1. Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot–Marie–Tooth type 1 patients. (19th April 2013) Authors: Koutsis, G; Pandraud, A; Karadima, G; Panas, M; Reilly, MM; Floroskufi, P; Wood, NW; Houlden, H Journal: Clinical genetics Issue: Volume 83:Number 4(2013:Apr.) Page Start: 388 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Spinal muscular atrophy, Dandy-Walker complex, and cataracts in two siblings: a new entity?. Issue 8 (15th July 2005) Authors: Panas, M; Spengos, K; Tsivgoulis, G; Kalfakis, N; Sfagos, C; Vassilopoulos, D; Markomichelakis, N Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 76:Issue 8(2005) Page Start: 1183 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot–Marie–Tooth type 1 patients. (5th July 2012) Authors: Koutsis, G; Pandraud, A; Karadima, G; Panas, M; Reilly, MM; Floroskufi, P; Wood, NW; Houlden, H Journal: Clinical genetics Issue: Volume 83:Number 4(2013:Apr.) Page Start: 388 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗