1. Advances in epilepsy gene discovery and implications for epilepsy diagnosis and treatment. Issue 2 (April 2017) Authors: Symonds, Joseph D.; Zuberi, Sameer M.; Johnson, Michael R. Journal: Current opinion in neurology Issue: Volume 30:Issue 2(2017:Apr.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Biological concepts in human sodium channel epilepsies and their relevance in clinical practice. (23rd February 2020) Authors: Brunklaus, Andreas; Du, Juanjiangmeng; Steckler, Felix; Ghanty, Ismael I.; Johannesen, Katrine M.; Fenger, Christina Dühring; Schorge, Stephanie; Baez‐Nieto, David; Wang, Hao‐Ran; Allen, Andrew; Pan, Jen Q.; Lerche, Holger; Heyne, Henrike; Symonds, Joseph D.; Zuberi, Sameer M.; Sanders, Stephan; ... Journal: Epilepsia Issue: Volume 61:issue 3(2020) Page Start: 387 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 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) ↗
4. Development and Validation of a Prediction Model for Early Diagnosis of SCN1A-Related Epilepsies. (15th March 2022) Authors: Brunklaus, Andreas; Pérez-Palma, Eduardo; Ghanty, Ismael; Xinge, Ji; Brilstra, Eva; Ceulemans, Berten; Chemaly, Nicole; de Lange, Iris; Depienne, Christel; Guerrini, Renzo; Mei, Davide; Møller, Rikke S.; Nabbout, Rima; Regan, Brigid M.; Schneider, Amy L.; Scheffer, Ingrid E.; Schoonjans, An-Sofie... Journal: Neurology Issue: Volume 98:Number 11(2022) Page Start: e1163 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Development and Validation of a Prediction Model for Early Diagnosis of SCN1A-Related Epilepsies. (15th March 2022) Authors: Brunklaus, Andreas; Pérez-Palma, Eduardo; Ghanty, Ismael; Xinge, Ji; Brilstra, Eva; Ceulemans, Berten; Chemaly, Nicole; de Lange, Iris; Depienne, Christel; Guerrini, Renzo; Mei, Davide; Møller, Rikke S.; Nabbout, Rima; Regan, Brigid M.; Schneider, Amy L.; Scheffer, Ingrid E.; Schoonjans, An-Sofie... Journal: Neurology Issue: Volume 98:Number 11(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Dravet syndrome and its mimics: Beyond SCN1A. (7th September 2017) Authors: Steel, Dora; Symonds, Joseph D.; Zuberi, Sameer M.; Brunklaus, Andreas Journal: Epilepsia Issue: Volume 58:issue 11(2017) Page Start: 1807 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. 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) ↗
8. Genetics update: Monogenetics, polygene disorders and the quest for modifying genes. (April 2018) Authors: Symonds, Joseph D.; Zuberi, Sameer M. Journal: Neuropharmacology Issue: Volume 132(2018) Page Start: 3 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk. (6th June 2018) Authors: Myers, Kenneth A.; Bello‐Espinosa, Luis E.; Symonds, Joseph D.; Zuberi, Sameer M.; Clegg, Robin; Sadleir, Lynette G.; Buchhalter, Jeffrey; Scheffer, Ingrid E. Journal: Epilepsia Issue: Volume 59:issue 7(2018) Page Start: 1372 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases. (6th February 2017) Authors: Symonds, Joseph D.; Joss, Shelagh; Metcalfe, Kay A.; Somarathi, Suresh; Cruden, Jamie; Devlin, Anita M.; Donaldson, Alan; DiDonato, Nataliya; Fitzpatrick, David; Kaiser, Frank J.; Lampe, Anne K.; Lees, Melissa M.; McLellan, Ailsa; Montgomery, Tara; Mundada, Vivek; Nairn, Lesley; Sarkar, Ajoy; Sch... Journal: Epilepsia Issue: Volume 58:issue 4(2017) Page Start: 565 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗