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. Corrigendum to "Epilepsy and developmental disorders: Next generation sequencing in the clinic" [Eur. J. Paediatr. Neurol. (2019) 15–23]. (January 2021) Authors: Symonds, Joseph D.; McTague, Amy Journal: European journal of paediatric neurology Issue: Volume 30(2021) Page Start: 170 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. Epilepsy and developmental disorders: Next generation sequencing in the clinic. (January 2020) Authors: Symonds, Joseph D.; McTague, Amy Journal: European journal of paediatric neurology Issue: Volume 24(2020) Page Start: 15 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Episodic dyscontrol syndrome. Issue 10 (1st June 2010) Authors: McTague, Amy; Appleton, Richard Journal: Archives of disease in childhood Issue: Volume 95:Issue 10(2010) Page Start: 841 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. Gain-of-function GABRB3 variants identified in vigabatrin-hypersensitive epileptic encephalopathies. Issue 2 (1st October 2020) Authors: Absalom, Nathan L; Liao, Vivian W Y; Kothur, Kavitha; Indurthi, Dinesh C; Bennetts, Bruce; Troedson, Christopher; Mohammad, Shekeeb S; Gupta, Sachin; McGregor, Iain S; Bowen, Michael T; Lederer, Damien; Mary, Sandrine; De Waele, Liesbeth; Jansen, Katrien; Gill, Deepak; Kurian, Manju A; McTague, A... Journal: Brain communications Issue: Volume 2:Issue 2(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome. (April 2017) Authors: Danti, Federica Rachele; Galosi, Serena; Romani, Marta; Montomoli, Martino; Carss, Keren J.; Raymond, F. Lucy; Parrini, Elena; Bianchini, Claudia; McShane, Tony; Dale, Russell C.; Mohammad, Shekeeb S.; Shah, Ubaid; Mahant, Neil; Ng, Joanne; McTague, Amy; Samanta, Rajib; Vadlamani, Gayatri; Valent... Journal: Neurology Issue: Volume 3:Number 2(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. 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) ↗
10. Myoclonic epilepsy in a child with 17q22–q23.1 deletion. Issue 8 (21st June 2013) Authors: Coppola, Antonietta; Tostevin, Anna; McTague, Amy; Pressler, Ronit M.; Cross, J. Helen; Sisodiya, Sanjay M. Journal: American journal of medical genetics Issue: Volume 161:Issue 8(2013:Aug.) Page Start: 2036 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗