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TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.
Chakravarthi SV, Kannabiran C, Sridhar MS, Vemuganti GK. Chakravarthi SV, et al. Invest Ophthalmol Vis Sci. 2005 Jan;46(1):121-5. doi: 10.1167/iovs.04-0440. Invest Ophthalmol Vis Sci. 2005. PMID: 15623763
Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy.
Kannabiran C, Sridhar MS, Chakravarthi SK, Vemuganti GK, Lakshmipathi M. Kannabiran C, et al. Arch Ophthalmol. 2005 Aug;123(8):1127-33. doi: 10.1001/archopht.123.8.1127. Arch Ophthalmol. 2005. PMID: 16087849
Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11.
Jiao X, Sultana A, Garg P, Ramamurthy B, Vemuganti GK, Gangopadhyay N, Hejtmancik JF, Kannabiran C. Jiao X, et al. J Med Genet. 2007 Jan;44(1):64-8. doi: 10.1136/jmg.2006.044644. Epub 2006 Jul 6. J Med Genet. 2007. PMID: 16825429 Free PMC article.
Phenotypic characterization of retinoblastoma for the presence of putative cancer stem-like cell markers by flow cytometry.
Balla MM, Vemuganti GK, Kannabiran C, Honavar SG, Murthy R. Balla MM, et al. Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1506-14. doi: 10.1167/iovs.08-2356. Epub 2008 Nov 21. Invest Ophthalmol Vis Sci. 2009. PMID: 19029022
Histopathologic risk factors in retinoblastoma in India.
Gupta R, Vemuganti GK, Reddy VA, Honavar SG. Gupta R, et al. Arch Pathol Lab Med. 2009 Aug;133(8):1210-4. doi: 10.1043/1543-2165-133.8.1210. Arch Pathol Lab Med. 2009. PMID: 19653711
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