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

The TransEuro open-label trial of human fetal ventral mesencephalic transplantation in patients with moderate Parkinson's disease

TransEuro 是一项开放标签试验,旨在研究人类胎儿腹侧中脑移植治疗中度帕金森病患者的疗效。

Barker, Roger A; Lao-Kaim, Nicholas P; Guzman, Natalie Valle; Athauda, Dilan; Bjartmarz, Hjalmar; Björklund, Anders; Church, Alistair; Cutting, Emma; Daft, Danielle; Dayal, Viswas; Dunnett, Stephen; Evans, Amy; Grealish, Shane; Hannaway, Naomi; He, Xiaoling; Hewitt, Sam; Kefalopoulou, Zinovia; Mahlknecht, Philipp; Martín-Bastida, Antonio; Farrell, Krista; Moore, Sarah; Bulstrode, Harry; Nakornchai, Tagore; Nelander-Wahlestedt, Jenny; Roupé, Linnea; Paul, Gesine; Peall, Kathryn; Rosser, Anne; Roca-Fernández, Adriana; Rowlands, Sophie; McGorrian, Anne-Marie; Scherf, Caroline; Vinh, Ngoc Nga; Roberton, Victoria; Kelly, Claire; Lelos, Mariah; Torres, Eduardo; Shires, Kate; Hills, Rachel; Williams, Debbie; Roussakis, Andreas-Antonios; Sibley, Krista; Tyers, Pamela; Wijeyekoon, Ruwani; Williams-Gray, Caroline; Foltynie, Thomas; Piccini, Paola; Morris, Robert; Lazic, Stanley E; Lindvall, Olle; Parmar, Malin; Widner, Hakan

Coronary Artery Calcification on Non-Cardiac Gated CT Thorax Scans: A Single Tertiary Centre Retrospective Observational Study

非心脏门控胸部CT扫描中冠状动脉钙化:一项单中心回顾性观察研究

Doyle, Robert S; Jain, Divyanshu; Devitt, Patrick; Hartnett, Jack; Temperley, Hugo C; McGorrian, Catherine

MiR-93-5p is a novel predictor of coronary in-stent restenosis

miR-93-5p是冠状动脉支架内再狭窄的新型预测因子

O'Sullivan, John F; Neylon, Antoinette; Fahy, Eoin F; Yang, Pengyi; McGorrian, Catherine; Blake, Gavin J

Transitioning high sensitivity cardiac troponin I (hs-cTnI) into routine diagnostic use: More than just a sensitivity issue

将高敏性心肌肌钙蛋白 I (hs-cTnI) 转化为常规诊断用途:不仅仅是敏感性问题

Graham R Lee, Tara Ca Browne, Berna Guest, Imran Khan, Eamon Murphy, Catherine McGorrian, Niall G Mahon, Maria C Fitzgibbon

NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment

NAA10 突变导致一种新型智力障碍综合征,因 N 端乙酰转移酶受损而出现 QT 间期延长

Jillian P Casey, Svein I Støve, Catherine McGorrian, Joseph Galvin, Marina Blenski, Aimee Dunne, Sean Ennis, Francesca Brett, Mary D King, Thomas Arnesen, Sally Ann Lynch

Getting to the heart of cardiac remodeling; how collagen subtypes may contribute to phenotype

了解心脏重塑的核心;胶原蛋白亚型如何影响表型

P Collier, C J Watson, M H van Es, D Phelan, C McGorrian, M Tolan, M T Ledwidge, K M McDonald, J A Baugh

Clinical and myopathological characteristics of desminopathy caused by a mutation in desmin tail domain

由结蛋白尾部结构域突变引起的结蛋白病的临床和肌病理学特征

Maddison, Paul; Damian, Maxwell S; Sewry, Caroline; McGorrian, Catherine; Winer, John B; Odgerel, Zagaa; Shatunov, Alexey; Lee, Hee Suk; Goldfarb, Lev G