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Shweta Birla

Showing results (11-20 of 22) with videos related to

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Indian Journal of Endocrinology and Metabolism|April 9, 2013
Genetic characterization of growth hormone 1 gene in patients with isolated growth hormone deficiencyShweta Birla, P Vieveka Jyotsana, Arundhati Sharma, et al.
Industrial Psychiatry Journal|May 16, 2025
Classifying opioid use disorder based on diagnostic criteria items using cluster analysisShweta Birla, Vinit Patel, Dinesh Gupta, et al.
Indian Journal of Ophthalmology|June 27, 2019
Molecular characterization of a rare phenotype of X-linked retinoschisis with angle-closure glaucomaHarathy Selvan, Anshul Sharma, Shweta Birla, et al.
Indian Journal of Endocrinology and Metabolism|October 2, 2015
Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 familiesSarita Yadav, Shweta Birla, Eunice Marumudi, et al.
The British Journal of Ophthalmology|September 30, 2019
Classifying juvenile onset primary open angle glaucoma using cluster analysisShweta Birla, Dinesh Gupta, Bindu I Somarajan, et al.
Endocrine Pathology|June 18, 2025
A Novel Three-Stage AI-Assisted Approach for Accurate Differential Diagnosis and Classification of NIFTP and Thyroid NeoplasmsShweta Birla, Nimisha Tiwari, Pragati Shyamal, et al.
Indian Journal of Ophthalmology|March 8, 2024
Machine learning-assisted prediction of trabeculectomy outcomes among patients of juvenile glaucoma by using 5-year follow-up dataShweta Birla, Toshit Varshney, Abhishek Singh, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|April 27, 2016
Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiencyShweta Birla, Rajesh Khadgawat, Viveka P Jyotsna, et al.
Clinical Kidney Journal|April 13, 2018
Mutations in <i>membrane cofactor protein</i> (<i>CD46</i>) gene in Indian children with hemolytic uremic syndromePriyanka Khandelwal, Shweta Birla, Divya Bhatia, et al.
Indian Journal of Ophthalmology|December 26, 2023
In vivo identification of angle dysgenesis and its relation to genetic markers associated with glaucoma using artificial intelligenceViney Gupta, Shweta Birla, Toshit Varshney, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Indian Journal of Endocrinology and Metabolism|April 9, 2013
Genetic characterization of growth hormone 1 gene in patients with isolated growth hormone deficiencyShweta Birla, P Vieveka Jyotsana, Arundhati Sharma, et al.
Industrial Psychiatry Journal|May 16, 2025
Classifying opioid use disorder based on diagnostic criteria items using cluster analysisShweta Birla, Vinit Patel, Dinesh Gupta, et al.
Indian Journal of Ophthalmology|June 27, 2019
Molecular characterization of a rare phenotype of X-linked retinoschisis with angle-closure glaucomaHarathy Selvan, Anshul Sharma, Shweta Birla, et al.
Indian Journal of Endocrinology and Metabolism|October 2, 2015
Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 familiesSarita Yadav, Shweta Birla, Eunice Marumudi, et al.
The British Journal of Ophthalmology|September 30, 2019
Classifying juvenile onset primary open angle glaucoma using cluster analysisShweta Birla, Dinesh Gupta, Bindu I Somarajan, et al.
Endocrine Pathology|June 18, 2025
A Novel Three-Stage AI-Assisted Approach for Accurate Differential Diagnosis and Classification of NIFTP and Thyroid NeoplasmsShweta Birla, Nimisha Tiwari, Pragati Shyamal, et al.
Indian Journal of Ophthalmology|March 8, 2024
Machine learning-assisted prediction of trabeculectomy outcomes among patients of juvenile glaucoma by using 5-year follow-up dataShweta Birla, Toshit Varshney, Abhishek Singh, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|April 27, 2016
Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiencyShweta Birla, Rajesh Khadgawat, Viveka P Jyotsna, et al.
Clinical Kidney Journal|April 13, 2018
Mutations in <i>membrane cofactor protein</i> (<i>CD46</i>) gene in Indian children with hemolytic uremic syndromePriyanka Khandelwal, Shweta Birla, Divya Bhatia, et al.
Indian Journal of Ophthalmology|December 26, 2023
In vivo identification of angle dysgenesis and its relation to genetic markers associated with glaucoma using artificial intelligenceViney Gupta, Shweta Birla, Toshit Varshney, et al.
Pageof 3