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Meeting Abstract (5)
Journal Articles (3)

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Investigative Ophthalmology & Visual Science (8)

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ARVO Annual Meeting Abstract (5)
Anatomy and Pathology/Oncology (1)
Cornea (1)
Immunology and Microbiology (1)

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Eye Anatomy and Disorders (2)
Genetics (2)
Biochemistry and Molecular Biology (1)
Cornea (1)
Immunology and Microbiology (1)
Oncology (1)

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genes (2)
bap1 gene (1)
complement system proteins (1)
cornea (1)
endothelium (1)
femtosecond pulsed lasers (1)
genotype (1)
hereditary retinal dystrophy (1)
intraocular melanoma (1)
microscopy, confocal (1)

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Showing 1 – 8 of 8

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Immunology and Microbiology February 2025

Elevated Plasma Complement Factors in CRB1 -Associated Inherited Retinal Dystrophies

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Lude Moekotte; Joke H. de Boer; Sanne Hiddingh; Aafke de Ligt; Xuan-Thanh-An Nguyen; Carel B. Hoyng; Chris F. Inglehearn; Martin McKibbin; Tina M. Lamey; Jennifer A. Thompson; Fred K. Chen; Terri L. McLaren; Alaa AlTalbishi; Daan M. Panneman; Erica G. M. Boonen; Sandro Banfi; Béatrice Bocquet; Isabelle Meunier; Elfride De Baere; Robert Koenekoop; Monika Ołdak; Carlo Rivolta; Lisa Roberts; Raj Ramesar; Rasa Strupaitė-Šileikienė; Susanne Kohl; G. Jane Farrar; Marion van Vugt; Jessica van Setten; Susanne Roosing; L. Ingeborgh van den Born; Camiel J. F. Boon; Maria M. van Genderen; Jonas J. W. Kuiper
TAGS: complement system proteins, hereditary retinal dystrophy, plasma, proteins, genotype, proteome, genes
Invest. Ophthalmol. Vis. Sci.. 2025; 66(2):55. https://doi.org/10.1167/iovs.66.2.55

Includes: Supplemental Content

Anatomy and Pathology/Oncology April 2016

Metastatic Disease in Polyploid Uveal Melanoma Patients Is Associated With BAP1 Mutations

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Serdar Yavuzyigitoglu; Hanneke W. Mensink; Kyra N. Smit; Jolanda Vaarwater; Robert M. Verdijk; Berna Beverloo; Hennie T. Brüggenwirth; Ronald van Marion; Hendrikus J. Dubbink; Dion Paridaens; Nicole C. Naus; Annelies de Klein; Emine Kiliç; for the Rotterdam Ocular Melanoma Study Group (ROMS),
TAGS: bap1 gene, intraocular melanoma, mutation, neoplasm metastasis, neoplasms, polyploidy, ploidies, genes
Invest. Ophthalmol. Vis. Sci.. 2016; 57(4):2232-2239. https://doi.org/10.1167/iovs.15-18608

Includes: Supplemental Content

Cornea August 2014

Surface Metrology and 3-Dimensional Confocal Profiling of Femtosecond Laser and Mechanically Dissected Ultrathin Endothelial Lamellae

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Mor M. Dickman; Marc P. F. H. L. van Maris; Friso W. van Marion; Yvonne Schuchard; Petra Steijger-Vermaat; Frank J. H. M. van den Biggelaar; Tos T. J. M. Berendschot; Rudy M. M. A. Nuijts
TAGS: cornea, endothelium, femtosecond pulsed lasers, tissue dissection, reconstructive surgical procedures, microscopy, confocal, optics
Invest. Ophthalmol. Vis. Sci.. 2014; 55(8):5183-5190. https://doi.org/10.1167/iovs.14-14309

ARVO Annual Meeting Abstract April 2014

Phenotypic features related to Wolfram syndrome in 17 families

Stephanie Leruez; Verschoore Marion; Johanna Grenier; Xavier Zanlonghi; Christian P Hamel; Christophe Orssaud; Catherine Vignal-Clermont; Vincent Pascal Procaccio Reynier; Patrizia Dominique Bonneau; Dan Milea

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):6423.

ARVO Annual Meeting Abstract April 2014

Pre-Descemetic Automated Endothelial Keratoplasty (PDAEK), towards an automated DMEK preparation technique

Mor Dickman; Jurriaan Brekelmans; Petra Steijger-Vermaat; Teja Wesseling; Friso W.F. van Marion; Frank Van den Biggelaar; Tos TJM Berendschot; Rudy M Nuijts

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):2699.

ARVO Annual Meeting Abstract April 2011

Bardet Biedl Syndrome Chaperonin-like Proteins Depletion Induces Photoreceptor Cells Death Due To Endoplasmic Reticulum Stress

Helene Dollfus; Anais Mockel; Dominique Schlicht; Nadia Messaddeq; Vincent Marion

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5414.

ARVO Annual Meeting Abstract April 2010

Confirmation of ADAMTSL4 Mutations for Autosomal Recessive Isolated Bilateral Ectopia Lentis

H. Dollfus; V. Bennouna Greene; V. Marion; V. Pelletier; C. Stoetzel

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):3079.

ARVO Annual Meeting Abstract May 2008

Mutational Load in a Series of 140 Bardet Biedl Syndrome Families Mutated in Known BBS Genes (BBS1-BBS12)

H. Dollfus; C. Stoetzel; S. Hellé; J.-M. Danse; C. Dalloz; V. Marion; M.-C. Vincent; M. Cossée; J.-L. Mandel

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):453.

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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