Aruna Gowdra
Bengaluru, KA, India
Last Updated: 09/26/2026
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Found 9 publications
A multiplexed LC-MS/MS assay for comprehensive screening of amino acid metabolism disorders.
Journal: Talanta open
Published: June 01, 2026
Use of untargeted metabolomics for the study of pediatric neurometabolic disorders: A review.
Journal: Molecular genetics and metabolism
Published: October 19, 2025
Lack of association of Stevens-Johnson syndrome/toxic epidermal necrolysis due to aromatic anticonvulsants and HLA-B alleles in South Indian children.
Journal: International journal of dermatology
Published: January 24, 2024
Identification of a rare [Gγ(Aγδβ)0] -thalassemia using tandem mass spectrometry.
Journal: Proteomics
Published: November 04, 2023
Filaggrin gene polymorphisms in Indian children with atopic dermatitis: A cross-sectional multicentre study.
Journal: Indian journal of dermatology, venereology and leprology
Published: January 09, 2022
Pseudodominant inheritance of self-improving collodion ichthyosis with homozygous mutation in the ALOX12B gene.
Journal: Indian journal of dermatology, venereology and leprology
Published: December 01, 2020
Clinicogenetic Profile, Treatment Modalities, and Mortality Predictors of Gaucher Disease: A 15-Year Retrospective Study.
Journal: Public health genomics
Published: September 03, 2020
A novel homozygous frameshift mutation in DSG1 gene in an Indian consanguineous family with severe dermatitis, multiple allergies and metabolic wasting syndrome.
Journal: Indian journal of dermatology, venereology and leprology
Published: May 01, 2019
A Clinical Study on Congenital Diaphragmatic Hernia in Neonates: Our Institutional Experience.
Journal: Journal of Indian Association of Pediatric Surgeons
Published: July 28, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026