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

Urinary albumin/creatinine ratio tertiles predict risk of diabetic retinopathy progression: a natural history study from the Adolescent Cardio-Renal Intervention Trial (AdDIT) observational cohort

尿白蛋白/肌酐比值三分位数可预测糖尿病视网膜病变进展风险:一项来自青少年心肾干预试验(AdDIT)观察队列的自然史研究

Benitez-Aguirre, Paul Z; Marcovecchio, M Loredana; Chiesa, Scott T; Craig, Maria E; Wong, Tien Y; Davis, Elizabeth A; Cotterill, Andrew; Couper, Jenny J; Cameron, Fergus J; Mahmud, Farid H; Neil, H Andrew W; Jones, Timothy W; Hodgson, Lauren A B; Dalton, R Neil; Marshall, Sally M; Deanfield, John; Dunger, David B; Donaghue, Kim C

Effect of atorvastatin on glycaemia progression in patients with diabetes: an analysis from the Collaborative Atorvastatin in Diabetes Trial (CARDS)

阿托伐他汀对糖尿病患者血糖进展的影响:来自阿托伐他汀治疗糖尿病协作试验(CARDS)的分析

Livingstone, Shona J; Looker, Helen C; Akbar, Tahira; Betteridge, D John; Durrington, Paul N; Hitman, Graham A; Neil, H Andrew W; Fuller, John H; Colhoun, Helen M

Effect of atorvastatin on C-reactive protein and benefits for cardiovascular disease in patients with type 2 diabetes: analyses from the Collaborative Atorvastatin Diabetes Trial

阿托伐他汀对2型糖尿病患者C反应蛋白的影响及其对心血管疾病的益处:来自阿托伐他汀糖尿病协作试验的分析

Soedamah-Muthu, Sabita S; Livingstone, Shona J; Charlton-Menys, Valentine; Betteridge, D John; Hitman, Graham A; Neil, H Andrew W; Bao, Weihang; DeMicco, David A; Preston, Gregory M; Fuller, John H; Stehouwer, Coen D A; Schalkwijk, Casper G; Durrington, Paul N; Colhoun, Helen M

Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations

对LDLR/APOB/PCSK9突变阴性的家族性高胆固醇血症患者进行全外显子组测序

Futema, Marta; Plagnol, Vincent; Li, KaWah; Whittall, Ros A; Neil, H Andrew W; Seed, Mary; Bertolini, Stefano; Calandra, Sebastiano; Descamps, Olivier S; Graham, Colin A; Hegele, Robert A; Karpe, Fredrik; Durst, Ronen; Leitersdorf, Eran; Lench, Nicholas; Nair, Devaki R; Soran, Handrean; Van Bockxmeer, Frank M; Humphries, Steve E

Analysis of the frequency and spectrum of mutations recognised to cause familial hypercholesterolaemia in routine clinical practice in a UK specialist hospital lipid clinic

对英国一家专科医院脂质诊所常规临床实践中已知的导致家族性高胆固醇血症的突变频率和谱系进行分析

Futema, Marta; Whittall, Ros A; Kiley, Amy; Steel, Louisa K; Cooper, Jackie A; Badmus, Ebele; Leigh, Sarah E; Karpe, Fredrik; Neil, H Andrew W; Humphries, Steve E

Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia

利用靶向外显子测序作为家族性高胆固醇血症的诊断工具

Futema, Marta; Plagnol, Vincent; Whittall, Ros A; Neil, H Andrew W; Humphries, Steve Eric

Normal levels of inflammatory markers in treated patients with familial hypercholesterolaemia: a cross-sectional study.

家族性高胆固醇血症患者接受治疗后炎症标志物水平正常:一项横断面研究

Seed Mary, Betteridge D John, Cooper Jackie, Caslake Muriel, Durrington Paul N, Thompson Gilbert R, Sattar Naveed, Humphries Steve E, Neil H Andrew W