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Saba Samad Memon

Showing results (51-60 of 74) with videos related to

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Nuklearmedizin. Nuclear Medicine|September 26, 2025
Outcomes of 68Ga-NODAGA-Exendin-4 PET/CT Guided Surgical Management of Insulinomas in MEN1: A Preliminary StudyKetki Sunil Ambulkar, Ravikumar Shah, Anurag Lila, et al.
Pituitary|June 8, 2024
Pituitary apoplexy in cushing's disease: a single center study and systematic literature reviewDivya C Ragate, Saba Samad Memon, Vijaya Sarathi, et al.
Indian Journal of Endocrinology and Metabolism|March 18, 2022
The Utility of <sup>68</sup>Ga-DOTATATE PET/CT in Localizing Primary/Metastatic Pheochromocytoma and Paraganglioma: Asian Indian ExperienceSanjeet Kumar Jaiswal, Vijaya Sarathi, Gaurav Malhotra, et al.
Journal of Endocrinological Investigation|April 28, 2025
Pediatric and adolescent von Hippel-Lindau disease: tumor profiles, genotype-phenotype correlation and comparison with adultsAnima Sharma, Ketki Ambulkar, Manjiri Karlekar, et al.
Endocrine Connections|August 20, 2024
LHCGR inactivating variants: single center experience and systematic review of phenotype-genotype of 46,XY and 46,XX patientsRohit Barnabas, Swati Jadhav, Anurag Ranjan Lila, et al.
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 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.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
Nuklearmedizin. Nuclear Medicine|September 26, 2025
Outcomes of 68Ga-NODAGA-Exendin-4 PET/CT Guided Surgical Management of Insulinomas in MEN1: A Preliminary StudyKetki Sunil Ambulkar, Ravikumar Shah, Anurag Lila, et al.
Pituitary|June 8, 2024
Pituitary apoplexy in cushing's disease: a single center study and systematic literature reviewDivya C Ragate, Saba Samad Memon, Vijaya Sarathi, et al.
Indian Journal of Endocrinology and Metabolism|March 18, 2022
The Utility of <sup>68</sup>Ga-DOTATATE PET/CT in Localizing Primary/Metastatic Pheochromocytoma and Paraganglioma: Asian Indian ExperienceSanjeet Kumar Jaiswal, Vijaya Sarathi, Gaurav Malhotra, et al.
Journal of Endocrinological Investigation|April 28, 2025
Pediatric and adolescent von Hippel-Lindau disease: tumor profiles, genotype-phenotype correlation and comparison with adultsAnima Sharma, Ketki Ambulkar, Manjiri Karlekar, et al.
Endocrine Connections|August 20, 2024
LHCGR inactivating variants: single center experience and systematic review of phenotype-genotype of 46,XY and 46,XX patientsRohit Barnabas, Swati Jadhav, Anurag Ranjan Lila, et al.
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 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.
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