1. CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis. Issue 8 (27th November 2014) Authors: Fridman, V; Bundy, B; Reilly, M M; Pareyson, D; Bacon, C; Burns, J; Day, J; Feely, S; Finkel, R S; Grider, T; Kirk, C A; Herrmann, D N; Laurá, M; Li, J; Lloyd, T; Sumner, C J; Muntoni, F; Piscosquito, G; Ramchandren, S; Shy, R Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 86:Issue 8(2015) Page Start: 873 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families. Issue 1 (1st July 1997) Authors: Uziel, G; Moroni, I; Lamantea, E; Fratta, G M; Ciceri, E; Carrara, F; Zeviani, M Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 63:Issue 1(1997) Page Start: 16 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗