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Overview
Dr Abhishek Kulkarni is a distinguished Paediatric Endocrinology based at Apollo Hospitals Navi Mumbai. With an impressive 10 years of experience in the medical field, he has dedicated his career to providing exceptional healthcare services to patients. He holds MD, PDCCVisiting Fellowship RCPCH, UK, showcasing his extensive training and commitment to medical excellence. He is proficient in multiple languages, ensuring effective communication with a diverse range of patients.
He is known for his patient-centric approach, emphasizing the importance of understanding each patient’s unique needs and medical history. He expertise encompasses a wide range of conditions related to Paediatric Endocrinology, enabling he to deliver precise diagnoses and treatments. He ensures that patients receive care tailored to their individual health requirements.
In his practice, Dr Abhishek Kulkarni goes beyond treatments by educating patients about their health conditions. This empowers individuals to take active roles in managing their health and making informed decisions. By fostering a supportive and understanding environment, he builds trust and ensures long-term health management strategies for patients.
Dedicated to staying updated with advancements in his field, Dr Abhishek Kulkarni actively collaborates with other healthcare professionals to provide comprehensive care. He commitment to improving health outcomes continues to leave a lasting impact on the lives of his patients, solidifying his reputation as a trusted name in Paediatric Endocrinology.
Memberships
- Membership: Indian Academy Paediatrics, Indian Society of Paediatric & Adolescent Endocrinology, Asia Pacific Paediatric Endocrine Society, Growth Hormone Research Society, India
- National Executive Council Member- Indian Society Paediatric & Adolescent Endocrinology 2017- 2018 & 2012 & 2013
Research and Publication
1. Diabetes in young: Beyond type 1
Anju Virmani and Abhishek Kulkarni1Indian J Endocrinol Metab. 2012 Dec; 16(Suppl 2): S256–S25810.4103/2230-8210.104. PMCID: PMC3603041
2. Neonatal severe hyperparathyroidism due to compound heterozygous mutation of calcium sensing receptor (CaSR) gene presenting as encephalopathy.
Kulkarni A, Mohite M, Vijaykumar R, Bansode P, Murade S, Tamhankar PM.
Indian J Pediatr. 2014 Nov;81(11):1228-9. doi: 10.1007/s12098-014-1442-3. Epub 2014 Apr 26.
3. Fetal intracranial calcification: pseudo-TORCH phenotype and discussion of related phenotypes.Kulkarni AM, Baskar S, Kulkarni ML, Kulkarni AJ, Mahuli AV, Vittalrao S, Kulkarni PM. Am J Med Genet A. 2010 Apr;152 A(4):930-7.doi: 10.1002/ajmg.a.33358.
4. First Author - Chapter on “Hypocalcemia in infants and children” – Indian Academy Pediatrics, Specialty series text book of Pediatric Endocrinology. 1st Edition 2012
5. Co Author -Chapter on “Calcium metabolism disorders in infants & children”. Practical Pediatric Endocrinology text book for resource limited countries
Editor- Associate. Prof Margaret Zaccharin. RCH, Melbourne. Elsevier,1st Edition 2013.
6. RESEARCH PAPER: Title: Growth and obesity status of middle socio-economic group children in Lucknow: a comparative analysis with upper socio-economic group studies , NMJI
7.Cystic bone tuberculosis.Kulkarni ML, Kulkarni AJ, Pujar MS, Patil AK, Shanbhag MM, Singanal H, Kulkarni AM. Indian J Pediatr. 2011 Nov;78(11):1431-2. doi: 10.1007/s12098-011-0455-4. Epub 2011 Jun 10.
8. Co author - Text book on Pediatric Toxicology, Paras Publication, 1st ed, 2011
9.17 alpha hydroxylase deficiency a rare cause of pediatric hypertension ,
A case report.-2 nd biennial meet of Indian Society Pediatric Endocrinology, Calicut 2011
Special Interests
- Growth diosders,
- Juvenile diabetes mellitus,
- Thyroid disorders,
- Pubertal disorders
- Metabolic bone disease
- Infantile and child hood obesity
- Neonatal diabetes
