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

PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker features.

PRNP E146G 突变遗传性朊病毒病:独特的临床、病理和体液生物标志物特征

Coysh Thomas, Jaunmuktane Zane, Hosszu Laszlo L P, Majbour Nour, Zhang Fuquan, Campbell Tracy, Darwent Lee, Matus Marcelo Barria, Chan Edgar, Holm-Mercer Leah, Mok Tze How, Wadsworth Jonathan D F, Bieschke Jan, Nithi Kannan, Brandner Sebastian, Smith Colin, Esiri Margaret, Collinge John, Mead Simon

Inherited prion disease caused by a novel frameshift mutation of PRNP resulting in protein truncation at codon 157

由PRNP基因新型移码突变引起的遗传性朊病毒病,导致第157位密码子处蛋白质截断。

Holm-Mercer, Leah; Mok, Tze How; Sequeira, Danielle; Coysh, Thomas; Rudge, Peter; Ramadan, Hawraman; Darwent, Lee; Campbell, Tracy; Murphy, Thomas; Smith, Colin; Ritchie, Diane; Brandner, Sebastian; Jaunmuktane, Zane; Collinge, John; Mead, Simon

Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort Study

朊病毒病运动障碍的患病率和治疗:一项纵向队列研究

Sequeira, Danielle; Nihat, Akin; Mok, Tzehow; Coysh, Thomas; Rudge, Peter; Collinge, John; Mead, Simon

The Future of Seed Amplification Assays and Clinical Trials

种子扩增检测和临床试验的未来

Coysh, Thomas; Mead, Simon

A nationwide analysis of successful litigation claims in neurological practice

一项针对神经科诊疗实践中成功诉讼案例的全国性分析

Coysh, Thomas; Breen, David P