Berson EL - Search Results

1

Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa.

Dryja TP, Finn JT, Peng YW, McGee TL, Berson EL, Yau KW. Dryja TP, et al. Among authors: berson el. Proc Natl Acad Sci U S A. 1995 Oct 24;92(22):10177-81. doi: 10.1073/pnas.92.22.10177. Proc Natl Acad Sci U S A. 1995. PMID: 7479749 Free PMC article.

2

Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.

DeAngelis MM, Grimsby JL, Sandberg MA, Berson EL, Dryja TP. DeAngelis MM, et al. Among authors: berson el. Arch Ophthalmol. 2002 Mar;120(3):369-75. doi: 10.1001/archopht.120.3.369. Arch Ophthalmol. 2002. PMID: 11879142

3

Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis.

Rivolta C, Ayyagari R, Sieving PA, Berson EL, Dryja TP. Rivolta C, et al. Among authors: berson el. Mol Vis. 2003 Feb 18;9:49-51. Mol Vis. 2003. PMID: 12592226 Free article.

4

Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseases.

Nishiguchi KM, Berson EL, Dryja TP. Nishiguchi KM, et al. Among authors: berson el. Mol Vis. 2004 Jan 26;10:62-4. Mol Vis. 2004. PMID: 14758335 Free article.

5

Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.

Seyedahmadi BJ, Rivolta C, Keene JA, Berson EL, Dryja TP. Seyedahmadi BJ, et al. Among authors: berson el. Exp Eye Res. 2004 Aug;79(2):167-73. doi: 10.1016/j.exer.2004.03.005. Exp Eye Res. 2004. PMID: 15325563

6

Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function.

Nishiguchi KM, Friedman JS, Sandberg MA, Swaroop A, Berson EL, Dryja TP. Nishiguchi KM, et al. Among authors: berson el. Proc Natl Acad Sci U S A. 2004 Dec 21;101(51):17819-24. doi: 10.1073/pnas.0408183101. Epub 2004 Dec 9. Proc Natl Acad Sci U S A. 2004. PMID: 15591106 Free PMC article.

7

Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.

Nishiguchi KM, Sandberg MA, Gorji N, Berson EL, Dryja TP. Nishiguchi KM, et al. Among authors: berson el. Hum Mutat. 2005 Mar;25(3):248-58. doi: 10.1002/humu.20142. Hum Mutat. 2005. PMID: 15712225

8

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.

Dryja TP, McGee TL, Berson EL, Fishman GA, Sandberg MA, Alexander KR, Derlacki DJ, Rajagopalan AS. Dryja TP, et al. Among authors: berson el. Proc Natl Acad Sci U S A. 2005 Mar 29;102(13):4884-9. doi: 10.1073/pnas.0501233102. Epub 2005 Mar 21. Proc Natl Acad Sci U S A. 2005. PMID: 15781871 Free PMC article.

9

Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.

Rivolta C, McGee TL, Rio Frio T, Jensen RV, Berson EL, Dryja TP. Rivolta C, et al. Among authors: berson el. Hum Mutat. 2006 Jul;27(7):644-53. doi: 10.1002/humu.20325. Hum Mutat. 2006. PMID: 16708387

10

Retinitis pigmentosa.

Hartong DT, Berson EL, Dryja TP. Hartong DT, et al. Among authors: berson el. Lancet. 2006 Nov 18;368(9549):1795-809. doi: 10.1016/S0140-6736(06)69740-7. Lancet. 2006. PMID: 17113430 Review.

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