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Patch testing with the Indian standard series in New Delhi.
Sharma VK, Sethuraman G, Garg T, Verma KK, Ramam M. Sharma VK, et al. Among authors: sethuraman g. Contact Dermatitis. 2004 Nov-Dec;51(5-6):319-21. doi: 10.1111/j.0105-1873.2004.0459k.x. Contact Dermatitis. 2004. PMID: 15606668 No abstract available.
Molecular basis of lipoid proteinosis in two Indian siblings.
Chan I, Sethuraman G, Sharma VK, Bruning E, Hamada T, McGrath JA. Chan I, et al. Among authors: sethuraman g. J Dermatol. 2004 Sep;31(9):764-6. doi: 10.1111/j.1346-8138.2004.tb00593.x. J Dermatol. 2004. PMID: 15628326 No abstract available.
Five new homozygous mutations in the KIND1 gene in Kindler syndrome.
Lai-Cheong JE, Liu L, Sethuraman G, Kumar R, Sharma VK, Reddy SR, Vahlquist A, Pather S, Arita K, Wessagowit V, McGrath JA. Lai-Cheong JE, et al. Among authors: sethuraman g. J Invest Dermatol. 2007 Sep;127(9):2268-70. doi: 10.1038/sj.jid.5700830. Epub 2007 Apr 26. J Invest Dermatol. 2007. PMID: 17460733 Free article. No abstract available.
Skin tuberculosis in children: learning from India.
Sethuraman G, Ramesh V, Ramam M, Sharma VK. Sethuraman G, et al. Dermatol Clin. 2008 Apr;26(2):285-94, vii. doi: 10.1016/j.det.2007.11.006. Dermatol Clin. 2008. PMID: 18346559 Review.
Novel and recurrent FERMT1 gene mutations in Kindler syndrome.
Techanukul T, Sethuraman G, Zlotogorski A, Horev L, Macarov M, Trainer A, Fong K, Lens M, Medenica L, Ramesh V, McGrath JA, Lai-Cheong JE. Techanukul T, et al. Among authors: sethuraman g. Acta Derm Venereol. 2011 May;91(3):267-70. doi: 10.2340/00015555-1063. Acta Derm Venereol. 2011. PMID: 21336475 Free article.
222 results