Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
4 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
Mol Vis. 2007 Sep 24;13:1777-82.
Mol Vis. 2007.
PMID: 17960116
Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.
Aldave AJ, Yellore VS, Bourla N, Momi RS, Khan MA, Salem AK, Rayner SA, Glasgow BJ, Kurtz I.
Aldave AJ, et al. Among authors: momi rs.
Cornea. 2007 Aug;26(7):896-900. doi: 10.1097/ICO.0b013e318074bb01.
Cornea. 2007.
PMID: 17667634
Item in Clipboard
No pathogenic mutations identified in the COL8A2 gene or four positional candidate genes in patients with posterior polymorphous corneal dystrophy.
Yellore VS, Rayner SA, Emmert-Buck L, Tabin GC, Raber I, Hannush SB, Stulting RD, Sampat K, Momi R, Principe AH, Aldave AJ.
Yellore VS, et al.
Invest Ophthalmol Vis Sci. 2005 May;46(5):1599-603. doi: 10.1167/iovs.04-1321.
Invest Ophthalmol Vis Sci. 2005.
PMID: 15851557
Item in Clipboard
Review of ranibizumab trials for neovascular age-related macular degeneration.
Patel RD, Momi RS, Hariprasad SM.
Patel RD, et al. Among authors: momi rs.
Semin Ophthalmol. 2011 Nov;26(6):372-9. doi: 10.3109/08820538.2011.570845.
Semin Ophthalmol. 2011.
PMID: 22044335
Review.
Item in Clipboard
Cite
Cite