Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Publications

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Dewan R. et al, (2021), Neuron, 109, 448 - 460.e4

To Zoom or Not to Zoom: The Should I Travel Index Revisited during the Coronavirus Disease Pandemic.

Rutkove SB. et al, (2021), Ann Neurol

Efficient homing of antibody-secreting cells to the bone marrow requires RNA-binding protein ZFP36L1

Saveliev A. et al, (2021), Journal of Experimental Medicine, 218

Improving clinical trial outcomes in amyotrophic lateral sclerosis.

Kiernan MC. et al, (2020), Nat Rev Neurol

Characterising neuropsychiatric disorders in patients with COVID-19 - Authors' reply.

Varatharaj A. et al, (2020), Lancet Psychiatry, 7, 934 - 935

Grand rounds: a precious resource to be nurtured.

Ross Russell AL. et al, (2020), Pract Neurol, 20, 342 - 344

Amyotrophic lateral sclerosis with a heterozygous D91A SOD1 variant and classical ALS-TDP neuropathology.

Feneberg E. et al, (2020), Neurology, 95, 595 - 596

An ALS-linked mutation in TDP-43 disrupts normal protein interactions in the motor neuron response to oxidative stress.

Feneberg E. et al, (2020), Neurobiol Dis

Methods for quantitative susceptibility and R2* mapping in whole post-mortem brains at 7T applied to amyotrophic lateral sclerosis.

Wang C. et al, (2020), Neuroimage, 222

Quantitative patterns of motor cortex proteinopathy across ALS genotypes.

Nolan M. et al, (2020), Acta Neuropathol Commun, 8

Reply to: Early white matter changes on diffusion tensor imaging in amyotrophic lateral sclerosis.

Gabel MC. et al, (2020), Ann Clin Transl Neurol, 7, 1266 - 1267

Neurological and neuropsychiatric complications of COVID-19 in 153 patients: a UK-wide surveillance study.

Varatharaj A. et al, (2020), Lancet Psychiatry

Correction of amyotrophic lateral sclerosis related phenotypes in induced pluripotent stem cell-derived motor neurons carrying a hexanucleotide expansion mutation in C9orf72 by CRISPR/Cas9 genome editing using homology-directed repair.

Ababneh NA. et al, (2020), Hum Mol Genet

A Data-Driven Characterisation of the Evolution of White Matter Damage in Amyotrophic Lateral Sclerosis

Leigh P. et al, (2020), NEUROLOGY, 94

Primary lateral sclerosis: diagnosis and management.

Turner MR. and Talbot K., (2020), Pract Neurol

Dynamic Post-Transcriptional Events Governing CD8+ T Cell Homeostasis and Effector Function

Salerno F. et al, (2020), Trends in Immunology, 41, 240 - 254

Occasional essay: Upper motor neuron syndrome in amyotrophic lateral sclerosis.

Swash M. et al, (2020), J Neurol Neurosurg Psychiatry, 91, 227 - 234

The Duty to Look for Incidental Findings in Imaging Research.

Koplin JJ. et al, (2020), Ethics Hum Res, 42, 2 - 12

Polypyrimidine tract-binding proteins are essential for B cell development

Monzón-Casanova E. et al, (2020), eLife, 9

Primary lateral sclerosis: consensus diagnostic criteria.

Turner MR. et al, (2020), J Neurol Neurosurg Psychiatry

Load More

1
2
3
4
5
6
7
...
»

Include forthcoming?