1. Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy. (2nd January 2018) Authors: McTague, Amy; Nair, Umesh; Malhotra, Sony; Meyer, Esther; Trump, Natalie; Gazina, Elena V.; Papandreou, Apostolos; Ngoh, Adeline; Ackermann, Sally; Ambegaonkar, Gautam; Appleton, Richard; Desurkar, Archana; Eltze, Christin; Kneen, Rachel; Kumar, Ajith V.; Lascelles, Karine; Montgomery, Tara; Rame... Journal: Neurology Issue: Volume 90:Number 1(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical Reasoning: A Teenage Girl With Progressive Hyperkinetic Movements, Seizures, and Encephalopathy. (3rd January 2023) Authors: Khamis, Sonia; Mitakidou, Maria R.; Champion, Michael; Goyal, Sushma; Jones, Rachel L.; Siddiqui, Ata; Sabanathan, Saraswathy; Hedderly, Tammy; Lin, Jean-Pierre; Jungbluth, Heinz; Papandreou, Apostolos Journal: Neurology Issue: Volume 100:Number 1(2023) Page Start: 30 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Delineation of the movement disorders associated with FOXG1 mutations. (10th May 2016) Authors: Papandreou, Apostolos; Schneider, Ruth B.; Augustine, Erika F.; Ng, Joanne; Mankad, Kshitij; Meyer, Esther; McTague, Amy; Ngoh, Adeline; Hemingway, Cheryl; Robinson, Robert; Varadkar, Sophia M.; Kinali, Maria; Salpietro, Vincenzo; O'Driscoll, Margaret C.; Basheer, S. Nigel; Webster, Richard I.; M... Journal: Neurology Issue: Volume 86:Number 19(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Diagnostic workup and management of patients with suspected Niemann-Pick type C disease. (May 2016) Authors: Papandreou, Apostolos; Gissen, Paul Journal: Therapeutic advances in neurological disorders Issue: Volume 9:Number 3(2016:May) Page Start: 216 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Familial recurrences of FOXG1‐related disorder: Evidence for mosaicism. (14th September 2015) Authors: McMahon, Kelly Q.; Papandreou, Apostolos; Ma, Mandy; Barry, Brenda J.; Mirzaa, Ghayda M.; Dobyns, William B.; Scott, Richard H.; Trump, Natalie; Kurian, Manju A.; Paciorkowski, Alex R. Journal: American journal of medical genetics Issue: Volume 167:Number 12(2015:Dec.) Page Start: 3096 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. GABRB3 mutations: a new and emerging cause of early infantile epileptic encephalopathy. (9th December 2015) Authors: Papandreou, Apostolos; McTague, Amy; Trump, Natalie; Ambegaonkar, Gautam; Ngoh, Adeline; Meyer, Esther; Scott, Richard H; Kurian, Manju A Journal: Developmental medicine & child neurology Issue: Volume 58:Number 4(2016:Apr.) Page Start: 416 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. Issue 5 (18th March 2016) Authors: Trump, Natalie; McTague, Amy; Brittain, Helen; Papandreou, Apostolos; Meyer, Esther; Ngoh, Adeline; Palmer, Rodger; Morrogh, Deborah; Boustred, Christopher; Hurst, Jane A; Jenkins, Lucy; Kurian, Manju A; Scott, Richard H Journal: Journal of medical genetics Issue: Volume 53:Issue 5(2016) Page Start: 310 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia. Issue 10 (25th July 2022) Authors: Reid, Kimberley M.; Spaull, Robert; Salian, Smrithi; Barwick, Katy; Meyer, Esther; Zhen, Juan; Hirata, Hiromi; Sheipouri, Diba; Benkerroum, Hind; Gorman, Kathleen M.; Papandreou, Apostolos; Simpson, Michael A.; Hirano, Yoshinobu; Farabella, Irene; Topf, Maya; Grozeva, Detelina; Carss, Keren; Smit... Journal: Movement disorders Issue: Volume 37:Issue 10(2022) Page Start: 2139 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Niemann–Pick type C disease as proof‐of‐concept for intelligent biomarker panel selection in neurometabolic disorders. (14th July 2022) Authors: Papandreou, Apostolos; Doykov, Ivan; Spiewak, Justyna; Komarov, Nikita; Habermann, Stephanie; Kurian, Manju A.; Mills, Philippa B.; Mills, Kevin; Gissen, Paul; Heywood, Wendy E. Journal: Developmental medicine & child neurology Issue: Volume 64:Number 12(2022) Page Start: 1539 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Physiological Adaptations to High-Intensity Interval and Continuous Training in Kayak Athletes. Issue 8 (August 2020) Authors: Papandreou, Apostolos; Philippou, Anastassios; Zacharogiannis, Elias; Maridaki, Maria Journal: Journal of strength and conditioning research Issue: Volume 34:Issue 8(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗