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Year Number of Results
2010 1
2011 1
2014 1
2018 1
2020 1
2021 2
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Page 1
Genetic analysis in Bartter syndrome from India.
Sharma PK, Saikia B, Sharma R, Ankur K, Khilnani P, Aggarwal VK, Cheong H. Sharma PK, et al. Among authors: ankur k. Indian J Pediatr. 2014 Oct;81(10):1095-8. doi: 10.1007/s12098-014-1379-6. Epub 2014 Apr 4. Indian J Pediatr. 2014. PMID: 24696311
Complexities of pyridoxine response in PNPO deficiency.
Farmania R, Gupta A, Ankur K, Chetry S, Sharma S. Farmania R, et al. Among authors: ankur k. Epilepsy Behav Rep. 2021 Apr 3;16:100443. doi: 10.1016/j.ebr.2021.100443. eCollection 2021. Epilepsy Behav Rep. 2021. PMID: 33981986 Free PMC article.