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

Factor H-related 1 and heparan sulfate architecture contribute to complement dysregulation in C3 glomerulopathy.

因子 H 相关 1 和硫酸乙酰肝素结构导致 C3 肾小球病中的补体失调

Slagle Amanda K, Ghiringhelli Borsa Nicolo, Wang Kai, Taylor Amanda O, Meyer Nicole C, Jones Michael B, Walls William D, Nelson Angela F M, Roberts Sarah M, Sun Mingyao, Goicoechea de Jorge Elena, Rodriguez de Cordoba Santiago, Jalal Diana I, Nester Carla M, Zhang Yuzhou, Smith Richard J H

Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 Glomerulopathy

将肾炎因子定义为C3肾小球病中系统性补体失调的多种驱动因素

Hauer, Jill J; Zhang, Yuzhou; Goodfellow, Renee; Taylor, Amanda; Meyer, Nicole C; Roberts, Sarah; Shao, Dingwu; Fergus, Lauren; Borsa, Nicolo Ghiringhelli; Hall, Monica; Nester, Carla M; Smith, Richard J H

Factor H Autoantibodies and Complement-Mediated Diseases

因子H自身抗体和补体介导疾病

Zhang, Yuzhou; Ghiringhelli Borsa, Nicolo; Shao, Dingwu; Dopler, Arthur; Jones, Michael B; Meyer, Nicole C; Pitcher, Gabriella R; Taylor, Amanda O; Nester, Carla M; Schmidt, Christoph Q; Smith, Richard J H

Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic Syndrome

对 400 名患者的基因分析加深了对非典型溶血性尿毒综合征的理解,并揭示了一种与该疾病相关的新基因

Bu, Fengxiao; Zhang, Yuzhou; Wang, Kai; Borsa, Nicolo Ghiringhelli; Jones, Michael B; Taylor, Amanda O; Takanami, Erika; Meyer, Nicole C; Frees, Kathy; Thomas, Christie P; Nester, Carla; Smith, Richard J H

C3 glomerulonephritis secondary to mutations in factors H and I: rapid recurrence in deceased donor kidney transplant effectively treated with eculizumab

由H因子和I因子突变引起的C3肾小球肾炎:已故供体肾移植后迅速复发,但依库珠单抗可有效治疗

Garg, Neetika; Zhang, Yuzhou; Nicholson-Weller, Anne; Khankin, Eliyahu V; Borsa, Nicolò Ghiringhelli; Meyer, Nicole C; McDermott, Susan; Stillman, Isaac E; Rennke, Helmut G; Smith, Richard J; Pavlakis, Martha

CPR in medical TV shows: non-health care student perspective

医疗类电视节目中的心肺复苏术:非医疗专业学生的视角

Alismail, Abdullah; Meyer, Nicole C; Almutairi, Waleed; Daher, Noha S

C4 Nephritic Factors in C3 Glomerulopathy: A Case Series

C3肾小球病中的C4肾炎因子:病例系列

Zhang, Yuzhou; Meyer, Nicole C; Fervenza, Fernando C; Lau, Winnie; Keenan, Adam; Cara-Fuentes, Gabriel; Shao, Dingwu; Akber, Aalia; Fremeaux-Bacchi, Veronique; Sethi, Sanjeev; Nester, Carla M; Smith, Richard J H

High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies.

血栓性微血管病和 C3 肾小球病的高通量基因检测

Bu Fengxiao, Borsa Nicolo Ghiringhelli, Jones Michael B, Takanami Erika, Nishimura Carla, Hauer Jill J, Azaiez Hela, Black-Ziegelbein Elizabeth A, Meyer Nicole C, Kolbe Diana L, Li Yingyue, Frees Kathy, Schnieders Michael J, Thomas Christie, Nester Carla, Smith Richard J H

PDZD7 and hearing loss: More than just a modifier

PDZD7 与听力损失:不仅仅是修饰基因

Booth, Kevin T; Azaiez, Hela; Kahrizi, Kimia; Simpson, Allen C; Tollefson, William T A; Sloan, Christina M; Meyer, Nicole C; Babanejad, Mojgan; Ardalani, Fariba; Arzhangi, Sanaz; Schnieders, Michael J; Najmabadi, Hossein; Smith, Richard J H

Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome

非典型溶血性尿毒综合征中补体和凝血基因的全面遗传分析

Bu, Fengxiao; Maga, Tara; Meyer, Nicole C; Wang, Kai; Thomas, Christie P; Nester, Carla M; Smith, Richard J H