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

Impact of Race on the Outcomes of Retinoblastoma Treated With Primary Enucleation: A Global Study of 1426 Patients

种族对视网膜母细胞瘤原发性眼球摘除术治疗结果的影响:一项纳入1426例患者的全球研究

Kaliki, Swathi; Vempuluru, Vijitha S; Ahmad, Alia; Berry, Jesse L; Diaz-Coronado, Rosdali; Eiger-Moscovich, Maya; Fabian, Ido Didi; Grossniklaus, Hans; Baker Hubbard, G 3rd; Mohammad, Mona; Pe'er, Jacob; Reddy, M Ashwin; Sagoo, Mandeep S; Shields, Carol L; Staffieri, Sandra E; Tanabe, Mika; Ushakova, Tatiana; Yousef, Yacoub A

Leber Hereditary Optic Neuropathy: Support, Genetic Prediction and Accurate Genetic Counselling Enhance Family Planning Choices

莱伯遗传性视神经病变:支持、基因预测和精准的基因咨询增强了家庭计划的选择

Kearns, Lisa S; Staffieri, Sandra E; Mackey, David A

Building capacity to treat childhood cancer in Papua New Guinea: 'It's a multidisciplinary village'

在巴布亚新几内亚建立儿童癌症治疗能力:“这是一个多学科协作的村庄”

Raj, Trisha A Soosay; Harrison, Jayne; Wakefield, Claire E; Daur, Benjamin; Felmingham, Ben; Casey, Michele; McLoone, Jordana K; Sullivan, Michael; Staffieri, Sandra E; Anga, Gwenda

Adherence to the recommended diabetic retinopathy screening guidelines in pregnant women with pregestational diabetes: a cross-sectional survey study

妊娠前糖尿病孕妇对推荐的糖尿病视网膜病变筛查指南的依从性:一项横断面调查研究

Widyaputri, Felicia; Rogers, Sophie L; Nankervis, Alison J; Conn, Jennifer J; Shub, Alexis; Staffieri, Sandra E; Sasongko, Muhammad B; Fagan, Xavier J; Symons, Robert C A; Lim, Lyndell L

At the epicentre: a qualitative study of how parents of a child with de novo retinoblastoma experience the diagnostic process and primary treatment

聚焦中心:一项关于患有新生视网膜母细胞瘤的儿童的父母如何体验诊断过程和初步治疗的定性研究

Lou, Stina; Carstensen, Kathrine; Mikkelsen, Pernille Aakjær; Jensen, Peter Skov; Høgild, Morten Lyng; Christensen, Rasmus Thøger; Overgaard, Jens; Urbak, Steen Fiil; Staffieri, Sandra E; Gregersen, Pernille Axél

HIGH-RISK HISTOPATHOLOGICAL FEATURES OF RETINOBLASTOMA FOLLOWING PRIMARY ENUCLEATION: A Global Study Of 1,426 Patients From 5 Continents

原发性眼球摘除术后视网膜母细胞瘤的高危组织病理学特征:一项来自五大洲1426例患者的全球研究

Kaliki, Swathi; Vempuluru, Vijitha S; Bakal, Komal Rajendra; Dorji, Samten; Tanna, Vishakha; Shields, Charlotte N; Fallon, Samuel J; Raval, Vishal; Ahmad, Alia; Mushtaq, Asma; Hussain, Mahvish; Yousef, Yacoub A; Mohammad, Mona; Roy, Soma Rani; Huque, Fahmida; Tatiana, Ushakova; Yuri, Serov; Vladimir, Polyakov; Zambrano, Sandro Casavilca; Alarcón-León, Sandra; Valdiviezo-Zapata, Cinthya; Vargas-Martorellet, Maria; Gutierrez-Chira, Cynthia; Buitrago, Mario; Ortiz, Joana Sánchez; Diaz-Coronado, Rosdali; Tripathy, Devjyoti; Rath, Suryasnata; Patil, Gaurav; Berry, Jesse L; Pike, Sarah; Brown, Brianne; Tanabe, Mika; Frenkel, Shahar; Eiger-Moscovich, Maya; Pe'er, Jacob; Shields, Carol L; Eagle, Ralph C Jr; Laiton, Andrea; Velasco, Ana Maria; Vega, Katherine; DeSimone, Joseph; Bejjanki, Kavya Madhuri; Kapoor, Anasua Ganguly; Venkataraman, Anusha; Bryant, Victoria; Reddy, M Ashwin; Sagoo, Mandeep S; Hubbard, G Baker 3rd; Azarcon, Corrina P; Olson, Thomas A; Grossniklaus, Hans; Rolfe, Olivia; Staffieri, Sandra E; O'Day, Roderick; Mathew, Anu A; Elder, James E; McKenzie, John D; Fabian, Ido Didi; Shemesh, Rachel; Vishnevskia-Dai, Vicktoria; Ali, Mohammed Hasnat; Jakati, Saumya; Mishra, Dilip K; Palkonda, Vijay Anand Reddy

Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?

莱伯遗传性视神经病变的患病风险和外显率真的低吗?

Mackey, David A; Ong, Jue-Sheng; MacGregor, Stuart; Whiteman, David C; Craig, Jamie E; Lopez Sanchez, M Isabel G; Kearns, Lisa S; Staffieri, Sandra E; Clarke, Linda; McGuinness, Myra B; Meteoukki, Wafaa; Samuel, Sona; Ruddle, Jonathan B; Chen, Celia; Fraser, Clare L; Harrison, John; Howell, Neil; Hewitt, Alex W

Danish heritable retinoblastoma survivors' perspectives on reproductive choices: "It's important for me, not to pass on this condition"

丹麦遗传性视网膜母细胞瘤幸存者对生育选择的看法:“对我来说,重要的是不要把这种疾病遗传给下一代”

Gregersen, Pernille A; Funding, Mikkel; Alsner, Jan; Olsen, Maja H; Overgaard, Jens; Urbak, Steen F; Staffieri, Sandra E; Lou, Stina

Quality of life in children with glaucoma: a qualitative interview study in Australia

澳大利亚青光眼儿童的生活质量:一项定性访谈研究

Knight, Lachlan S W; Ridge, Bronwyn; Staffieri, Sandra E; Craig, Jamie E; Prem Senthil, Mallika; Souzeau, Emmanuelle

Pathogenic genetic variants identified in Australian families with paediatric cataract

在澳大利亚患有儿童白内障的家族中发现了致病性基因变异

Jones, Johanna L; McComish, Bennet J; Staffieri, Sandra E; Souzeau, Emmanuelle; Kearns, Lisa S; Elder, James E; Charlesworth, Jac C; Mackey, David A; Ruddle, Jonathan B; Taranath, Deepa; Pater, John; Casey, Theresa; Craig, Jamie E; Burdon, Kathryn P