1) M.P.Desai, R.Sharma, I.Riaz, S.Sudhanshu, R.Parikh, V.Bhatia. Newborn Screening Guidelines for Congenital Hypothyroidism in India: Recommendations of the Indian Society for Pediatric and Adolescent Endocrinology. Indian J Pediatr. 2018 Jun;85(6):440-447 & Indian J Pediatr. 2018 Jun;85(6):448-453.
2) Shah R, Rao S, Parikh R, Sophia T, Khalid H. Fanconi Bickel Syndrome with hypercalciuria due to GLUT 2 Mutation. Indian Pediatr. 2016 Sep 8;53(9):829-830.
3) Singh P, Rao SC, Parikh R. Neonatal Diabetes with intractable Epilepsy: DEND Syndrome. Indian J Pediatr. 2014 Dec;81(12):1387-8.
4) Daphne Y, Kevin C, Anuja N, Ruchi P, Natalie C, Mohammed D, Senthil S, Indraneel B. Congenital Hyperinsulinism due to mutations in HNF1A. Accepted for publication in European Journal of Medical Genetics, April 2020.
5) Article on McCune Albright Syndrome published in CAPENEWS, Newsletter of ISPAE, September 2014, Volume 18, Issue 2. Pages 6-8.
6) Chapter Author, “Hypoglycemia in an Older child”, IAP Textbook of Pediatric Endocrinology, Vaman Khadilkar, Anurag Bajpai, Hemchand Prasad. Released in 2019. Chapter 46.
7) Chapter author along with Dr Meena Desai, “Normal Puberty” - Disorders of the Endocrine Gland for the Postgraduate Textbook of Pediatrics, Piyush Gupta, PSN Menon, Siddarth Ramji, Rakesh Lodha. Released in 2015. Chapter 44.10,Sec-44 (1-33).indd 2326-2330.
8) Chapter author along with Dr Meena Desai, “Disorders of Thyroid Gland” IAP Textbook of Pediatrics 7th Edition, Piyush Gupta, PSN Menon. Chapter13.5