Bingham EL - Search Results

1

Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene.

Ayyagari R, Kakuk LE, Coats CL, Bingham EL, Toda Y, Felius J, Sieving PA. Ayyagari R, et al. Among authors: bingham el. Mol Vis. 1999 Jul 28;5:13. Mol Vis. 1999. PMID: 10427103 Free article.

2

Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene.

Ayyagari R, Griesinger IB, Bingham E, Lark KK, Moroi SE, Sieving PA. Ayyagari R, et al. Arch Ophthalmol. 2000 Jan;118(1):85-92. doi: 10.1001/archopht.118.1.85. Arch Ophthalmol. 2000. PMID: 10636420

3

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy.

Ayyagari R, Kakuk LE, Bingham EL, Szczesny JJ, Kemp J, Toda Y, Felius J, Sieving PA. Ayyagari R, et al. Among authors: bingham el. Hum Genet. 2000 Jul;107(1):75-82. doi: 10.1007/s004390000338. Hum Genet. 2000. PMID: 10982039 Free article.

4

Clinical course and visual function in a family with mutations in the RPE65 gene.

Felius J, Thompson DA, Khan NW, Bingham EL, Jamison JA, Kemp JA, Sieving PA. Felius J, et al. Among authors: bingham el. Arch Ophthalmol. 2002 Jan;120(1):55-61. doi: 10.1001/archopht.120.1.55. Arch Ophthalmol. 2002. PMID: 11786058

5

X-linked recessive atrophic macular degeneration from RPGR mutation.

Ayyagari R, Demirci FY, Liu J, Bingham EL, Stringham H, Kakuk LE, Boehnke M, Gorin MB, Richards JE, Sieving PA. Ayyagari R, et al. Among authors: bingham el. Genomics. 2002 Aug;80(2):166-71. doi: 10.1006/geno.2002.6815. Genomics. 2002. PMID: 12160730

6

Sorsby's fundus dystrophy in a family with a Ser-181-CVS mutation in the TIMP-3 gene: poor outcome after laser photocoagulation.

Sieving PA, Boskovich S, Bingham E, Pawar H. Sieving PA, et al. Trans Am Ophthalmol Soc. 1996;94:275-94; discussion 295-7. Trans Am Ophthalmol Soc. 1996. PMID: 8981701 Free PMC article.

7

Refined genetic mapping of juvenile X-linked retinoschisis.

Pawar H, Bingham EL, Lunetta KL, Segal M, Richards JE, Boehnke M, Sieving PA. Pawar H, et al. Among authors: bingham el. Hum Hered. 1995 Jul-Aug;45(4):206-10. doi: 10.1159/000154290. Hum Hered. 1995. PMID: 7558052

8

Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.

Sieving PA, Richards JE, Naarendorp F, Bingham EL, Scott K, Alpern M. Sieving PA, et al. Among authors: bingham el. Proc Natl Acad Sci U S A. 1995 Jan 31;92(3):880-4. doi: 10.1073/pnas.92.3.880. Proc Natl Acad Sci U S A. 1995. PMID: 7846071 Free PMC article.

9

Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave.

Sieving PA, Bingham EL, Kemp J, Richards J, Hiriyanna K. Sieving PA, et al. Among authors: bingham el. Am J Ophthalmol. 1999 Aug;128(2):179-84. doi: 10.1016/s0002-9394(99)00144-0. Am J Ophthalmol. 1999. PMID: 10458173

10

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change.

Hiriyanna KT, Bingham EL, Yashar BM, Ayyagari R, Fishman G, Small KW, Weinberg DV, Weleber RG, Lewis RA, Andreasson S, Richards JE, Sieving PA. Hiriyanna KT, et al. Among authors: bingham el. Hum Mutat. 1999;14(5):423-7. doi: 10.1002/(SICI)1098-1004(199911)14:5<423::AID-HUMU8>3.0.CO;2-D. Hum Mutat. 1999. PMID: 10533068 Free article.

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

39 results

Search Page

Filters