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Influence of open-source virtual-reality based gaze training on navigation performance in Retinitis pigmentosa patients in a crossover randomized controlled trial

PloS one, 2024-02, Vol.19 (2), p.e0291902-e0291902

2024

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Subretinal electronic chips allow blind patients to read letters and combine them to words

Proceedings of the Royal Society. B, Biological sciences, 2011-05, Vol.278 (1711), p.1489

2011

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Subretinal Visual Implant Alpha IMS – Clinical trial interim report

Vision research (Oxford), 2015-06, Vol.111 (Pt B), p.149-160

2015

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HLA Polymorphisms and Clinical Manifestations in IgA Vasculitis

International journal of molecular sciences, 2024-01, Vol.25 (2), p.882

2024

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Genetic architecture of inherited retinal degeneration in Germany: A large cohort study from a single diagnostic center over a 9‐year period

Human mutation, 2020-09, Vol.41 (9), p.1514-1527

2020

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Oscillatory Potentials in Achromatopsia as a Tool for Understanding Cone Retinal Functions

International journal of molecular sciences, 2021-11, Vol.22 (23), p.12717

2021

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Various approaches for accessing the influence of human leukocyte antigens disparity in haploidentical stem cell transplantation

International journal of laboratory hematology, 2022-06, Vol.44 (3), p.547-557

2022

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Interim Results of a Multicenter Trial with the New Electronic Subretinal Implant Alpha AMS in 15 Patients Blind from Inherited Retinal Degenerations

Frontiers in neuroscience, 2017-08, Vol.11, p.445-445

2017

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Clinical Characteristics of POC1B-Associated Retinopathy and Assignment of Pathogenicity to Novel Deep Intronic and Non-Canonical Splice Site Variants

International journal of molecular sciences, 2021-05, Vol.22 (10), p.5396

2021

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RPE65-retinal Dystrophies: From the Spectrum of the Clinical Picture to Gene Therapy

Klinische Monatsblatter fur Augenheilkunde, 2024-03, Vol.241 (3), p.257

2024

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X-Linked Retinitis Pigmentosa Caused by Non-Canonical Splice Site Variants in RPGR

International journal of molecular sciences, 2021-01, Vol.22 (2), p.850

2021

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Splicing defects and CRISPR-Cas9 correction in isogenic homozygous photoreceptor precursors harboring clustered deep-intronic ABCA4 variants

Molecular therapy. Nucleic acids, 2024-03, Vol.35 (1), p.102113-102113, Article 102113

2024

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Population receptive field analysis of the primary visual cortex complements perimetry in patients with homonymous visual field defects

Proceedings of the National Academy of Sciences - PNAS, 2014-04, Vol.111 (16), p.E1656-E1665

2014

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Effective splicing restoration of a deep-intronic ABCA4 variant in cone photoreceptor precursor cells by CRISPR/SpCas9 approaches

Molecular therapy. Nucleic acids, 2022-09, Vol.29, p.511-524

2022

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Biallelic Variants in TULP1 Are Associated with Heterogeneous Phenotypes of Retinal Dystrophy

International journal of molecular sciences, 2023-01, Vol.24 (3), p.2709

2023

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Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction

International journal of molecular sciences, 2022-06, Vol.23 (12), p.6868

2022

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Spatial resolution and perception of patterns mediated by a subretinal 16-electrode array in patients blinded by hereditary retinal dystrophies

Investigative ophthalmology & visual science, 2011-07, Vol.52 (8), p.5995-6003

2011

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CDHR1 mutations in retinal dystrophies

Scientific reports, 2017-08, Vol.7 (1), p.6992-6992, Article 6992

2017

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Molecular Properties of Human Guanylate Cyclase-Activating Protein 3 (GCAP3) and Its Possible Association with Retinitis Pigmentosa

International journal of molecular sciences, 2022-03, Vol.23 (6), p.3240

2022

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Defining reference values of arterioles in healthy individuals for studies with adaptive optics imaging

Frontiers in ophthalmology, 2024-03, Vol.4

2024

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A Novel, Apparently Silent Variant in MFSD8 Causes Neuronal Ceroid Lipofuscinosis with Marked Intrafamilial Variability

International journal of molecular sciences, 2022-02, Vol.23 (4), p.2271

2022

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Influence of Systematic Gaze Patterns in Navigation and Search Tasks with Simulated Retinitis Pigmentosa

Brain sciences, 2021-02, Vol.11 (2), p.223

2021

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German reference network for rare eye diseases (DRN-EYE). The way to national networking

Die Ophthalmologie, 2022-10, Vol.119 (10), p.1017-1021

2022

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Deutsches Referenznetzwerk für Seltene Augenerkrankungen (DRN-EYE). Der Weg zur bundesweiten Vernetzung

Die Ophthalmologie, 2022-10, Vol.119 (10), p.1017-1021

2022

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Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush

International journal of molecular sciences, 2021-09, Vol.22 (19), p.10352

2021

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Influence of open-source virtual-reality based gaze training on navigation performance in Retinitis pigmentosa patients in a crossover randomized controlled trial

Subretinal electronic chips allow blind patients to read letters and combine them to words

Subretinal Visual Implant Alpha IMS – Clinical trial interim report

HLA Polymorphisms and Clinical Manifestations in IgA Vasculitis

Genetic architecture of inherited retinal degeneration in Germany: A large cohort study from a single diagnostic center over a 9‐year period

Oscillatory Potentials in Achromatopsia as a Tool for Understanding Cone Retinal Functions

Various approaches for accessing the influence of human leukocyte antigens disparity in haploidentical stem cell transplantation

Interim Results of a Multicenter Trial with the New Electronic Subretinal Implant Alpha AMS in 15 Patients Blind from Inherited Retinal Degenerations

Clinical Characteristics of POC1B-Associated Retinopathy and Assignment of Pathogenicity to Novel Deep Intronic and Non-Canonical Splice Site Variants

RPE65-retinal Dystrophies: From the Spectrum of the Clinical Picture to Gene Therapy

X-Linked Retinitis Pigmentosa Caused by Non-Canonical Splice Site Variants in RPGR

Splicing defects and CRISPR-Cas9 correction in isogenic homozygous photoreceptor precursors harboring clustered deep-intronic ABCA4 variants

Population receptive field analysis of the primary visual cortex complements perimetry in patients with homonymous visual field defects

Effective splicing restoration of a deep-intronic ABCA4 variant in cone photoreceptor precursor cells by CRISPR/SpCas9 approaches

Biallelic Variants in TULP1 Are Associated with Heterogeneous Phenotypes of Retinal Dystrophy

Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction

Spatial resolution and perception of patterns mediated by a subretinal 16-electrode array in patients blinded by hereditary retinal dystrophies

CDHR1 mutations in retinal dystrophies

Molecular Properties of Human Guanylate Cyclase-Activating Protein 3 (GCAP3) and Its Possible Association with Retinitis Pigmentosa

Defining reference values of arterioles in healthy individuals for studies with adaptive optics imaging

A Novel, Apparently Silent Variant in MFSD8 Causes Neuronal Ceroid Lipofuscinosis with Marked Intrafamilial Variability

Influence of Systematic Gaze Patterns in Navigation and Search Tasks with Simulated Retinitis Pigmentosa

German reference network for rare eye diseases (DRN-EYE). The way to national networking

Deutsches Referenznetzwerk für Seltene Augenerkrankungen (DRN-EYE). Der Weg zur bundesweiten Vernetzung

Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush

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