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

Risk factors and surrogate indicators for cardiovascular disease are prevalent in Common Variable Immunodeficiency and associate with inflammatory phenotype

常见变异型免疫缺陷病中普遍存在心血管疾病的风险因素和替代指标,且与炎症表型相关。

Yu, Aidan Jia Sheng; Moreira, Fernando; Symes, Andrew; Curlewis, Keegan; O'Sullivan, Mary; Jayasundera, Joseph; El Rhermoul, Fatema-Zahra; Lever, Charley; Stoenchev, Kostadin; Chow, Ke Li; Uysal, Omer Faruk; Alharbi, Ahmad M; Workman, Sarita; Halliday, Neil; Laurence, Arian; Verma, Nisha; Tadros, Susan; Kiani-Alikhan, Sorena; Barnett, Joseph; Burns, Siobhan O; Hurst, John R; Lowe, David M

MODELING NATURAL HISTORY AND COST-EFFECTIVENESS OF GENE-AGNOSTIC TREATMENT IN RETINITIS PIGMENTOSA

视网膜色素变性自然史建模及基因非诊断治疗的成本效益分析

Sullivan, Patrick W; Wertheimer, Albert I; Grover, Sandeep; Jayasundera, Kanishka T

Functional Vision Assessment Over 4 Years in USH2A Using the Veteran Affairs Low-Vision Visual Functioning Questionnaire

使用退伍军人事务部低视力视觉功能问卷对美国退伍军人事务部第二阶段医疗援助计划 (USH2A) 中的患者进行为期 4 年的功能性视觉评估

Parekh, Bela; Peck-Dimit, Nicholas; Duncan, Jacque L; Samarakoon, Lassana; Abalem, Maria Fernanda; Andrews, Chris A; Audo, Isabelle; Ayala, Allison R; Bradley, Chris; Cheetham, Janet K; Dagnelie, Gislin; Durham, Todd A; Huckfeldt, Rachel M; Lacy, Gabrielle D; Malbin, Brett; Michaelides, Michel; Musch, David C; Stingl, Katarina; Weng, Christina Y; Zmejkoski, Alex Z; Melia, Michele; Jayasundera, K Thiran

Characterization of Visual Field Loss Over 4 Years in the Rate of Progression in USH2A-Related Retinal Degeneration (RUSH2A) Study

USH2A相关视网膜变性(RUSH2A)进展速度研究中4年内视野缺损的特征分析

Duncan, Jacque L; Maguire, Maureen G; McDaniel, Lee S; Doucet, Nicole R; Audo, Isabelle; Ayala, Allison R; Cheetham, Janet K; Cheng, Peiyao; Durham, Todd A; Huckfeldt, Rachel M; Hufnagel, Robert B; Jayasundera, K Thiran; Khan, Naheed; Malbin, Brett; Maldonado, Ramiro S; Michaelides, Michel; Pennesi, Mark E; Weng, Christina Y; Zmejkoski, Alex; Aravind, Shobana; Ishikawa, Hiroshi; Birch, David G

Grid-Based Software for Quantification of Diabetic Retinal Nonperfusion on Ultra-Widefield Fluorescein Angiography

基于网格的软件用于量化超广角荧光血管造影中糖尿病视网膜无灌注区

Omari, Amro; Cooper, Caitlyn; Desjarlais, Eric B; Cook, Maverick; Abalem, Maria Fernanda; Andrews, Chris A; Joltikov, Katherine; Khan, Rida M; Chen, Andy; DeOrio, Andrew; Gardner, Thomas W; Paulus, Yannis M; Jayasundera, K Thiran

Addressing Challenges in Developing Treatments for Inherited Retinal Diseases: Recommendations From the Third Monaciano Symposium

应对遗传性视网膜疾病治疗研发中的挑战:第三届莫纳恰诺研讨会的建议

Thompson, Debra A; Jayasundera, K Thiran; Alekseev, Oleg; Ali, Robin R; Amato, Alessia; Arshavsky, Vadim Y; Audo, Isabelle S; Auricchio, Alberto; Bainbridge, James W B; Banin, Eyal; Besirli, Cagri G; Birch, David G; Branham, Kari E; Cideciyan, Artur V; Daiger, Stephen P; Duncan, Jacque L; Fahim, Abigail T; Flannery, John G; Gattegna, Roberto; Heckenlively, John R; Héon, Elise; Iannaccone, Alessandro; Khan, Naheed W; Khateb, Samer; Klassen, Henry J; Leroy, Bart P; Marangoni, Dario; Michaelides, Michel; Musch, David C; Pennesi, Mark E; Petersen-Jones, Simon M; Pierce, Eric A; Rao, Rajesh C; Sahel, José-Alain; Sieving, Paul A; Strettoi, Enrica; Strong, Cameron R; Wubben, Thomas J; Yang, Paul; Zacks, David N

Female Simplex Carriers of X-Linked Retinal Dystrophies: A Case Series

X连锁视网膜营养不良症女性单纯携带者:病例系列

Delaney, Adrienne; Branham, Kari E; Jayasundera, K Thiran; Khan, Naheed W; Fahim, Abigail T

CEDART Study: protocol for a non-randomized feasibility study

CEDART 研究:非随机可行性研究方案

Kwak, Jung; Jafari, Aveen; Salter, Allison; Perry, Andrea; de Montfort Shepherd, Alexis; Jayasundera, Menaka; Stayer, Sarah; Brode, Mike; Patel, Snehal; Kvale, Elizabeth

Gene Editing for CEP290-Associated Retinal Degeneration

基因编辑治疗CEP290相关视网膜变性

Pierce, Eric A; Aleman, Tomas S; Jayasundera, Kanishka T; Ashimatey, Bright S; Kim, Keunpyo; Rashid, Alia; Jaskolka, Michael C; Myers, Rene L; Lam, Byron L; Bailey, Steven T; Comander, Jason I; Lauer, Andreas K; Maguire, Albert M; Pennesi, Mark E

Racial Disparities in Genetic Detection Rates for Inherited Retinal Diseases

遗传性视网膜疾病基因检测率的种族差异

Abuzaitoun, Rebhi O; Branham, Kari H; Lacy, Gabrielle D; Hufnagel, Robert B; Kumar, Meenakshi M; Koskenvuo, Juha W; Tuupanen, Sari; Durham, Todd; Zhao, Peter Y; Abalem, Maria Fernanda; Andrews, Chris A; Schlegel, Dana; Khan, Naheed W; Fahim, Abigail T; Heckenlively, John R; Musch, David C; Jayasundera, K Thiran