1. A novel mutation deep within intron 7 of the GBA gene causes Gaucher disease. Issue 3 (14th January 2020) Authors: Malekkou, Anna; Sevastou, Ioanna; Mavrikiou, Gavriella; Georgiou, Theodoros; Vilageliu, Lluisa; Moraitou, Marina; Michelakakis, Helen; Prokopiou, Chrystalla; Drousiotou, Anthi Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 3(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Alpha-synuclein dimerization in erythrocytes of patients with genetic and non-genetic forms of Parkinson's Disease. (13th April 2018) Authors: Papagiannakis, Nikolaos; Koros, Christos; Stamelou, Maria; Simitsi, Athina-Maria; Maniati, Matina; Antonelou, Roubina; Papadimitriou, Dimitra; Dermentzaki, Georgia; Moraitou, Marina; Michelakakis, Helen; Stefanis, Leonidas Journal: Neuroscience letters Issue: Volume 672(2018) Page Start: 145 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Circulating Brain‐Enriched MicroRNAs for Detection and Discrimination of Idiopathic and Genetic Parkinson's Disease. Issue 3 (4th December 2019) Authors: Ravanidis, Stylianos; Bougea, Anastasia; Papagiannakis, Nikolaos; Maniati, Matina; Koros, Christos; Simitsi, Athina‐Maria; Bozi, Maria; Pachi, Ioanna; Stamelou, Maria; Paraskevas, George P.; Kapaki, Elisabeth; Moraitou, Marina; Michelakakis, Helen; Stefanis, Leonidas; Doxakis, Epaminondas Journal: Movement disorders Issue: Volume 35:Issue 3(2020) Page Start: 457 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Lysosomal alterations in peripheral blood mononuclear cells of Parkinson's disease patients. Issue 13 (November 2015) Authors: Papagiannakis, Nikolaos; Xilouri, Maria; Koros, Christos; Stamelou, Maria; Antonelou, Roubina; Maniati, Matina; Papadimitriou, Dimitra; Moraitou, Marina; Michelakakis, Helen; Stefanis, Leonidas Journal: Movement disorders Issue: Volume 30:Issue 13(2015) Page Start: 1830 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Synergistic use of glycomics and single‐molecule molecular inversion probes for identification of congenital disorders of glycosylation type‐1. Issue 4 (28th March 2022) Authors: Abu Bakar, Nurulamin; Ashikov, Angel; Brum, Jaime Moritz; Smeets, Roel; Kersten, Marjan; Huijben, Karin; Keng, Wee Teik; Speck‐Martins, Carlos Eduardo; de Carvalho, Daniel Rocha; de Rizzo, Isabela Maria Pinto Oliveira; de Mello, Walquiria Domingues; Heiner‐Fokkema, Rebecca; Gorman, Kathleen; Grun... Journal: Journal of inherited metabolic disease Issue: Volume 45:Issue 4(2022) Page Start: 769 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Toward understanding tissue‐specific symptoms in dolichol‐phosphate‐mannose synthesis disorders; insight from DPM3‐CDG. Issue 5 (23rd April 2019) Authors: van Tol, Walinka; Michelakakis, Helen; Georgiadou, Elissavet; van den Bergh, Peter; Moraitou, Marina; Papadimas, George K.; Papadopoulos, Constantinos; Huijben, Karin; Alsady, Mohammad; Willemsen, Michèl A.; Lefeber, Dirk J. Journal: Journal of inherited metabolic disease Issue: Volume 42:Issue 5(2019) Page Start: 984 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Α-Synuclein dimerization in erythrocytes of Gaucher disease patients: correlation with lipid abnormalities and oxidative stress. (2nd February 2016) Authors: Moraitou, Marina; Dermentzaki, Georgia; Dimitriou, Evangelia; Monopolis, Ioannis; Dekker, Nick; Aerts, Hans; Stefanis, Leonidas; Michelakakis, Helen Journal: Neuroscience letters Issue: Volume 613(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗