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Author/Creator Patil, Virendra

1. 17β hydroxysteroid dehydrogenase 3 deficiency in 46, XY disorders of sex development: Our experience and a gender role‐focused systematic review. (27th February 2022)

Authors:
Krishnappa, Brijesh; Arya, Sneha; Lila, Anurag R.; Sarathi, Vijaya; Memon, Saba S.; Barnabas, Rohit; Kumbhar, Bajarang V.; Bhandare, Vishwambhar V.; Patil, Virendra; Shah, Nalini S.; Kunwar, Ambarish; Bandgar, Tushar
Journal:
Clinical endocrinology
Issue:
Volume 97:Number 1(2022)
Page Start:
43
Record Type:
Journal Article
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3. 68Ga‐DOTATATE PET/CT imaging in endogenous hyperinsulinemic hypoglycemia: A tertiary endocrine centre experience. (8th September 2021)

Authors:
Shah, Ravikumar; Sehemby, Manjeetkaur; Garg, Robin; Purandare, Nilendu; Hira, Priya; Mahajan, Abhishek; Lele, Vikram; Malhotra, Gaurav; Verma, Priyanka; Rojekar, Amey; Dalvi, Abhay; Uchino, Shinya; Rastogi, Shivam; Lila, Anurag; Patil, Virendra; Shah, Nalini; Bandgar, Tushar
Journal:
Clinical endocrinology
Issue:
Volume 96:Number 2(2022)
Page Start:
190
Record Type:
Journal Article
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4. Cabergoline may act as a radioprotective agent in Cushing's disease. (22nd November 2019)

Authors:
Thakkar, Kunal; Lila, Anurag; Sarathi, Vijaya; Ramteke‐Jadhav, Swati; Goroshi, Manjunath; Memon, Saba Samad; Krishnatry, Rahul; Gupta, Tejpal; Jalali, Rakesh; Goel, Atul; Shah, Abhidha; Sankhe, Shilpa; Patil, Virendra; Bandgar, Tushar; Shah, Nalini S.
Journal:
Clinical endocrinology
Issue:
Volume 92:Number 1(2020)
Page Start:
55
Record Type:
Journal Article
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7. Exendin‐4‐based imaging in endogenous hyperinsulinemic hypoglycaemia cohort: A tertiary Endocrine centre experience. (6th August 2020)

Authors:
Garg, Robin; Shah, Ravikumar; Tiwari, Ankita; Purandare, Nilendu; Lele, Vikram R.; Malhotra, Gaurav; Verma, Priyanka; Gosavi, Vikrant; Dalvi, Abhay; Kumar Jaiswal, Sanjeet; Patil, Virendra; Ramteke‐Jadhav, Swati; Lila, Anurag; Shah, Nalini; Bandgar, Tushar
Journal:
Clinical endocrinology
Issue:
Volume 93:Number 6(2020)
Page Start:
678
Record Type:
Journal Article
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9. Expanding genetic spectrum and discriminatory role of steroid profiling by LC‐MS/MS in 11β‐hydroxylase deficiency. (4th December 2020)

Authors:
Karlekar, Manjiri Pramod; Sarathi, Vijaya; Lila, Anurag; Rai, Khushnandan; Arya, Sneha; Bhandare, Vishwambhar Vishnu; Atluri, Sridevi; Patil, Virendra; Ramteke‐Jadhav, Swati; Shah, Nalini S.; Kunwar, Ambarish; Bandgar, Tushar
Journal:
Clinical endocrinology
Issue:
Volume 94:Number 4(2021)
Page Start:
533
Record Type:
Journal Article
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10. Homozygous p.Val89Leu plays an important pathogenic role in 5α-reductase type 2 deficiency patients with homozygous p.Arg246Gln in SRD5A2. Issue 3 (September 2020)

Authors:
Arya, Sneha; Tiwari, Ankita; Lila, Anurag Ranjan; Sarathi, Vijaya; Bhandare, Vishwambhar Vishnu; Kumbhar, Bajarang Vasant; Rai, Khushnandan; Kunwar, Ambarish; Thakkar, Hemangini; Thakkar, Kunal; Memon, Saba Samad; Patil, Virendra; Khadilkar, Kranti; Jadhav, Swati S; Shah, Nalini S; Bandgar, Tushar
Journal:
European journal of endocrinology
Issue:
Volume 183:Issue 3(2020)
Page Start:
275
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗