Case Reports:
- 1. Posterior reversible encephalopathy syndrome a rare presentation of post-streptococcal glomerulonephritis. Indian J Child Health. 2020;
- 2. Valproate-induced hyperammonemic encephalopathy in a child without hepatic failure: A case report. Indian J Case Reports. 2020;
- 3.Dengue encephalitis in children “Not an uncommon entity but is rarely thought of”: A case report. J Pediatr Neurosci 2020; 15(3):301-303. DOI:10.4103/jpn_7_20. PMCID:PMC7847127
- 4. A Great Masquerader: Acute Respiratory Failure as the Only Initial Presentation for Juvenile Myasthenia Gravis. J Clin and Diagn Research.2020:14(5);SD03-SD04. DOI: 10.7860/JCDR/2020/44145.13712
- 5.Hyperacute Gullian Barre Syndrome mimic acute spinal cord lesion: A rare case report. Perspectives in Medical Research 2020; 8(1):
- 6.Isolated Myoclonus Following Dengue Infection. Pediatr oncall J.2020:17;54-55
DOI:https://doi.org/10.7199/ped.oncall.2020.25
- 7. A Case Report of Idiopathic Ketotic Hypoglycemia Masquerading as Epilepsy. J Pediatr Epilepsy.
DOI https://doi.org/10.1055/s-0040-1710043.
- 8. Hereditary spastic paraplegia associated with a rare endoplasmic reticulum lipid raft-associated protein 2 mutation. Int J Contem Pediatr 2020;7:2077-9
- 9. Acute Encephalopathic Presentation of 3-Methylglutaconic Aciduria Type I With a Novel Mutation in AUH Gene. Cureus 12(12): e11951. DOI 10.7759/cureus.11951. PMCID:PMC7785470
- 10. A Forkhead box G1 (FOXG1) gene mutation in an Indian patient with a congenital variant of Rett syndrome.. Pediatric Rev Int J Pediatr Res. 2020;7(8):442-445..
- 11. A Novel Mutation in KCDT7 Gene in an Indian Girl With Progressive Myoclonus Epilepsy. Cureus 13(2): e13447. DOI 10.7759/cureus.13447. PMCID:PMC7982382
- 12. Homozygous Phosphatidylinositol Glycan Class T Mutation in an Indian Girl With Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3. Cureus 13(4): e14727. DOI 10.7759/cureus.14727. PMCID:PMC8163346
- 13. Dudipala S, Reddy R, Shankar R (April 24, 2023) Hyperekplexia: A Treatable Seizure Mimicker in Infants. Cureus 15(4): e38082. DOI 10.7759/cureus.38082