Traboulsi E - Search Results

1

Cutis marmorata telangiectatica congenita: a focus on its diagnosis, ophthalmic anomalies, and possible etiologic factors.

Elitt MS, Tamburro JE, Moran RT, Traboulsi E. Elitt MS, et al. Among authors: traboulsi e. Ophthalmic Genet. 2020 Apr;41(2):101-107. doi: 10.1080/13816810.2020.1744018. Epub 2020 Mar 31. Ophthalmic Genet. 2020. PMID: 32233697 Review.

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. Among authors: traboulsi e. 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. 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

Color vision testing.

Melamud A, Hagstrom S, Traboulsi E. Melamud A, et al. Among authors: traboulsi e. Ophthalmic Genet. 2004 Sep;25(3):159-87. doi: 10.1080/13816810490498341. Ophthalmic Genet. 2004. PMID: 15512994 Review.

7

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

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

8

The value of keratometry and central corneal thickness measurements in the clinical diagnosis of Marfan syndrome.

Heur M, Costin B, Crowe S, Grimm RA, Moran R, Svensson LG, Traboulsi EI. Heur M, et al. Am J Ophthalmol. 2008 Jun;145(6):997-1001. doi: 10.1016/j.ajo.2008.01.028. Epub 2008 Apr 18. Am J Ophthalmol. 2008. PMID: 18378212

9

Update on the morning glory disc anomaly.

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

10

Aicardi syndrome in a genotypic male.

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

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