1. B48 DNA repair pathways as a common genetic mechanism modulating the age at onset in polyglutamine diseases. (13th September 2016) Authors: Bettencourt, Conceição; Moss, Davina Hensman; Flower, Michael; Wiethoff, Sarah; Brice, Alexis; Goizet, Cyril; Stevanin, Giovanni; Koutsis, Georgios; Karadima, Georgia; Panas, Marios; Yescas-Gómez, Petra; García-Velázquez, Lizbeth Esmeralda; Alonso-Vilatela, María Elisa; Lima, Manuela; Raposo, Maf... Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87(2016)Supplement 1 Page Start: A26 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases. Issue 6 (6th May 2016) Authors: Bettencourt, Conceição; Hensman‐Moss, Davina; Flower, Michael; Wiethoff, Sarah; Brice, Alexis; Goizet, Cyril; Stevanin, Giovanni; Koutsis, Georgios; Karadima, Georgia; Panas, Marios; Yescas‐Gómez, Petra; García‐Velázquez, Lizbeth Esmeralda; Alonso‐Vilatela, María Elisa; Lima, Manuela; Raposo, Maf... Journal: Annals of neurology Issue: Volume 79:Issue 6(2016:Jun.) Page Start: 983 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Elevated Serum α-Synuclein Levels in Huntington's Disease Patients. (1st April 2020) Authors: Breza, Marianthi; Emmanouilidou, Evangelia; Leandrou, Emmanouela; Kartanou, Chrisoula; Bougea, Anastasia; Panas, Marios; Stefanis, Leonidas; Karadima, Georgia; Vekrellis, Kostas; Koutsis, Georgios Journal: Neuroscience Issue: Volume 431(2020) Page Start: 34 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Evidence for Cognitive Deficits in X-Linked Charcot-Marie-Tooth Disease. (17th March 2020) Authors: Kasselimis, Dimitrios; Karadima, Georgia; Angelopoulou, Georgia; Breza, Marianthi; Tsolakopoulos, Dimitrios; Potagas, Constantin; Panas, Marios; Koutsis, Georgios Journal: Journal of the International Neuropsychological Society Issue: Volume 26:Number 3(2020) Page Start: 294 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. From Mild Ataxia to Huntington Disease Phenocopy: The Multiple Faces of Spinocerebellar Ataxia 17. (2nd October 2014) Authors: Koutsis, Georgios; Panas, Marios; Paraskevas, George P.; Bougea, Anastasia M.; Kladi, Athina; Karadima, Georgia; Kapaki, Elisabeth Other Names: Koide Reiji Academic Editor. Journal: Case reports in neurological medicine Issue: Volume 2014(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. HINT1‐related neuropathy in Greek patients with Charcot‐Marie‐Tooth disease. Issue 4 (29th October 2021) Authors: Kontogeorgiou, Zoi; Voudommatis, Charalampos; Kartanou, Chrisoula; Pandis, Dionysis; Breza, Marianthi; Zambelis, Thomas; Stefanis, Leonidas; Panas, Marios; Koutsis, Georgios; Karadima, Georgia Journal: Journal of the peripheral nervous system Issue: Volume 26:Issue 4(2021) Page Start: 444 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. J4 Huntington's disease in the greek population: 21 years of clinical assessment and genetic testing at a national reference centre. (13th September 2016) Authors: Koutsis, Georgios; Karadima, Georgia; Kladi, Athina; Breza, Marianthi; Kartanou, Chrisoula; Panas, Marios Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87(2016)Supplement 1 Page Start: A76 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mutational analysis of Greek patients with suspected hereditary neuropathy with liability to pressure palsies (HNPP): a 15‐year experience. Issue 2 (June 2015) Authors: Karadima, Georgia; Koutsis, Georgios; Raftopoulou, Maria; Karletidi, Karolina‐Maria; Zambelis, Thomas; Karandreas, Nikolaos; Panas, Marios Journal: Journal of the peripheral nervous system Issue: Volume 20:Issue 2(2015) Page Start: 79 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Relapsing Remitting Multiple Sclerosis in X-Linked Charcot-Marie-Tooth Disease with Central Nervous System Involvement. (25th March 2015) Authors: Koutsis, Georgios; Karadima, Georgia; Floroskoufi, Paraskewi; Raftopoulou, Maria; Panas, Marios Other Names: Toft Mathias Academic Editor. Journal: Case reports in neurological medicine Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Relapsing Remitting Multiple Sclerosis in X-Linked Charcot-Marie-Tooth Disease with Central Nervous System Involvement. (25th March 2015) Authors: Koutsis, Georgios; Karadima, Georgia; Floroskoufi, Paraskewi; Raftopoulou, Maria; Panas, Marios Other Names: Toft Mathias Academic Editor. Journal: Case reports in neurological medicine Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗