Traboulsi EI - Search Results

1

A novel mutation in the RDS/Peripherin gene causes adult-onset foveomacular dystrophy.

Yang Z, Lin W, Moshfeghi DM, Thirumalaichary S, Li X, Jiang L, Zhang H, Zhang S, Kaiser PK, Traboulsi EI, Zhang K. Yang Z, et al. Among authors: traboulsi ei. Am J Ophthalmol. 2003 Feb;135(2):213-8. doi: 10.1016/s0002-9394(02)01815-9. Am J Ophthalmol. 2003. PMID: 12566026

2

Evaluation of choroidal thickness in retinitis pigmentosa using enhanced depth imaging optical coherence tomography.

Dhoot DS, Huo S, Yuan A, Xu D, Srivistava S, Ehlers JP, Traboulsi E, Kaiser PK. Dhoot DS, et al. Br J Ophthalmol. 2013 Jan;97(1):66-9. doi: 10.1136/bjophthalmol-2012-301917. Epub 2012 Oct 23. Br J Ophthalmol. 2013. PMID: 23093617

3

Mutation screen of the membrane-type frizzled-related protein (MFRP) gene in patients with inherited retinal degenerations.

Pauer GJ, Xi Q, Zhang K, Traboulsi EI, Hagstrom SA. Pauer GJ, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2005 Dec;26(4):157-61. doi: 10.1080/13816810500374425. Ophthalmic Genet. 2005. PMID: 16352475

4

Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration.

Stefko ST, Zhang K, Gorin MB, Traboulsi EI. Stefko ST, et al. Among authors: traboulsi ei. Am J Ophthalmol. 2000 Aug;130(2):203-8. doi: 10.1016/s0002-9394(00)00562-6. Am J Ophthalmol. 2000. PMID: 11004295

5

Lymphedema-distichiasis syndrome and FOXC2 gene mutation.

Traboulsi EI, Al-Khayer K, Matsumoto M, Kimak MA, Crowe S, Wilson SE, Finegold DN, Ferrell RE, Meisler DM. Traboulsi EI, et al. Am J Ophthalmol. 2002 Oct;134(4):592-6. doi: 10.1016/s0002-9394(02)01642-2. Am J Ophthalmol. 2002. PMID: 12383817

6

A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).

Yazdani A, Chung DC, Abbaszadegan MR, Al-Khayer K, Chan WM, Yazdani M, Ghodsi K, Engle EC, Traboulsi EI. Yazdani A, et al. Among authors: traboulsi ei. Am J Ophthalmol. 2003 Nov;136(5):861-5. doi: 10.1016/s0002-9394(03)00891-2. Am J Ophthalmol. 2003. PMID: 14597037

7

Dominant radial drusen and Arg345Trp EFEMP1 mutation.

Matsumoto M, Traboulsi EI. Matsumoto M, et al. Among authors: traboulsi ei. Am J Ophthalmol. 2001 Jun;131(6):810-2. doi: 10.1016/s0002-9394(00)00926-0. Am J Ophthalmol. 2001. PMID: 11384588

8

Bilateral macular lesions in a 10-year-old girl.

Radhakrishnan S, Bala E, Peachey NS, Lewis H, Traboulsi EI. Radhakrishnan S, et al. Among authors: traboulsi ei. Am J Ophthalmol. 2007 Jan;143(1):184-5. doi: 10.1016/j.ajo.2006.07.035. Epub 2006 Sep 1. Am J Ophthalmol. 2007. PMID: 17188069

9

Thirty-year follow-up of a patient with leber congenital amaurosis and novel RPE65 mutations.

Al-Khayer K, Hagstrom S, Pauer G, Zegarra H, Sears J, Traboulsi EI. Al-Khayer K, et al. Among authors: traboulsi ei. Am J Ophthalmol. 2004 Feb;137(2):375-7. doi: 10.1016/S0002-9394(03)00913-9. Am J Ophthalmol. 2004. PMID: 14962443

10

A new locus for dominant drusen and macular degeneration maps to chromosome 6q14.

Kniazeva M, Traboulsi EI, Yu Z, Stefko ST, Gorin MB, Shugart YY, O'Connell JR, Blaschak CJ, Cutting G, Han M, Zhang K. Kniazeva M, et al. Among authors: traboulsi ei. Am J Ophthalmol. 2000 Aug;130(2):197-202. doi: 10.1016/s0002-9394(00)00585-7. Am J Ophthalmol. 2000. PMID: 11004294

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