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Cornea|August 28, 2007
Keratoconus is not associated with mutations in COL8A1 and COL8A2Anthony J Aldave, Nirit Bourla, Vivek S Yellore, et al.
Retina (Philadelphia, Pa.)|June 15, 2007
Risk for eye splash injury during administration of intraocular injections: a study of retina specialists and fellowsDan H Bourla, Robert S Wirthlin, Nirit Bourla, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 28, 2011
Staphylolysin is an effective therapeutic agent for Staphylococcus aureus experimental keratitisIrina S Barequet, Nirit Bourla, Yuval N Pessach, et al.
Ophthalmic Genetics|June 15, 2007
Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2Anthony J Aldave, Baris Sonmez, Nirit Bourla, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI geneAnthony J Aldave, Vivek S Yellore, Baris Sonmez, et al.
Cornea|August 2, 2007
Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11Anthony J Aldave, Vivek S Yellore, Nirit Bourla, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal herniaAnthony J Aldave, Vivek S Yellore, Fei Yu, et al.
Molecular Vision|October 26, 2007
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophyVivek S Yellore, M Ali Khan, Nirit Bourla, et al.
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