1. A RETT-LOOK-ALIKE WITH BRAIN IRON ACCUMULATION. Issue 11 (9th October 2013) Authors: Crisp, Sarah; Meyer, Esther; Gregory, Allison; Archer, Hayley; Hayflick, Susan; Kurian, Manju A; de Silva, Rajith Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 84:Issue 11(2013) Page Start: e2 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum. (31st October 2013) Authors: Peall, Kathryn J; Lumsden, Daniel; Kneen, Rachel; Madhu, Rajesh; Peake, Deirdre; Gibbon, Frances; Lewis, Hilary; Hedderly, Tammy; Meyer, Esther; Robb, Stephanie A; Lynch, Bryan; King, Mary D; Lin, Jean‐Pierre; Morris, Huw R; Jungbluth, Heinz; Kurian, Manju A Journal: Developmental medicine & child neurology Issue: Volume 56:Number 7(2014:Jul.) Page Start: 642 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Beta‐propeller–associated neurodegeneration can present with dominant or isolated parkinsonism. Issue 4 (28th February 2018) Authors: Morales‐Briceño, Hugo; Sanchez‐Hernandez, Beatriz E.; Meyer, Esther; Kurian, Manju A.; Fois, Alessandro F.; Rodriguez‐Violante, Mayela; Leal‐Ortega, Roberto; Perez‐Lohman, Christian; Mohammad, Shekeeb; Fung, Victor S.C. Other Names: Weintraub, MD Daniel guestEditor.; Litvan, MD Irene guestEditor.; Hamilton, PhD Jamie L. guestEditor. Journal: Movement disorders Issue: Volume 33:Issue 4(2018) Page Start: 654 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗
5. Clinical features of childhood‐onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. (30th January 2013) Authors: Silveira‐Moriyama, Laura; Gardiner, Alice R; Meyer, Esther; King, Mary D; Smith, Martin; Rakshi, Karl; Parker, Alasdair; Mallick, Andrew A; Brown, Richard; Vassallo, Grace; Jardine, Philip E; Guerreiro, Marilisa M; Lees, Andrew J; Houlden, Henry; Kurian, Manju A Journal: Developmental medicine & child neurology Issue: Volume 55:Number 4(2013:Apr.) Page Start: 327 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. 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) ↗
7. Designing a Transformative Epistemology of the Problematic: A Perspective for Transdisciplinary Sustainability Research. (3rd July 2020) Authors: Meyer, Esther; Peukert, Daniela Journal: Social epistemology Issue: Volume 34:Number 4(2020) Page Start: 346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Designing a Transformative Epistemology of the Problematic: A Perspective for Transdisciplinary Sustainability Research. (3rd July 2020) Authors: Meyer, Esther; Peukert, Daniela Journal: Social epistemology Issue: Volume 34:Number 4(2020) Page Start: 346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. DNAJC6 Mutations Disrupt Dopamine Homeostasis in Juvenile Parkinsonism‐Dystonia. Issue 8 (30th May 2020) Authors: Ng, Joanne; Cortès‐Saladelafont, Elisenda; Abela, Lucia; Termsarasab, Pichet; Mankad, Kshitij; Sudhakar, Sniya; Gorman, Kathleen M.; Heales, Simon J.R.; Pope, Simon; Biassoni, Lorenzo; Csányi, Barbara; Cain, John; Rakshi, Karl; Coutts, Helen; Jayawant, Sandeep; Jefferson, Rosalind; Hughes, Debora... Journal: Movement disorders Issue: Volume 35:Issue 8(2020) Page Start: 1357 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. 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) ↗