Detalhe da pesquisa
1.
A Novel Large Deletion in the EVER1 Gene in a Family With Epidermodysplasia Verruciformis From India.
Am J Dermatopathol
; 2024 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38574087
2.
Incidence, Intrapartum Risk Factors, and Prognosis of Neonatal Hypoxic-Ischemic Encephalopathy Among Infants Born at 35 Weeks Gestation or More.
J Obstet Gynaecol Can
; 42(12): 1489-1497, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33039315
3.
Epitope-based immunoinformatics approach on RNA-dependent RNA polymerase (RdRp) protein complex of Nipah virus (NiV).
J Cell Biochem
; 120(5): 7082-7095, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30417438
4.
Congenital Adrenal Hyperplasia - A Comprehensive Review of Genetic Studies on 21-Hydroxylase Deficiency from India.
Indian J Endocrinol Metab
; 28(2): 117-128, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38911104
5.
Clinical, Hormonal, and Genetic Spectrum of 46 XY Disorders of Sexual Development (DSD) Patients.
Indian J Pediatr
; 2024 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38761274
6.
High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal Hyperplasia.
Endocrine
; 2024 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38441846
7.
The BRCA mutation spectrum among breast and ovarian cancers in India: highlighting the need to screen BRCA1 185delAG among South Indians.
Eur J Hum Genet
; 2024 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38538877
8.
Clinical Features of Unrecognized Congenital Adrenal Hyperplasia Due to 17α-hydroxylase Deficiency Since Adolescence: A Case Report.
J ASEAN Fed Endocr Soc
; 38(2): 131-134, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38045661
9.
Allele-specific and multiplex PCR based tools for cost-effective and comprehensive genetic testing in Congenital Adrenal Hyperplasia.
MethodsX
; 9: 101748, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35756349
10.
Genetic Heterogeneity and Challenges in the Management of Permanent Neonatal Diabetes Mellitus: A Single-Centre Study from South India.
Indian J Endocrinol Metab
; 26(1): 79-86, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35662751
11.
WFS1 Gene-associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India.
J Clin Endocrinol Metab
; 107(5): 1328-1336, 2022 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35018440
12.
Allele-specific PCR and Next-generation sequencing based genetic screening for Congenital Adrenal Hyperplasia in India.
Eur J Med Genet
; 64(12): 104369, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34718183
13.
Non-alcoholic fatty liver disease and outcomes in persons with acute coronary syndromes: insights from the GRACE-ALT analysis.
Heart Asia
; 4(1): 137-40, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-27326050