Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Varsha, Jagtap"'
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 21, Iss 2, Pp 360-362 (2017)
Externí odkaz:
https://doaj.org/article/d325622ff7264ce9a65021a0fe89fa67
Autor:
Anurag Ranjan Lila, Vijaya Sarathi, Varsha Jagtap, Tushar Bandgar, Padma S Menon, Nalini Samir Shah
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 2, Pp 258-262 (2012)
Primary hyperparathyroidism (PHPT) is associated with nephrolithiasis and nephrocalcinosis. Hypercalciuria is one of the multiple factors that is implicated in the complex pathophysiology of stone formation. The presence of a renal stone (symptomatic
Externí odkaz:
https://doaj.org/article/d9431c6c3dfe46a89b4aee0c753f9496
Autor:
Nihal Shah, Sumiran A. Mahajan, Sampada Karne, Chandrakant Chavan, Arundhati Diwan, Varsha Jagtap, Preeti Dave
Publikováno v:
International Journal of Advances in Medicine. 8:611
Pheochromocytomas are rare catecholamine secreting neuroendocrine tumors that can cause intracerebral hemorrhage sometimes and can very rarely cause cardiomyopathy simulating hypertrophic obstructive cardiomyopathy. We report a case of combination of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53c9474d17e7cdaca4a05450ea860874
https://doi.org/10.18203/2349-3933.ijam20211065
https://doi.org/10.18203/2349-3933.ijam20211065
Publikováno v:
The Journal of the Association of Physicians of India. 64(8)
Thyrotoxic crisis is a life threatening medical condition that requires urgent diagnosis and treatment. Because of the wide variety of presenting symptoms, its diagnosis can be difficult in some cases and a high index of suspicion is required for dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d99e92c92e0fd4e01d1d973068f64ea5
https://pubmed.ncbi.nlm.nih.gov/27762123
https://pubmed.ncbi.nlm.nih.gov/27762123
Autor:
Harshada Kudalkar, Varsha Jagtap
Publikováno v:
A Complete Textbook for GNM Internship
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85c260a2a993cd45ccfc4cacd689d5cb
https://doi.org/10.5005/jp/books/12602_22
https://doi.org/10.5005/jp/books/12602_22
Autor:
Gaurav, Malhotra, Archi, Agrawal, Nirmala A, Jambhekar, Vijaya, Sarathi, Varsha, Jagtap, Manish G, Agarwal, Mukta, Kulkarni, Ramesh V, Asopa, Nalini S, Shah
Publikováno v:
Clinical nuclear medicine. 35(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3595b94932640061118ac6b56d0de3da
https://pubmed.ncbi.nlm.nih.gov/20940555
https://pubmed.ncbi.nlm.nih.gov/20940555
Autor:
Vaman Khadilkar, Ketki Kelkar-Ramanan, Nikhil Phadke, Anuradha Khadilkar, Kavita Khatod, John Mathew, Varsha Jagtap
Publikováno v:
International Journal of Pediatric Endocrinology
Prader-Willi syndrome (PWS) is caused by loss of function of genes on chromosome 15; most cases occur when a segment of the paternal chromosome 15 is absent/inactivated. Recently few cases have been identified with truncating mutations in MAGEL2 gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a45439b07f470c5478bd4cd4e795ad9