| Treatment of mitochondrial disorders S Avula, S Parikh, S Demarest, J Kurz, A Gropman Current treatment options in neurology 16, 1-20, 2014 | 120 | 2014 |
| Novel homozygous mutation in the FBXL4 gene is associated with mitochondria DNA depletion syndrome-13 S Wang, L Lin, Y Wang, A Wang, Z Liu, S Wu, X Lan, J Jia, Y Zhang, ... Journal of the Neurological Sciences 416, 116948, 2020 | 11 | 2020 |
| Wernicke-Korsakoff Syndrome From Hyperemesis Gravidarum VJ Patel, J Vu, G Mercado, S Avula, S Deering Maternal-Fetal Medicine 6 (01), 54-56, 2024 | 2 | 2024 |
| Neurobiology of common sleep disorders Z Liu, A Tolaymat, SK Avula Journal of Neuroscience and Neurological Disorders 2 (2), 039-046, 2018 | 2 | 2018 |
| A Case of a Seven-Year-old boy with Epilepsy with Myoclonic Absence: Importance of Seizure Semiology, Genetic Etiology, and Electroencephalogram Correlation for Timely Intervention I Frydson, S Avula, SF Ahmad Child Neurology Open 9, 2329048X221131738, 2022 | 1 | 2022 |
| Sleep disorders in childhood epileptic disorders Z Liu, S Avula, A Tolaymat SM J Sleep Disord 3 (2), 1013, 2017 | 1 | 2017 |
| Epilepsia Partialis Continua that Improved in a Pediatric Patient with Sub-dural Empyema J Schall, S Ahmad, S Avula Child Neurology Open 10, 2329048X231205416, 2023 | | 2023 |
| Novel Pathogenic Variants in the SURF1 Gene Cause Leigh Syndrome: A Case Report and Review of Literature Y Chen, C Wang, S Wang, L Lin, Y Wang, A Wang, Z Liu, S Wu, X Lan, ... Frontiers in Pediatrics 8, 592, 2020 | | 2020 |
| Fainting in Teenagers is Not Always Faking S Avula, M Moodley ANNALS OF NEUROLOGY 76, S240-S240, 2014 | | 2014 |
| “Fainting in Teenagers Is Not Always Faking”(P6. 101) S Avula, M Moodley Neurology 82 (10_supplement), P6. 101, 2014 | | 2014 |
Scott DemarestUniveristy of Colorado在 UCDENVER.EDU 的电子邮件经过验证
