Pennesi ME - Search Results

1

Results at 5 Years After Gene Therapy for RPE65-Deficient Retinal Dystrophy.

Pennesi ME, Weleber RG, Yang P, Whitebirch C, Thean B, Flotte TR, Humphries M, Chegarnov E, Beasley KN, Stout JT, Chulay JD. Pennesi ME, et al. Hum Gene Ther. 2018 Dec;29(12):1428-1437. doi: 10.1089/hum.2018.014. Epub 2018 Jul 24. Hum Gene Ther. 2018. PMID: 29869534 Clinical Trial.

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: pennesi me. Ophthalmology. 2010 Jun;117(6):1190-8. doi: 10.1016/j.ophtha.2009.09.056. Epub 2010 Jan 15. Ophthalmology. 2010. PMID: 20079931

3

High-resolution optical coherence tomography shows new aspects of Bietti crystalline retinopathy.

Pennesi ME, Weleber RG. Pennesi ME, et al. Retina. 2010 Mar;30(3):531-2. doi: 10.1097/IAE.0b013e3181c96a15. Retina. 2010. PMID: 20139800 No abstract available.

4

The 'dark' side of sedation: 12 years of office-based pediatric deep sedation for electroretinography in the dark.

Lalwani K, Tompkins BD, Burnes K, Krahmer MR, Pennesi ME, Weleber RG. Lalwani K, et al. Among authors: pennesi me. Paediatr Anaesth. 2011 Jan;21(1):65-71. doi: 10.1111/j.1460-9592.2010.03462.x. Paediatr Anaesth. 2011. PMID: 21155929

5

Residual electroretinograms in young Leber congenital amaurosis patients with mutations of AIPL1.

Pennesi ME, Stover NB, Stone EM, Chiang PW, Weleber RG. Pennesi ME, et al. Invest Ophthalmol Vis Sci. 2011 Oct 17;52(11):8166-73. doi: 10.1167/iovs.11-8298. Invest Ophthalmol Vis Sci. 2011. PMID: 21900377 Free PMC article.

6

Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies.

Fletcher AL, Pennesi ME, Harding CO, Weleber RG, Gillingham MB. Fletcher AL, et al. Among authors: pennesi me. Mol Genet Metab. 2012 May;106(1):18-24. doi: 10.1016/j.ymgme.2012.02.015. Epub 2012 Mar 8. Mol Genet Metab. 2012. PMID: 22459206 Free PMC article. Review.

7

Ophthalmic findings in an infant with phosphomannomutase deficiency.

Messenger WB, Yang P, Pennesi ME. Messenger WB, et al. Among authors: pennesi me. Doc Ophthalmol. 2014 Apr;128(2):149-53. doi: 10.1007/s10633-014-9427-0. Epub 2014 Feb 4. Doc Ophthalmol. 2014. PMID: 24493206 Free PMC article.

8

Retinal morphology of patients with achromatopsia during early childhood: implications for gene therapy.

Yang P, Michaels KV, Courtney RJ, Wen Y, Greninger DA, Reznick L, Karr DJ, Wilson LB, Weleber RG, Pennesi ME. Yang P, et al. Among authors: pennesi me. JAMA Ophthalmol. 2014 Jul;132(7):823-31. doi: 10.1001/jamaophthalmol.2014.685. JAMA Ophthalmol. 2014. PMID: 24676353 Free PMC article.

9

Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium.

Thompson DA, Ali RR, Banin E, Branham KE, Flannery JG, Gamm DM, Hauswirth WW, Heckenlively JR, Iannaccone A, Jayasundera KT, Khan NW, Molday RS, Pennesi ME, Reh TA, Weleber RG, Zacks DN; Monaciano Consortium. Thompson DA, et al. Among authors: pennesi me. Invest Ophthalmol Vis Sci. 2015 Feb 9;56(2):918-31. doi: 10.1167/iovs.14-16049. Invest Ophthalmol Vis Sci. 2015. PMID: 25667399 Free PMC article. Review.

10

Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation.

Yang P, Chiang PW, Weleber RG, Pennesi ME. Yang P, et al. Among authors: pennesi me. JAMA Ophthalmol. 2015 Jun;133(6):653-61. doi: 10.1001/jamaophthalmol.2015.0357. JAMA Ophthalmol. 2015. PMID: 25789692 Free PMC article.

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