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

Familial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated Cholesterol

家族性高胆固醇血症变异型与高胆固醇患者的心血管风险

Zhang, Yiyi; Dron, Jacqueline S; Bellows, Brandon K; Khera, Amit V; Liu, Junxiu; Balte, Pallavi P; Oelsner, Elizabeth C; Amr, Sami Samir; Lebo, Matthew S; Nagy, Anna; Peloso, Gina M; Natarajan, Pradeep; Rotter, Jerome I; Willer, Cristen; Boerwinkle, Eric; Ballantyne, Christie M; Lutsey, Pamela L; Fornage, Myriam; Lloyd-Jones, Donald M; Hou, Lifang; Psaty, Bruce M; Bis, Joshua C; Floyd, James S; Vasan, Ramachandran S; Heard-Costa, Nancy L; Carson, April P; Hall, Michael E; Rich, Stephen S; Guo, Xiuqing; Kazi, Dhruv S; de Ferranti, Sarah D; Moran, Andrew E

Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease

严重高胆固醇血症和家族性高胆固醇血症基因型与冠心病风险的关联

Zhang, Yiyi; Dron, Jacqueline S; Bellows, Brandon K; Khera, Amit V; Liu, Junxiu; Balte, Pallavi P; Oelsner, Elizabeth C; Amr, Sami Samir; Lebo, Matthew S; Nagy, Anna; Peloso, Gina M; Natarajan, Pradeep; Rotter, Jerome I; Willer, Cristen; Boerwinkle, Eric; Ballantyne, Christie M; Lutsey, Pamela L; Fornage, Myriam; Lloyd-Jones, Donald M; Hou, Lifang; Psaty, Bruce M; Bis, Joshua C; Floyd, James S; Vasan, Ramachandran S; Heard-Costa, Nancy L; Carson, April P; Hall, Michael E; Rich, Stephen S; Guo, Xiuqing; Kazi, Dhruv S; de Ferranti, Sarah D; Moran, Andrew E

Development, implementation, and evaluation of a competency-based didactic and simulation-focused boot camp for incoming urology residents: Report of the first three years

针对泌尿外科新住院医师,开发、实施和评估以能力为导向的教学和模拟训练营:前三年报告

Wang, Yuding; Hoogenes, Jen; Clark, Roderick; Wong, Nathan C; Blankstein, Udi; Randhawa, Harkanwal; Lovatt, Catherine; Kim, Kevin; Stern, Noah; Law, Jeffrey; Sami, Samir; Uy, Michael; Moore, Courtney; Shayegan, Bobby; Kapoor, Anil; Lambe, Shahid; Davies, Timothy; Dave, Sumit; Sener, Alp; Matsumoto, Edward D

A Novel Variant in the TBC1D24 Lipid-Binding Pocket Causes Autosomal Dominant Hearing Loss: Evidence for a Genotype-Phenotype Correlation

TBC1D24脂质结合口袋中的一种新型变异导致常染色体显性遗传性听力损失:基因型-表型相关性的证据

Parzefall, Thomas; Frohne, Alexandra; Koenighofer, Martin; Neesen, Juergen; Laccone, Franco; Eckl-Dorna, Julia; Waters, Jonathan J; Schreiner, Markus; Amr, Sami Samir; Ashton, Emma; Schoefer, Christian; Gstœttner, Wolfgang; Frei, Klemens; Lucas, Trevor

Histopathology of the Inner Ear in Charcot-Marie-Tooth Syndrome Caused by a Missense Variant (p.Thr65Ala) in the MPZ Gene

MPZ 基因错义变异 (p.Thr65Ala) 导致的 Charcot-Marie-Tooth 综合征的内耳组织病理学

Joseph B Nadol Jr, E Tessa Hedley-Whyte, Sami Samir Amr, Jennifer T O Apos Malley, Takefumi Kamakura