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

Is congenital thrombotic thrombocytopenic purpura a risk factor for ischemic osteonecrosis of the hip joint (Legg-Calvé-Perthes disease)?

先天性血栓性血小板减少性紫癜是髋关节缺血性骨坏死(Legg-Calvé-Perthes病)的危险因素吗?

Laemmle, Alexander; Lämmle, Bernhard

Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration

通过基因组、表型、功能、结构和深度学习整合,将甲状腺激素转运蛋白MCT8的变异与疾病严重程度联系起来。

Groeneweg, Stefan; van Geest, Ferdy S; Martín, Mariano; Dias, Mafalda; Frazer, Jonathan; Medina-Gomez, Carolina; Sterenborg, Rosalie B T M; Wang, Hao; Dolcetta-Capuzzo, Anna; de Rooij, Linda J; Teumer, Alexander; Abaci, Ayhan; van den Akker, Erica L T; Ambegaonkar, Gautam P; Armour, Christine M; Bacos, Iiuliu; Bakhtiani, Priyanka; Barca, Diana; Bauer, Andrew J; van den Berg, Sjoerd A A; van den Berge, Amanda; Bertini, Enrico; van Beynum, Ingrid M; Brunetti-Pierri, Nicola; Brunner, Doris; Cappa, Marco; Cappuccio, Gerarda; Castellotti, Barbara; Castiglioni, Claudia; Chatterjee, Krishna; Chesover, Alexander; Christian, Peter; Coenen-van der Spek, Jet; de Coo, Irenaeus F M; Coutant, Regis; Craiu, Dana; Crock, Patricia; DeGoede, Christian; Demir, Korcan; Dewey, Cheyenne; Dica, Alice; Dimitri, Paul; Dremmen, Marjolein H G; Dubey, Rachana; Enderli, Anina; Fairchild, Jan; Gallichan, Jonathan; Garibaldi, Luigi; George, Belinda; Gevers, Evelien F; Greenup, Erin; Hackenberg, Annette; Halász, Zita; Heinrich, Bianka; Hurst, Anna C; Huynh, Tony; Isaza, Amber R; Klosowska, Anna; van der Knoop, Marieke M; Konrad, Daniel; Koolen, David A; Krude, Heiko; Kulkarni, Abhishek; Laemmle, Alexander; LaFranchi, Stephen H; Lawson-Yuen, Amy; Lebl, Jan; Leeuwenburgh, Selmar; Linder-Lucht, Michaela; López Martí, Anna; Lorea, Cláudia F; Lourenço, Charles M; Lunsing, Roelineke J; Lyons, Greta; Malikova, Jana Krenek; Mancilla, Edna E; McCormick, Kenneth L; McGowan, Anne; Mericq, Veronica; Lora, Felipe Monti; Moran, Carla; Muller, Katalin E; Nicol, Lindsey E; Oliver-Petit, Isabelle; Paone, Laura; Paul, Praveen G; Polak, Michel; Porta, Francesco; Poswar, Fabiano O; Reinauer, Christina; Rozenkova, Klara; Seckold, Rowen; Seven Menevse, Tuba; Simm, Peter; Simon, Anna; Singh, Yogen; Spada, Marco; Stals, Milou A M; Stegenga, Merel T; Stoupa, Athanasia; Subramanian, Gopinath M; Szeifert, Lilla; Tonduti, Davide; Turan, Serap; Vanderniet, Joel; van der Walt, Adri; Wémeau, Jean-Louis; van Wermeskerken, Anne-Marie; Wierzba, Jolanta; de Wit, Marie-Claire Y; Wolf, Nicole I; Wurm, Michael; Zibordi, Federica; Zung, Amnon; Zwaveling-Soonawala, Nitash; Rivadeneira, Fernando; Meima, Marcel E; Marks, Debora S; Nicola, Juan P; Chen, Chi-Hua; Medici, Marco; Visser, W Edward

Newborn Screening Alone Cannot Prevent Most Cases of Severe Vitamin B12 Deficiency in the First Year of Life

仅靠新生儿筛查无法预防大多数婴儿出生第一年内发生的严重维生素B12缺乏症。

Kaufman, Christina; Margreitter, Julian; Herle, Marion; Bonfig, Walter; Däster, Corinne; Heinrich, Bianka; Karall, Daniela; Kogler, Hubert; Konstantopoulou, Vassiliki; Laemmle, Alexander; Malär, Reta; Müller, Pascal; Pöll, Veronika; Poms, Martin; Righini-Grunder, Franziska; Saurenmann, Rotraud K; Sluka, Susanna; von der Weid, Nicolas; Zeyda, Maximilian; Baumgartner, Matthias R; Huemer, Martina

Novel Treatment Strategy for Patients With Urea Cycle Disorders: Pharmacological Chaperones Enhance Enzyme Stability and Activity in Patient-Derived Liver Disease Models

尿素循环障碍患者的新型治疗策略:药理学伴侣增强患者来源肝病模型中酶的稳定性和活性

Ramosaj, Adhuresa; Borsuk, Mariia; Underhaug, Jarl; Mathis, Déborah; Matsumoto, Shirou; Keogh, Adrian; Banz, Vanessa; Pandey, Amit V; Gougeard, Nadine; Rubio, Vicente; Martinez, Aurora; Allegri, Gabriella; Poms, Martin; Thöny, Beat; Häberle, Johannes; Laemmle, Alexander

Diagnostic challenges in ornithine transcarbamylase deficiency lacking genetic confirmation: liver biopsy versus human induced pluripotent stem cell technology

缺乏基因确诊的鸟氨酸转氨甲酰酶缺乏症的诊断挑战:肝活检与人诱导多能干细胞技术

Laemmle, Alexander; Naef, Niklas

Induced pluripotent stem cell-derived hepatocytes reveal TCA cycle disruption and the potential basis for triheptanoin treatment for malate dehydrogenase 2 deficiency

诱导性多能干细胞来源的肝细胞揭示 TCA 循环中断和三庚酸甘油酯治疗苹果酸脱氢酶 2 缺乏症的潜在基础

Déborah Mathis, Jasmine Koch, Sophie Koller, Kay Sauter, Christa Flück, Anne-Christine Uldry, Patrick Forny, D Sean Froese, Alexander Laemmle

Health of children who experienced Australian immigration detention

曾遭受澳大利亚移民拘留的儿童的健康状况

Tosif, Shidan; Graham, Hamish; Kiang, Karen; Laemmle-Ruff, Ingrid; Heenan, Rachel; Smith, Andrea; Volkman, Thomas; Connell, Tom; Paxton, Georgia

Induced pluripotent stem cell technology as diagnostic tool in patients with suspected ornithine transcarbamylase deficiency lacking genetic confirmation

诱导多能干细胞技术可作为诊断工具,用于疑似鸟氨酸转氨甲酰酶缺乏症但缺乏基因检测结果的患者。

Ramosaj, Adhuresa; Singhal, Palak; Schaller, André; Laemmle, Alexander

Aquaporin 9 induction in human iPSC-derived hepatocytes facilitates modeling of ornithine transcarbamylase deficiency

在人诱导多能干细胞来源的肝细胞中诱导水通道蛋白9的表达,有助于构建鸟氨酸转氨甲酰酶缺乏症的模型。

Laemmle, Alexander; Poms, Martin; Hsu, Bernadette; Borsuk, Mariia; Rüfenacht, Véronique; Robinson, Joshua; Sadowski, Martin C; Nuoffer, Jean-Marc; Häberle, Johannes; Willenbring, Holger

Vaccine safety in Australia during the COVID-19 pandemic: Lessons learned on the frontline

新冠疫情期间澳大利亚疫苗安全:一线经验教训

Laemmle-Ruff, Ingrid; Lewis, Georgina; Clothier, Hazel J; Dimaguila, Gerardo Luis; Wolthuizen, Michelle; Buttery, Jim; Crawford, Nigel W