Traboulsi EI - Search Results

1

Bilateral angle closure glaucoma in a 28-year-old Cohen syndrome patient.

Li A, Gandhi A, Wang H, Traboulsi EI. Li A, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2018 Oct;39(5):657-658. doi: 10.1080/13816810.2018.1495746. Epub 2018 Jul 9. Ophthalmic Genet. 2018. PMID: 29985682 No abstract available.

2

Morning glory disk anomaly, choroidal coloboma, and congenital constrictive malformations of the internal carotid arteries (moyamoya disease).

Krishnan C, Roy A, Traboulsi E. Krishnan C, et al. Ophthalmic Genet. 2000 Mar;21(1):21-4. Ophthalmic Genet. 2000. PMID: 10779846

3

Colobomatous microphthalmia and orbital neuroglial cyst: case report.

Garcia LM, Castro E, Foster JA, Green RW, Traboulsi EI. Garcia LM, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2002 Mar;23(1):37-42. doi: 10.1076/opge.23.1.37.2205. Ophthalmic Genet. 2002. PMID: 11910557

4

Presenting signs and clinical diagnosis in individuals referred to rule out Marfan syndrome.

Hamod A, Moodie D, Clark B, Traboulsi EI. Hamod A, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2003 Mar;24(1):35-9. doi: 10.1076/opge.24.1.35.13892. Ophthalmic Genet. 2003. PMID: 12660864

5

Ocular findings in ichthyosis follicularis-alopecia-photophobia (IFAP) syndrome.

Traboulsi E, Waked N, Mégarbané H, Mégarbané A. Traboulsi E, et al. Ophthalmic Genet. 2004 Jun;25(2):153-6. doi: 10.1080/13816810490514405. Ophthalmic Genet. 2004. PMID: 15370546

6

Optic disc coloboma and localized chorioretinal defects in constitutional partial trisomy 8 mosaicism.

Taban M, Marcotty A, Traboulsi EI. Taban M, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2006 Sep;27(3):103-5. doi: 10.1080/13816810600862543. Ophthalmic Genet. 2006. PMID: 17050287

7

Cohen syndrome: report of nine cases and review of the literature, with emphasis on ophthalmic features.

Taban M, Memoracion-Peralta DS, Wang H, Al-Gazali LI, Traboulsi EI. Taban M, et al. Among authors: traboulsi ei. J AAPOS. 2007 Oct;11(5):431-7. doi: 10.1016/j.jaapos.2007.01.118. Epub 2007 Mar 26. J AAPOS. 2007. PMID: 17383910

8

Update on the morning glory disc anomaly.

Lee BJ, Traboulsi EI. Lee BJ, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2008 Jun;29(2):47-52. doi: 10.1080/13816810801901876. Ophthalmic Genet. 2008. PMID: 18484308 Review.

9

Aicardi syndrome in a genotypic male.

Chappelow AV, Reid J, Parikh S, Traboulsi EI. Chappelow AV, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2008 Dec;29(4):181-3. doi: 10.1080/13816810802320209. Ophthalmic Genet. 2008. PMID: 19005990

10

Coats' disease, megalopapilla and Cornelia de Lange syndrome.

Barakat MR, Traboulsi EI, Sears JE. Barakat MR, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2009 Jun;30(2):106-8. doi: 10.1080/13816810902744613. Ophthalmic Genet. 2009. PMID: 19373684

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