Items where authors include "Hewamadduma, C.A."

Article

Hewamadduma, C.A., Hoggard, N. orcid.org/0000-0002-6447-7639, O'Malley, R. et al. (13 more authors) (2018) Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations. Neurology Genetics, 4 (6). e279.

Proceedings Paper

Hewamadduma, C.A., Omalley, R., Robinson, M. et al. (7 more authors) (2017) Mutations in SPG7 as an important cause of spastic-ataxia in a large british cohort: Hybrid phenotype helps direct screening. In: Journal of the Neurological Sciences. World Congress of Neurology (WCN 2017), 16-21 Sep 2017, Kyoto, Japan. Elsevier , pp. 304-305.