Pennesi ME - Search Results

1

Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations.

Zou G, Zhang T, Cheng X, Igelman AD, Wang J, Qian X, Fu S, Wang K, Koenekoop RK, Fishman GA, Yang P, Li Y, Pennesi ME, Chen R. Zou G, et al. Among authors: pennesi me. Mol Vis. 2021 Mar 18;27:95-106. eCollection 2021. Mol Vis. 2021. PMID: 33907365 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

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.

4

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.

5

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.

6

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.

7

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.

8

Sarpogrelate, a 5-HT2A Receptor Antagonist, Protects the Retina From Light-Induced Retinopathy.

Tullis BE, Ryals RC, Coyner AS, Gale MJ, Nicholson A, Ku C, Regis D, Sinha W, Datta S, Wen Y, Yang P, Pennesi ME. Tullis BE, et al. Among authors: pennesi me. Invest Ophthalmol Vis Sci. 2015 Jul;56(8):4560-9. doi: 10.1167/iovs.15-16378. Invest Ophthalmol Vis Sci. 2015. PMID: 26200496 Free PMC article.

9

Molecular and Clinical Findings in Patients With Knobloch Syndrome.

Hull S, Arno G, Ku CA, Ge Z, Waseem N, Chandra A, Webster AR, Robson AG, Michaelides M, Weleber RG, Davagnanam I, Chen R, Holder GE, Pennesi ME, Moore AT. Hull S, et al. Among authors: pennesi me. JAMA Ophthalmol. 2016 Jul 1;134(7):753-62. doi: 10.1001/jamaophthalmol.2016.1073. JAMA Ophthalmol. 2016. PMID: 27259167

10

OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY OF CHOROIDAL NEOVASCULARIZATION IN FOUR INHERITED RETINAL DYSTROPHIES.

Patel RC, Gao SS, Zhang M, Alabduljalil T, Al-Qahtani A, Weleber RG, Yang P, Jia Y, Huang D, Pennesi ME. Patel RC, et al. Among authors: pennesi me. Retina. 2016 Dec;36(12):2339-2347. doi: 10.1097/IAE.0000000000001159. Retina. 2016. PMID: 27336230 Free PMC article.

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