Berson EL - Search Results

1

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

2

Histopathologic study of variation in severity of retinitis pigmentosa due to the dominant rhodopsin mutation Pro23His.

To K, Adamian M, Dryja TP, Berson EL. To K, et al. Among authors: berson el. Am J Ophthalmol. 2002 Aug;134(2):290-3. doi: 10.1016/s0002-9394(02)01545-3. Am J Ophthalmol. 2002. PMID: 12140048

3

Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutations.

Berson EL, Rosner B, Weigel-DiFranco C, Dryja TP, Sandberg MA. Berson EL, et al. Invest Ophthalmol Vis Sci. 2002 Sep;43(9):3027-36. Invest Ophthalmol Vis Sci. 2002. PMID: 12202526

4

Paternal uniparental heterodisomy with partial isodisomy of chromosome 1 in a patient with retinitis pigmentosa without hearing loss and a missense mutation in the Usher syndrome type II gene USH2A.

Rivolta C, Berson EL, Dryja TP. Rivolta C, et al. Among authors: berson el. Arch Ophthalmol. 2002 Nov;120(11):1566-71. doi: 10.1001/archopht.120.11.1566. Arch Ophthalmol. 2002. PMID: 12427073

5

Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.

Sharon D, Sandberg MA, Caruso RC, Berson EL, Dryja TP. Sharon D, et al. Among authors: berson el. Arch Ophthalmol. 2003 Sep;121(9):1316-23. doi: 10.1001/archopht.121.9.1316. Arch Ophthalmol. 2003. PMID: 12963616

6

RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa.

Sharon D, Sandberg MA, Rabe VW, Stillberger M, Dryja TP, Berson EL. Sharon D, et al. Among authors: berson el. Am J Hum Genet. 2003 Nov;73(5):1131-46. doi: 10.1086/379379. Epub 2003 Oct 16. Am J Hum Genet. 2003. PMID: 14564670 Free PMC article.

7

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.

8

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

9

Clinical trial of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment.

Berson EL, Rosner B, Sandberg MA, Weigel-DiFranco C, Moser A, Brockhurst RJ, Hayes KC, Johnson CA, Anderson EJ, Gaudio AR, Willett WC, Schaefer EJ. Berson EL, et al. Arch Ophthalmol. 2004 Sep;122(9):1297-305. doi: 10.1001/archopht.122.9.1297. Arch Ophthalmol. 2004. PMID: 15364708 Clinical Trial.

10

Further evaluation of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment: subgroup analyses.

Berson EL, Rosner B, Sandberg MA, Weigel-DiFranco C, Moser A, Brockhurst RJ, Hayes KC, Johnson CA, Anderson EJ, Gaudio AR, Willett WC, Schaefer EJ. Berson EL, et al. Arch Ophthalmol. 2004 Sep;122(9):1306-14. doi: 10.1001/archopht.122.9.1306. Arch Ophthalmol. 2004. PMID: 15364709 Clinical Trial.

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