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

Selecting patients with sickle cell disease for gene addition or gene editing-based therapeutic approaches: Report on behalf of a joint EHA Specialized Working Group and EBMT Hemoglobinopathies Working Party consensus conference

选择镰状细胞病患者进行基因添加或基因编辑治疗:欧洲血液学协会 (EHA) 专业工作组和欧洲骨髓移植协会 (EBMT) 血红蛋白病工作组联合共识会议报告

de Franceschi, Lucia; Locatelli, Franco; Rees, David; Chabannon, Christian; Dalle, Jean-Hugues; Rivella, Stefano; Iolascon, Achille; Lobitz, Stephan; Abboud, Miguel R; de la Fuente, Josu; Flevari, Pagona; Angelucci, Emanuele; de Montalembert, Mariane

Gene therapy in transfusion-dependent non-β0/β0 genotype β-thalassemia: first real-world experience of beti-cel

输血依赖型非β0/β0基因型β地中海贫血的基因治疗:Beti-cel的首个真实世界经验

Mirza, Adil; Ritsert, Mona-Lisa; Tao, Gloria; Thakar, Himal; Lobitz, Stephan; Heine, Sabine; Koscher, Leila; Dürken, Matthias; Schmitt, Anita; Schmitt, Michael; Pavel, Petra; Laier, Sascha; Jakoby, Donate; Greil, Johann; Kunz, Joachim; Kulozik, Andreas

Approaches to Invasive Fungal Diseases in Paediatric Cancer Centres: An Analysis of Current Practices and Challenges in Germany, Austria and Switzerland

儿科癌症中心侵袭性真菌病的治疗方法:德国、奥地利和瑞士的现状分析及挑战

Seidel, Danila; Pana, Zoi Dorothea; Ebrahimi-Fakhari, Daniel; Butzer, Sarina K; Mehler, Katrin; Reinhold, Ilana; Simon, Arne; Dohna-Schwake, Christian; Mack, Ines; Bodmer, Nicole; Niehues, Tim; Claviez, Alexander; Längler, Alfred; Leipold, Alfred; Prokop, Aram; Brummel, Bastian; Winkler, Beate; Gruhn, Bernd; Classen, Carl Friedrich; Friedrich, Carsten; Koenig, Christa; Flotho, Christian; Poyer, Fiona; Schilling, Freimut; Calaminus, Gabriele; Sieben, Geeke; Schwabe, Georg C; Reinhard, Harald; Teltschik, Heiko-Manuel; Hengartner, Heinz; Stursberg, Jana; Greiner, Jeanette; Greil, Johann; Leyh, Jörg; Kühl, Jörn-Sven; Ehlert, Karoline; Bochennek, Konrad; Rohde, Marius; Demmert, Martin; Stiefel, Martina; Eyrich, Matthias; Siepermann, Meinolf; Frühwald, Michael; Döring, Michaela; Nathrath, Michaela; Minkov, Milen; Streiter, Monika; Jones, Neil; Naumann-Bartsch, Nora; Jorch, Norbert; Beck, Olaf; Beier, Rita; Crazzolara, Roman; Kietz, Silke; Vieth, Simon; Fröhling, Stefan; Lobitz, Stephan; Ghosh, Sujal; Vallée, Tanja C; Müller, Thilo; Wiesel, Thomas; Däbritz, Tobias; Kontny, Udo; Thiel, Uwe; Strenger, Volker; Eberl, Wolfgang R; Cornely, Oliver A; Groll, Andreas H; Lehrnbecher, Thomas

Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea

胎儿血红蛋白的遗传修饰因子会影响接受羟基脲治疗的镰状细胞病患者的病情进程

Allard, Pierre; Alhaj, Nareen; Lobitz, Stephan; Cario, Holger; Jarisch, Andreas; Grosse, Regine; Oevermann, Lena; Hakimeh, Dani; Tagliaferri, Laura; Kohne, Elisabeth; Kopp-Schneider, Annette; Kulozik, Andreas E; Kunz, Joachim B

Introduction of Universal Newborn Screening for Sickle Cell Disease in Germany-A Brief Narrative Review

德国引入新生儿镰状细胞病普遍筛查——简要叙述性回顾

Lobitz, Stephan; Kunz, Joachim B; Cario, Holger; Hakimeh, Dani; Jarisch, Andrea; Kulozik, Andreas E; Oevermann, Lena; Grosse, Regine

Benefits of a Disease Management Program for Sickle Cell Disease in Germany 2011-2019: The Increased Use of Hydroxyurea Correlates with a Reduced Frequency of Acute Chest Syndrome

德国2011-2019年镰状细胞病疾病管理项目的益处:羟基脲使用量的增加与急性胸部综合征发生率的降低相关

Kunz, Joachim B; Schlotmann, Andreas; Daubenbüchel, Andrea; Lobitz, Stephan; Jarisch, Andrea; Grosse, Regine; Cario, Holger; Oevermann, Lena; Hakimeh, Dani; Tagliaferri, Laura; Kulozik, Andreas E

High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers

高灵敏度微卫星不稳定性评估用于检测双等位基因生殖系错配修复突变携带者正常组织中的错配修复缺陷

González-Acosta, Maribel; Marín, Fátima; Puliafito, Benjamin; Bonifaci, Nuria; Fernández, Anna; Navarro, Matilde; Salvador, Hector; Balaguer, Francesc; Iglesias, Silvia; Velasco, Angela; Grau Garces, Elia; Moreno, Victor; Gonzalez-Granado, Luis Ignacio; Guerra-García, Pilar; Ayala, Rosa; Florkin, Benoît; Kratz, Christian; Ripperger, Tim; Rosenbaum, Thorsten; Januszkiewicz-Lewandowska, Danuta; Azizi, Amedeo A; Ragab, Iman; Nathrath, Michaela; Pander, Hans-Jürgen; Lobitz, Stephan; Suerink, Manon; Dahan, Karin; Imschweiler, Thomas; Demirsoy, Ugur; Brunet, Joan; Lázaro, Conxi; Rueda, Daniel; Wimmer, Katharina; Capellá, Gabriel; Pineda, Marta

A Medication Adherence App for Children With Sickle Cell Disease: Qualitative Study

一款针对镰状细胞病患儿的用药依从性应用程序:定性研究

Curtis, Kristina; Lebedev, Anastasiya; Aguirre, Elisa; Lobitz, Stephan

Newborn Screening for Sickle Cell Disease in Europe

欧洲新生儿镰状细胞病筛查

Daniel, Yvonne; Elion, Jacques; Allaf, Bichr; Badens, Catherine; Bouva, Marelle J; Brincat, Ian; Cela, Elena; Coppinger, Cathy; de Montalembert, Mariane; Gulbis, Béatrice; Henthorn, Joan; Ketelslegers, Olivier; McMahon, Corrina; Streetly, Allison; Colombatti, Raffaella; Lobitz, Stephan

Thalassemias: An Overview

地中海贫血症概述

Angastiniotis, Michael; Lobitz, Stephan