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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1984 6
1985 11
1986 9
1987 7
1988 12
1989 4
1990 7
1991 3
1992 9
1993 12
1994 3
1995 5
1996 2
1997 2
1998 7
1999 4
2000 8
2001 6
2002 4
2003 11
2004 10
2005 12
2006 18
2007 10
2008 13
2009 12
2010 11
2011 12
2012 15
2013 9
2014 10
2015 8
2016 11
2017 10
2018 12
2019 13
2020 10
2021 6
2022 10
2023 4
2024 0

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320 results

Results by year

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Page 1
Cohen Syndrome.
Wang H, Falk MJ, Wensel C, Traboulsi EI. Wang H, et al. Among authors: traboulsi ei. 2006 Aug 29 [updated 2016 Jul 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2006 Aug 29 [updated 2016 Jul 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301655 Free Books & Documents. Review.
Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.
Fujinami K, Strauss RW, Chiang JP, Audo IS, Bernstein PS, Birch DG, Bomotti SM, Cideciyan AV, Ervin AM, Marino MJ, Sahel JA, Mohand-Said S, Sunness JS, Traboulsi EI, West S, Wojciechowski R, Zrenner E, Michaelides M, Scholl HPN; ProgStar Study Group; ProgStar Study Group. Fujinami K, et al. Among authors: traboulsi ei. Br J Ophthalmol. 2019 Mar;103(3):390-397. doi: 10.1136/bjophthalmol-2018-312064. Epub 2018 Jun 20. Br J Ophthalmol. 2019. PMID: 29925512 Free PMC article.
Gene therapy for RPE65-related retinal disease.
Miraldi Utz V, Coussa RG, Antaki F, Traboulsi EI. Miraldi Utz V, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2018 Dec;39(6):671-677. doi: 10.1080/13816810.2018.1533027. Epub 2018 Oct 18. Ophthalmic Genet. 2018. PMID: 30335549 Review.
Effective gene therapy of Stargardt disease with PEG-ECO/pGRK1-ABCA4-S/MAR nanoparticles.
Sun D, Sun W, Gao SQ, Lehrer J, Naderi A, Wei C, Lee S, Schilb AL, Scheidt J, Hall RC, Traboulsi EI, Palczewski K, Lu ZR. Sun D, et al. Among authors: traboulsi ei. Mol Ther Nucleic Acids. 2022 Aug 24;29:823-835. doi: 10.1016/j.omtn.2022.08.026. eCollection 2022 Sep 13. Mol Ther Nucleic Acids. 2022. PMID: 36159595 Free PMC article.
Ocular manifestations of the autoinflammatory syndromes.
Tarabishy AB, Hise AG, Traboulsi EI. Tarabishy AB, et al. Among authors: traboulsi ei. Ophthalmic Genet. 2012 Dec;33(4):179-86. doi: 10.3109/13816810.2012.695421. Epub 2012 Aug 27. Ophthalmic Genet. 2012. PMID: 22924780 Review.
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
Solaki M, Baumann B, Reuter P, Andreasson S, Audo I, Ayuso C, Balousha G, Benedicenti F, Birch D, Bitoun P, Blain D, Bocquet B, Branham K, Català-Mora J, De Baere E, Dollfus H, Falana M, Giorda R, Golovleva I, Gottlob I, Heckenlively JR, Jacobson SG, Jones K, Jägle H, Janecke AR, Kellner U, Liskova P, Lorenz B, Martorell-Sampol L, Messias A, Meunier I, Belga Ottoni Porto F, Papageorgiou E, Plomp AS, de Ravel TJL, Reiff CM, Renner AB, Rosenberg T, Rudolph G, Salati R, Sener EC, Sieving PA, Stanzial F, Traboulsi EI, Tsang SH, Varsanyi B, Weleber RG, Zobor D, Stingl K, Wissinger B, Kohl S. Solaki M, et al. Among authors: traboulsi ei. Hum Mutat. 2022 Jul;43(7):832-858. doi: 10.1002/humu.24371. Epub 2022 Apr 14. Hum Mutat. 2022. PMID: 35332618 Review.
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.
320 results