Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Puja M Thadani"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f7b69b994f9ffbdd089e6164136db15
https://doi.org/10.1007/s11102-021-01140-9
https://doi.org/10.1007/s11102-021-01140-9
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbfd4fea78b93fcdcde49a055d4b568a
https://doi.org/10.1007/s11102-020-01078-4
https://doi.org/10.1007/s11102-020-01078-4
Autor:
Virendra Patil, Atul Goel, Tushar Bandgar, Swati Ramteke-Jadhav, Nalini S. Shah, Naina Goel, Shilpa Sankhe, Sridhar Epari, Saba Samad Memon, Kunal Thakkar, Anurag R. Lila, Nilesh Lomte, Rajeev Kasaliwal, Puja M Thadani
Publikováno v:
Endocrine Connections, Vol 9, Iss 2, Pp 111-121 (2020)
Endocrine Connections
Endocrine Connections
Background Most common incidentally detected sellar-suprasellar region (SSR) masses are pituitary adenomas, followed by craniopharyngioma, rathke’s cleft cyst, hypophysitis, and meningioma. Besides these, certain unusual SSR lesions can sometimes p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96406d9e855cbd681b5c81ebfda98952
https://doi.org/10.1530/ec-19-0497
https://doi.org/10.1530/ec-19-0497
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f85f99fa171cc6d9ab7356eeac9be410
https://pubmed.ncbi.nlm.nih.gov/33742319
https://pubmed.ncbi.nlm.nih.gov/33742319
Autor:
Hemraj B. Chandalia, Puja M. Thadani
Publikováno v:
International Journal of Diabetes in Developing Countries. 36:359-369
Target setting is an important strategy in diabetes. The commonly used glycemic targets are blood glucose and HbA1c. The target values can be fixed based upon normative data or outcome data. Individualization of glycemic targets is based upon age of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2b9eb3fbd8cc714c28d18605622352d
https://doi.org/10.1007/s13410-016-0467-8
https://doi.org/10.1007/s13410-016-0467-8