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Meeting Abstract (6)
Journal Articles (5)

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Investigative Ophthalmology & Visual Science (11)

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ARVO Annual Meeting Abstract (6)
Biochemistry and Molecular Biology (2)
Eye Movements, Strabismus, Amblyopia and Neuro-ophthalmology (2)
Retina (1)

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Eye Anatomy and Disorders (3)
Genetics (3)
Biochemistry and Molecular Biology (2)
Eye Movements, Strabismus, Amblyopia and Neuro-ophthalmology (2)
Retina (2)
Imaging (1)
Low Vision (1)
Retinal Imaging (1)

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mutation (3)
genes (2)
screening (2)
amblyopia (1)
artifacts (1)
autosomal recessive inheritance (1)
child (1)
cohort studies (1)
congenital abnormality (1)
diagnostic imaging (1)

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Eye Movements, Strabismus, Amblyopia and Neuro-ophthalmology May 2011

Heartbeat-Induced Axial Motion Artifacts in Optical Coherence Tomography Measurements of the Retina

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Roy de Kinkelder; Jeroen Kalkman; Dirk J. Faber; Olaf Schraa; Pauline H. B. Kok; Frank D. Verbraak; Ton G. van Leeuwen
TAGS: artifacts, motion, optical coherence tomography, retina, diagnostic imaging, heart rate
Invest. Ophthalmol. Vis. Sci.. 2011; 52(6):3908-3913. https://doi.org/10.1167/iovs.10-6738

ARVO Annual Meeting Abstract April 2011

Reproducibility Measurements Of RNFL Segmentation Software Of SD-OCT Systems With A Phantom Eye Model

Roy de Kinkelder; Daniel M. de Bruin; Frank D. Verbraak; Ton G. van Leeuwen; Dirk J. Faber

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):3671.

Biochemistry and Molecular Biology April 2011

High-Resolution Homozygosity Mapping Is a Powerful Tool to Detect Novel Mutations Causative of Autosomal Recessive RP in the Dutch Population

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Rob W. J. Collin; L. Ingeborgh van den Born; B. Jeroen Klevering; Marta de Castro-Miró; Karin W. Littink; Kentar Arimadyo; Maleeha Azam; Volkan Yazar; Marijke N. Zonneveld; Codrut C. Paun; Anna M. Siemiatkowska; Tim M. Strom; Jayne Y. Hehir-Kwa; Hester Y. Kroes; Jan-Tjeerd H. N. de Faber; Mary J. van Schooneveld; John R. Heckenlively; Carel B. Hoyng; Anneke I. den Hollander; Frans P. M. Cremers
TAGS: autosomal recessive inheritance, dutch, homozygote, mutation, genes, proteins
Invest. Ophthalmol. Vis. Sci.. 2011; 52(5):2227-2239. https://doi.org/10.1167/iovs.10-6185

Biochemistry and Molecular Biology January 2011

Expanding the Spectrum of FOXC1 and PITX2 Mutations and Copy Number Changes in Patients with Anterior Segment Malformations

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Barbara D'haene; Françoise Meire; Ilse Claerhout; Hester Y. Kroes; Astrid Plomp; Yvonne H. Arens; Thomy de Ravel; Ingele Casteels; Sarah De Jaegere; Sally Hooghe; Wim Wuyts; Jenneke van den Ende; Françoise Roulez; Hermine E. Veenstra-Knol; Rogier A. Oldenburg; Jacques Giltay; Johanna B. G. M. Verheij; Jan-Tjeerd de Faber; Björn Menten; Anne De Paepe; Philippe Kestelyn; Bart P. Leroy; Elfride De Baere
TAGS: congenital abnormality, mutation, screening
Invest. Ophthalmol. Vis. Sci.. 2011; 52(1):324-333. https://doi.org/10.1167/iovs.10-5309

Includes: Supplemental Content

Eye Movements, Strabismus, Amblyopia and Neuro-ophthalmology July 2010

Rotterdam AMblyopia Screening Effectiveness Study: Detection and Causes of Amblyopia in a Large Birth Cohort

PDF

Johanna H. Groenewoud; Angela M. Tjiam; V. Kathleen Lantau; W. Christina Hoogeveen; Jan Tjeerd H. N. de Faber; Rikard E. Juttmann; Harry J. de Koning; Huibert J. Simonsz
TAGS: amblyopia, child, cohort studies, screening, vision screening, visual acuity
Invest. Ophthalmol. Vis. Sci.. 2010; 51(7):3476-3484. https://doi.org/10.1167/iovs.08-3352

ARVO Annual Meeting Abstract April 2010

Heartbeat-Induced Axial Eye Motion Artifacts During Optical Coherence Tomography Measurements

R. de Kinkelder; J. Kalkman; P. H. Kok; O. Schraa; D. J. Faber; F. D. Verbraak; T. G. van Leeuwen

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):2530.

ARVO Annual Meeting Abstract April 2009

Post-acquisition Analysis of RNFL in SD-OCT (3DOCT-1000 of Topcon) Acquired Volumes

R. de Kinkelder; J. Kalkman; D. J. Faber; P. H. B. Kok; F. D. Verbraak; T. G. van Leeuwen

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):354.

ARVO Annual Meeting Abstract April 2009

Measuring Cell Death in Human RPE Cells Using Optical Coherence Tomography

D. M. de Bruin; M. Broekgaarden; T. Gorgels; T. G. van Leeuwen; D. J. Faber

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):5551.

ARVO Annual Meeting Abstract May 2008

A Comparison of Fourier Domain , Slitlamp Mounted, Optical Coherence Tomography Scans With Scans Made by an OCT Stratus (Zeiss) , and a 3D OCT-1000 (Topcon)

F. D. Verbraak; P. H. B. Kok; D. J. Faber; H. R. de Vries; H. W. van Dijk; M. E. J. van Velthoven; T. G. van Leeuwen

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):1846.

ARVO Annual Meeting Abstract May 2008

Sensitivity Estimation of Nanoparticle Assisted Optical Molecular Imaging (NAOMI) Using Layered Retinal Tissue-Simulating Phantoms

D. M. de Bruin; D. J. Faber; T. Gorgels; F. Verbraak; T. G. van Leeuwen

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):4806.

Retina March 2006

Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis

PDF

Suzanne Yzer; Bart P. Leroy; Elfride De Baere; Thomy J. de Ravel; Marijke N. Zonneveld; Krysta Voesenek; Ulrich Kellner; Jose P. Martinez Ciriano; Jan-Tjeerd H. N. de Faber; Klaus Rohrschneider; Ronald Roepman; Anneke I. den Hollander; Johannes R. Cruysberg; Françoise Meire; Ingele Casteels; Norka G. van Moll-Ramirez; Rando Allikmets; L. Ingeborgh van den Born; Frans P. M. Cremers
TAGS: genotype, leber's amaurosis, mutation, phenotype, genes, ophthalmoscopy, eye
Invest. Ophthalmol. Vis. Sci.. 2006; 47(3):1167-1176. https://doi.org/10.1167/iovs.05-0848

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