Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ramdas Barure"'
Autor:
Sridevi Atluri, Vijaya Sarathi, Amit Goel, Shivaprasad Channabasappa, Shailaja Alapaty, Melkunte S Dhananjaya, Ramdas Barure, Gautam Kolla
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 26, Iss 1, Pp 38-43 (2022)
Context: As synacthen use is not licensed in India and there are concerns about the safety of the insulin tolerance test (ITT), an alternative dynamic test to diagnose adrenal insufficiency (AI) is required. Objective: The study aimed to evaluate the
Externí odkaz:
https://doaj.org/article/65e5f771592c4b9f83117f43efd4b470
Autor:
Ramdas, Barure, Dhananjaya Melkunte, Shanthaiah, Sridevi, Atluri, Shivaprasad, Channabasappa, Gautam, Kolla, S L Sagar, Reddy, Vijaya, Sarathi
Publikováno v:
Indian journal of endocrinology and metabolism. 26(4)
The American Diabetes Association recommends statin therapy for young type 2 diabetes mellitus (T2DM) adults only if one additional cardiovascular (CV) risk factor coexists. The data regarding CV risk factors in young Indian T2DM adults is limited. H
Autor:
Amey Joshi, Anupam Bhambhani, Ramdas Barure, Samhitha Gonuguntla, Vijaya Sarathi, Abdelrahman M Attia, Abhigan Babu Shrestha, Vikash Jaiswal
Publikováno v:
Medicine. 102:e32735
Autor:
Vijaya Sarathi, Sridevi Atluri, Amit Goel, Shivaprasad Channabasappa, Shailaja Alapaty, MelkunteS Dhananjaya, Ramdas Barure, Gautam Kolla
Publikováno v:
Indian journal of endocrinology and metabolism. 26(1)
As synacthen use is not licensed in India and there are concerns about the safety of the insulin tolerance test (ITT), an alternative dynamic test to diagnose adrenal insufficiency (AI) is required.The study aimed to evaluate the diagnostic performan
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Autor:
S K, Sharma, Sangram, Mangudkar, Mehul, Rathod, Amrita, Verma, R L V, Phanikumar, Subodh, Garg, Ajinkya, Dhakne, Ramdas, Barure
Publikováno v:
The Journal of the Association of Physicians of India. 62(3)
Hereditary hemochromatosis (HH) is manifested as iron overload in different organs due to homozygosity of a single autosomal mutation. Two different mutations C282Y and H63D in the HFE gene have been associated with hereditary hemochromatosis cases.
Autor:
Shivaprasad C; Department of Endocrinology, Vydehi Institute of Medical Sciences and Research Centre, Bangalore, Karnataka, India., Aiswarya Y; Department of Endocrinology, Vydehi Institute of Medical Sciences and Research Centre, Bangalore, Karnataka, India., Kejal S; Department of Internal Medicine, Vydehi Institute of Medical Sciences and Research Centre, Bangalore, Karnataka, India., Sridevi A; Department of Endocrinology, Vydehi Institute of Medical Sciences and Research Centre, Bangalore, Karnataka, India., Anupam B; Department of Endocrinology, Vydehi Institute of Medical Sciences and Research Centre, Bangalore, Karnataka, India., Ramdas B; Department of Endocrinology, Vydehi Institute of Medical Sciences and Research Centre, Bangalore, Karnataka, India., Gautham K; Department of Endocrinology, Vydehi Institute of Medical Sciences and Research Centre, Bangalore, Karnataka, India., Aarudhra P; Department of Internal Medicine, Vydehi Institute of Medical Sciences and Research Centre, Bangalore, Karnataka, India.
Publikováno v:
Journal of diabetes science and technology [J Diabetes Sci Technol] 2021 Jan; Vol. 15 (1), pp. 134-140. Date of Electronic Publication: 2019 Jul 07.