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Items: 1 to 50 of 119

1.

ENHANCED S-CONE SYNDROME: VISUAL FUNCTION, CROSS-SECTIONAL IMAGING, AND CELLULAR STRUCTURE WITH ADAPTIVE OPTICS OPHTHALMOSCOPY.

Ammar MJ, Scavelli KT, Uyhazi KE, Bedoukian EC, Serrano LW, Edelstein ID, Vergilio G, Cooper RF, Morgan JIW, Kumar P, Aleman TS.

Retin Cases Brief Rep. 2019 Jul 10. doi: 10.1097/ICB.0000000000000891. [Epub ahead of print]

PMID:
31306293
2.

Visual Function at the Atrophic Border in Choroideremia Assessed with Adaptive Optics Microperimetry.

Tuten WS, Vergilio GK, Young GJ, Bennett J, Maguire AM, Aleman TS, Brainard DH, Morgan JIW.

Ophthalmol Retina. 2019 May 8. pii: S2468-6530(19)30014-4. doi: 10.1016/j.oret.2019.05.002. [Epub ahead of print]

PMID:
31235310
3.

Detailed retinal phenotype of Boucher-Neuhäuser syndrome associated with mutations in PNPLA6 mimicking choroideremia.

O'Neil E, Serrano L, Scoles D, Cunningham KE, Han G, Chiang J, Bennett J, Aleman TS.

Ophthalmic Genet. 2019 Jun;40(3):267-275. doi: 10.1080/13816810.2019.1605392. Epub 2019 May 28.

PMID:
31135245
4.

Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.

Garnai SJ, Brinkmeier ML, Emery B, Aleman TS, Pyle LC, Veleva-Rotse B, Sisk RA, Rozsa FW, Ozel AB, Li JZ, Moroi SE, Archer SM, Lin CM, Sheskey S, Wiinikka-Buesser L, Eadie J, Urquhart JE, Black GCM, Othman MI, Boehnke M, Sullivan SA, Skuta GL, Pawar HS, Katz AE, Huryn LA, Hufnagel RB; Genomic Ascertainment Cohort, Camper SA, Richards JE, Prasov L.

PLoS Genet. 2019 May 2;15(5):e1008130. doi: 10.1371/journal.pgen.1008130. eCollection 2019 May.

5.

Persistent and Progressive Outer Retina Thinning in Frontotemporal Degeneration.

Kim BJ, Grossman M, Song D, Saludades S, Pan W, Dominguez-Perez S, Dunaief JL, Aleman TS, Ying GS, Irwin DJ.

Front Neurosci. 2019 Apr 4;13:298. doi: 10.3389/fnins.2019.00298. eCollection 2019.

6.

RDH12 Mutations Cause a Severe Retinal Degeneration With Relatively Spared Rod Function.

Aleman TS, Uyhazi KE, Serrano LW, Vasireddy V, Bowman SJ, Ammar MJ, Pearson DJ, Maguire AM, Bennett J.

Invest Ophthalmol Vis Sci. 2018 Oct 1;59(12):5225-5236. doi: 10.1167/iovs.18-24708.

PMID:
30372751
7.

Absent Foveal Pit, Also Known as Fovea Plana, in a Child without Associated Ocular or Systemic Findings.

Hernandez-Moreno L, Moreno Perdomo N, Aleman TS, Baskaran K, Macedo AF.

Case Rep Ophthalmol Med. 2018 Jul 26;2018:2146826. doi: 10.1155/2018/2146826. eCollection 2018.

8.

Diagnostic and Therapeutic Challenges.

Tripathy K, Aleman TS.

Retina. 2018 Aug 1. doi: 10.1097/IAE.0000000000002277. [Epub ahead of print] No abstract available.

PMID:
30074523
9.

Identification of a novel pathogenic missense mutation in PRPF31 using whole exome sequencing: a case report.

Bryant L, Lozynska O, Marsh A, Papp TE, van Gorder L, Serrano LW, Gai X, Maguire AM MD, Aleman TS, Bennett J.

Br J Ophthalmol. 2019 Jun;103(6):761-767. doi: 10.1136/bjophthalmol-2017-311405. Epub 2018 Jul 20.

10.

Comparing Clinical Perimetry and Population Receptive Field Measures in Patients with Choroideremia.

Silson EH, Aleman TS, Willett A, Serrano LW, Pearson DJ, Rauschecker AM, Maguire AM, Baker CI, Bennett J, Ashtari M.

Invest Ophthalmol Vis Sci. 2018 Jul 2;59(8):3249-3258. doi: 10.1167/iovs.18-23929.

11.

Structural and Electrophysiologic Outcomes in a Patient with Retinal Metallosis.

Sulewski ME Jr, Serrano LW, Han G, Aleman TS, Nichols CW.

Ophthalmol Retina. 2018 Feb;2(2):173-175. doi: 10.1016/j.oret.2017.07.014. Epub 2017 Sep 28. No abstract available.

12.

Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness.

Song JY, Aravand P, Nikonov S, Leo L, Lyubarsky A, Bennicelli JL, Pan J, Wei Z, Shpylchak I, Herrera P, Bennett DJ, Commins N, Maguire AM, Pham J, den Hollander AI, Cremers FPM, Koenekoop RK, Roepman R, Nishina P, Zhou S, Pan W, Ying GS, Aleman TS, de Melo J, McNamara I, Sun J, Mills J, Bennett J.

Mol Ther. 2018 Jun 6;26(6):1581-1593. doi: 10.1016/j.ymthe.2018.03.015. Epub 2018 Mar 21.

13.

Early photoreceptor outer segment loss and retinoschisis in Cohen syndrome.

Uyhazi KE, Binenbaum G, Carducci N, Zackai EH, Aleman TS.

Ophthalmic Genet. 2018 Jun;39(3):399-404. doi: 10.1080/13816810.2018.1459735. Epub 2018 Apr 10.

PMID:
29634382
14.

Prescreening whole exome sequencing results from patients with retinal degeneration for variants in genes associated with retinal degeneration.

Bryant L, Lozynska O, Maguire AM, Aleman TS, Bennett J.

Clin Ophthalmol. 2017 Dec 29;12:49-63. doi: 10.2147/OPTH.S147684. eCollection 2018.

15.

FREQUENT SUBCLINICAL MACULAR CHANGES IN COMBINED BRAF/MEK INHIBITION WITH HIGH-DOSE HYDROXYCHLOROQUINE AS TREATMENT FOR ADVANCED METASTATIC BRAF MUTANT MELANOMA: Preliminary Results From a Phase I/II Clinical Treatment Trial.

Nti AA, Serrano LW, Sandhu HS, Uyhazi KE, Edelstein ID, Zhou EJ, Bowman S, Song D, Gangadhar TC, Schuchter LM, Mitnick S, Huang A, Nichols CW, Amaravadi RK, Kim BJ, Aleman TS.

Retina. 2019 Mar;39(3):502-513. doi: 10.1097/IAE.0000000000002027.

16.

Optical coherence tomography identifies outer retina thinning in frontotemporal degeneration.

Kim BJ, Irwin DJ, Song D, Daniel E, Leveque JD, Raquib AR, Pan W, Ying GS, Aleman TS, Dunaief JL, Grossman M.

Neurology. 2017 Oct 10;89(15):1604-1611. doi: 10.1212/WNL.0000000000004500. Epub 2017 Sep 8.

17.

Quantitative Assessment of Microstructural Changes of the Retina in Infants With Congenital Zika Syndrome.

Aleman TS, Ventura CV, Cavalcanti MM, Serrano LW, Traband A, Nti AA, Gois AL, Bravo-Filho V, Martins TT, Nichols CW, Maia M, Belfort R Jr.

JAMA Ophthalmol. 2017 Oct 1;135(10):1069-1076. doi: 10.1001/jamaophthalmol.2017.3292.

18.

Localized Bilateral Juxtafoveal Photoreceptor Loss in POEMS: A New Association.

Hwang CK, Kolomeyer AM, Brucker AJ, Morgan JIW, Nichols CW, Aleman TS.

Retina. 2017 Jul;37(7):e91-e92. doi: 10.1097/IAE.0000000000001666. No abstract available.

19.

Optical coherence tomography and visual evoked potentials in pediatric MS.

Waldman AT, Liu GT, Lavery AM, Liu G, Gaetz W, Aleman TS, Banwell BL.

Neurol Neuroimmunol Neuroinflamm. 2017 Jun 5;4(4):e356. doi: 10.1212/NXI.0000000000000356. eCollection 2017 Jul.

20.

ACUTE EXUDATIVE PARANEOPLASTIC POLYMORPHOUS VITELLIFORM MACULOPATHY DURING VEMURAFENIB AND PEMBROLIZUMAB TREATMENT FOR METASTATIC MELANOMA.

Sandhu HS, Kolomeyer AM, Lau MK, Shields CL, Schuchter LM, Nichols CW, Aleman TS.

Retin Cases Brief Rep. 2019 Spring;13(2):103-107. doi: 10.1097/ICB.0000000000000604.

PMID:
28614138
21.

Acute Zonal Cone Photoreceptor Outer Segment Loss.

Aleman TS, Sandhu HS, Serrano LW, Traband A, Lau MK, Adamus G, Avery RA.

JAMA Ophthalmol. 2017 May 1;135(5):487-490. doi: 10.1001/jamaophthalmol.2017.0451.

22.

Evaluation of Optical Coherence Tomography to Detect Elevated Intracranial Pressure in Children.

Swanson JW, Aleman TS, Xu W, Ying GS, Pan W, Liu GT, Lang SS, Heuer GG, Storm PB, Bartlett SP, Katowitz WR, Taylor JA.

JAMA Ophthalmol. 2017 Apr 1;135(4):320-328. doi: 10.1001/jamaophthalmol.2017.0025.

23.

Natural History of the Central Structural Abnormalities in Choroideremia: A Prospective Cross-Sectional Study.

Aleman TS, Han G, Serrano LW, Fuerst NM, Charlson ES, Pearson DJ, Chung DC, Traband A, Pan W, Ying GS, Bennett J, Maguire AM, Morgan JI.

Ophthalmology. 2017 Mar;124(3):359-373. doi: 10.1016/j.ophtha.2016.10.022. Epub 2016 Dec 13.

24.

Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularization.

Fuerst NM, Serrano L, Han G, Morgan JI, Maguire AM, Leroy BP, Kim BJ, Aleman TS.

Ophthalmic Genet. 2016 Dec;37(4):445-452. Epub 2016 Mar 30.

25.

Evaluation of Dose and Safety of AAV7m8 and AAV8BP2 in the Non-Human Primate Retina.

Ramachandran PS, Lee V, Wei Z, Song JY, Casal G, Cronin T, Willett K, Huckfeldt R, Morgan JI, Aleman TS, Maguire AM, Bennett J.

Hum Gene Ther. 2017 Feb;28(2):154-167. doi: 10.1089/hum.2016.111. Epub 2016 Oct 17. Review.

26.

Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations.

Jacobson SG, McGuigan DB 3rd, Sumaroka A, Roman AJ, Gruzensky ML, Sheplock R, Palma J, Schwartz SB, Aleman TS, Cideciyan AV.

Invest Ophthalmol Vis Sci. 2016 Sep 1;57(11):4847-4858. doi: 10.1167/iovs.16-19890.

27.

Diagnostic and Therapeutic Challenges.

Ratra D, Dhabalia DM, Sahu ES, Aleman TS.

Retina. 2017 May;37(5):1008-1017. doi: 10.1097/IAE.0000000000001212. No abstract available.

PMID:
27467378
28.

SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa.

Matsui R, McGuigan Iii DB, Gruzensky ML, Aleman TS, Schwartz SB, Sumaroka A, Koenekoop RK, Cideciyan AV, Jacobson SG.

Ophthalmic Genet. 2016 Sep;37(3):333-8. doi: 10.3109/13816810.2015.1130154. Epub 2016 Feb 8.

29.

Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell Loss.

Bonafede L, Ficicioglu CH, Serrano L, Han G, Morgan JI, Mills MD, Forbes BJ, Davidson SL, Binenbaum G, Kaplan PB, Nichols CW, Verloo P, Leroy BP, Maguire AM, Aleman TS.

Invest Ophthalmol Vis Sci. 2015 Dec;56(13):7875-87. doi: 10.1167/iovs.15-17857.

30.

Diagnostic and Therapeutic Challenges.

Elshatory YM, Carver A, Shah VA, Aleman TS.

Retina. 2016 Apr;36(4):840-5. doi: 10.1097/IAE.0000000000000704. No abstract available.

PMID:
26225484
31.

Relationship Between Optic Nerve Appearance and Retinal Nerve Fiber Layer Thickness as Explored with Spectral Domain Optical Coherence Tomography.

Aleman TS, Huang J, Garrity ST, Carter SB, Aleman WD, Ying GS, Tamhankar MA.

Transl Vis Sci Technol. 2014 Nov 3;3(6):4. eCollection 2014 Oct.

32.

Obstructive sleep apnea and central serous chorioretinopathy.

Brodie FL, Charlson ES, Aleman TS, Salvo RT, Gewaily DY, Lau MK, Farren ND, Engelhard SB, Pistilli M, Brucker AJ.

Retina. 2015 Feb;35(2):238-43. doi: 10.1097/IAE.0000000000000326.

33.

Retinal Structure in Cobalamin C Disease: Mechanistic and Therapeutic Implications.

Aleman TS, Brodie F, Garvin C, Gewaily DY, Ficicioglu CH, Mills MD, Forbes BJ, Maguire AM, Davidson SL.

Ophthalmic Genet. 2015;36(4):339-48. doi: 10.3109/13816810.2014.885059. Epub 2014 Feb 10.

PMID:
24512365
34.

Retinal structure in vitamin A deficiency as explored with multimodal imaging.

Aleman TS, Garrity ST, Brucker AJ.

Doc Ophthalmol. 2013 Dec;127(3):239-43. doi: 10.1007/s10633-013-9403-0. Epub 2013 Jul 31.

PMID:
23900584
35.

Traumatic arteriovenous fistula of the superficial temporal artery: a histopathologic report.

Moran AM, Aleman TS, Gausas RE, Fogt F.

Ophthalmic Plast Reconstr Surg. 2013 Sep-Oct;29(5):e126-8. doi: 10.1097/IOP.0b013e31827ab9ef.

PMID:
23235516
36.

Evidence of recurrent microvascular occlusions associated with acute branch retinal artery occlusion demonstrated with spectral-domain optical coherence tomography.

Aleman TS, Tapino PJ, Brucker AJ.

Retina. 2012 Sep;32(8):1687-8. doi: 10.1097/IAE.0b013e318260aef9. No abstract available.

PMID:
22869026
37.

Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa.

Beltran WA, Cideciyan AV, Lewin AS, Iwabe S, Khanna H, Sumaroka A, Chiodo VA, Fajardo DS, Román AJ, Deng WT, Swider M, Alemán TS, Boye SL, Genini S, Swaroop A, Hauswirth WW, Jacobson SG, Aguirre GD.

Proc Natl Acad Sci U S A. 2012 Feb 7;109(6):2132-7. doi: 10.1073/pnas.1118847109. Epub 2012 Jan 23.

38.

Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trials.

Cideciyan AV, Swider M, Aleman TS, Feuer WJ, Schwartz SB, Russell RC, Steinberg JD, Stone EM, Jacobson SG.

Invest Ophthalmol Vis Sci. 2012 Feb 21;53(2):841-52. doi: 10.1167/iovs.11-8415. Print 2012 Feb.

39.

Gene therapy for retinitis pigmentosa caused by MFRP mutations: human phenotype and preliminary proof of concept.

Dinculescu A, Estreicher J, Zenteno JC, Aleman TS, Schwartz SB, Huang WC, Roman AJ, Sumaroka A, Li Q, Deng WT, Min SH, Chiodo VA, Neeley A, Liu X, Shu X, Matias-Florentino M, Buentello-Volante B, Boye SL, Cideciyan AV, Hauswirth WW, Jacobson SG.

Hum Gene Ther. 2012 Apr;23(4):367-76. doi: 10.1089/hum.2011.169. Epub 2012 Jan 26.

40.

Characterisation of a C1qtnf5 Ser163Arg knock-in mouse model of late-onset retinal macular degeneration.

Shu X, Luhmann UF, Aleman TS, Barker SE, Lennon A, Tulloch B, Chen M, Xu H, Jacobson SG, Ali R, Wright AF.

PLoS One. 2011;6(11):e27433. doi: 10.1371/journal.pone.0027433. Epub 2011 Nov 16.

41.

Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years.

Jacobson SG, Cideciyan AV, Ratnakaram R, Heon E, Schwartz SB, Roman AJ, Peden MC, Aleman TS, Boye SL, Sumaroka A, Conlon TJ, Calcedo R, Pang JJ, Erger KE, Olivares MB, Mullins CL, Swider M, Kaushal S, Feuer WJ, Iannaccone A, Fishman GA, Stone EM, Byrne BJ, Hauswirth WW.

Arch Ophthalmol. 2012 Jan;130(1):9-24. doi: 10.1001/archophthalmol.2011.298. Epub 2011 Sep 12.

42.

Retinal disease course in Usher syndrome 1B due to MYO7A mutations.

Jacobson SG, Cideciyan AV, Gibbs D, Sumaroka A, Roman AJ, Aleman TS, Schwartz SB, Olivares MB, Russell RC, Steinberg JD, Kenna MA, Kimberling WJ, Rehm HL, Williams DS.

Invest Ophthalmol Vis Sci. 2011 Oct 7;52(11):7924-36. doi: 10.1167/iovs.11-8313.

43.

Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model.

Aleman TS, Cideciyan AV, Aguirre GK, Huang WC, Mullins CL, Roman AJ, Sumaroka A, Olivares MB, Tsai FF, Schwartz SB, Vandenberghe LH, Limberis MP, Stone EM, Bell P, Wilson JM, Jacobson SG.

Invest Ophthalmol Vis Sci. 2011 Aug 29;52(9):6898-910. doi: 10.1167/iovs.11-7701.

44.

The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65.

Lopes VS, Gibbs D, Libby RT, Aleman TS, Welch DL, Lillo C, Jacobson SG, Radu RA, Steel KP, Williams DS.

Hum Mol Genet. 2011 Jul 1;20(13):2560-70. doi: 10.1093/hmg/ddr155. Epub 2011 Apr 14.

45.

Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy.

Cideciyan AV, Rachel RA, Aleman TS, Swider M, Schwartz SB, Sumaroka A, Roman AJ, Stone EM, Jacobson SG, Swaroop A.

Hum Mol Genet. 2011 Apr 1;20(7):1411-23. doi: 10.1093/hmg/ddr022. Epub 2011 Jan 18.

46.

Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome.

Stone EM, Cideciyan AV, Aleman TS, Scheetz TE, Sumaroka A, Ehlinger MA, Schwartz SB, Fishman GA, Traboulsi EI, Lam BL, Fulton AB, Mullins RF, Sheffield VC, Jacobson SG.

Arch Ophthalmol. 2011 Jan;129(1):81-7. doi: 10.1001/archophthalmol.2010.330.

47.

Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remaining.

Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Roman AJ, Swider M, Schwartz SB, Banin E, Stone EM.

Invest Ophthalmol Vis Sci. 2011 Jan 5;52(1):70-9. doi: 10.1167/iovs.10-6127.

PMID:
20702822
48.

Molecular anthropology meets genetic medicine to treat blindness in the North African Jewish population: human gene therapy initiated in Israel.

Banin E, Bandah-Rozenfeld D, Obolensky A, Cideciyan AV, Aleman TS, Marks-Ohana D, Sela M, Boye S, Sumaroka A, Roman AJ, Schwartz SB, Hauswirth WW, Jacobson SG, Hemo I, Sharon D.

Hum Gene Ther. 2010 Dec;21(12):1749-57. doi: 10.1089/hum.2010.047. Epub 2010 Nov 3.

PMID:
20604683
49.

Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutations.

Caruso RC, Aleman TS, Cideciyan AV, Roman AJ, Sumaroka A, Mullins CL, Boye SL, Hauswirth WW, Jacobson SG.

Invest Ophthalmol Vis Sci. 2010 Oct;51(10):5304-13. doi: 10.1167/iovs.10-5559. Epub 2010 May 19.

PMID:
20484585
50.

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.

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

PMID:
20079931

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