| Coronavirus infections in the nervous system of children: a scoping review making the case for long-term neurodevelopmental surveillance TG Singer, KD Evankovich, K Fisher, GJ Demmler-Harrison, SR Risen Pediatric neurology 117, 47-63, 2021 | 54 | 2021 |
| Current advances in pediatric onset multiple sclerosis KS Fisher, FX Cuascut, VM Rivera, GJ Hutton Biomedicines 8 (4), 71, 2020 | 41 | 2020 |
| Evidence of neuroinflammation and immunotherapy responsiveness in individuals with down syndrome regression disorder JD Santoro, R Partridge, R Tanna, D Pagarkar, M Khoshnood, ... Journal of Neurodevelopmental Disorders 14 (1), 35, 2022 | 26 | 2022 |
| Pediatric ocular myasthenia gravis K Fisher, V Shah Current Treatment Options in Neurology 21, 1-11, 2019 | 14 | 2019 |
| NAXE deficiency: A neurometabolic disorder of NAD (P) HX repair amenable for metabolic correction J Manor, D Calame, C Gijavanekar, K Fisher, J Hunter, E Mizerik, ... Molecular genetics and metabolism 136 (2), 101-110, 2022 | 11 | 2022 |
| Clinical profile and long-term outcome in neonatal cerebral sinus venous thrombosis I Herman, C Karakas, TA Webber, SF Kralik, DS Takacs, KS Fisher, ... Pediatric Neurology 121, 20-25, 2021 | 10 | 2021 |
| Multiple sclerosis in a multi-ethnic population in Houston, Texas: a retrospective analysis V Mercado, D Dongarwar, K Fisher, HM Salihu, GJ Hutton, FX Cuascut Biomedicines 8 (12), 534, 2020 | 10 | 2020 |
| Pediatric autoimmune ocular myasthenia gravis: evaluation of presentation and treatment outcomes in a large cohort KS Fisher, J Gill, HF Todd, MB Yang, MA Lopez, F Abid, T Lotze, VS Shah Pediatric Neurology 118, 12-19, 2021 | 7 | 2021 |
| Fulminant anti-myelin oligodendrocyte glycoprotein-associated cerebral cortical encephalitis: Case series of a severe pediatric myelin oligodendrocyte glycoprotein antibody … V Kannan, AJ Sandweiss, TA Erickson, JM Yarimi, A Ankar, VA Hardwick, ... Pediatric Neurology 147, 36-43, 2023 | 6 | 2023 |
| Longitudinal neurological analysis of moderate and severe pediatric cerebral visual impairment A Jimenez-Gomez, KS Fisher, KX Zhang, C Liu, Q Sun, VS Shah Frontiers in Human Neuroscience 16, 772353, 2022 | 5 | 2022 |
| Impact of COVID-19 on HIV treatment interruption in seven PEPFAR countries, April-June 2020. N Mehta, A Stewart, K Fisher, S Ghosh, L Santos, P Harvey, M Li, ... Journal of the International AIDS Society 24 (S4), 76-78, 2021 | 3 | 2021 |
| Bimodal Presentation of First Relapse in Paediatric MOGAD: A Single Center Retrospective Study J Yarimi, K Salazar, V Kannan, V Hardwick, N Shukla, T Lotze, K Fisher MULTIPLE SCLEROSIS JOURNAL 29, 157-157, 2023 | 1 | 2023 |
| Evidence for different gene rare variants contributing to early onset neurological autoimmune disease D Calame, I Herman, I Fatih, K Fisher, Z Akdemir, H Du, S Jhangiani, ... ANNALS OF NEUROLOGY 90, S72-S74, 2021 | 1 | 2021 |
| Effect of Rituximab on Immunoglobulin levels in Pediatric Multiple Sclerosis Patients (4398) N Mehta, A Balasa, N Shukla, K Fisher, T Lotze Neurology 96 (15 Supplement), 2021 | 1 | 2021 |
| Increased Likelihood of Relapse in Pediatric Anti-MOG Acute Disseminated Encephalomyelitis (ADEM) and Optic Neuritis (ON) vs. Seronegative ADEM and ON Patients (1061) K Fisher, A Balasa, N Shukla, T Lotze Neurology 94 (15 Supplement), 2020 | 1 | 2020 |
| A Retrospective Analysis of Clinical Features, Neuroimaging Findings and Long-term Outcome in Pediatric Cerebral Venous Sinus Thrombosis C Karakas, D Takacs, E Edmondson, K Fisher, N Shukla, G Clark, ... ANNALS OF NEUROLOGY 86, S161-S162, 2019 | 1 | 2019 |
| Retrospective cohort analysis in neonatal cerebral sinus venous thrombosis (P2. 3-053) C Karakas, D Takacs, E Edmondson, K Fisher, N Shukla, G Clark, ... Neurology 92 (15_supplement), P2. 3-053, 2019 | 1 | 2019 |
| Clinical Presentation, Neuroimaging Characteristics and Long-term Outcome in Pediatric Cerebral Venous Sinus Thrombosis: A Retrospective Study (P2. 3-052) C Karakas, D Takacs, E Edmondson, K Fisher, N Shukla, G Clark, ... Neurology 92 (15_supplement), P2. 3-052, 2019 | 1 | 2019 |
| Biallelic mutations in SUPV3L1 cause an inherited neurodevelopmental disorder with variable leukodystrophy due to aberrant mitochondrial double stranded RNA processing L Green, N Hamilton, M Elpidorou, R Maroofian, AGL Douglas, K Õunap, ... | | 2024 |
| Initial MRI, EEG, and CSF White Cell Count Are Abnormal in Children with Anti-NMDA Receptor Encephalitis with Isolated Psychiatric Symptoms (P6-14.020) G Gombolay, J Brenton, J Santoro, C Stredny, R Kammeyer, K Fisher, ... Neurology 102 (17_supplement_1), 1248, 2024 | | 2024 |
