1. Recurrent headache in a five year old boy. Saini L, Kumar RM, Chakrabarty B,
Gulati S Ann Indian Acad Neurol. 2016 Jan-Mar;19(1):143-5.
2. A 7-year-old girl with recurrent episodes of abdominal pain, seizures, and loss of
vision: Primary diffuse leptomeningeal primitive neuroectodermal tumor masquerading
as chronic meningitis. Nambirajan A, Suri V, Sharma MC, Kumar R, Garg A, Gulati S,
Tandon V. Neurol India. 2015 Sep-Oct;63(5):736-42.
3. A Trembling Child at Rest, Action, and Intention: A Unique Treatable Entity. Dubey
R, Saini L, Manokaran RK, Chakrabarty B, Agrawal D, Kumar A, Gulati S. Pediatr
Neurol. 2015 Sep;53(3):268-9.
4. A Combination of Moyamoya Pattern and Cerebral Venous Sinus Thrombosis: A
Case of Tubercular Vasculopathy. Kumar RM, Saini L, Kaushik JS, Chakrabarty B,
Kumar A, Gulati S. J Trop Pediatr. 2015 Oct;61(5):393-6.
5. Sleep and drug resistant epilepsy in Children: Sleep Medicine and Disorders:
International Journal: Manuscript accepted: Manokaran RK, Gulati S. Sleep and drug
resistant epilepsy in children. Sleep Med Dis Int J. 2018;2(4):96‒98. DOI:
10.15406/smdij.2018.02.00050
6. Development and validation of DSM-5 based diagnostic tool for children with
Autism Spectrum Disorder: Gulati S, Kaushik JS, Saini L, Sondhi V, Madaan P, et al.
(2019) Development and validation of DSM-5 based diagnostic tool for children with
Autism Spectrum Disorder. PLOS ONE 14(3):
e0213242. https://doi.org/10.1371/journal.pone.0213242
7. Cerebral venous sinus thrombosis in Lesch Nyhan Syndrome: Article accepted in
Neurology India
8. Sleep abnormalities and polysomnographic profile in children with drug resistant
epilepsy for epilepsy & behavior (Manuscript submitted to Epilepsy and behavior)
9. Prevalence of smooth muscle dysfucntion among children with duchenne muscular
dystrophy (Manuscript submitted to Muscle and Nerve)

10. "Phenytoin induced status dystonicus: A rare manifestation of phenytoin toxicity in
a child with autism spectrum disorder." "AIAN_674_19". (Manuscript under
publication – Annals of Indian Academy of Neurology
11. "An atypical presentation of Joubert syndrome due to a novel mutation in ZNF 423
gene "JPN_168_19". (Manuscript under Publication – Journal of Pediatric
Neurosciences.

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