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Clinical application of a novel next generation sequencing assay for CYP21A2 gene in 310 cases of 21- hydroxylase congenital adrenal hyperplasia from India.
Gangodkar P, Khadilkar V, Raghupathy P, Kumar R, Dayal AA, Dayal D, Ayyavoo A, Godbole T, Jahagirdar R, Bhat K, Gupta N, Kamalanathan S, Jagadeesh S, Ranade S, Lohiya N, Oke RL, Ganesan K, Khatod K, Agarwal M, Phadke N, Khadilkar A. Gangodkar P, et al. Among authors: khadilkar a, khadilkar v. Endocrine. 2021 Jan;71(1):189-198. doi: 10.1007/s12020-020-02494-z. Epub 2020 Sep 18. Endocrine. 2021. PMID: 32948948
Long-term Growth in Congenital Adrenal Hyperplasia.
Maheshwari A, Khadilkar V, Gangodkar P, Khadilkar A. Maheshwari A, et al. Among authors: khadilkar a, khadilkar v. Indian J Pediatr. 2019 Feb;86(2):154-158. doi: 10.1007/s12098-018-2753-6. Epub 2018 Aug 10. Indian J Pediatr. 2019. PMID: 30097840
Growth charts: A diagnostic tool.
Khadilkar V, Khadilkar A. Khadilkar V, et al. Among authors: khadilkar a. Indian J Endocrinol Metab. 2011 Sep;15 Suppl 3(Suppl3):S166-71. doi: 10.4103/2230-8210.84854. Indian J Endocrinol Metab. 2011. PMID: 22029020 Free PMC article.
Field Testing of IAP2015 Charts.
Lohiya N, Khadilkar V, Pawar S, Khadilkar A, Chiplonkar S, Jahagirdar R. Lohiya N, et al. Among authors: khadilkar a, khadilkar v. Indian J Pediatr. 2018 Sep;85(9):723-728. doi: 10.1007/s12098-018-2621-4. Epub 2018 Jan 24. Indian J Pediatr. 2018. PMID: 29368106
Genetic Analysis and Clinical Presentation in Silver Russell Syndrome.
Lohiya N, Lote-Oke R, Agarwal M, Phadke N, Khadilkar V, Khadilkar A. Lohiya N, et al. Among authors: khadilkar a, khadilkar v. Indian J Pediatr. 2018 Dec;85(12):1141-1142. doi: 10.1007/s12098-018-2738-5. Epub 2018 Jul 23. Indian J Pediatr. 2018. PMID: 30039337 No abstract available.
300 results