Search | IOVS | ARVO Journals

Showing 1 – 20 of 34

SORT: Best Match Most Recent Oldest

VIEW: Basic | Expanded

ARVO Annual Meeting Abstract June 2022

Clinical utility of Spectral-Domain Optical Coherence Tomography (SD-OCT) marker Disorganization of Retinal Inner Layers (DRIL) in Diabetic Retinopathy (DR)

Srinidhi Singuri; Shiming Luo; Dilara Hatipoglu; Amy Nowacki; Riya Patel; Andrew Schachat; Aleksandra V Rachitskaya; Justis P Ehlers; Sumit Sharma; Peter K Kaiser; Sunil K Srivastava; Elias I Traboulsi; Daniel F Martin; Rishi P Singh; Bela Anand-Apte; Alex Yuan

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):2517 – F0243. doi:

ARVO Annual Meeting Abstract June 2022

Retinal Mitochondrial Flavoprotein Fluorescence in Patients with Genetically Confirmed Retinal Dystrophies

Matthew Russell; Justin Muste; Collin Rich; Kurt Riegger; Rishi P Singh; Elias I Traboulsi

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):4094 – F0058. doi:

ARVO Annual Meeting Abstract June 2021

Visual field and Visual Acuity changes in the Natural History of Choroideremia

Emily Liu; Joshua Boyer; Rachel M. Huckfeldt; Elise Heon; Paul F Kenna; Isabelle Audo; Ruifang Sui; Elias I Traboulsi; Paul S Bernstein; Tim Stout; Kathy Reape; Daniel C Chung

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3506. doi:

Eye Movements, Strabismus, Amblyopia and Neuro-ophthalmology August 2020

Recurrent Rare Copy Number Variants Increase Risk for Esotropia

PDF

Mary C. Whitman; Silvio Alessandro Di Gioia; Wai-Man Chan; Alon Gelber; Brandon M. Pratt; Jessica L. Bell; Thomas E. Collins; James A. Knowles; Christopher Armoskus; Michele Pato; Carlos Pato; Sherin Shaaban; Sandra Staffieri; Sarah MacKinnon; Gail D. E. Maconachie; James E. Elder; Elias I. Traboulsi; Irene Gottlob; David A. Mackey; David G. Hunter; Elizabeth C. Engle; for the Strabismus Genetics Research Consortium
TAGS: copy number polymorphism, esotropia, recurrence
Invest. Ophthalmol. Vis. Sci.. 2020; 61(10):22. doi: https://doi.org/10.1167/iovs.61.10.22

ARVO Annual Meeting Abstract July 2019

Novel mutation in CTNNB1 causing familial exudative vitreoretinopathy and microcephaly

Razek Georges Coussa; Yue Zhao; Meghan J DeBenedictis; Allison Babiuch; Jonathan E Sears; Elias I Traboulsi

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2947. doi:

Genetics August 2018

Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect

PDF

Sherin Shaaban; Sarah MacKinnon; Caroline Andrews; Sandra E. Staffieri; Gail D. E. Maconachie; Wai-Man Chan; Mary C. Whitman; Sarah U. Morton; Seyhan Yazar; Stuart MacGregor; James E. Elder; Elias I. Traboulsi; Irene Gottlob; Alex W. Hewitt; Strabismus Genetics Research Consortium; David G. Hunter; David A. Mackey; Elizabeth C. Engle
TAGS: cohort studies, disease susceptibility, esotropia, genetics, genome-wide association study, parent, single nucleotide polymorphism, meta-analysis, strabismus, genome
Invest. Ophthalmol. Vis. Sci.. 2018; 59(10):4054-4064. doi: https://doi.org/10.1167/iovs.18-24082

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2018

Progression of Stargardt disease as measured by spectral-domain optical coherence tomography (SD-OCT) in the ProgStar Study

Rupert Wolfgang Strauss; Xiangrong Kong; Beatriz E Munoz; Sheila K West; Michael S Ip; Alexander Ho; Anamika Jha; Paul S Bernstein; David G Birch; Artur V Cideciyan; Michel Michaelides; José-Alain Sahel; Janet S Sunness; Elias I Traboulsi; Eberhart Zrenner; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1568. doi:

ARVO Annual Meeting Abstract June 2017

Genetic characteristics of an international large cohort with Stargardt disease: The ProgStar study

Kaoru Fujinami; Rupert Wolfgang Strauss; John Chiang; Isabelle S Audo; Paul S Bernstein; David G Birch; Samuel G Jacobson; Brian C Mansfield; Meghan J Marino; Jose Alain Sahel; Saddek Mohand-Said; Janet S Sunness; Elias I Traboulsi; Eberhart Zrenner; Michel Michaelides; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4638. doi:

ARVO Annual Meeting Abstract September 2016

Progression of atrophic lesions prospectively determined by fundus autofluorescence: the natural history of the progression of atrophy secondary to Stargardt disease (ProgStar) study

Rupert Wolfgang Strauss; Xiangrong Kong; Anamika Jha; Paul S Bernstein; Michel Michaelides; Jose Sahel; Elias I Traboulsi; Eberhart Zrenner; Sheila K West; Srinivas R Sadda; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12) doi:

ARVO Annual Meeting Abstract September 2016

Visual acuity loss during one year in Stargardt Disease: ProgStar Prospective Study

Xiangrong Kong; Rupert Wolfgang Strauss; Ann-Margret Ervin; Paul S Bernstein; Artur V Cideciyan; Janet S Sunness; Elias I Traboulsi; Beatriz E Munoz; Mohamed Ahmed; Sheila K West; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12) doi:

ARVO Annual Meeting Abstract September 2016

Associations between fundus autofluorescence and spectral-domain optical coherence tomography in Stargardt disease at baseline of the prospective ProgStar study.

Yulia Wolfson; Beatriz E Munoz; Rupert Wolfgang Strauss; Alexander Ho; Anamika Jha; Elias I Traboulsi; Artur V Cideciyan; Michel Michaelides; Srinivas R Sadda; Sheila K West; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12) doi:

ARVO Annual Meeting Abstract September 2016

Ellipsoid Zone Mapping and Outer Retinal Assessment in Stargardt disease

Sruthi Arepalli; Elias I Traboulsi; Justis P Ehlers

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2692. doi:

ARVO Annual Meeting Abstract September 2016

Retinal Histopathology in Eyes from Patients with Stargardt Disease.

Mary E Rayborn; Vera L Bonilha; Brent A Bell; Meghan J Marino; Elias I Traboulsi; Stephanie A Hagstrom; Joe G Hollyfield

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):6597. doi:

ARVO Annual Meeting Abstract June 2015

A Novel CRX Mutation in a Family with Findings Suggestive of Benign Concentric Annular Macular Dystrophy

Joseph F Griffith; Meghan J Marino; Elias I Traboulsi

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2868. doi:

ARVO Annual Meeting Abstract June 2015

Retinitis Pigmentosa or Sperm Dysfunction as the Only Signs of BBS2 Mutations

Brian D Perkins; Meghan J Marino; Gayle J T Pauer; John (pei wen) Chiang; Glenn Lobo; Joseph Fogerty; Stephanie A Hagstrom; Elias I Traboulsi

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2869. doi:

ARVO Annual Meeting Abstract June 2015

Retinal Histopathology in Eyes from a Patient with Cone Dystrophy.

Meghan J Marino; Vera L Bonilha; Mary E Rayborn; Brent A Bell; Elias I Traboulsi; Stephanie A Hagstrom; Joe G Hollyfield

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2402. doi:

ARVO Annual Meeting Abstract April 2014

A Novel Nonsense Mutation in KCNJ13 Causes Leber Congenital Amaurosis

Bikash R Pattnaik; Meghan J Marino; John Chiang; De-Ann M Pillers; Elias I Traboulsi

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3283. doi:

ARVO Annual Meeting Abstract April 2014

Retinal Histopathology in Eyes from a Patient with Digenic Usher Syndrome Caused by Mutations in USH2A and GPR98 .

Meghan J Marino; Vera L Bonilha; Mary E Rayborn; Brent A Bell; William J Kimberling; Elias I Traboulsi; Stephanie A Hagstrom; Joe G Hollyfield

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):6331. doi:

ARVO Annual Meeting Abstract April 2014

Retinal Histopathology in Eyes from Patients with Best Disease Caused by VMD2 Mutations

Mary E Rayborn; Vera L Bonilha; Brent A Bell; Meghan J Marino; Gayle J T Pauer; Elias I Traboulsi; Craig D Beight; Stephanie A Hagstrom; Gerald A Fishman; Joe G Hollyfield

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):6332. doi:

ARVO Annual Meeting Abstract April 2014

Retinal Histopathology in Eyes from a Carrier of XLRP with an RP2 Mutation

Gayle J T Pauer; Vera L Bonilha; Mary E Rayborn; Brent A Bell; Meghan J Marino; John R Heckenlively; Elias I Traboulsi; Stephanie A Hagstrom; Joe G Hollyfield

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):6338. doi:

1 2

Next 20 Results »

NARROW

Content Type

Journal

Article Type

Topics

Tags

Specify Date Range

Clinical utility of Spectral-Domain Optical Coherence Tomography (SD-OCT) marker Disorganization of Retinal Inner Layers (DRIL) in Diabetic Retinopathy (DR)

Retinal Mitochondrial Flavoprotein Fluorescence in Patients with Genetically Confirmed Retinal Dystrophies

Visual field and Visual Acuity changes in the Natural History of Choroideremia

Recurrent Rare Copy Number Variants Increase Risk for Esotropia

Novel mutation in CTNNB1 causing familial exudative vitreoretinopathy and microcephaly

Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect

Progression of Stargardt disease as measured by spectral-domain optical coherence tomography (SD-OCT) in the ProgStar Study

Genetic characteristics of an international large cohort with Stargardt disease: The ProgStar study

Progression of atrophic lesions prospectively determined by fundus autofluorescence: the natural history of the progression of atrophy secondary to Stargardt disease (ProgStar) study

Visual acuity loss during one year in Stargardt Disease: ProgStar Prospective Study

Associations between fundus autofluorescence and spectral-domain optical coherence tomography in Stargardt disease at baseline of the prospective ProgStar study.

Ellipsoid Zone Mapping and Outer Retinal Assessment in Stargardt disease

Retinal Histopathology in Eyes from Patients with Stargardt Disease.

A Novel CRX Mutation in a Family with Findings Suggestive of Benign Concentric Annular Macular Dystrophy

Retinitis Pigmentosa or Sperm Dysfunction as the Only Signs of BBS2 Mutations

Retinal Histopathology in Eyes from a Patient with Cone Dystrophy.

A Novel Nonsense Mutation in KCNJ13 Causes Leber Congenital Amaurosis

Retinal Histopathology in Eyes from a Patient with Digenic Usher Syndrome Caused by Mutations in USH2A and GPR98 .

Retinal Histopathology in Eyes from Patients with Best Disease Caused by VMD2 Mutations

Retinal Histopathology in Eyes from a Carrier of XLRP with an RP2 Mutation

To View More...

You must be signed into an individual account to use this feature.