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A cross-linked hyaluronic acid hydrogel (Healaflow®) as a novel vitreous substitute

Graefe's archive for clinical and experimental ophthalmology, 2016-04, Vol.254 (4), p.697-703

2016

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A five-year follow-up of ABCA4 carriers showing deterioration of retinal function and increased structural changes

Molecular vision, 2022, Vol.28, p.300-316

2022

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homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene

Proceedings of the National Academy of Sciences - PNAS, 2009-11, Vol.106 (46), p.19581-19586

2009

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Full-Field Electroretinography Changes Associated with Age-Related Macular Degeneration: A Systematic Review with Meta-Analyses

Ophthalmologica (Basel), 2022-06, Vol.245 (3), p.195-203

2022

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A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing

Genes, 2023-07, Vol.14 (7), p.1413

2023

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Do variants in IRF2BPL cause both neurological disorders and keratoconus 8?

Parkinsonism & related disorders, 2020-10, Vol.79, p.138-140

2020

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Cone implicit time as a predictor of visual outcome in macular hole surgery

Graefe's archive for clinical and experimental ophthalmology, 2014-12, Vol.252 (12), p.1903-1909

2014

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Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene

Ophthalmic genetics, 2021-04, Vol.42 (2), p.161-169

2021

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The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial

Investigative ophthalmology & visual science, 2017-02, Vol.58 (2), p.821-832

2017

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Increased Plasma cGMP in a Family With Autosomal Recessive Retinitis Pigmentosa Due to Homozygous Mutations in the PDE6A Gene

Investigative ophthalmology & visual science, 2016-11, Vol.57 (14), p.6048-6057

2016

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Attenuation of the retinal nerve fibre layer and reduced retinal function assessed by optical coherence tomography and full‐field electroretinography in patients exposed to vigabatrin medication

Acta ophthalmologica (Oxford, England), 2014-03, Vol.92 (2), p.149-157

2014

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Full‐field electroretinography in age‐related macular degeneration: an overall retinal response

Acta ophthalmologica (Oxford, England), 2021-03, Vol.99 (2), p.e253-e259

2021

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Macular function measured by binocular mfERG and compared with macular structure in healthy children

Documenta ophthalmologica, 2015-12, Vol.131 (3), p.169-176

2015

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Retinal Function and Morphology in the Rabbit Eye after Intravitreal Injection of the TNF Alpha Inhibitor Adalimumab

Current eye research, 2014-11, Vol.39 (11), p.1106-1116

2014

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A novel phenotype associated with the R162W variant in the KCNJ13 gene

Ophthalmic genetics, 2022-07, Vol.43 (4), p.1-507

2022

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Full‐field Electroretinography in Age‐related Macular Degeneration: can retinal electrophysiology predict the subjective visual outcome of cataract surgery?

Acta ophthalmologica (Oxford, England), 2020-11, Vol.98 (7), p.693-700

2020

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Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC

Neurobiology of disease, 2017-02, Vol.98, p.36-51

2017

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Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease

Investigative ophthalmology & visual science, 2012-12, Vol.53 (13), p.8232-8237

2012

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Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophy

Graefe's archive for clinical and experimental ophthalmology, 2016-02, Vol.254 (2), p.215-221

2016

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Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa

Molecular vision, 2016-05, Vol.22, p.362-373

2016

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Alteration of vitreal retinoschisin level in human primary retinal detachment

JAMA ophthalmology, 2014-03, Vol.132 (3), p.353

2014

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Vitreous levels of oxidative stress biomarkers and the radical-scavenger α1-microglobulin/A1M in human rhegmatogenous retinal detachment

Graefe's archive for clinical and experimental ophthalmology, 2013-03, Vol.251 (3), p.725-732

2013

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A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa

Ophthalmic genetics, 2019-03, Vol.40 (2), p.177-181

2019

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A cross-linked hyaluronic acid hydrogel (Healaflow®) as a novel vitreous substitute

A five-year follow-up of ABCA4 carriers showing deterioration of retinal function and increased structural changes

homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene

Full-Field Electroretinography Changes Associated with Age-Related Macular Degeneration: A Systematic Review with Meta-Analyses

A Description of the Yield of Genetic Reinvestigation in Patients with Inherited Retinal Dystrophies and Previous Inconclusive Genetic Testing

Do variants in IRF2BPL cause both neurological disorders and keratoconus 8?

Cone implicit time as a predictor of visual outcome in macular hole surgery

Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene

Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing

The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial

Increased Plasma cGMP in a Family With Autosomal Recessive Retinitis Pigmentosa Due to Homozygous Mutations in the PDE6A Gene

Attenuation of the retinal nerve fibre layer and reduced retinal function assessed by optical coherence tomography and full‐field electroretinography in patients exposed to vigabatrin medication

Full‐field electroretinography in age‐related macular degeneration: an overall retinal response

Macular function measured by binocular mfERG and compared with macular structure in healthy children

Retinal Function and Morphology in the Rabbit Eye after Intravitreal Injection of the TNF Alpha Inhibitor Adalimumab

A novel phenotype associated with the R162W variant in the KCNJ13 gene

Full‐field Electroretinography in Age‐related Macular Degeneration: can retinal electrophysiology predict the subjective visual outcome of cataract surgery?

Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC

Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease

Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects

Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophy

Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa

Alteration of vitreal retinoschisin level in human primary retinal detachment

Vitreous levels of oxidative stress biomarkers and the radical-scavenger α1-microglobulin/A1M in human rhegmatogenous retinal detachment

A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa

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