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

Year Number of Results
1980 1
1987 1
1989 3
1990 3
1991 3
1992 7
1993 4
1994 4
1995 5
1996 3
1997 4
1998 4
1999 5
2000 3
2001 7
2002 7
2003 6
2004 4
2005 8
2006 4
2007 4
2008 6
2009 7
2010 6
2011 10
2012 17
2013 17
2014 24
2015 15
2016 21
2017 16
2018 17
2019 10
2020 13
2021 17
2022 11
2023 13
2024 21
2025 16
2026 2

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Search Results

318 results

Results by year

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Page 1
Gene Editing for CEP290-Associated Retinal Degeneration.
Pierce EA, Aleman TS, Jayasundera KT, Ashimatey BS, Kim K, Rashid A, Jaskolka MC, Myers RL, Lam BL, Bailey ST, Comander JI, Lauer AK, Maguire AM, Pennesi ME. Pierce EA, et al. Among authors: lam bl. N Engl J Med. 2024 Jun 6;390(21):1972-1984. doi: 10.1056/NEJMoa2309915. Epub 2024 May 6. N Engl J Med. 2024. PMID: 38709228 Free PMC article. Clinical Trial.
Initial results from a first-in-human gene therapy trial on X-linked retinitis pigmentosa caused by mutations in RPGR.
Cehajic-Kapetanovic J, Xue K, Martinez-Fernandez de la Camara C, Nanda A, Davies A, Wood LJ, Salvetti AP, Fischer MD, Aylward JW, Barnard AR, Jolly JK, Luo E, Lujan BJ, Ong T, Girach A, Black GCM, Gregori NZ, Davis JL, Rosa PR, Lotery AJ, Lam BL, Stanga PE, MacLaren RE. Cehajic-Kapetanovic J, et al. Among authors: lam bl. Nat Med. 2020 Mar;26(3):354-359. doi: 10.1038/s41591-020-0763-1. Epub 2020 Feb 24. Nat Med. 2020. PMID: 32094925 Free PMC article. Clinical Trial.
Association of Maintenance Intravenous Immunoglobulin With Prevention of Relapse in Adult Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.
Chen JJ, Huda S, Hacohen Y, Levy M, Lotan I, Wilf-Yarkoni A, Stiebel-Kalish H, Hellmann MA, Sotirchos ES, Henderson AD, Pittock SJ, Bhatti MT, Eggenberger ER, Di Nome M, Kim HJ, Kim SH, Saiz A, Paul F, Dale RC, Ramanathan S, Palace J, Camera V, Leite MI, Lam BL, Bennett JL, Mariotto S, Hodge D, Audoin B, Maillart E, Deschamps R, Pique J, Flanagan EP, Marignier R. Chen JJ, et al. Among authors: lam bl. JAMA Neurol. 2022 May 1;79(5):518-525. doi: 10.1001/jamaneurol.2022.0489. JAMA Neurol. 2022. PMID: 35377395 Free PMC article.
Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies.
Schwartz SD, Regillo CD, Lam BL, Eliott D, Rosenfeld PJ, Gregori NZ, Hubschman JP, Davis JL, Heilwell G, Spirn M, Maguire J, Gay R, Bateman J, Ostrick RM, Morris D, Vincent M, Anglade E, Del Priore LV, Lanza R. Schwartz SD, et al. Among authors: lam bl. Lancet. 2015 Feb 7;385(9967):509-16. doi: 10.1016/S0140-6736(14)61376-3. Epub 2014 Oct 15. Lancet. 2015. PMID: 25458728 Clinical Trial.
Effect of acetazolamide on visual function in patients with idiopathic intracranial hypertension and mild visual loss: the idiopathic intracranial hypertension treatment trial.
NORDIC Idiopathic Intracranial Hypertension Study Group Writing Committee; Wall M, McDermott MP, Kieburtz KD, Corbett JJ, Feldon SE, Friedman DI, Katz DM, Keltner JL, Schron EB, Kupersmith MJ. NORDIC Idiopathic Intracranial Hypertension Study Group Writing Committee, et al. JAMA. 2014 Apr 23-30;311(16):1641-51. doi: 10.1001/jama.2014.3312. JAMA. 2014. PMID: 24756514 Free PMC article. Clinical Trial.
Choroideremia Gene Therapy.
Lam BL, Davis JL, Gregori NZ. Lam BL, et al. Int Ophthalmol Clin. 2021 Oct 1;61(4):185-193. doi: 10.1097/IIO.0000000000000385. Int Ophthalmol Clin. 2021. PMID: 34584056 Free PMC article. No abstract available.
Reply.
Feuer WJ, Guy J, Gonzalez P, Koilkonda R, Porciatti V, Yuan H, Davis JL, Lam BL. Feuer WJ, et al. Among authors: lam bl. Ophthalmology. 2017 Mar;124(3):e22-e23. doi: 10.1016/j.ophtha.2016.07.003. Ophthalmology. 2017. PMID: 28219503 No abstract available.
Reply.
Guy J, Feuer WJ, Davis JL, Porciatti V, Gonzalez PJ, Koilkonda RD, Yuan H, Hauswirth WW, Lam BL. Guy J, et al. Among authors: lam bl. Ophthalmology. 2018 Feb;125(2):e15-e16. doi: 10.1016/j.ophtha.2017.08.041. Ophthalmology. 2018. PMID: 29389414 No abstract available.
Extreme Phenotypic Variability of ACTG1-Related Disorders in Hearing Loss.
Bernardi MT, Ramzan M, Calderon L, Salvatore F, De Rosa MA, Bivona S, Armando R, Vazquez N, Azcoiti ME, Marti MA, Arberas C, Ropelato MG, Olha S, Lam BL, Telischi FF, Tekin M, Walz K. Bernardi MT, et al. Among authors: lam bl. Adv Genet (Hoboken). 2024 Dec 5;5(4):2400040. doi: 10.1002/ggn2.202400040. eCollection 2024 Dec. Adv Genet (Hoboken). 2024. PMID: 39734360 Free PMC article.
318 results