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Items: 1 to 50 of 217

1.

A Review of Next-Generation Sequencing (NGS): Applications to the Diagnosis of Ocular Infectious Diseases.

Ma L, Jakobiec FA, Dryja TP.

Semin Ophthalmol. 2019;34(4):223-231. doi: 10.1080/08820538.2019.1620800. Epub 2019 Jun 6. Review.

PMID:
31170015
2.

A Review of the Role of Cytogenetics in the Diagnosis of Orbital Rhabdomyosarcoma.

Cortes Barrantes P, Jakobiec FA, Dryja TP.

Semin Ophthalmol. 2019;34(4):243-251. doi: 10.1080/08820538.2019.1620802. Epub 2019 May 30. Review.

PMID:
31146616
3.

Using Healthcare Databases to Refine Understanding of Exploratory Associations Between Drugs and Progression of Open-Angle Glaucoma.

Wang SV, Li N, Rice DS, Grosskreutz CL, Dryja TP, Prasanna G, Lii J, Gagne JJ.

Clin Pharmacol Ther. 2019 Apr 30. doi: 10.1002/cpt.1490. [Epub ahead of print]

PMID:
31038730
4.

Lens regeneration in children.

Vavvas DG, Dryja TP, Wilson ME, Olsen TW, Shah A, Jurkunas U, Pineda R, Poulaki V, Palioura S, Veldman P, Moreno-Montañés J, Pinazo-Duran MD, Pastor JC, Tsilimbaris M, Rhee D, Colby K, Hunter DG, Thanos S, Sakamoto T, Pasquale LR, Miller JW, VanderVeen D, Lambert SR.

Nature. 2018 Apr 4;556(7699):E2-E3. doi: 10.1038/nature26149. No abstract available.

PMID:
29620729
5.

Induction of Ocular Complement Activation by Inflammatory Stimuli and Intraocular Inhibition of Complement Factor D in Animal Models.

Crowley MA, Delgado O, Will-Orrego A, Buchanan NM, Anderson K, Jaffee BD, Dryja TP, Liao SM.

Invest Ophthalmol Vis Sci. 2018 Feb 1;59(2):940-951. doi: 10.1167/iovs.17-22605.

PMID:
29450541
6.

Systemic Medication Associations with Presumed Advanced or Uncontrolled Primary Open-Angle Glaucoma.

Zheng W, Dryja TP, Wei Z, Song D, Tian H, Kahler KH, Khawaja AP.

Ophthalmology. 2018 Jul;125(7):984-993. doi: 10.1016/j.ophtha.2018.01.007. Epub 2018 Feb 9.

7.

Multiple Eyelid Cysts (Apocrine and Eccrine Hidrocystomas, Trichilemmal Cyst, and Hybrid Cyst) in a Patient With a Prolactinoma.

Ma L, Jakobiec FA, Wolkow N, Dryja TP, Borodic GE.

Ophthalmic Plast Reconstr Surg. 2018 May/Jun;34(3):e83-e85. doi: 10.1097/IOP.0000000000001069.

PMID:
29351118
8.

Mild Complications or Unusual Persistence of Porcine Collagen and Hyaluronic Acid Gel Following Periocular Filler Injections.

Wolkow N, Jakobiec FA, Dryja TP, Lefebvre DR.

Ophthalmic Plast Reconstr Surg. 2018 Sep/Oct;34(5):e143-e146. doi: 10.1097/IOP.0000000000001029. Review.

PMID:
29319639
9.

Specific correlation between the major chromosome 10q26 haplotype conferring risk for age-related macular degeneration and the expression of HTRA1.

Liao SM, Zheng W, Zhu J, Lewis CA, Delgado O, Crowley MA, Buchanan NM, Jaffee BD, Dryja TP.

Mol Vis. 2017 Jun 14;23:318-333. eCollection 2017.

10.

A Compact Whole-Eye Perfusion System to Evaluate Pharmacologic Responses of Outflow Facility.

Zhou EH, Paolucci M, Dryja TP, Manley T, Xiang C, Rice DS, Prasanna G, Chen A.

Invest Ophthalmol Vis Sci. 2017 Jun 1;58(7):2991-3003. doi: 10.1167/iovs.16-20974.

PMID:
28605810
11.

Long-acting protein drugs for the treatment of ocular diseases.

Ghosh JG, Nguyen AA, Bigelow CE, Poor S, Qiu Y, Rangaswamy N, Ornberg R, Jackson B, Mak H, Ezell T, Kenanova V, de la Cruz E, Carrion A, Etemad-Gilbertson B, Caro RG, Zhu K, George V, Bai J, Sharma-Nahar R, Shen S, Wang Y, Subramanian KK, Fassbender E, Maker M, Hanks S, Vrouvlianis J, Leehy B, Long D, Prentiss M, Kansara V, Jaffee B, Dryja TP, Roguska M.

Nat Commun. 2017 Mar 23;8:14837. doi: 10.1038/ncomms14837.

12.

Early Insight Into Neovascular Age-Related Macular Degeneration.

Dryja TP.

JAMA Ophthalmol. 2016 Nov 1;134(11):1281-1282. doi: 10.1001/jamaophthalmol.2016.3031. No abstract available.

PMID:
27657333
13.

Dry Eye Signs and Symptoms Persist During Systemic Neutralization of IL-1β by Canakinumab or IL-17A by Secukinumab.

Grosskreutz CL, Hockey HU, Serra D, Dryja TP.

Cornea. 2015 Dec;34(12):1551-6. doi: 10.1097/ICO.0000000000000627.

14.

AAV-mediated RLBP1 gene therapy improves the rate of dark adaptation in Rlbp1 knockout mice.

Choi VW, Bigelow CE, McGee TL, Gujar AN, Li H, Hanks SM, Vrouvlianis J, Maker M, Leehy B, Zhang Y, Aranda J, Bounoutas G, Demirs JT, Yang J, Ornberg R, Wang Y, Martin W, Stout KR, Argentieri G, Grosenstein P, Diaz D, Turner O, Jaffee BD, Police SR, Dryja TP.

Mol Ther Methods Clin Dev. 2015 Jul 8;2:15022. doi: 10.1038/mtm.2015.22. eCollection 2015.

15.

Reliability of the mouse model of choroidal neovascularization induced by laser photocoagulation.

Poor SH, Qiu Y, Fassbender ES, Shen S, Woolfenden A, Delpero A, Kim Y, Buchanan N, Gebuhr TC, Hanks SM, Meredith EL, Jaffee BD, Dryja TP.

Invest Ophthalmol Vis Sci. 2014 Sep 9;55(10):6525-34. doi: 10.1167/iovs.14-15067.

PMID:
25205860
16.

Interview with Thaddeus P. Dryja, MD. Interviewed by George B. Bartley.

Dryja TP.

Arch Ophthalmol. 2012 Jan;130(1):111-2. doi: 10.1001/archophthalmol.2011.382. No abstract available.

PMID:
22232480
17.

Effects of AIN457, a fully human antibody to interleukin-17A, on psoriasis, rheumatoid arthritis, and uveitis.

Hueber W, Patel DD, Dryja T, Wright AM, Koroleva I, Bruin G, Antoni C, Draelos Z, Gold MH; Psoriasis Study Group, Durez P, Tak PP, Gomez-Reino JJ; Rheumatoid Arthritis Study Group, Foster CS, Kim RY, Samson CM, Falk NS, Chu DS, Callanan D, Nguyen QD; Uveitis Study Group, Rose K, Haider A, Di Padova F.

Sci Transl Med. 2010 Oct 6;2(52):52ra72. doi: 10.1126/scitranslmed.3001107.

18.

Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.

McGee TL, Seyedahmadi BJ, Sweeney MO, Dryja TP, Berson EL.

J Med Genet. 2010 Jul;47(7):499-506. doi: 10.1136/jmg.2009.075143. Epub 2010 May 27.

19.

Response of choroidal leiomyoma to treatment with proton beam radiation.

Kiss S, Gragoudas ES, Dryja TP, Jakobiec FA.

Retin Cases Brief Rep. 2010 Spring;4(2):168-73. doi: 10.1097/ICB.0b013e3181a7d066.

PMID:
25390394
20.

Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutation.

Hartong DT, McGee TL, Sandberg MA, Berson EL, Asselbergs FW, van der Harst P, De Vivo I, Dryja TP.

Mol Vis. 2009;15:592-7. Epub 2009 Mar 27.

21.

A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.

den Hollander AI, McGee TL, Ziviello C, Banfi S, Dryja TP, Gonzalez-Fernandez F, Ghosh D, Berson EL.

Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1864-72. doi: 10.1167/iovs.08-2497. Epub 2008 Dec 13.

22.

Diagnosis in a patient with fundus albipunctatus and atypical fundus changes.

Hajali M, Fishman GA, Dryja TP, Sweeney MO, Lindeman M.

Doc Ophthalmol. 2009 Jun;118(3):233-8. doi: 10.1007/s10633-008-9151-8. Epub 2008 Oct 24.

PMID:
18949499
23.

Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle.

Hartong DT, Dange M, McGee TL, Berson EL, Dryja TP, Colman RF.

Nat Genet. 2008 Oct;40(10):1230-4. doi: 10.1038/ng.223. Epub 2008 Sep 21.

24.

Comprehensive analysis of CRP, CFH Y402H and environmental risk factors on risk of neovascular age-related macular degeneration.

Kim IK, Ji F, Morrison MA, Adams S, Zhang Q, Lane AM, Capone A, Dryja TP, Ott J, Miller JW, DeAngelis MM.

Mol Vis. 2008 Aug 11;14:1487-95.

25.

Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.

Sandberg MA, Rosner B, Weigel-DiFranco C, McGee TL, Dryja TP, Berson EL.

Invest Ophthalmol Vis Sci. 2008 Dec;49(12):5532-9. doi: 10.1167/iovs.08-2009. Epub 2008 Jul 18.

26.

[Acute coronary syndrome with persistent ST-elevation and normal coronary angiography].

Goracy J, Lewandowski M, Dryja T, Kaliszczak R.

Kardiol Pol. 2007 Dec;65(12):1515-8; discussion 1519. Polish. No abstract available.

PMID:
18181063
27.

Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration.

Deangelis MM, Ji F, Adams S, Morrison MA, Harring AJ, Sweeney MO, Capone A Jr, Miller JW, Dryja TP, Ott J, Kim IK.

Ophthalmology. 2008 Jul;115(7):1209-1215.e7. doi: 10.1016/j.ophtha.2007.10.032. Epub 2007 Dec 27.

28.

Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.

Thiagalingam S, McGee TL, Weleber RG, Sandberg MA, Trzupek KM, Berson EL, Dryja TP.

Ophthalmic Genet. 2007 Sep;28(3):135-42. Erratum in: Ophthalmic Genet. 2007 Dec;28(4):231.

PMID:
17896311
29.

Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene.

Iannaccone A, Tedesco SA, Gallaher KT, Yamamoto H, Charles S, Dryja TP.

Doc Ophthalmol. 2007 Sep;115(2):111-6. Epub 2007 May 3.

PMID:
17476461
31.

Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.

Sandberg MA, Rosner B, Weigel-DiFranco C, Dryja TP, Berson EL.

Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1298-304.

PMID:
17325176
32.

Cigarette smoking, CFH, APOE, ELOVL4, and risk of neovascular age-related macular degeneration.

DeAngelis MM, Ji F, Kim IK, Adams S, Capone A Jr, Ott J, Miller JW, Dryja TP.

Arch Ophthalmol. 2007 Jan;125(1):49-54.

PMID:
17210851
33.

Solitary myofibroma of the sclera.

Choopong P, Nielsen PG, Perlman EM, Huang JJ, Dryja TP, Foster CS.

Cornea. 2007 Jan;26(1):114-6.

PMID:
17198028
35.

A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosa.

Mylvaganam GH, McGee TL, Berson EL, Dryja TP.

Mol Vis. 2006 Dec 4;12:1496-8.

36.

Retinitis pigmentosa.

Hartong DT, Berson EL, Dryja TP.

Lancet. 2006 Nov 18;368(9549):1795-809. Review.

PMID:
17113430
37.

Conjunctival non-caseating granulomas in a human immunodeficiency virus (HIV) positive patient attributed to sarcoidosis.

Papadaki TG, Kafkala C, Zacharopoulos IP, Seyedahmadi B J, Dryja T, Foster CS.

Ocul Immunol Inflamm. 2006 Oct;14(5):309-11.

PMID:
17056466
38.

Treatment of acute ST-segment elevation myocardial infarction in West Pomerania province of Poland. Comparison between primary coronary intervention and thrombolytic therapy.

Dryja T, Kornacewicz-Jach Z, Goracy J, Przybycień K, Jodko L, Skowronek A, Kurowski M, Zinka E.

Kardiol Pol. 2006 Jun;64(6):591-9; discussion 600-1.

PMID:
16810577
39.

Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.

Rivolta C, McGee TL, Rio Frio T, Jensen RV, Berson EL, Dryja TP.

Hum Mutat. 2006 Jul;27(7):644-53.

PMID:
16708387
40.

Case records of the Massachusetts General Hospital. Case 5-2006. An 11-year-old girl with loss of vision in the right eye.

Walton DS, Mukai S, Grabowski EF, Munzenrider JE, Dryja TP.

N Engl J Med. 2006 Feb 16;354(7):741-8. No abstract available.

PMID:
16481642
41.

Melanocytoma of the optic nerve associated with sound-induced phosphenes.

Kim IK, Dryja TP, Lessell S, Gragoudas ES.

Arch Ophthalmol. 2006 Feb;124(2):273-7. No abstract available.

PMID:
16476900
42.

Importance of genotyping in clinical trials of inherited and orphan retinal diseases.

Dryja TP.

Retina. 2005 Dec;25(8 Suppl):S74. Review. No abstract available.

PMID:
16374348
43.

Photoreceptor cell rescue in inherited and orphan retinal diseases: disease-specific requirements.

Dryja TP.

Retina. 2005 Dec;25(8 Suppl):S13-S14. Review. No abstract available.

PMID:
16374317
44.

Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.

Schatz P, Ponjavic V, Andréasson S, McGee TL, Dryja TP, Abrahamson M.

Ophthalmic Genet. 2005 Sep;26(3):119-24.

PMID:
16272056
45.

Histopathologic-genotypic correlations in retinitis pigmentosa and allied diseases.

Ben-Arie-Weintrob Y, Berson EL, Dryja TP.

Ophthalmic Genet. 2005 Jun;26(2):91-100.

PMID:
16020312
46.

Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophy.

Lin J, Nishiguchi KM, Nakamura M, Dryja TP, Berson EL, Miyake Y.

J Med Genet. 2005 Jun;42(6):e38.

47.

Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.

Wada Y, Sandberg MA, McGee TL, Stillberger MA, Berson EL, Dryja TP.

Invest Ophthalmol Vis Sci. 2005 May;46(5):1735-41.

PMID:
15851576
48.

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.

Dryja TP, McGee TL, Berson EL, Fishman GA, Sandberg MA, Alexander KR, Derlacki DJ, Rajagopalan AS.

Proc Natl Acad Sci U S A. 2005 Mar 29;102(13):4884-9. Epub 2005 Mar 21.

49.
50.

Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function.

Nishiguchi KM, Friedman JS, Sandberg MA, Swaroop A, Berson EL, Dryja TP.

Proc Natl Acad Sci U S A. 2004 Dec 21;101(51):17819-24. Epub 2004 Dec 9.

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