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Publications (11)
- Delay in diagnosis is the most important proximate reason for mortality in hereditary angio-oedema: our experience at Chandigarh, India Save
- Familial aggregation of diffuse cutaneous systemic sclerosis: Interplay of C1r gene defect, susceptible HLA haplotype and autoantibodies Save
- Heterozygous RAD50 gene variant in a family with systemic sclerosis suggests role of impaired DNA repair mechanisms in disease pathogenesis Save
- Ophthalmologic profile of patients with systemic sclerosis Save
- Recalcitrant skin ulcers in a patient with Papillon–Lefèvre syndrome: an unusual novel presentation Save
- Transmission patterns of C1-INH deficiency hereditary angioedema favors a wild-type male offspring: Our experience at Chandigarh, India Save
- Human leukocyte antigen association in systemic sclerosis patients: our experience at a tertiary care center in North India Save
- Antinuclear antibody pattern and autoantibody profiling of systemic sclerosis patients in a tertiary referral center in North India Save
- Detection of Epstein–Barr virus in systemic sclerosis patients: A molecular and serological based study Save
- An improved and easy protocol for primary epithelial cell culture from atretic tissue in biliary atresia Save