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F Boon

Showing results (191-200 of 293) with videos related to

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Plos One|June 4, 2016
Analysis of Risk Alleles and Complement Activation Levels in Familial and Non-Familial Age-Related Macular DegenerationNicole T M Saksens, Yara T E Lechanteur, Sanne K Verbakel, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 12, 2012
Clinical evaluation of 3 families with basal laminar drusen caused by novel mutations in the complement factor H geneJohannes P H van de Ven, Camiel J F Boon, Sacha Fauser, et al.
Molecular Genetics & Genomic Medicine|February 7, 2019
Exome sequencing in families with chronic central serous chorioretinopathyRosa L Schellevis, Elon H C van Dijk, Myrte B Breukink, et al.
The British Journal of Ophthalmology|May 17, 2007
Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatusCamiel J F Boon, Mary J van Schooneveld, Anneke I den Hollander, et al.
Progress in Retinal and Eye Research|June 21, 2022
The retinal pigmentation pathway in human albinism: Not so black and whiteReinier Bakker, Ellie L Wagstaff, Charlotte C Kruijt, et al.
Ophthalmic Genetics|May 26, 2025
Pseudocolobomatous autosomal dominant atrophic maculopathy (PADAM)Jonathan Hensman, Mary J van Schooneveld, Roselie M H Diederen, et al.
Molecular Immunology|March 20, 2009
The spectrum of phenotypes caused by variants in the CFH geneCamiel J F Boon, Nicole C van de Kar, B Jeroen Klevering, et al.
Ophthalmology|April 13, 2010
Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophyJudith C Booij, Camiel J F Boon, Mary J van Schooneveld, et al.
Ophthalmology Science|September 11, 2025
Bile Acid Metabolism Changes in Patients with a <i>CRB1</i>-Associated Inherited Retinal DegenerationLude Moekotte, Joke H de Boer, Sanne Hiddingh, et al.
American Journal of Ophthalmology|July 2, 2021
Half-Dose Photodynamic Therapy Versus Eplerenone in Chronic Central Serous Chorioretinopathy (SPECTRA): A Randomized Controlled TrialThomas J van Rijssen, Elon H C van Dijk, Roula Tsonaka, et al.
Pageof 30

Showing results (191-200 of 293) with videos related to

Sort By:
Pageof 30
Plos One|June 4, 2016
Analysis of Risk Alleles and Complement Activation Levels in Familial and Non-Familial Age-Related Macular DegenerationNicole T M Saksens, Yara T E Lechanteur, Sanne K Verbakel, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 12, 2012
Clinical evaluation of 3 families with basal laminar drusen caused by novel mutations in the complement factor H geneJohannes P H van de Ven, Camiel J F Boon, Sacha Fauser, et al.
Molecular Genetics & Genomic Medicine|February 7, 2019
Exome sequencing in families with chronic central serous chorioretinopathyRosa L Schellevis, Elon H C van Dijk, Myrte B Breukink, et al.
The British Journal of Ophthalmology|May 17, 2007
Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatusCamiel J F Boon, Mary J van Schooneveld, Anneke I den Hollander, et al.
Progress in Retinal and Eye Research|June 21, 2022
The retinal pigmentation pathway in human albinism: Not so black and whiteReinier Bakker, Ellie L Wagstaff, Charlotte C Kruijt, et al.
Ophthalmic Genetics|May 26, 2025
Pseudocolobomatous autosomal dominant atrophic maculopathy (PADAM)Jonathan Hensman, Mary J van Schooneveld, Roselie M H Diederen, et al.
Molecular Immunology|March 20, 2009
The spectrum of phenotypes caused by variants in the CFH geneCamiel J F Boon, Nicole C van de Kar, B Jeroen Klevering, et al.
Ophthalmology|April 13, 2010
Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophyJudith C Booij, Camiel J F Boon, Mary J van Schooneveld, et al.
Ophthalmology Science|September 11, 2025
Bile Acid Metabolism Changes in Patients with a <i>CRB1</i>-Associated Inherited Retinal DegenerationLude Moekotte, Joke H de Boer, Sanne Hiddingh, et al.
American Journal of Ophthalmology|July 2, 2021
Half-Dose Photodynamic Therapy Versus Eplerenone in Chronic Central Serous Chorioretinopathy (SPECTRA): A Randomized Controlled TrialThomas J van Rijssen, Elon H C van Dijk, Roula Tsonaka, et al.
Pageof 30