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Molecular genetics for the pediatric ophthalmologist.
Bollinger K, Traboulsi EI. Bollinger K, et al. Among authors: traboulsi ei. J Pediatr Ophthalmol Strabismus. 2007 Jul-Aug;44(4):209-15; quiz 241-2. doi: 10.3928/01913913-20070701-01. J Pediatr Ophthalmol Strabismus. 2007. PMID: 17694825 Review.
Hypermetropia and esotropia in myotonic dystrophy.
Bollinger KE, Kattouf V, Arthur B, Weiss AH, Kivlin J, Kerr N, West CE, Kipp M, Traboulsi EI. Bollinger KE, et al. Among authors: traboulsi ei. J AAPOS. 2008 Feb;12(1):69-71. doi: 10.1016/j.jaapos.2007.08.005. Epub 2007 Oct 29. J AAPOS. 2008. PMID: 18029209
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.
Robitaille JM, Gillett RM, LeBlanc MA, Gaston D, Nightingale M, Mackley MP, Parkash S, Hathaway J, Thomas A, Ells A, Traboulsi EI, Héon E, Roy M, Shalev S, Fernandez CV, MacGillivray C, Wallace K, Fahiminiya S, Majewski J, McMaster CR, Bedard K. Robitaille JM, et al. Among authors: traboulsi ei. JAMA Ophthalmol. 2014 Dec;132(12):1393-9. doi: 10.1001/jamaophthalmol.2014.2814. JAMA Ophthalmol. 2014. PMID: 25124931
Molecular biology and genetics of embryonic eyelid development.
Rubinstein TJ, Weber AC, Traboulsi EI. Rubinstein TJ, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2016 Sep;37(3):252-9. doi: 10.3109/13816810.2015.1071409. Epub 2016 Feb 11. Ophthalmic Genet. 2016. PMID: 26863902 Review.
Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task Force.
Drack AV, Miraldi Utz V, Wang K, Alcorn DM, Brooks BP, Costakos DM, Couser NL, Heon E, Levin AV, Lloyd IC, Morse CL, Schmitt MA, Whitman MC, Traboulsi EI. Drack AV, et al. Among authors: traboulsi ei. J AAPOS. 2019 Aug;23(4):226-228.e1. doi: 10.1016/j.jaapos.2019.04.005. Epub 2019 Jun 21. J AAPOS. 2019. PMID: 31233830
348 results