Detalhe da pesquisa
1.
Characterization of a Novel POU1F1 Mutation Identified on Screening 160 Growth Hormone Deficiency Patients.
Horm Metab Res
; 51(4): 248-255, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31022740
2.
Novel MEN 1 gene findings in rare sporadic insulinoma--a case control study.
BMC Endocr Disord
; 15: 44, 2015 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26307114
3.
Machine learning-assisted prediction of trabeculectomy outcomes among patients of juvenile glaucoma by using 5-year follow-up data.
Indian J Ophthalmol
; 72(7): 987-993, 2024 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38454857
4.
In vivo identification of angle dysgenesis and its relation to genetic markers associated with glaucoma using artificial intelligence.
Indian J Ophthalmol
; 72(3): 339-346, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38146977
5.
Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency.
J Pediatr Endocrinol Metab
; 25(11-12): 1185-90, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23329769
6.
Latent Tuberculosis Infection Diagnosis among Household Contacts in a High Tuberculosis-Burden Area: a Comparison between Transcript Signature and Interferon Gamma Release Assay.
Microbiol Spectr
; 10(2): e0244521, 2022 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35416716
7.
Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotype.
Mol Hum Reprod
; 17(6): 372-8, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21242195
8.
Screening Malaria-box compounds to identify potential inhibitors against SARS-CoV-2 Mpro, using molecular docking and dynamics simulation studies.
Eur J Pharmacol
; 890: 173664, 2021 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33131721
9.
Dataset of mutational analysis, miRNAs targeting SARS-CoV-2 genes and host gene expression in SARS-CoV and SARS-CoV-2 infections.
Data Brief
; 32: 106207, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32864402
10.
Integrative analyses of SARS-CoV-2 genomes from different geographical locations reveal unique features potentially consequential to host-virus interaction, pathogenesis and clues for novel therapies.
Heliyon
; 6(9): e04658, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32844125
11.
Classifying juvenile onset primary open angle glaucoma using cluster analysis.
Br J Ophthalmol
; 104(6): 827-835, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31563868
12.
Rare manifestation of multiple endocrine neoplasia type 2A & cutaneous lichen amyloidosis in a family with RET gene mutation.
Indian J Med Res
; 139(5): 779-81, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25027091
13.
Molecular characterization of a rare phenotype of X-linked retinoschisis with angle-closure glaucoma.
Indian J Ophthalmol
; 67(7): 1226-1229, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31238476
14.
Mutations in membrane cofactor protein (CD46) gene in Indian children with hemolytic uremic syndrome.
Clin Kidney J
; 11(2): 198-203, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29644059
15.
Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiency.
Growth Horm IGF Res
; 29: 50-56, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27114065
16.
Impact of a novel 14âbp MEN1 deletion in a patient with hyperparathyroidism and gastrinoma.
Endocrinol Diabetes Metab Case Rep
; 2015: 150011, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26191410
17.
Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 families.
Indian J Endocrinol Metab
; 19(5): 644-8, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26425475
18.
Rare association of acromegaly with left atrial myxoma in Carney's complex due to novel PRKAR1A mutation.
Endocrinol Diabetes Metab Case Rep
; 2014: 140023, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25298879
19.
Genetic characterization of growth hormone 1 gene in patients with isolated growth hormone deficiency.
Indian J Endocrinol Metab
; 16(Suppl 2): S310-2, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23565410