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GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and Anemia GLUT1缺乏综合征伴发运动障碍和贫血 Yoganathan, Sangeetha; AlFaris, Haya S.; Menetrey, Anika; Chowdhury, Sayoni Roy; Vogt, Lindsey; Dickson, Jolynn; Owusu, Karen; Krishnan, Pradeep; Sharma, Suvasini; Aljouda, Liali; Pabari, Reena; Yoon, Grace; Gorodetsky, Carolina 分享 收藏
Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature Review 杂合变异AFG3L2基因患者的表型探索:病例系列及文献综述 Yoganathan, Sangeetha; Tochen, Laura; Ganguly, Jacky; Chowdhury, Sayoni Roy; AlFaris, Haya S.; Pai, Vivek; LeBlanc-Millar, Andrea; Breitbart, Sara; Kumar, Hrishikesh; Shroff, Manohar; Reginald, Arun; Yoon, Grace; Fasano, Alfonso; Ibrahim, George M.; Gorodetsky, Carolina 分享 收藏
Individual and Socioecological Resilience in Childhood-Onset Systemic Lupus Erythematosus: Associations With Patient Characteristics and Psychosocial Patient-Reported Outcomes 儿童期发病系统性红斑狼疮中的个体与社会生态韧性:与患者特征及心理社会患者报告结局的关联 Zaffino, Isabella; Boulard, Louise; Law, Joanna; Danguecan, Ashley; Jeyanathan, Asha; Ng, Lawrence; Williams-Reid, Sandra; Reid, Kiah; Cortes, Angela; Cortes, Eugene; Levy, Deborah M.; Hiraki, Linda T.; Knight, Andrea M. 分享 收藏
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8-Shogaol, a natural compound derived from Zingiber officinale , ameliorates rheumatoid arthritis by targeting TAK1 8-姜烯酚,一种从姜黄中提取的天然化合物,通过靶向TAK1改善类风湿关节炎 Sohn, S-A; Jo, S.; Samarpita, S.; Lee, J. S.; Lee, J. Y.; Son, J. E.; Jeong, M.; Kim, J. H.; Hong, S.; Yoo, S-A; Kim, W-U; Rasool, M.; Byun, S. 分享 收藏
Patterns of Children With Complex Chronic Conditions: A Latent Class Analysis 复杂慢性病患儿的模式:一项潜在类别分析 Cohen, Eyal; Osipovich, Maria; Benjamin, Hallie; Bayer, Nathaniel D.; Pulcini, Christian D.; Colvin, Jeffrey D.; Coller, Ryan J.; Leary, Jana C.; Malecki, Sarah; Morrison, John M.; Hall, Matt; Berry, Jay G. 分享 收藏
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ROME, an Ancient Gene with a Novel Function in Vertebrates, Is a Key Modulator of Embryonal Development and Cancer Metastasis ROME,一种在脊椎动物中具有新颖功能的古老基因,是胚胎发育和癌症转移的关键调节因子 Molotkova, Anna; Deniz, Emre; Swift, Matthew; Glasgow, Eric; Ma, Junfeng; Petro, Jeffrey A.; Frye, Isabel; Ozdemirli, Metin; Pesic, Dusan; Ahern, Gerard P.; Suter, Robert K.; Tiwari, Purushottam B.; Shlien, Adam; Toretsky, Jeffrey; Uren, Aykut 分享 收藏
Development of an educational video to support guideline panels in incorporating patient values and preferences into recommendation-making: qualitative one-on-one interviews and brainstorming meetings 开发支持指南专家组将患者价值观和偏好纳入建议制定的教育视频:定性的一对一访谈和头脑风暴会议 Zeng, Linan; Li, Ranyi; Li, Shelly-Anne; Clarissa, Sherinne; Agoritsas, Thomas; Chen, Jingjing; Li, Xiayan; Vandvik, Per O.; Brignardello-Petersen, Romina; Li, Xiaoyu; Zhang, Lingli; Guyatt, Gordon 分享 收藏
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Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia DENND2B基因的变异与神经发育障碍、精神病和紧张症的易感性相关。Brain Murthy, Harsha; Hoang, Ny; Stark, Jamie C.; Cui, Sunny; Pannia, Emanuela; Tsoi, Chung Ting; Harris, Simon; Ceolin, C'airah; Verhaeghe, Lauren; Scholten, Sydney; Baribeau, Danielle; Summers, Jane; Costain, Gregory; Selvanayagam, Thanuja; Howe, Jennifer L.; Lewis, M. E. Suzanne; Brunet, Theresa; Rieger, Susanne; Rosenfeld, Jill A.; Craigen, William J.; Burrage, Lindsay C.; Christie, Michelle R.; Baldwin, Deborah; Wentzensen, Ingrid M.; Keren, Boris; Cogne, Benjamin; Isidor, Bertrand; Afenjar, Alexandra; Elshafie, Reem M.; Bastaki, Laila; Alkanderi, Sumaya; Myers, Kenneth A.; Demarest, Scott; Angione, Katie; Abbott, Megan; Campeau, Philippe M.; Dowling, James J.; Mendoza-Londono, Roberto; Scherer, Stephen W.; Deshwar, Ashish R.; Vorstman, Jacob 分享 收藏