Akın Nihat (Akin Nihat)

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 6

Top Topics

Endothelial Cells

Amyotrophic Lateral Sclerosis

Top Venues

Journal of neurology, neurosurgery, and psychiatry

Genome medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Akın Nihat, Janice M Ranson, Dominique Harris, Kirsty McNiven, TzeHow Mok, Peter Rudge, John Collinge, David J Llewellyn, Simon Mead
Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease. Brain communications 4 (4) (2022)
Akın Nihat, Tze How Mok, Hans Odd, Andrew Geoffrey Bourne Thompson, Diana Caine, Kirsty McNiven, Veronica O'Donnell, Selam Tesfamichael, Peter Rudge, John Collinge, Simon Mead
Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease. Journal of neurology, neurosurgery, and psychiatry 93 (4) (2022)
Andrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, Ines Whitworth, Annapurna Nayak, Akın Nihat, Tze How Mok, Peter Rudge, Jonathan D F Wadsworth, Jonathan Rohrer, Jonathan M Schott, Amanda Heslegrave, Henrik Zetterberg, John Collinge, Graham S Jackson, Simon Mead
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases. Molecular psychiatry (2021)
Emmanuel A Asante, Jacqueline M Linehan, Andrew Tomlinson, Tatiana Jakubcova, Shyma Hamdan, Andrew Grimshaw, Michelle Smidak, Asif Jeelani, Akın Nihat, Simon Mead, Sebastian Brandner, Jonathan D F Wadsworth, John Collinge
Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS. PLoS biology 18 (6) (2020)
Akın Nihat, Simon Mead
Detection of Creutzfeldt-Jakob disease prions in skin: implications for healthcare. Genome medicine 10 (1) (2018)
Diana Caine, Akın Nihat, Philippa Crabb, Peter Rudge, Lisa Cipolotti, John Collinge, Simon Mead
The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature. PloS one 13 (1) (2018)