Pennesi ME - Search Results

1

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.

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

Inherited retinal degenerations with systemic manifestations.

Courtney RJ, Pennesi ME. Courtney RJ, et al. Among authors: pennesi me. Int Ophthalmol Clin. 2012 Winter;52(1):119-47. doi: 10.1097/IIO.0b013e31823bbe56. Int Ophthalmol Clin. 2012. PMID: 22124242 Review. No abstract available.

7

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.

8

Long-term characterization of retinal degeneration in rd1 and rd10 mice using spectral domain optical coherence tomography.

Pennesi ME, Michaels KV, Magee SS, Maricle A, Davin SP, Garg AK, Gale MJ, Tu DC, Wen Y, Erker LR, Francis PJ. Pennesi ME, et al. Invest Ophthalmol Vis Sci. 2012 Jul 10;53(8):4644-56. doi: 10.1167/iovs.12-9611. Invest Ophthalmol Vis Sci. 2012. PMID: 22562504 Free PMC article.

9

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.

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.

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

168 results

Search Page