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Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Tze How Mok

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Neurobiology of Aging|June 5, 2018

Evaluating the causality of novel sequence variants in the prion protein gene by exampleTze How Mok, Carolin Koriath, Zane Jaunmuktane, et al.

Viruses|September 28, 2021

Characterization of Prion Disease Associated with a Two-Octapeptide Repeat InsertionNicholas Brennecke, Ignazio Cali, Tze How Mok, et al.

Molecular Psychiatry|March 6, 2021

Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.

Neurology|July 13, 2026

Performance of Alzheimer Disease Plasma Biomarkers in Patients With Prion DiseasesThomas Coysh, Rhiannon Laban, Elena Veleva, et al.

Journal of Neurogenetics|January 10, 2025

The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's diseaseLeah Holm-Mercer, Thomas Coysh, Tze How Mok, et al.

Journal of Neurology|March 29, 2025

PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker featuresThomas Coysh, Zane Jaunmuktane, Laszlo L P Hosszu, et al.

Neuroimage. Clinical|November 18, 2019

Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian processLiane S Canas, Carole H Sudre, Enrico De Vita, et al.

JAMA Neurology|February 24, 2016

Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob DiseaseSimon Mead, Matthew Burnell, Jessica Lowe, et al.

Brain : a Journal of Neurology|March 28, 2023

Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion diseaseTze How Mok, Akin Nihat, Nour Majbour, et al.

The Lancet. Neurology|September 19, 2020

Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association studyEmma Jones, Holger Hummerich, Emmanuelle Viré, et al.

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Search research articles

Showing results (11-20 of 20) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 20 results.

Neurobiology of Aging|June 5, 2018

Evaluating the causality of novel sequence variants in the prion protein gene by exampleTze How Mok, Carolin Koriath, Zane Jaunmuktane, et al.

Viruses|September 28, 2021

Characterization of Prion Disease Associated with a Two-Octapeptide Repeat InsertionNicholas Brennecke, Ignazio Cali, Tze How Mok, et al.

Molecular Psychiatry|March 6, 2021

Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.

Neurology|July 13, 2026

Performance of Alzheimer Disease Plasma Biomarkers in Patients With Prion DiseasesThomas Coysh, Rhiannon Laban, Elena Veleva, et al.

Journal of Neurogenetics|January 10, 2025

The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's diseaseLeah Holm-Mercer, Thomas Coysh, Tze How Mok, et al.

Journal of Neurology|March 29, 2025

PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker featuresThomas Coysh, Zane Jaunmuktane, Laszlo L P Hosszu, et al.

Neuroimage. Clinical|November 18, 2019

Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian processLiane S Canas, Carole H Sudre, Enrico De Vita, et al.

JAMA Neurology|February 24, 2016

Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob DiseaseSimon Mead, Matthew Burnell, Jessica Lowe, et al.

Brain : a Journal of Neurology|March 28, 2023

Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion diseaseTze How Mok, Akin Nihat, Nour Majbour, et al.

The Lancet. Neurology|September 19, 2020

Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association studyEmma Jones, Holger Hummerich, Emmanuelle Viré, et al.

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