Lam BL - Search Results

1

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.

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

Retinitis pigmentosa associated with a dominant mutation in codon 46 of the peripherin/RDS gene (arginine-46-stop).

Lam BL, Vandenburgh K, Sheffield VC, Stone EM. Lam BL, et al. Am J Ophthalmol. 1995 Jan;119(1):65-71. doi: 10.1016/s0002-9394(14)73815-2. Am J Ophthalmol. 1995. PMID: 7825692

5

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

6

Mutation analysis of 3 genes in patients with Leber congenital amaurosis.

Lotery AJ, Namperumalsamy P, Jacobson SG, Weleber RG, Fishman GA, Musarella MA, Hoyt CS, Héon E, Levin A, Jan J, Lam B, Carr RE, Franklin A, Radha S, Andorf JL, Sheffield VC, Stone EM. Lotery AJ, et al. Arch Ophthalmol. 2000 Apr;118(4):538-43. doi: 10.1001/archopht.118.4.538. Arch Ophthalmol. 2000. PMID: 10766140

7

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2).

Nishimura DY, Searby CC, Carmi R, Elbedour K, Van Maldergem L, Fulton AB, Lam BL, Powell BR, Swiderski RE, Bugge KE, Haider NB, Kwitek-Black AE, Ying L, Duhl DM, Gorman SW, Heon E, Iannaccone A, Bonneau D, Biesecker LG, Jacobson SG, Stone EM, Sheffield VC. Nishimura DY, et al. Among authors: lam bl. Hum Mol Genet. 2001 Apr 1;10(8):865-74. doi: 10.1093/hmg/10.8.865. Hum Mol Genet. 2001. PMID: 11285252

8

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

9

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

10

Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic wavelets.

Aleman TS, Lam BL, Cideciyan AV, Sumaroka A, Windsor EA, Roman AJ, Schwartz SB, Stone EM, Jacobson SG. Aleman TS, et al. Among authors: lam bl. Eye (Lond). 2009 Jan;23(1):230-3. doi: 10.1038/eye.2008.264. Epub 2008 Aug 15. Eye (Lond). 2009. PMID: 18704120

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

302 results

Search Page

Filters