

Dougherty, Gerard W; Ostrowski, Lawrence E; Nöthe-Menchen, Tabea; Raidt, Johanna; Schramm, Andre; Olbrich, Heike; Yin, Weining; Sears, Patrick R; Dang, Hong; Smith, Amanda J; Beule, Achim G; Hjeij, Rim; Rutjes, Niels; Haarman, Eric G; Maas, Saskia M; Ferkol, Thomas W; Noone, Peadar G; Olivier, Kenneth N; Bracht, Diana C; Barbry, Pascal; Zaragosi, Laure-Emmanuelle; Fierville, Morgane; Kliesch, Sabine; Wohlgemuth, Kai; König, Julia; George, Sebastian; Loges, Niki T; Ceppe, Agathe; Markovetz, Matthew R; Luo, Hong; Guo, Ting; Rizk, Hoda; Eldesoky, Tarek; Dahlke, Katrin; Boldt, Karsten; Ueffing, Marius; Hill, David B; Pang, Yuan-Ping; Knowles, Michael R; Zariwala, Maimoona A; Omran, Heymut

Development of a Patient Journey Map for Improving Patient Experience and Quality of Atopic Dermatitis Care

制定患者就医流程图,以改善特应性皮炎患者的就医体验和护理质量

Roustán, Gastón; Loro, Marta; Rosell, Ángel; Menchen, Belén; Vicente, Olga; Elosua-González, Marta; Castaño, Juan L; Peña, Catalina; Isidoro, Olga

Nudging recommendation algorithms increases news consumption and diversity on YouTube

通过引导式推荐算法来增加 YouTube 上的新闻消费量和新闻多样性。

Yu, Xudong; Haroon, Muhammad; Menchen-Trevino, Ericka; Wojcieszak, Magdalena

Controversies in the management of anti-TNF therapy in patients with Crohn's disease: a Delphi consensus

克罗恩病患者抗TNF治疗管理中的争议:德尔菲共识

González-Lama, Yago; Ricart, Elena; Carpio, Daniel; Bastida, Guillermo; Ceballos, Daniel; Ginard, Daniel; Marin-Jimenez, Ignacio; Menchen, Luis; Muñoz, Fernando

Non-News Websites Expose People to More Political Content Than News Websites: Evidence from Browsing Data in Three Countries

非新闻网站比新闻网站向人们展示更多政治内容:来自三个国家浏览数据的证据

Wojcieszak, Magdalena; Menchen-Trevino, Ericka; Clemm von Hohenberg, Bernhard; de Leeuw, Sjifra; Gonçalves, João; Davidson, Sam; Gonçalves, Alexandre

Protection against Aβ-induced neuronal damage by KU-32: PDHK1 inhibition as important target

KU-32 预防 Aβ 诱导的神经元损伤:PDHK1 抑制是重要靶点

Ranu Pal, Dongwei Hui, Heather Menchen, Huiping Zhao, Olivier Mozziconacci, Heather Wilkins, Brian S J Blagg, Christian Schöneich, Russell H Swerdlow, Mary L Michaelis, Elias K Michaelis

Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility

CCDC39、CCDC40、RSPH1、RSPH9、HYDIN 和 SPEF2 中的致病基因变异会导致精子鞭毛组成缺陷和男性不育。

Aprea, I; Wilken, A; Krallmann, C; Nöthe-Menchen, T; Olbrich, H; Loges, N T; Dougherty, G W; Bracht, D; Brenker, C; Kliesch, S; Strünker, T; Tüttelmann, F; Raidt, J; Omran, H

[Short term effects of an initial COVID-19 outbreak on breast cancer care. A brief report]

[新冠疫情初期爆发对乳腺癌治疗的短期影响:简要报告]

Barco Nebreda, Israel; García-Fernández, Antonio; Menchen Palau, Lidia; Giménez Gómez, Nuria; Fraile López-Amor, Manel