A clinical approach to diagnosis of autoimmune encephalitis F Graus, MJ Titulaer, R Balu, S Benseler, CG Bien, T Cellucci, I Cortese, ... The lancet neurology 15 (4), 391-404, 2016 | 3558 | 2016 |
International Pediatric Multiple Sclerosis Study Group criteria for pediatric multiple sclerosis and immune-mediated central nervous system demyelinating disorders: revisions … LB Krupp, M Tardieu, MP Amato, B Banwell, T Chitnis, RC Dale, A Ghezzi, ... Multiple Sclerosis Journal 19 (10), 1261-1267, 2013 | 1160 | 2013 |
Acute disseminated encephalomyelitis, multiphasic disseminated encephalomyelitis and multiple sclerosis in children RC Dale, C De Sousa, WK Chong, TCS Cox, B Harding, BGR Neville Brain 123 (12), 2407-2422, 2000 | 921 | 2000 |
MOG encephalomyelitis: international recommendations on diagnosis and antibody testing S Jarius, F Paul, O Aktas, N Asgari, RC Dale, J De Seze, D Franciotta, ... Journal of neuroinflammation 15, 1-10, 2018 | 722 | 2018 |
Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling GI Rice, Y del Toro Duany, EM Jenkinson, GMA Forte, BH Anderson, ... Nature genetics 46 (5), 503-509, 2014 | 595 | 2014 |
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1 YJ Crow, DS Chase, J Lowenstein Schmidt, M Szynkiewicz, GMA Forte, ... American journal of medical genetics Part A 167 (2), 296-312, 2015 | 572 | 2015 |
Clinical course, therapeutic responses and outcomes in relapsing MOG antibody-associated demyelination S Ramanathan, S Mohammad, E Tantsis, TK Nguyen, V Merheb, ... Journal of Neurology, Neurosurgery & Psychiatry 89 (2), 127-137, 2018 | 515 | 2018 |
Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study GI Rice, GMA Forte, M Szynkiewicz, DS Chase, A Aeby, MS Abdel-Hamid, ... The lancet neurology 12 (12), 1159-1169, 2013 | 429 | 2013 |
Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunity RC Dale, AJ Church, RAH Surtees, AJ Lees, JE Adcock, B Harding, ... Brain 127 (1), 21-33, 2004 | 429 | 2004 |
Self-antigen tetramers discriminate between myelin autoantibodies to native or denatured protein KC O'Connor, KA McLaughlin, PL De Jager, T Chitnis, E Bettelli, C Xu, ... Nature medicine 13 (2), 211-217, 2007 | 423 | 2007 |
Antibodies to surface dopamine-2 receptor in autoimmune movement and psychiatric disorders RC Dale, V Merheb, S Pillai, D Wang, L Cantrill, TK Murphy, H Ben-Pazi, ... Brain 135 (11), 3453-3468, 2012 | 401 | 2012 |
Radiological differentiation of optic neuritis with myelin oligodendrocyte glycoprotein antibodies, aquaporin-4 antibodies, and multiple sclerosis S Ramanathan, K Prelog, EH Barnes, EM Tantsis, SW Reddel, ... Multiple Sclerosis Journal 22 (4), 470-482, 2016 | 346 | 2016 |
Antibodies to MOG are transient in childhood acute disseminated encephalomyelitis AK Pröbstel, K Dornmair, R Bittner, P Sperl, D Jenne, S Magalhaes, ... Neurology 77 (6), 580-588, 2011 | 342 | 2011 |
Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS disease RC Dale, F Brilot, LV Duffy, M Twilt, AT Waldman, S Narula, E Muscal, ... Neurology 83 (2), 142-150, 2014 | 337 | 2014 |
Antibodies to native myelin oligodendrocyte glycoprotein in children with inflammatory demyelinating central nervous system disease F Brilot, RC Dale, RC Selter, V Grummel, S Reddy Kalluri, M Aslam, ... Annals of Neurology: Official Journal of the American Neurological …, 2009 | 334 | 2009 |
Maternal immune activation and neuroinflammation in human neurodevelopmental disorders VX Han, S Patel, HF Jones, RC Dale Nature Reviews Neurology 17 (9), 564-579, 2021 | 324 | 2021 |
Anti–basal ganglia antibodies in acute and persistent Sydenham’s chorea AJ Church, F Cardoso, RC Dale, AJ Lees, EJ Thompson, G Giovannoni Neurology 59 (2), 227-231, 2002 | 320 | 2002 |
Anti-MOG antibody: the history, clinical phenotype, and pathogenicity of a serum biomarker for demyelination S Ramanathan, RC Dale, F Brilot Autoimmunity reviews 15 (4), 307-324, 2016 | 299 | 2016 |
Autoimmune encephalitis: proposed best practice recommendations for diagnosis and acute management H Abboud, JC Probasco, S Irani, B Ances, DR Benavides, M Bradshaw, ... Journal of Neurology, Neurosurgery & Psychiatry 92 (7), 757-768, 2021 | 285 | 2021 |
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia K Tuschl, E Meyer, LE Valdivia, N Zhao, C Dadswell, A Abdul-Sada, ... Nature communications 7 (1), 11601, 2016 | 284 | 2016 |