Pennesi ME - Search Results

1

REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.

Langlo CS, Erker LR, Parker M, Patterson EJ, Higgins BP, Summerfelt P, Razeen MM, Collison FT, Fishman GA, Kay CN, Zhang J, Weleber RG, Yang P, Pennesi ME, Lam BL, Chulay JD, Dubra A, Hauswirth WW, Wilson DJ, Carroll J; ACHM-001 study group. Langlo CS, et al. Among authors: pennesi me. Retina. 2017 Oct;37(10):1956-1966. doi: 10.1097/IAE.0000000000001434. Retina. 2017. PMID: 28145975 Free PMC article. 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

Diagnostic and therapeutic challenges.

Genead MA, Fishman GA, Landeman M, Pennesi ME, Traboulsi EI. Genead MA, et al. Among authors: pennesi me. Retina. 2011 Feb;31(2):413-8. doi: 10.1097/IAE.0b013e3181dc58db. Retina. 2011. PMID: 20458258 No abstract available.

5

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

6

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.

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

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.

10

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.

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