Weleber RG - Search Results

1

Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older.

Grover S, Fishman GA, Anderson RJ, Tozatti MS, Heckenlively JR, Weleber RG, Edwards AO, Brown J Jr. Grover S, et al. Among authors: weleber rg. Ophthalmology. 1999 Sep;106(9):1780-5. doi: 10.1016/S0161-6420(99)90342-1. Ophthalmology. 1999. PMID: 10485550

2

Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa.

Walia S, Fishman GA, Jacobson SG, Aleman TS, Koenekoop RK, Traboulsi EI, Weleber RG, Pennesi ME, Heon E, Drack A, Lam BL, Allikmets R, Stone EM. Walia S, et al. Among authors: weleber rg. Ophthalmology. 2010 Jun;117(6):1190-8. doi: 10.1016/j.ophtha.2009.09.056. Epub 2010 Jan 15. Ophthalmology. 2010. PMID: 20079931

3

Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290.

McAnany JJ, Genead MA, Walia S, Drack AV, Stone EM, Koenekoop RK, Traboulsi EI, Smith A, Weleber RG, Jacobson SG, Fishman GA. McAnany JJ, et al. Among authors: weleber rg. JAMA Ophthalmol. 2013 Feb;131(2):178-82. doi: 10.1001/2013.jamaophthalmol.354. JAMA Ophthalmol. 2013. PMID: 23411883 Free PMC article.

4

Comparison of the clinical expression of retinitis pigmentosa associated with rhodopsin mutations at codon 347 and codon 23.

Oh KT, Longmuir R, Oh DM, Stone EM, Kopp K, Brown J, Fishman GA, Sonkin P, Gehrs KM, Weleber RG. Oh KT, et al. Among authors: weleber rg. Am J Ophthalmol. 2003 Aug;136(2):306-13. doi: 10.1016/s0002-9394(03)00206-x. Am J Ophthalmol. 2003. PMID: 12888054

5

Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia.

Roberts MF, Fishman GA, Roberts DK, Heckenlively JR, Weleber RG, Anderson RJ, Grover S. Roberts MF, et al. Among authors: weleber rg. Br J Ophthalmol. 2002 Jun;86(6):658-62. doi: 10.1136/bjo.86.6.658. Br J Ophthalmol. 2002. PMID: 12034689 Free PMC article.

6

Effect of methazolamide on chronic macular edema in patients with retinitis pigmentosa.

Fishman GA, Gilbert LD, Anderson RJ, Marmor MF, Weleber RG, Viana MA. Fishman GA, et al. Among authors: weleber rg. Ophthalmology. 1994 Apr;101(4):687-93. doi: 10.1016/s0161-6420(94)31277-2. Ophthalmology. 1994. PMID: 8152764 Clinical Trial.

7

Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease.

Branham K, Othman M, Brumm M, Karoukis AJ, Atmaca-Sonmez P, Yashar BM, Schwartz SB, Stover NB, Trzupek K, Wheaton D, Jennings B, Ciccarelli ML, Jayasundera KT, Lewis RA, Birch D, Bennett J, Sieving PA, Andreasson S, Duncan JL, Fishman GA, Iannaccone A, Weleber RG, Jacobson SG, Heckenlively JR, Swaroop A. Branham K, et al. Among authors: weleber rg. Invest Ophthalmol Vis Sci. 2012 Dec 13;53(13):8232-7. doi: 10.1167/iovs.12-11025. Invest Ophthalmol Vis Sci. 2012. PMID: 23150612 Free PMC article.

8

Randomized trial of ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for retinitis pigmentosa.

Birch DG, Weleber RG, Duncan JL, Jaffe GJ, Tao W; Ciliary Neurotrophic Factor Retinitis Pigmentosa Study Groups. Birch DG, et al. Among authors: weleber rg. Am J Ophthalmol. 2013 Aug;156(2):283-292.e1. doi: 10.1016/j.ajo.2013.03.021. Epub 2013 May 10. Am J Ophthalmol. 2013. PMID: 23668681 Free PMC article. Clinical Trial.

9

Effect of Oral Valproic Acid vs Placebo for Vision Loss in Patients With Autosomal Dominant Retinitis Pigmentosa: A Randomized Phase 2 Multicenter Placebo-Controlled Clinical Trial.

Birch DG, Bernstein PS, Iannacone A, Pennesi ME, Lam BL, Heckenlively J, Csaky K, Hartnett ME, Winthrop KL, Jayasundera T, Hughbanks-Wheaton DK, Warner J, Yang P, Fish GE, Teske MP, Sklaver NL, Erker L, Chegarnov E, Smith T, Wahle A, VanVeldhuisen PC, McCormack J, Lindblad R, Bramer S, Rose S, Zilliox P, Francis PJ, Weleber RG. Birch DG, et al. Among authors: weleber rg. JAMA Ophthalmol. 2018 Aug 1;136(8):849-856. doi: 10.1001/jamaophthalmol.2018.1171. JAMA Ophthalmol. 2018. PMID: 29879277 Free PMC article. Clinical Trial.

10

Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14.

Edwards AO, Miedziak A, Vrabec T, Verhoeven J, Acott TS, Weleber RG, Donoso LA. Edwards AO, et al. Among authors: weleber rg. Am J Ophthalmol. 1999 Apr;127(4):426-35. doi: 10.1016/s0002-9394(98)00331-6. Am J Ophthalmol. 1999. PMID: 10218695

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