Original Articles:

  • 1. Gratification phenomena in children: a report of nineteen children and review of the literature. Int J Contemp Pediatr 2021;8:333-6.
    DOI: https://dx.doi.org/10.18203/2349-3291.ijcp20210124
  • 2. Clinical profile of acute drug-induced dystonia in children. Indian J Child Health 7(5), 220-222.
    DOI: https://doi.org/10.32677/IJCH.2020.v07.i05.007
  • 3. Eucalyptus Oil-Induced Seizures in Children: Case Reports and Review of the Literature. J Neurosci Rural Pract:2021;12:112–115.
    DOI: https://doi.org/ 10.1055/s-0040-1721199. PMCID: PMC7846315
  • 4. Eucalyptus Oil-Induced Seizures in Children: A Single-Center Prospective Study. Cureus 13(3): e14109.,
    DOI 10.7759/cureus.14109. PMCID:PMC8075753
  • 5. Randomized placebo controlled clinical study on the role of zinc in low birth weight neonates. Inj J Pharm Sci Nanotech Vo7;Issue 2, April 2014/2425-2428 (International Journal) – Won best paper of the year for 2014

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
  • 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