Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 270

1.

A Professionalism Curricular Model to Promote Transformative Learning Among Residents.

Foshee CM, Mehdi A, Bierer SB, Traboulsi EI, Isaacson JH, Spencer A, Calabrese C, Burkey BB.

J Grad Med Educ. 2017 Jun;9(3):351-356. doi: 10.4300/JGME-D-16-00421.1.

PMID:
28638516
2.

ELLIPSOID ZONE MAPPING AND OUTER RETINAL ASSESSMENT IN STARGARDT DISEASE.

Arepalli S, Traboulsi EI, Ehlers JP.

Retina. 2017 Jun 6. doi: 10.1097/IAE.0000000000001716. [Epub ahead of print]

PMID:
28613213
3.

Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy.

Jiao X, Li A, Jin ZB, Wang X, Iannaccone A, Traboulsi EI, Gorin MB, Simonelli F, Hejtmancik JF.

Eur J Hum Genet. 2017 Apr;25(4):461-471. doi: 10.1038/ejhg.2016.184. Epub 2017 Jan 4.

4.

Correlation of ultra-widefield fundus autofluorescence patterns with the underlying genotype in retinal dystrophies and retinitis pigmentosa.

Trichonas G, Traboulsi EI, Ehlers JP.

Ophthalmic Genet. 2016 Nov 23:1-5. doi: 10.1080/13816810.2016.1227450. [Epub ahead of print]

PMID:
27880076
5.

Authors' response to Finsterer and Zarrouk-Mahjoub's comments.

Parikh S, Zhu CC, Traboulsi EI.

Ophthalmic Genet. 2017 May-Jun;38(3):299. doi: 10.1080/13816810.2016.1193882. Epub 2016 Jul 21. No abstract available.

PMID:
27442076
6.

Cohen Syndrome.

Wang H, Falk MJ, Wensel C, Traboulsi EI.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2006 Aug 29 [updated 2016 Jul 21].

7.

Associated systemic and ocular disorders in patients with congenital unilateral cataracts: the Infant Aphakia Treatment Study experience.

Traboulsi EI, Vanderveen D, Morrison D, Drews-Botsch CD, Lambert SR; Infant Aphakia Treatment Study Group.

Eye (Lond). 2016 Sep;30(9):1170-4. doi: 10.1038/eye.2016.124. Epub 2016 Jun 17.

PMID:
27315350
8.

Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome.

Ansari M, Rainger J, Hanson IM, Williamson KA, Sharkey F, Harewood L, Sandilands A, Clayton-Smith J, Dollfus H, Bitoun P, Meire F, Fantes J, Franco B, Lorenz B, Taylor DS, Stewart F, Willoughby CE, McEntagart M, Khaw PT, Clericuzio C, Van Maldergem L, Williams D, Newbury-Ecob R, Traboulsi EI, Silva ED, Madlom MM, Goudie DR, Fleck BW, Wieczorek D, Kohlhase J, McTrusty AD, Gardiner C, Yale C, Moore AT, Russell-Eggitt I, Islam L, Lees M, Beales PL, Tuft SJ, Solano JB, Splitt M, Hertz JM, Prescott TE, Shears DJ, Nischal KK, Doco-Fenzy M, Prieur F, Temple IK, Lachlan KL, Damante G, Morrison DA, van Heyningen V, FitzPatrick DR.

PLoS One. 2016 Apr 28;11(4):e0153757. doi: 10.1371/journal.pone.0153757. eCollection 2016.

9.

Ultra-widefield fundus autofluorescence patterns in retinitis pigmentosa and other retinal dystrophies.

Trichonas G, Traboulsi EI, Ehlers JP.

Ophthalmic Genet. 2017 Jan-Feb;38(1):98-100. doi: 10.3109/13816810.2015.1137328. Epub 2016 Apr 6. No abstract available.

PMID:
27049178
10.

Ophthalmological findings in 74 patients with mitochondrial disease.

Zhu CC, Traboulsi EI, Parikh S.

Ophthalmic Genet. 2017 Jan-Feb;38(1):67-69. doi: 10.3109/13816810.2015.1130153. Epub 2016 Mar 30.

PMID:
27029465
11.

Molecular biology and genetics of embryonic eyelid development.

Rubinstein TJ, Weber AC, Traboulsi EI.

Ophthalmic Genet. 2016 Sep;37(3):252-9. doi: 10.3109/13816810.2015.1071409. Epub 2016 Feb 11.

PMID:
26863902
12.

The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1.

Strauss RW, Ho A, Muñoz B, Cideciyan AV, Sahel JA, Sunness JS, Birch DG, Bernstein PS, Michaelides M, Traboulsi EI, Zrenner E, Sadda S, Ervin AM, West S, Scholl HP; Progression of Stargardt Disease Study Group.

Ophthalmology. 2016 Apr;123(4):817-28. doi: 10.1016/j.ophtha.2015.12.009. Epub 2016 Jan 16.

PMID:
26786511
13.

The Use of a Mobile Van for School Vision Screening: Results of 63 841 Evaluations.

Griffith JF, Wilson R, Cimino HC, Patthoff M, Martin DF, Traboulsi EI.

Am J Ophthalmol. 2016 Mar;163:108-14.e1. doi: 10.1016/j.ajo.2015.11.026. Epub 2015 Nov 24.

PMID:
26621684
14.

Corneal Deformation Response and Ocular Geometry: A Noninvasive Diagnostic Strategy in Marfan Syndrome.

Beene LC, Traboulsi EI, Seven I, Ford MR, Sinha Roy A, Butler RS, Dupps WJ Jr.

Am J Ophthalmol. 2016 Jan;161:56-64.e1. doi: 10.1016/j.ajo.2015.09.027. Epub 2015 Oct 24.

15.

Retinal histopathology in eyes from patients with autosomal dominant retinitis pigmentosa caused by rhodopsin mutations.

Bonilha VL, Rayborn ME, Bell BA, Marino MJ, Beight CD, Pauer GJ, Traboulsi EI, Hollyfield JG, Hagstrom SA.

Graefes Arch Clin Exp Ophthalmol. 2015 Dec;253(12):2161-9. doi: 10.1007/s00417-015-3099-7. Epub 2015 Jul 23.

PMID:
26202387
16.

A Novel KCNJ13 Nonsense Mutation and Loss of Kir7.1 Channel Function Causes Leber Congenital Amaurosis (LCA16).

Pattnaik BR, Shahi PK, Marino MJ, Liu X, York N, Brar S, Chiang J, Pillers DA, Traboulsi EI.

Hum Mutat. 2015 Jul;36(7):720-7. doi: 10.1002/humu.22807. Epub 2015 May 20.

PMID:
25921210
17.

Bilateral conjunctival follicular lymphoma in a child.

Wall PB, Traboulsi EI, Hsi ED, Singh AD.

J AAPOS. 2015 Apr;19(2):183-5. doi: 10.1016/j.jaapos.2014.10.030. Epub 2015 Mar 29.

PMID:
25824110
18.

Histopathology of the Retina from a Three Year-Old Suspected to Have Joubert Syndrome.

Bonilha VL, Rayborn ME, Bell BA, Marino MJ, Traboulsi EI, Hagstrom SA, Hollyfield JG.

Austin J Clin Ophthalmol. 2015;2(4). pii: 1057. Epub 2015 Sep 21.

19.

Histopathological comparison of eyes from patients with autosomal recessive retinitis pigmentosa caused by novel EYS mutations.

Bonilha VL, Rayborn ME, Bell BA, Marino MJ, Pauer GJ, Beight CD, Chiang J, Traboulsi EI, Hollyfield JG, Hagstrom SA.

Graefes Arch Clin Exp Ophthalmol. 2015 Feb;253(2):295-305. doi: 10.1007/s00417-014-2868-z. Epub 2014 Dec 11.

PMID:
25491159
20.

The effects of surgical factors on postoperative astigmatism in patients enrolled in the Infant Aphakia Treatment Study (IATS).

Wall PB, Lee JA, Lynn MJ, Lambert SR, Traboulsi EI; Infant Aphakia Treatment Study Group.

J AAPOS. 2014 Oct;18(5):441-5. doi: 10.1016/j.jaapos.2014.06.016. Epub 2014 Sep 27.

Supplemental Content

Loading ...
Support Center