Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 11/12, p. 1185, doi. 10.1515/jpem-2012-0152
- By:
- Publication type:
- Article
Works by Birla, Shweta
Results: 14
1
2
Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation.
- Published in:
- Indian Journal of Medical Research, 2014, v. 139, n. 5, p. 779
- By:
- Publication type:
- Article
3
Calcium sensing receptor expression is downregulated in gastroenteropancreatic neuroendocrine tumours via epigenetic mechanisms.
- Published in:
- International Journal of Cancer, 2025, v. 156, n. 5, p. 980, doi. 10.1002/ijc.35264
- By:
- Publication type:
- Article
4
Novel MEN 1 gene findings in rare sporadic insulinoma--a case control study.
- Published in:
- BMC Endocrine Disorders, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12902-015-0041-2
- By:
- Publication type:
- Article
5
Mutations in membrane cofactor protein (CD46) gene in Indian children with hemolytic uremic syndrome.
- Published in:
- Clinical Kidney Journal, 2018, v. 11, n. 2, p. 198, doi. 10.1093/ckj/sfx078
- By:
- Publication type:
- Article
6
Machine learning-assisted prediction of trabeculectomy outcomes among patients of juvenile glaucoma by using 5-year follow-up data.
- Published in:
- Indian Journal of Ophthalmology, 2024, v. 72, n. 7, p. 987, doi. 10.4103/IJO.IJO_2009_23
- By:
- Publication type:
- Article
7
In vivo identification of angle dysgenesis and its relation to genetic markers associated with glaucoma using artificial intelligence.
- Published in:
- Indian Journal of Ophthalmology, 2024, v. 72, n. 3, p. 339, doi. 10.4103/IJO.IJO_1456_23
- By:
- Publication type:
- Article
8
Molecular characterization of a rare phenotype of X-linked retinoschisis with angle-closure glaucoma.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
9
Classifying opioid use disorder based on diagnostic criteria items using cluster analysis.
- Published in:
- Industrial Psychiatry Journal, 2025, v. 34, n. 1, p. 32, doi. 10.4103/ipj.ipj_430_24
- By:
- Publication type:
- Article
10
Deep learning model to identify angle dysgenesis on ASOCT images.
- Published in:
- 2022
- By:
- Publication type:
- Abstract
11
Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotype.
- Published in:
- Molecular Human Reproduction, 2011, v. 17, n. 6, p. 372, doi. 10.1093/molehr/gar002
- By:
- Publication type:
- Article
12
Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 families.
- Published in:
- Indian Journal of Endocrinology & Metabolism, 2015, v. 19, n. 5, p. 644, doi. 10.4103/2230-8210.163191
- By:
- Publication type:
- Article
13
Gene analysis of POU1F1 and PROP1 and prenatal diagnosis in combined pituitary hormone deficiency.
- Published in:
- Indian Journal of Endocrinology & Metabolism, 2012, v. 16, p. S515
- By:
- Publication type:
- Article
14
Genetic characterization of growth hormone 1 gene in patients with isolated growth hormone deficiency.
- Published in:
- Indian Journal of Endocrinology & Metabolism, 2012, v. 16, p. S310, doi. 10.4103/2230-8210.104071
- By:
- Publication type:
- Article