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ARVO Annual Meeting Abstract June 2024

AI-based identification of photoreceptor degeneration and retinal pigment epithelial atrophy in inherited macular dystrophies

Ulrich Kellner; Simone Kellner; Heidi Stöhrq; Christina Kiel; Silke Weinitz; Ghazaleh Farmand; Bernhard Hf Weber

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):3099.

ARVO Annual Meeting Abstract June 2023

Near-infrared autofluorescence in inherited retinal dystrophies

Simone Kellner; Heidi Stoehr; Christina Kiel; Silke Weinitz; Ghazaleh Farmand; Bernhard HF Weber; Ulrich Kellner

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4656.

ARVO Annual Meeting Abstract June 2023

Wide-field optical coherence tomography in retinitis pigmentosa

Ulrich Kellner; Heidi Stoehr; Christina Kiel; Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4655.

ARVO Annual Meeting Abstract June 2022

DNAJC30 disease-causing gene variants in a large Central European cohort of patients with inherited optic atrophy

Ting XIAO; Sinja Kieninger; Nicole Weisschuh; Susanne Kohl; Klaus Rüther; Peter Kroisel; Tobias Brockmann; Steffi Knappe; Ulrich Kellner; Wolf Lagrèze; Pascale Mazzola; Tobias Haack; Bernd Wissinger; Felix Tonagel

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1211 – A0211.

ARVO Annual Meeting Abstract June 2021

Autosomal dominant gyrate atrophy-like choroidal dystrophy revisited: 45 years follow-up and association with a novel missense variant

Ulrich Kellner; Nicole Weisschuh; Silke Weinitz; Ghazaleh Farmand; Sebastian Deutsch; Friederike Kortüm; Pascale Mazzola; Karin Schäferhoff; Valerio Marino; Daniele Dell`Orco

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3220.

ARVO Annual Meeting Abstract June 2020

Variation of Clinical Findings in Choroideremia Carriers - From normal to severe

Ulrich Kellner; Heidi Stoehr; Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3039.

ARVO Annual Meeting Abstract June 2020

Long-term follow-up and variable progression of ocular signs in two sisters with AHI1-gene associated Joubert syndrome

Simone Kellner; Heidi Stoehr; Silke Weinitz; Ghazaleh Farmand; Bernhard HF Weber; Ulrich Kellner

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3041.

ARVO Annual Meeting Abstract July 2019

North-Carolina Macular dystrophy like phenotype in a three generation pedigree wit autosomal dominant inheritance and exclusion of MCRD1

Ulrich Kellner; Heidi Stohr; Birgit Budde; Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Birgit Lindau; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4482.

ARVO Annual Meeting Abstract July 2018

Molecular Genetic Screening In A Series Of 852 Patients With Inherited Retinal Dystrophies From One German Reference Center

Ulrich Kellner; Heidi Stoehr; Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Birgit Lindau; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):18.

ARVO Annual Meeting Abstract July 2018

Acute Fingolimod Associated Macular Edema 2 Days After Onset Of Treatment And Gradual Resolution Under Ketorolac Therapy Over 5 Months

Simone Kellner; Sonja Slowik; Mahmoud Mokhtar Elhelbawi; Silke Weinitz; Ghazaleh Farmand; Ulrich Kellner

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3151.

ARVO Annual Meeting Abstract June 2017

Comparison Of 2 Techniques Of Optical Coherence Tomography Angiography (Zeiss & Heidelberg Engineering) In A Series Of Patients With Neovascular Age-Related Macular Degeneration

Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Ulrich Kellner

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):30.

Visual Neuroscience February 2017

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

PDF

Ditta Zobor; Annette Werner; Franco Stanzial; Francesco Benedicenti; Günther Rudolph; Ulrich Kellner; Christian Hamel; Sten Andréasson; Gergely Zobor; Torsten Strasser; Bernd Wissinger; Susanne Kohl; Eberhart Zrenner; for the RD-CURE Consortium
TAGS: achromatopsia, genes, vif, phenotype, psychophysics, retinal cone, electroretinography, rod photoreceptors, atrophy, electrophysiology
Invest. Ophthalmol. Vis. Sci.. 2017; 58(2):821-832. https://doi.org/10.1167/iovs.16-20427

Includes: Supplemental Content

Genetics January 2017

Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort—Impact of Selected Deep Intronic Variants and Common SNPs

PDF

Heidi L. Schulz; Felix Grassmann; Ulrich Kellner; Georg Spital; Klaus Rüther; Herbert Jägle; Karsten Hufendiek; Philipp Rating; Cord Huchzermeyer; Maria J. Baier; Bernhard H. F. Weber; Heidi Stöhr

Invest. Ophthalmol. Vis. Sci.. 2017; 58(1):394-403. https://doi.org/10.1167/iovs.16-19936

Includes: Supplemental Content

ARVO Annual Meeting Abstract September 2016

Wide-field MultiColor Spectral Imaging and Wide-field Spectral Domain Optical Coherence Tomography Imaging in Retinitis Pigmentosa

Ulrich Kellner; Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Birgit Lindau; Heidi Barbara Stoehr; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):146.

ARVO Annual Meeting Abstract September 2016

Wide-field MultiColor Spectral Imaging and Wide-field Spectral Domain Optical Coherence Tomography Imaging in ABCA4-related retinal dystrophies

Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Heidi Barbara Stoehr; Bernhard HF Weber; Ulrich Kellner

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):147.

ARVO Annual Meeting Abstract September 2016

Investigating the pathomechanism of FAM161A -associated retinal disease in primary ciliated cells

Heidi Barbara Stoehr; Marlene Schwarzfischer; Lisa-Marie Braun; Alexander Aslanidis; Thomas Langmann; Ulrich Kellner

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3192.

ARVO Annual Meeting Abstract June 2015

Comparison Of Spectralis Fundus Autofluorescence Blue (486 nm) And Green Mode (518 nm) In A Consecutive Series Of Patients With Retinal Disorders

Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Ulrich Kellner

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):5904.

ARVO Annual Meeting Abstract June 2015

A Decade Of Diagnosing Inherited Retinal Dystrophies and Optic Atrophies: The Evolution Towards An Advanced Standardized Retinal Imaging and Molecular Genetic Approach

Ulrich Kellner; Heidi Stöhr; Susanne Kohl; Bernhard HF Weber; Bernd Wissinger; Teresa Neuhann; Silke Weinitz; Ghazaleh Farmand; Simone Kellner

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):3877.

ARVO Annual Meeting Abstract April 2014

Retinal structure and function in Achromatopsia: the CNGA3 phenotype

Ditta Zobor; Franco Stanzial; Ulrich Kellner; Günther Rudolph; Bernd Wissinger; Susanne Kohl; Eberhart Zrenner

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):346.

ARVO Annual Meeting Abstract April 2014

Risk Of Endophthalmitis In A Large Series (135.729 injections) Of Patients Treated With Intravitreal Anti-VEGF or Dexamethasone Injections

Ulrich Kellner; Ruth Kölb-Keerl; Detlef Engineer; Andreas Kersten; Norbert Körber; VOA Study Group

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):585.

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AI-based identification of photoreceptor degeneration and retinal pigment epithelial atrophy in inherited macular dystrophies

Near-infrared autofluorescence in inherited retinal dystrophies

Wide-field optical coherence tomography in retinitis pigmentosa

DNAJC30 disease-causing gene variants in a large Central European cohort of patients with inherited optic atrophy

Autosomal dominant gyrate atrophy-like choroidal dystrophy revisited: 45 years follow-up and association with a novel missense variant

Variation of Clinical Findings in Choroideremia Carriers - From normal to severe

Long-term follow-up and variable progression of ocular signs in two sisters with AHI1-gene associated Joubert syndrome

North-Carolina Macular dystrophy like phenotype in a three generation pedigree wit autosomal dominant inheritance and exclusion of MCRD1

Molecular Genetic Screening In A Series Of 852 Patients With Inherited Retinal Dystrophies From One German Reference Center

Acute Fingolimod Associated Macular Edema 2 Days After Onset Of Treatment And Gradual Resolution Under Ketorolac Therapy Over 5 Months

Comparison Of 2 Techniques Of Optical Coherence Tomography Angiography (Zeiss & Heidelberg Engineering) In A Series Of Patients With Neovascular Age-Related Macular Degeneration

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

Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort—Impact of Selected Deep Intronic Variants and Common SNPs

Wide-field MultiColor Spectral Imaging and Wide-field Spectral Domain Optical Coherence Tomography Imaging in Retinitis Pigmentosa

Wide-field MultiColor Spectral Imaging and Wide-field Spectral Domain Optical Coherence Tomography Imaging in ABCA4-related retinal dystrophies

Investigating the pathomechanism of FAM161A -associated retinal disease in primary ciliated cells

Comparison Of Spectralis Fundus Autofluorescence Blue (486 nm) And Green Mode (518 nm) In A Consecutive Series Of Patients With Retinal Disorders

A Decade Of Diagnosing Inherited Retinal Dystrophies and Optic Atrophies: The Evolution Towards An Advanced Standardized Retinal Imaging and Molecular Genetic Approach

Retinal structure and function in Achromatopsia: the CNGA3 phenotype

Risk Of Endophthalmitis In A Large Series (135.729 injections) Of Patients Treated With Intravitreal Anti-VEGF or Dexamethasone Injections

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