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pro vyhledávání: '"Saravanan Jothi"'
Autor:
P Sri Subiksha, Saravanan Jothi
Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 62, Iss 2, Pp 202-205 (2024)
Purpose: To compare the central foveal thickness (CFT) in diabetics without retinopathy versus nondiabetics using optical coherence tomography (OCT). Methods: The study was done as a comparative cross-sectional study among two groups with 30 subjects
Externí odkaz:
https://doaj.org/article/3926e3e877514147bac3761320a930b8
Autor:
Saravanan Jothi, Hemanandini Mangalanathan, Malligai Kamatchi, Vinetha Viswanathan, Swetha Karicheri
Publikováno v:
Kerala Journal of Ophthalmology, Vol 28, Iss 1, Pp 23-26 (2016)
Purpose: Retinopathy of prematurity (ROP) is a preventable cause of childhood blindness. Identification of risk factors is essential for its early detection and management. Aim: The aim of this study was to analyze the incidence and risk factors of R
Externí odkaz:
https://doaj.org/article/1e91fa976e7746598c9ef0680ea670d7
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 9, Pp LC01-LC05 (2016)
Introduction: National Old Age Pension Scheme (NOAPS) was aimed at providing a safety net for India’s aging population in terms of social, economical and moral support by helping eligible elderly citizens with direct cash benefit. Aim: To asses
Externí odkaz:
https://doaj.org/article/cb80c2583b31429984e6e63b6c8a3f9a
Autor:
Suneetha Vuppu, Saravanan Jothi
Publikováno v:
Biocatalysis and Biotransformation. 40:471-480
Microbial mediated, especially the fungi mediated asymmetric reduction of the ketone is one of the most promising tools for the synthesis of chiral alcohols. Many fungal cultures were isolated from soil and screened for the stereo selective bioreduct
Autor:
Saravanan, Jothi, Suneetha, Vuppu
Publikováno v:
Preparative biochemistrybiotechnology. 50(10)
Microbial asymmetric reduction of ketone is an efficient tool for the synthesis of chiral alcohols. This research focuses on exploring the soil fungal isolates for their ability toward the keto reduction of acetophenone and its derivatives to their c