Gene therapy for RPE65-related retinal disease
Miraldi Utz, Virginia, Coussa, Razek Georges, Antaki, Fares, Traboulsi, Elias I.
Published in Ophthalmic genetics (02.11.2018)
Published in Ophthalmic genetics (02.11.2018)
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Journal Article
Outcomes of Bilateral Cataracts Removed in Infants 1 to 7 Months of Age Using the Toddler Aphakia and Pseudophakia Treatment Study Registry
Bothun, Erick D., Wilson, M. Edward, Vanderveen, Deborah K., Plager, David A., Freedman, Sharon F., Trivedi, Rupal H., Traboulsi, Elias I., Anderson, Jill S., Loh, Allison R., Yen, Kimberly G., Weil, Natalie C., Morrison, David, Lambert, Scott R.
Published in Ophthalmology (Rochester, Minn.) (01.04.2020)
Published in Ophthalmology (Rochester, Minn.) (01.04.2020)
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Journal Article
Mitochondrial DNA A3243G variant-associated retinopathy: Current perspectives and clinical implications
Coussa, Razek Georges, Parikh, Sumit, Traboulsi, Elias I.
Published in Survey of ophthalmology (01.09.2021)
Published in Survey of ophthalmology (01.09.2021)
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Journal Article
Outcomes of Bilateral Cataract Surgery in Infants 7 to 24 Months of Age Using the Toddler Aphakia and Pseudophakia Treatment Study Registry
Bothun, Erick D., Wilson, M. Edward, Yen, Kimberly G., Anderson, Jill S., Weil, Natalie C., Loh, Allison R., Morrison, David, Freedman, Sharon F., Plager, David A., Vanderveen, Deborah K., Traboulsi, Elias I., Hodge, David O., Lambert, Scott R.
Published in Ophthalmology (Rochester, Minn.) (01.02.2021)
Published in Ophthalmology (Rochester, Minn.) (01.02.2021)
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Journal Article
Outcomes of Unilateral Cataracts in Infants and Toddlers 7 to 24 Months of Age: Toddler Aphakia and Pseudophakia Study (TAPS)
Bothun, Erick D, Wilson, M Edward, Traboulsi, Elias I, Diehl, Nancy N, Plager, David A, Vanderveen, Deborah K, Freedman, Sharon F, Yen, Kimberly G, Weil, Natalie C, Loh, Allison R, Morrison, David, Anderson, Jill S, Lambert, Scott R
Published in Ophthalmology (Rochester, Minn.) (01.08.2019)
Published in Ophthalmology (Rochester, Minn.) (01.08.2019)
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Journal Article
Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus
Mayer, Anja K, Mahajnah, Muhammad, Thomas, Mervyn G, Cohen, Yuval, Habib, Adib, Schulze, Martin, Maconachie, Gail D E, AlMoallem, Basamat, De Baere, Elfride, Lorenz, Birgit, Traboulsi, Elias I, Kohl, Susanne, Azem, Abdussalam, Bauer, Peter, Gottlob, Irene, Sharkia, Rajech, Wissinger, Bernd
Published in Brain (London, England : 1878) (01.06.2019)
Published in Brain (London, England : 1878) (01.06.2019)
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Journal Article
Ocular Findings in a Patient With KAT6A Mutation
Young, LeAnne, Brooks, Brian, Traboulsi, Elias I
Published in Journal of pediatric ophthalmology and strabismus (01.05.2021)
Published in Journal of pediatric ophthalmology and strabismus (01.05.2021)
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Journal Article
Stickler syndrome: exploring prophylaxis for retinal detachment
Coussa, Razek Georges, Sears, Jonathan, Traboulsi, Elias I
Published in Current opinion in ophthalmology (01.09.2019)
Published in Current opinion in ophthalmology (01.09.2019)
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Journal Article
Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome
Patel, Nisha, Khan, Arif O., Mansour, Ahmad, Mohamed, Jawahir Y., Al-Assiri, Abdullah, Haddad, Randa, Jia, Xiaofei, Xiong, Yong, Mégarbané, André, Traboulsi, Elias I., Alkuraya, Fowzan S.
Published in American journal of human genetics (01.05.2014)
Published in American journal of human genetics (01.05.2014)
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Journal Article
ELLIPSOID ZONE MAPPING AND OUTER RETINAL ASSESSMENT IN STARGARDT DISEASE
Arepalli, Sruthi, Traboulsi, Elias I, Ehlers, Justis P
Published in Retina (Philadelphia, Pa.) (01.07.2018)
Published in Retina (Philadelphia, Pa.) (01.07.2018)
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Journal Article