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

High-Level Alzheimer Disease Neuropathological Change Following Iatrogenic Exposure

医源性暴露后阿尔茨海默病高水平神经病理学改变

Banerjee, Gargi; Mok, Tze How; Hyare, Harpreet; Cousins, Oliver; Jaunmuktane, Zane; Mead, Simon; Collinge, John

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

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

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。

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

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

Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease

有患朊病毒病风险的个体的种子扩增和神经退行性标志物轨迹

Tze How Mok, Akin Nihat, Nour Majbour, Danielle Sequeira, Leah Holm-Mercer, Thomas Coysh, Lee Darwent, Mark Batchelor, Bradley R Groveman, Christina D Orr, Andrew G Hughson, Amanda Heslegrave, Rhiannon Laban, Elena Veleva, Ross W Paterson, Ashvini Keshavan, Jonathan M Schott, Imogen J Swift, Carolin

Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease

开发用于测量克雅氏病疾病严重程度的新型临床检查量表

Nihat, Akin; Mok, Tze How; Odd, Hans; Thompson, Andrew Geoffrey Bourne; Caine, Diana; McNiven, Kirsty; O'Donnell, Veronica; Tesfamichael, Selam; Rudge, Peter; Collinge, John; Mead, Simon

Assessing initial MRI reports for suspected CJD patients

评估疑似克雅氏病患者的初始MRI报告

Jesuthasan, Aaron; Sequeira, Danielle; Hyare, Harpreet; Odd, Hans; Rudge, Peter; Mok, Tze How; Nihat, Akin; Collinge, John; Mead, Simon

Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases

对人类朊病毒疾病12年临床队列中血浆tau蛋白和神经丝轻链生物标志物的评估

Thompson, Andrew G B; Anastasiadis, Prodromos; Druyeh, Ronald; Whitworth, Ines; Nayak, Annapurna; Nihat, Akin; Mok, Tze How; Rudge, Peter; Wadsworth, Jonathan D F; Rohrer, Jonathan; Schott, Jonathan M; Heslegrave, Amanda; Zetterberg, Henrik; Collinge, John; Jackson, Graham S; Mead, Simon

NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease Progression

NT1-Tau在克雅氏病患者的脑脊液和血浆中升高,且与疾病进展相关

Mengel, David; Mok, Tze How; Nihat, Akin; Liu, Wen; Rissman, Robert A; Galasko, Douglas; Zetterberg, Henrik; Mead, Simon; Collinge, John; Walsh, Dominic M