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

Beyond the interferon score: neurofilament light chain and glial fibrillary acidic protein capture immune-mediated neuroinjury and response to JAK inhibition in Aicardi-Goutières syndrome

除了干扰素评分之外:神经丝轻链和胶质纤维酸性蛋白可反映免疫介导的神经损伤以及Aicardi-Goutières综合征对JAK抑制剂的反应。

Wege, Lisa; Klemann, Christian; Siegert, Sandy; Bley, Annette; Koss, Sarah; Koy, Anne; Langer, Thorsten; Dunst, Franziska; Plecko, Barbara; Fleger, Martin; Speth, Fabian; Niehues, Tim; Kaufmann, Peter; Schultz, Jurek; Attia, Mohammed; Stoffels, Johannes; Wolska-Kuśnierz, Beata; Rolke, Roman; Reichelt, Gabriele; Blankenburg, Friederike; Brunner, Jürgen; Akgün, Katja; Wolf, Christine; Lee-Kirsch, Min Ae

Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy: A Nonrandomized Controlled Trial

新生儿脊髓性肌萎缩症筛查的临床有效性:一项非随机对照试验

Schwartz, Oliver; Vill, Katharina; Pfaffenlehner, Michelle; Behrens, Max; Weiß, Claudia; Johannsen, Jessika; Friese, Johannes; Hahn, Andreas; Ziegler, Andreas; Illsinger, Sabine; Smitka, Martin; von Moers, Arpad; Kölbel, Heike; Schreiber, Gudrun; Kaiser, Nadja; Wilichowski, Ekkehard; Flotats-Bastardas, Marina; Husain, Ralf A; Baumann, Matthias; Köhler, Cornelia; Trollmann, Regina; Schwerin-Nagel, Annette; Eisenkölbl, Astrid; Schimmel, Mareike; Fleger, Martin; Kauffmann, Birgit; Wiegand, Gert; Baumgartner, Manuela; Rauscher, Christian; Cirak, Sebahattin; Gläser, Dieter; Bernert, Günther; Hagenacker, Tim; Goldbach, Susanne; Probst-Schendzielorz, Kristina; Lochmüller, Hanns; Müller-Felber, Wolfgang; Schara-Schmidt, Ulrike; Walter, Maggie C; Kirschner, Janbernd; Pechmann, Astrid

Real-Time Temperature-Controlled Retinal Laser Irradiation in Rabbits

兔子的实时温控视网膜激光照射

von der Burchard, Claus; Kren, Christopher; Fleger, Jan-Erik; Theisen-Kunde, Dirk; Danicke, Veit; Abbas, Hossam S; Kleyman, Viktoria; Roider, Johann; Brinkmann, Ralf

Design and Use of a Gold Nanoparticle-Carbon Dot Hybrid for a FLIM-Based IMPLICATION Nano Logic Gate

基于FLIM的蕴含纳米逻辑门的金纳米粒子-碳点混合材料的设计和应用

Pawar, Shweta; Duadi, Hamootal; Fleger, Yafit; Fixler, Dror

Enhancing Light-Matter Interactions in MoS(2) by Copper Intercalation

铜插层增强 MoS(2) 中的光-物质相互作用

Stern, Chen; Twitto, Avraham; Snitkoff, Rifael Z; Fleger, Yafit; Saha, Sabyasachi; Boddapati, Loukya; Jain, Akash; Wang, Mengjing; Koski, Kristie J; Deepak, Francis Leonard; Ramasubramaniam, Ashwin; Naveh, Doron

Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder

BCAS3基因的双等位基因功能缺失变异会导致一种综合征性神经发育障碍

Hengel, Holger; Hannan, Shabab B; Dyack, Sarah; MacKay, Sara B; Schatz, Ulrich; Fleger, Martin; Kurringer, Andreas; Balousha, Ghassan; Ghanim, Zaid; Alkuraya, Fowzan S; Alzaidan, Hamad; Alsaif, Hessa S; Mitani, Tadahiro; Bozdogan, Sevcan; Pehlivan, Davut; Lupski, James R; Gleeson, Joseph J; Dehghani, Mohammadreza; Mehrjardi, Mohammad Y V; Sherr, Elliott H; Parks, Kendall C; Argilli, Emanuela; Begtrup, Amber; Galehdari, Hamid; Balousha, Osama; Shariati, Gholamreza; Mazaheri, Neda; Malamiri, Reza A; Pagnamenta, Alistair T; Kingston, Helen; Banka, Siddharth; Jackson, Adam; Osmond, Mathew; Rieß, Angelika; Haack, Tobias B; Nägele, Thomas; Schuster, Stefanie; Hauser, Stefan; Admard, Jakob; Casadei, Nicolas; Velic, Ana; Macek, Boris; Ossowski, Stephan; Houlden, Henry; Maroofian, Reza; Schöls, Ludger

Impaired glucose-1,6-biphosphate production due to bi-allelic PGM2L1 mutations is associated with a neurodevelopmental disorder

由PGM2L1双等位基因突变引起的葡萄糖-1,6-二磷酸生成受损与神经发育障碍有关。

Morava, Eva; Schatz, Ulrich A; Torring, Pernille M; Abbott, Mary-Alice; Baumann, Matthias; Brasch-Andersen, Charlotte; Chevalier, Nathalie; Dunkhase-Heinl, Ulrike; Fleger, Martin; Haack, Tobias B; Nelson, Stephen; Potelle, Sven; Radenkovic, Silvia; Bommer, Guido T; Van Schaftingen, Emile; Veiga-da-Cunha, Maria

Carbon Dots-Based Logic Gates

基于碳点的逻辑门

Pawar, Shweta; Duadi, Hamootal; Fleger, Yafit; Fixler, Dror

DNA-assembled superconducting 3D nanoscale architectures

DNA组装的超导三维纳米结构

Shani, Lior; Michelson, Aaron N; Minevich, Brian; Fleger, Yafit; Stern, Michael; Shaulov, Avner; Yeshurun, Yosef; Gang, Oleg

Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?

二氢嘧啶脱氢酶缺乏症:代谢性疾病还是生化表型?

Fleger, M; Willomitzer, J; Meinsma, R; Alders, M; Meijer, J; Hennekam, R C M; Huemer, M; van Kuilenburg, A B P