Lam BL - Search Results

1

Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia.

Langlo CS, Patterson EJ, Higgins BP, Summerfelt P, Razeen MM, Erker LR, Parker M, Collison FT, Fishman GA, Kay CN, Zhang J, Weleber RG, Yang P, Wilson DJ, Pennesi ME, Lam BL, Chiang J, Chulay JD, Dubra A, Hauswirth WW, Carroll J; ACHM-001 Study Group. Langlo CS, et al. Among authors: lam bl. Invest Ophthalmol Vis Sci. 2016 Aug 1;57(10):3984-95. doi: 10.1167/iovs.16-19313. Invest Ophthalmol Vis Sci. 2016. PMID: 27479814 Free PMC article.

2

Effect of mydriasis on visual field area in retinitis pigmentosa.

Lam BL, Fishman GA, Anderson RJ, Smith DA, Alexander KR. Lam BL, et al. Ophthalmology. 1992 Nov;99(11):1724-7. doi: 10.1016/s0161-6420(92)31740-3. Ophthalmology. 1992. PMID: 1454349 Clinical Trial.

3

Prevalence of foveal lesions in type 1 and type 2 Usher's syndrome.

Fishman GA, Anderson RJ, Lam BL, Derlacki DJ. Fishman GA, et al. Among authors: lam bl. Arch Ophthalmol. 1995 Jun;113(6):770-3. doi: 10.1001/archopht.1995.01100060096040. Arch Ophthalmol. 1995. PMID: 7786220

4

Racial differences in the prevalence of atrophic-appearing macular lesions between black and white patients with retinitis pigmentosa.

Fishman GA, Lam BL, Anderson RJ. Fishman GA, et al. Among authors: lam bl. Am J Ophthalmol. 1994 Jul 15;118(1):33-8. doi: 10.1016/s0002-9394(14)72839-9. Am J Ophthalmol. 1994. PMID: 8023873

5

An analysis of allelic variation in the ABCA4 gene.

Webster AR, Héon E, Lotery AJ, Vandenburgh K, Casavant TL, Oh KT, Beck G, Fishman GA, Lam BL, Levin A, Heckenlively JR, Jacobson SG, Weleber RG, Sheffield VC, Stone EM. Webster AR, et al. Among authors: lam bl. Invest Ophthalmol Vis Sci. 2001 May;42(6):1179-89. Invest Ophthalmol Vis Sci. 2001. PMID: 11328725

6

The a-wave latency in control subjects and patients with retinal diseases.

Hamasaki DI, Liu M, Qiu H, Fujiwara E, Lam BL. Hamasaki DI, et al. Among authors: lam bl. Jpn J Ophthalmol. 2002 Jul-Aug;46(4):433-42. doi: 10.1016/s0021-5155(02)00504-x. Jpn J Ophthalmol. 2002. PMID: 12225823

7

Atypical mild enhanced S-cone syndrome with novel compound heterozygosity of the NR2E3 gene.

Lam BL, Goldberg JL, Hartley KL, Stone EM, Liu M. Lam BL, et al. Am J Ophthalmol. 2007 Jul;144(1):157-9. doi: 10.1016/j.ajo.2007.03.012. Am J Ophthalmol. 2007. PMID: 17601449

8

Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa.

Walia S, Fishman GA, Jacobson SG, Aleman TS, Koenekoop RK, Traboulsi EI, Weleber RG, Pennesi ME, Heon E, Drack A, Lam BL, Allikmets R, Stone EM. Walia S, et al. Among authors: lam bl. Ophthalmology. 2010 Jun;117(6):1190-8. doi: 10.1016/j.ophtha.2009.09.056. Epub 2010 Jan 15. Ophthalmology. 2010. PMID: 20079931

9

Leber hereditary optic neuropathy gene therapy clinical trial recruitment: year 1.

Lam BL, Feuer WJ, Abukhalil F, Porciatti V, Hauswirth WW, Guy J. Lam BL, et al. Arch Ophthalmol. 2010 Sep;128(9):1129-35. doi: 10.1001/archophthalmol.2010.201. Arch Ophthalmol. 2010. PMID: 20837795 Free PMC article. Clinical Trial.

10

Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome.

Stone EM, Cideciyan AV, Aleman TS, Scheetz TE, Sumaroka A, Ehlinger MA, Schwartz SB, Fishman GA, Traboulsi EI, Lam BL, Fulton AB, Mullins RF, Sheffield VC, Jacobson SG. Stone EM, et al. Among authors: lam bl. Arch Ophthalmol. 2011 Jan;129(1):81-7. doi: 10.1001/archophthalmol.2010.330. Arch Ophthalmol. 2011. PMID: 21220633 Free PMC article.

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