Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jugal V. Gada"'
Autor:
Suhas S. Khaire, Jugal V. Gada, Ketaki V. Utpat, Nikita Shah, Premlata K. Varthakavi, Nikhil M. Bhagwat
Publikováno v:
Clinical Diabetes and Endocrinology, Vol 6, Iss 1, Pp 1-9 (2020)
Abstract Background Obstructive sleep apnea syndrome (OSAS) in association with Type 2 Diabetes Mellitus (DM) may result in increased glycemic variability affecting the glycemic control and hence increasing the risk of complications associated with d
Externí odkaz:
https://doaj.org/article/52d92061a82e40ff87d7b53d960ddd8d
Autor:
Prudwiraj Sanamandra, Jugal V Gada, Sukirti Misra, Sagar A Barasara, Premlata K Varthakavi, Nikhil M Bhagwat
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 27, Iss 2, Pp 170-176 (2023)
Context: It is postulated that 25(OH)D deficiency is associated with a worse prognosis of COVID-19. Aims: We aimed to find out whether baseline serum 25-hydroxy vitamin D levels were correlated with COVID-19 disease severity or not in Indian populati
Externí odkaz:
https://doaj.org/article/2feda5591c264ae4898911db1fc38b83
Autor:
Nikita Shah, Jugal V Gada, Vishwanath S Billa, Jatin Piyush Kothari, Shrirang D Bichu, Deepa H Usulumarty, Suhas S Khaire, Premlata K Varthakavi, Nikhil M Bhagwat
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 26, Iss 5, Pp 439-445 (2022)
Context: Glycemic variability plays a major role in the development as well as the progression of cardiovascular disease in diabetes. Aims: We compared the mean plasma glucose and glycemic variability (GV) parameters on and off hemodialysis (HD) in p
Externí odkaz:
https://doaj.org/article/9ab84fcf6e574d3a858795e6883f2b01
Autor:
Chakra Diwaker, Tushar Bandgar, Swati Jadhav, Anurag R. Lila, Virendra Patil, Jugal V Gada, Shantanu Kale, Puja M Thadani, Vijaya Sarathi, Nalini S. Shah, Sneha Arya
Publikováno v:
Pituitary. 24:657-669
POU1F1 mutations are prevalent in Indian CPHD cohorts. Genotype–phenotype correlation is not well-studied. To describe phenotypic and genotypic spectrum of POU1F1 mutations in our CPHD cohort and present systematic review as well as genotype–phen
Autor:
Manjunath Goroshi, Virendra Patil, Hiren Patt, Swati Jadhav, Shilpa Sankhe, Shantanu Kale, Vyankatesh Shivane, Jugal V Gada, Sweta Budyal, Nalini S. Shah, Tushar Bandgar, Vijaya Sarathi, Sneha Arya, Anurag R. Lila, Shrikrishna Acharya, Aparna A Kamble, Puja M Thadani, Vijaya Raghavan
Publikováno v:
Pituitary. 23:701-715
Regional variation in prevalence of genetic mutations in growth hormone deficiency (GHD) is known. Study phenotype and prevalence of mutations in GH1, GHRHR, POU1F1, PROP1 genes in GHD cohort. One hundred and two patients {Isolated GHD (IGHD): 79; co
Autor:
Swati, Jadhav, Chakra, Diwaker, Anurag R, Lila, Jugal V, Gada, Shantanu, Kale, Vijaya, Sarathi, Puja M, Thadani, Sneha, Arya, Virendra A, Patil, Nalini S, Shah, Tushar R, Bandgar
Publikováno v:
Pituitary. 24(5)
POU1F1 mutations are prevalent in Indian CPHD cohorts. Genotype-phenotype correlation is not well-studied.To describe phenotypic and genotypic spectrum of POU1F1 mutations in our CPHD cohort and present systematic review as well as genotype-phenotype
Publikováno v:
Neurology India. 68
Functioning pituitary tumors contribute to significant morbidity and mortality. Proper diagnostic approach and management is essential for optimal outcomes. Prolactinomas, the commonest of these, are the only tumors which can be managed medically. Ac
Publikováno v:
Growth Hormone & IGF Research. 59:101394
Aims The aim of the study was to evaluate the prevalence and predictors of abnormal glucose tolerance (Diabetes + Prediabetes) and its resolution in Acromegaly. Settings and design Retrospective observational study. Methods and material Ninety patien