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| Pediatric cerebral palsy in Africa: a systematic review KA Donald, P Samia, A Kakooza-Mwesige, D Bearden Seminars in pediatric neurology 21 (1), 30-35, 2014 | 203 | 2014 |
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| Global HIV neurology: a comprehensive review KT Thakur, A Boubour, D Saylor, M Das, DR Bearden, GL Birbeck Aids 33 (2), 163-184, 2019 | 105 | 2019 |
| Enteroviruses in X-linked agammaglobulinemia: update on epidemiology and therapy D Bearden, M Collett, PL Quan, BT Costa-Carvalho, KE Sullivan The Journal of Allergy and Clinical Immunology: In Practice 4 (6), 1059-1065, 2016 | 94 | 2016 |
| Treatment Responsiveness in KCNT1-Related Epilepsy MP Fitzgerald, M Fiannacca, DM Smith, TS Gertler, B Gunning, S Syrbe, ... Neurotherapeutics 16, 848-857, 2019 | 84 | 2019 |
| A recurrent de novo PACS2 heterozygous missense variant causes neonatal-onset developmental epileptic encephalopathy, facial dysmorphism, and cerebellar dysgenesis HE Olson, N Jean-Marçais, E Yang, D Heron, K Tatton-Brown, ... The American Journal of Human Genetics 102 (5), 995-1007, 2018 | 74 | 2018 |
| Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia D Ebrahimi-Fakhari, J Teinert, R Behne, M Wimmer, A D'amore, ... Brain 143 (10), 2929-2944, 2020 | 69 | 2020 |
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| KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum CM Bonardi, HO Heyne, M Fiannacca, MP Fitzgerald, E Gardella, ... Brain 144 (12), 3635-3650, 2021 | 65 | 2021 |
| A recurrent de novo variant in NACC1 causes a syndrome characterized by infantile epilepsy, cataracts, and profound developmental delay K Schoch, L Meng, S Szelinger, DR Bearden, A Stray-Pedersen, OL Busk, ... The American Journal of Human Genetics 100 (2), 343-351, 2017 | 58 | 2017 |
| Treatment of chronic enterovirus encephalitis with fluoxetine in a patient with X-linked agammaglobulinemia J Gofshteyn, AM Cárdenas, D Bearden Pediatric Neurology 64, 94-98, 2016 | 49 | 2016 |
| Isolated neonatal seizures: when to suspect inborn errors of metabolism C Ficicioglu, D Bearden Pediatric neurology 45 (5), 283-291, 2011 | 49 | 2011 |
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| KCNT1-related epilepsy T Gertler, D Bearden, A Bhattacharjee, G Carvill | 37 | 2018 |
| Risk factors for cerebral palsy in children in Botswana B Monokwane, A Johnson, C Gambrah-Sampaney, E Khurana, J Baier, ... Pediatric Neurology 77, 73-77, 2017 | 29 | 2017 |
| Severe 5, 10-methylenetetrahydrofolate reductase deficiency and two MTHFR variants in an adolescent with progressive myoclonic epilepsy ED Kristin, D Bearden, D Watkins, K Hyland, DS Rosenblatt, C Ficicioglu Pediatric neurology 51 (2), 266-270, 2014 | 29 | 2014 |
| Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders I Mannucci, NDP Dang, H Huber, JB Murry, J Abramson, T Althoff, ... Genome medicine 13 (1), 90, 2021 | 28 | 2021 |
| Pathogenic variants in fucokinase cause a congenital disorder of glycosylation BG Ng, JA Rosenfeld, L Emrick, M Jain, LC Burrage, B Lee, WJ Craigen, ... The American Journal of Human Genetics 103 (6), 1030-1037, 2018 | 24 | 2018 |
Sylvia Mwanza-KabagheLecturer: The University of Zambia/ Kansanshi Mining PLCEmail verificata su unza.zm