Willie Stewart

Cauda equina lymphoma – a rare presentation of primary central nervous system lymphoma: case report and literature review

C. Mathieson, M. Teo, R. Carruthers, 2012, British journal of neurosurgery.

ECEL 1 gene related contractural syndrome : long-term follow-up and update on clinical and pathological aspects

F. Muntoni, A. Manzur, M. Farrugia, 2018 .

Two recurrent mutations are associated with GNE myopathy in the North of Britain

K. Bushby, P. Chinnery, Hanns Lochmüller, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

A Cancer Research UK First Time in Human Phase I Trial of IMA950 (Novel Multipeptide Therapeutic Vaccine) in Patients with Newly Diagnosed Glioblastoma

O. Schoor, S. Halford, C. Twelves, 2016, Clinical Cancer Research.

Mutation Update and Genotype–Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies

E. Bertini, K. Pelin, E. Mercuri, 2014, Human mutation.

Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: an important cause of stroke in young people

C. Santosh, J. Goodfellow, K. Dani, 2012, Postgraduate Medical Journal.

The phenotypic and genotypic features of a Scottish cohort with McArdle disease

M. Farrugia, R. Quinlivan, V. Straub, 2021, Neuromuscular Disorders.

The validity of EORTC GBM prognostic calculator on survival of GBM patients in the West of Scotland

J. Paul, M. Teo, B. Clark, 2014, British journal of neurosurgery.

A survival analysis of GBM patients in the West of Scotland pre- and post-introduction of the Stupp regime

J. Paul, M. Teo, B. Clark, 2014, British journal of neurosurgery.