Lam BL - Search Results

1

REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.

Langlo CS, Erker LR, Parker M, Patterson EJ, Higgins BP, Summerfelt P, Razeen MM, Collison FT, Fishman GA, Kay CN, Zhang J, Weleber RG, Yang P, Pennesi ME, Lam BL, Chulay JD, Dubra A, Hauswirth WW, Wilson DJ, Carroll J; ACHM-001 study group. Langlo CS, et al. Among authors: lam bl. Retina. 2017 Oct;37(10):1956-1966. doi: 10.1097/IAE.0000000000001434. Retina. 2017. PMID: 28145975 Free PMC article. Clinical Trial.

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

Predicting the pathogenicity of RPE65 mutations.

Philp AR, Jin M, Li S, Schindler EI, Iannaccone A, Lam BL, Weleber RG, Fishman GA, Jacobson SG, Mullins RF, Travis GH, Stone EM. Philp AR, et al. Among authors: lam bl. Hum Mutat. 2009 Aug;30(8):1183-8. doi: 10.1002/humu.21033. Hum Mutat. 2009. PMID: 19431183 Free PMC article.

6

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

7

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.

8

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.

9

Autosomal recessive vitelliform macular dystrophy in a large cohort of vitelliform macular dystrophy patients.

Kinnick TR, Mullins RF, Dev S, Leys M, Mackey DA, Kay CN, Lam BL, Fishman GA, Traboulsi E, Iezzi R, Stone EM. Kinnick TR, et al. Among authors: lam bl. Retina. 2011 Mar;31(3):581-95. doi: 10.1097/IAE.0b013e318203ee60. Retina. 2011. PMID: 21273940

10

Autosomal recessive retinitis pigmentosa caused by mutations in the MAK gene.

Stone EM, Luo X, Héon E, Lam BL, Weleber RG, Halder JA, Affatigato LM, Goldberg JB, Sumaroka A, Schwartz SB, Cideciyan AV, Jacobson SG. Stone EM, et al. Among authors: lam bl. Invest Ophthalmol Vis Sci. 2011 Dec 28;52(13):9665-73. doi: 10.1167/iovs.11-8527. Invest Ophthalmol Vis Sci. 2011. PMID: 22110072 Free PMC article.

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