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Devi Dayal

Showing results (171-180 of 180) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|April 19, 2025
Clinical and genetic insights into congenital lipoid adrenal hyperplasia: a case series from a tertiary care center in North IndiaArun George, Anvitha Rallapalli, Pamali Mahasweta Nanda, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|May 12, 2025
Clinical and molecular spectrum of genetic hypertriglyceridaemia in North Indian children: a case seriesSayan Banerjee, Arun George, Pamali Mahaswata Nanda, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 26, 2023
<i>SHOX</i> Variations in Idiopathic Short Stature in North India and a Review of Cases from Asian CountriesPriyanka Srivastava, Ankita Tyagi, Chitra Bamba, et al.
Indian Journal of Pediatrics|February 24, 2025
CANDID Study: Clinical and Molecular Characterization of Congenital Arginine Vasopressin-Resistance and the Use of a Novel Diagnostic Biomarker in Indian ChildrenSayan Banerjee, Pratyush P Pathak, Rajni Sharma, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 25, 2024
Estrogen Receptor 1 Gene Polymorphism and its Association with Idiopathic Short Stature in a North Indian PopulationRavi Shankar Patel, Roshan Daniel, Chitra Bhardwaj, et al.
Journal of Diabetes and Its Complications|October 1, 2021
Insulin gene mutations linked to permanent neonatal diabetes mellitus in Indian populationSundaramoorthy Gopi, Palanisamy Gowri, Jayant Kumar Panda, et al.
AACE Clinical Case Reports|April 13, 2022
Camurati-Engelmann Disease Complicated by Hypopituitarism: Management Challenges and Literature Review of Outcomes With BisphosphonatesLiza Das, Vandana Dhiman, Pinaki Dutta, et al.
The Indian Journal of Medical Research|May 23, 2019
Role of anti-tissue transglutaminase IgA+IgG antibodies in detection of potential celiac disease in patients with type 1 diabetesNavchetan Kaur, Ranjana W Minz, Sanjay K Bhadada, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 10, 2021
Bone density and bone health alteration in boys with Duchenne Muscular Dystrophy: a prospective observational studyRenu Suthar, B V Chaithanya Reddy, Manisha Malviya, et al.
Endocrine|September 19, 2020
Clinical application of a novel next generation sequencing assay for CYP21A2 gene in 310 cases of 21- hydroxylase congenital adrenal hyperplasia from IndiaPriyanka Gangodkar, Vaman Khadilkar, P Raghupathy, et al.
Pageof 18

Showing results (171-180 of 180) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 180 results.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 19, 2025
Clinical and genetic insights into congenital lipoid adrenal hyperplasia: a case series from a tertiary care center in North IndiaArun George, Anvitha Rallapalli, Pamali Mahasweta Nanda, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|May 12, 2025
Clinical and molecular spectrum of genetic hypertriglyceridaemia in North Indian children: a case seriesSayan Banerjee, Arun George, Pamali Mahaswata Nanda, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 26, 2023
<i>SHOX</i> Variations in Idiopathic Short Stature in North India and a Review of Cases from Asian CountriesPriyanka Srivastava, Ankita Tyagi, Chitra Bamba, et al.
Indian Journal of Pediatrics|February 24, 2025
CANDID Study: Clinical and Molecular Characterization of Congenital Arginine Vasopressin-Resistance and the Use of a Novel Diagnostic Biomarker in Indian ChildrenSayan Banerjee, Pratyush P Pathak, Rajni Sharma, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 25, 2024
Estrogen Receptor 1 Gene Polymorphism and its Association with Idiopathic Short Stature in a North Indian PopulationRavi Shankar Patel, Roshan Daniel, Chitra Bhardwaj, et al.
Journal of Diabetes and Its Complications|October 1, 2021
Insulin gene mutations linked to permanent neonatal diabetes mellitus in Indian populationSundaramoorthy Gopi, Palanisamy Gowri, Jayant Kumar Panda, et al.
AACE Clinical Case Reports|April 13, 2022
Camurati-Engelmann Disease Complicated by Hypopituitarism: Management Challenges and Literature Review of Outcomes With BisphosphonatesLiza Das, Vandana Dhiman, Pinaki Dutta, et al.
The Indian Journal of Medical Research|May 23, 2019
Role of anti-tissue transglutaminase IgA+IgG antibodies in detection of potential celiac disease in patients with type 1 diabetesNavchetan Kaur, Ranjana W Minz, Sanjay K Bhadada, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 10, 2021
Bone density and bone health alteration in boys with Duchenne Muscular Dystrophy: a prospective observational studyRenu Suthar, B V Chaithanya Reddy, Manisha Malviya, et al.
Endocrine|September 19, 2020
Clinical application of a novel next generation sequencing assay for CYP21A2 gene in 310 cases of 21- hydroxylase congenital adrenal hyperplasia from IndiaPriyanka Gangodkar, Vaman Khadilkar, P Raghupathy, et al.
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