Lam BL - Search Results

1

C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations.

Gerth-Kahlert C, Tiwari A, Hanson JVM, Batmanabane V, Traboulsi E, Pennesi ME, Al-Qahtani AA, Lam BL, Heckenlively J, Zweifel SA, Vincent A, Fierz F, Barthelmes D, Branham K, Khan N, Bahr A, Baehr L, Magyar I, Koller S, Azzarello-Burri S, Niedrist D, Heon E, Berger W. Gerth-Kahlert C, et al. Among authors: lam bl. Invest Ophthalmol Vis Sci. 2017 Aug 1;58(10):3840-3850. doi: 10.1167/iovs.17-21597. Invest Ophthalmol Vis Sci. 2017. PMID: 28763557 Free 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

Early-onset autosomal dominant retinitis pigmentosa with severe hyperopia.

Lam BL, Judisch GF. Lam BL, et al. Am J Ophthalmol. 1991 Apr 15;111(4):454-6. doi: 10.1016/s0002-9394(14)72380-3. Am J Ophthalmol. 1991. PMID: 2012147

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

Low-frequency damped electroretinographic wavelets in young asymptomatic patients with dominant retinitis pigmentosa: a new electroretinographic finding.

Lam BL, Liu M, Hamasaki DI. Lam BL, et al. Ophthalmology. 1999 Jun;106(6):1109-13. doi: 10.1016/S0161-6420(99)90263-4. Ophthalmology. 1999. PMID: 10366078 Free article.

6

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

7

Ocular manifestations of Seckel syndrome.

Guirgis MF, Lam BL, Howard CW. Guirgis MF, et al. Among authors: lam bl. Am J Ophthalmol. 2001 Oct;132(4):596-7. doi: 10.1016/s0002-9394(01)01046-7. Am J Ophthalmol. 2001. PMID: 11589896

8

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

9

Electroretinographic monitoring in birdshot chorioretinopathy.

Sobrin L, Lam BL, Liu M, Feuer WJ, Davis JL. Sobrin L, et al. Among authors: lam bl. Am J Ophthalmol. 2005 Jul;140(1):52-64. doi: 10.1016/j.ajo.2005.01.053. Am J Ophthalmol. 2005. PMID: 16038651

10

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

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