Pennesi ME - Search Results

1

The Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 Gene.

Chung DC, Bertelsen M, Lorenz B, Pennesi ME, Leroy BP, Hamel CP, Pierce E, Sallum J, Larsen M, Stieger K, Preising M, Weleber R, Yang P, Place E, Liu E, Schaefer G, DiStefano-Pappas J, Elci OU, McCague S, Wellman JA, High KA, Reape KZ. Chung DC, et al. Among authors: pennesi me. Am J Ophthalmol. 2019 Mar;199:58-70. doi: 10.1016/j.ajo.2018.09.024. Epub 2018 Sep 28. Am J Ophthalmol. 2019. PMID: 30268864 Free PMC article.

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

Retinal dystrophy in 2 brothers with α-Mannosidosis.

Courtney RJ, Pennesi ME. Courtney RJ, et al. Among authors: pennesi me. Arch Ophthalmol. 2011 Jun;129(6):799-802. doi: 10.1001/archophthalmol.2011.134. Arch Ophthalmol. 2011. PMID: 21670350 No abstract available.

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

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.

8

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.

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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