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Saba Samad

Showing results (61-70 of 80) with videos related to

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Endocrine|July 8, 2025
Clinical and radiological insights into secondary hypophysitis: A single-center experience with a focus on tuberculosisArchana Rao, Anurag Ranjan Lila, Manjiri Karlekar, et al.
Journal of the Endocrine Society|February 18, 2022
17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of LiteratureMadhur Maheshwari, Sneha Arya, Anurag Ranjan Lila, et al.
Endocrine Connections|January 31, 2025
Bilateral macronodular adrenocortical disease: a single centre experienceAnuj Ban, Rohit Barnabas, Manjiri Karlekar, et al.
Endocrine Connections|January 8, 2020
Sellar surprises: a single-centre experience of unusual sellar massesKunal Thakkar, Swati Ramteke-Jadhav, Rajeev Kasaliwal, et al.
Annales D'Endocrinologie|June 22, 2023
46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parametersChethan Yami Channaiah, Saba Samad Memon, Vijaya Sarathi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 7, 2021
Genotype and phenotypic spectrum of vitamin D dependent rickets type 1A: our experience and systematic reviewManjunath Havalappa Dodamani, Manjeetkaur Sehemby, Saba Samad Memon, et al.
Annales D'Endocrinologie|April 25, 2025
46, XY under-virilization and NR5A1 variants: Monocentric Indian experience and systematic reviewSandeep Kumar, Reshma Pandit, Vijaya Sarathi, et al.
Endocrine|October 19, 2024
The polar vessel sign: insights from CT imaging analysis in Asian Indian primary hyperparathyroidismAnima Sharma, Saba Samad Memon, Manjunath Goroshi, et al.
Clinical Endocrinology|February 18, 2024
Steroidogenic acute regulatory protein (STAR) deficiency: Our experience and systematic review for phenotype-genotype correlationAditya Phadte, Charushila Dhole, Samiksha Hegishte, et al.
Calcified Tissue International|November 19, 2023
Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic ReviewManjunath Havalappa Dodamani, Saba Samad Memon, Manjiri Karlekar, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
Endocrine|July 8, 2025
Clinical and radiological insights into secondary hypophysitis: A single-center experience with a focus on tuberculosisArchana Rao, Anurag Ranjan Lila, Manjiri Karlekar, et al.
Journal of the Endocrine Society|February 18, 2022
17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of LiteratureMadhur Maheshwari, Sneha Arya, Anurag Ranjan Lila, et al.
Endocrine Connections|January 31, 2025
Bilateral macronodular adrenocortical disease: a single centre experienceAnuj Ban, Rohit Barnabas, Manjiri Karlekar, et al.
Endocrine Connections|January 8, 2020
Sellar surprises: a single-centre experience of unusual sellar massesKunal Thakkar, Swati Ramteke-Jadhav, Rajeev Kasaliwal, et al.
Annales D'Endocrinologie|June 22, 2023
46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parametersChethan Yami Channaiah, Saba Samad Memon, Vijaya Sarathi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 7, 2021
Genotype and phenotypic spectrum of vitamin D dependent rickets type 1A: our experience and systematic reviewManjunath Havalappa Dodamani, Manjeetkaur Sehemby, Saba Samad Memon, et al.
Annales D'Endocrinologie|April 25, 2025
46, XY under-virilization and NR5A1 variants: Monocentric Indian experience and systematic reviewSandeep Kumar, Reshma Pandit, Vijaya Sarathi, et al.
Endocrine|October 19, 2024
The polar vessel sign: insights from CT imaging analysis in Asian Indian primary hyperparathyroidismAnima Sharma, Saba Samad Memon, Manjunath Goroshi, et al.
Clinical Endocrinology|February 18, 2024
Steroidogenic acute regulatory protein (STAR) deficiency: Our experience and systematic review for phenotype-genotype correlationAditya Phadte, Charushila Dhole, Samiksha Hegishte, et al.
Calcified Tissue International|November 19, 2023
Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic ReviewManjunath Havalappa Dodamani, Saba Samad Memon, Manjiri Karlekar, et al.
Pageof 8