Akin Nihat

33 Cleveland Street, W1W 7FF
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 20 publications

A scalable, dividing cell model for the robust propagation and quantification of human sporadic Creutzfeldt-Jakob disease prions.

A scalable, dividing cell model for the robust propagation and quantification of human sporadic Creutzfeldt-Jakob disease prions.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: June 30, 2026

Strain-specific propagation of variant Creutzfeldt-Jakob disease prions in humanized neural cells.

Strain-specific propagation of variant Creutzfeldt-Jakob disease prions in humanized neural cells.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: June 11, 2026

Letter to the Editor Regarding Kortazar-Zubizarreta et al. 'The Risk of Transmission of Genetic Prion Diseases Is Greater Than 50%'.

Letter to the Editor Regarding Kortazar-Zubizarreta et al. 'The Risk of Transmission of Genetic Prion Diseases Is Greater Than 50%'.

Journal: European journal of neurology

Published: January 18, 2026

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

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

Journal: Brain : a journal of neurology

Published: November 09, 2022

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

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

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: March 24, 2022

Assessing initial MRI reports for suspected CJD patients.

Assessing initial MRI reports for suspected CJD patients.

Journal: Journal of neurology

Published: January 08, 2022

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

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

Journal: Cells

Published: November 10, 2021

Prion protein monoclonal antibody (PRN100) therapy for Creutzfeldt-Jakob disease: evaluation of a first-in-human treatment programme.

Prion protein monoclonal antibody (PRN100) therapy for Creutzfeldt-Jakob disease: evaluation of a first-in-human treatment programme.

Journal: The Lancet. Neurology

Published: October 22, 2021

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

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

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: August 29, 2021

Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases.

Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases.

Journal: Scientific reports

Published: August 10, 2020

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

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

Journal: Molecular psychiatry

Published: July 27, 2020

Cognitive decline heralds onset of symptomatic inherited prion disease.

Cognitive decline heralds onset of symptomatic inherited prion disease.

Journal: Brain : a journal of neurology

Published: June 19, 2020

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Last Updated: 09/26/2026