1. Congenital myasthenic syndrome due to DPAGT1 mutations mimicking congenital myopathy in an Irish family. (22nd January 2018) Authors: Bogdanova‐Mihaylova, P.; Murphy, R. P. J.; Alexander, M. D.; McHugh, J. C.; Foley, A. Reghan; Brett, F.; Murphy, S. M. Journal: European journal of neurology Issue: Volume 25:Number 2(2018) Page Start: e22 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Spastic ataxia associated with colour vision deficiency due to DDHD2 mutations. (18th September 2019) Authors: Bogdanova‐Mihaylova, P.; Austin, N.; Alexander, M. D.; Cassidy, L.; Murphy, R. P.; Walsh, R. A.; Murphy, S. M. Journal: European journal of neurology Issue: Volume 27:Number 1(2020) Page Start: e9 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The future of digital dermatology. (1st June 2021) Authors: Alexander, M. D. Journal: Clinical and experimental dermatology Issue: Volume 46:Number 4(2021) Page Start: 740 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The future of digital dermatology. (9th January 2021) Authors: Alexander, M. D. Journal: Clinical and experimental dermatology Issue: Volume 46:Number 4(2021) Page Start: 740 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗