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Comparing the Effectiveness of Bevacizumab to Ranibizumab in Patients with Exudative Age-Related Macular Degeneration. The BRAMD Study

PloS one, 2016-05, Vol.11 (5), p.e0153052

2016

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Genotype‐phenotype correlations of low‐frequency variants in the complement system in renal disease and age‐related macular degeneration

Clinical genetics, 2018-10, Vol.94 (3-4), p.330-338

2018

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Extramacular drusen are highly associated with age-related macular degeneration, but not with CFH and ARMS2 genotypes

British journal of ophthalmology, 2016-08, Vol.100 (8), p.1047-1051

2016

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Genotyping microarray (gene chip) for the ABCR (ABCA4) gene

Human mutation, 2003-11, Vol.22 (5), p.395-403

2003

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Aging and the Haptic Perception of Material Properties

Perception (London), 2016-12, Vol.45 (12), p.1387-1398

2016

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Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT)

Human molecular genetics, 2015-07, Vol.24 (13), p.3742-3751

2015

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Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy

Clinical genetics, 2018-08, Vol.94 (2), p.221-231

2018

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Systemic and ocular fluid compounds as potential biomarkers in age-related macular degeneration

Survey of ophthalmology, 2018-01, Vol.63 (1), p.9-39

2018

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Autosomal Recessive Retinitis Pigmentosa and Cone-rod Dystrophy Caused by Splice Site Mutations in the Stargardt's Disease Gene ABCR

Human molecular genetics, 1998-03, Vol.7 (3), p.355-362

1998

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Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus

British journal of ophthalmology, 2007-11, Vol.91 (11), p.1504-1511

2007

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The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease

American journal of human genetics, 1999-04, Vol.64 (4), p.1024-1035

1999

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Comparing the effectiveness and costs of Bevacizumab to Ranibizumab in patients with Diabetic Macular Edema: a randomized clinical trial (the BRDME study)

BMC ophthalmology, 2015-07, Vol.15 (1), p.71-71, Article 71

2015

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Mutations in the ABCA4 ( ABCR) Gene Are the Major Cause of Autosomal Recessive Cone-Rod Dystrophy

American journal of human genetics, 2000-10, Vol.67 (4), p.960-966

2000

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Analysis of visual pigment by fundus autofluorescence

Experimental eye research, 2008-02, Vol.86 (2), p.296-304

2008

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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

European journal of human genetics : EJHG, 2005-03, Vol.13 (3), p.302-308

2005

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Commentary on “Evidence of complement dysregulation in outer retina of Stargardt disease donor eyes”

Redox biology, 2021-09, Vol.45, p.101957-101957, Article 101957

2021

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Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)

Human molecular genetics, 2001-07, Vol.10 (15), p.1555-1562

2001

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253 Phase angle (PA) from bioelectrical impedance analysis (BIA) in children with cystic fibrosis (CF)

Journal of cystic fibrosis, 2012-06, Vol.11, p.S121-S121

2012

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Intravitreal triamcinolone for the treatment of refractory macular edema in idiopathic intermediate or posterior uveitis

European journal of ophthalmology, 2008-05, Vol.18 (3), p.429-434

2008

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The visual perception of distance ratios outdoors

Attention, perception & psychophysics, 2017-05, Vol.79 (4), p.1195-1203

2017

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Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Nature genetics, 1999-10, Vol.23 (2), p.217-221

1999

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Mutations in the CEP290 ( NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

American journal of human genetics, 2006-09, Vol.79 (3), p.556-561

2006

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Relationship between anticoagulant medication and massive intraocular hemorrhage in age-related macular degeneration

Graefe's archive for clinical and experimental ophthalmology, 2000-06, Vol.238 (6), p.482-485

2000

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Aging and visual 3-D shape recognition from motion

Attention, perception & psychophysics, 2017-11, Vol.79 (8), p.2467-2477

2017

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Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 ( CRB1) Gene

American journal of human genetics, 2001-07, Vol.69 (1), p.198-203

2001

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Comparing the Effectiveness of Bevacizumab to Ranibizumab in Patients with Exudative Age-Related Macular Degeneration. The BRAMD Study

Genotype‐phenotype correlations of low‐frequency variants in the complement system in renal disease and age‐related macular degeneration

Extramacular drusen are highly associated with age-related macular degeneration, but not with CFH and ARMS2 genotypes

Genotyping microarray (gene chip) for the ABCR (ABCA4) gene

Aging and the Haptic Perception of Material Properties

Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT)

Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy

Systemic and ocular fluid compounds as potential biomarkers in age-related macular degeneration

Autosomal Recessive Retinitis Pigmentosa and Cone-rod Dystrophy Caused by Splice Site Mutations in the Stargardt's Disease Gene ABCR

Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus

The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease

Comparing the effectiveness and costs of Bevacizumab to Ranibizumab in patients with Diabetic Macular Edema: a randomized clinical trial (the BRDME study)

Mutations in the ABCA4 ( ABCR) Gene Are the Major Cause of Autosomal Recessive Cone-Rod Dystrophy

Analysis of visual pigment by fundus autofluorescence

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

Commentary on “Evidence of complement dysregulation in outer retina of Stargardt disease donor eyes”

Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)

253 Phase angle (PA) from bioelectrical impedance analysis (BIA) in children with cystic fibrosis (CF)

Intravitreal triamcinolone for the treatment of refractory macular edema in idiopathic intermediate or posterior uveitis

The visual perception of distance ratios outdoors

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Mutations in the CEP290 ( NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

Relationship between anticoagulant medication and massive intraocular hemorrhage in age-related macular degeneration

Aging and visual 3-D shape recognition from motion

Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 ( CRB1) Gene

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