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Journal of the Neurological Sciences|October 15, 2005
Minimum prevalence of spinocerebellar ataxia 17 in the north east of EnglandKate Craig, Sharon M Keers, Timothy J Walls, et al.Annals of Neurology|September 5, 2002
Normokalemic periodic paralysis revisited: does it exist?Patrick F Chinnery, Timothy J Walls, Michael G Hanna, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Spectrum of movement disorders in neuroferritinopathyDouglas E Crompton, Patrick F Chinnery, David Bates, et al.Annals of Neurology|December 17, 2005
Motor neuron disease in a patient with a mitochondrial tRNAIle mutationGillian M Borthwick, Robert W Taylor, Timothy J Walls, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 2013
Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1Sarah Finlayson, Jacqueline Palace, Katsiaryna Belaya, et al.American Journal of Human Genetics|June 30, 2012
Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregatesKatsiaryna Belaya, Sarah Finlayson, Clarke R Slater, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 6, 2016
Clinical features of the myasthenic syndrome arising from mutations in GMPPBPedro M Rodríguez Cruz, Katsiaryna Belaya, Keivan Basiri, et al.Brain : a Journal of Neurology|July 3, 2015
Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathiesKatsiaryna Belaya, Pedro M Rodríguez Cruz, Wei Wei Liu, et al.Pageof 1