A. Renner

发表

Progression of retinal pigment epithelial alterations during long-term follow-up in female carriers of choroideremia and report of a novel CHM mutation.

B. Weber, B. Fiebig, U. Kellner, 2009, Archives of ophthalmology.

fMRI with Central Vision Loss: Effects of Fixation Locus and Stimulus Type.

M. Greenlee, H. Jägle, Tina Plank, 2017, Optometry and vision science : official publication of the American Academy of Optometry.

Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations.

B. Weber, B. Wissinger, S. Andréasson, 2009, American journal of ophthalmology.

Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.

E. Zrenner, V. Kitiratschky, R. Wilke, 2008, Investigative ophthalmology & visual science.

Neural correlates of visual search in patients with hereditary retinal dystrophies

M. Greenlee, Tina Plank, A. Renner, 2013, Human brain mapping.

ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies

A. Cideciyan, S. Jacobson, E. Zrenner, 2008, European Journal of Human Genetics.

Liver-specific increase of UTP and UDP-sugar concentrations in rats induced by dietary vitamin B6-deficiency and its relation to complex N-glycan structures of liver membrane-proteins

W. Reutter, A. Renner, D. Grunow, 2007, Glycoconjugate Journal.

[Dry eye syndrome and neurotrophic keratitis in childhood. Causes and therapy].

I. Oberacher-Velten, A. Renner, H. Helbig, 2010, Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft.

Fundus autofluorescence and mfERG for early detection of retinal alterations in patients using chloroquine/hydroxychloroquine.

U. Kellner, A. Renner, H. Tillack, 2006, Investigative ophthalmology & visual science.

Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia

P. Sieving, S. Jacobson, R. Salati, 2022, Human mutation.

[Evidence-based diagnostic approach to inherited retinal dystrophies 2009].

B. Fiebig, U. Kellner, A. Renner, 2009, Klinische Monatsblatter fur Augenheilkunde.

Recurrent episodes of night blindness in a patient with short bowel syndrome

H. Jägle, A. Renner, T. Dietrich-Ntoukas, 2015, Documenta Ophthalmologica.

Ten-year follow-up of two unrelated patients with Müller cell sheen dystrophy and first report of successful vitrectomy

H. Jägle, U. Kellner, A. Renner, 2014, Documenta Ophthalmologica.

ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT

B. Fiebig, U. Kellner, M. Foerster, 2008, Documenta Ophthalmologica.

Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram

U. Kellner, M. Foerster, A. Renner, 2006, Graefe's Archive for Clinical and Experimental Ophthalmology.

Retinoschisis: Formen, Manifestation, Therapiemöglichkeiten (Retinoschisis: Types, Morphological Characteristics, Therapeutic Options)

A. Renner, H. Helbig, 2009 .

A subgroup of age-related macular degeneration is associated with mono-allelic sequence variants in the ABCA4 gene.

C. Keilhauer, L. Fritsche, U. Mansmann, 2012, Investigative ophthalmology & visual science.

Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.

Olivier Poch, Sabine Defoort-Dhellemmes, Xavier Zanlonghi, 2012, American journal of human genetics.

[Hereditary retinal dystrophies].

U. Kellner, A. Renner, S. M. Herbst, 1997, Klinische Monatsblatter fur Augenheilkunde.

TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.

T. Léveillard, J. Sahel, S. Jacobson, 2009, American journal of human genetics.

FOVEAL CAVITATION AS AN OPTICAL COHERENCE TOMOGRAPHY FINDING IN CENTRAL CONE DYSFUNCTION

Dorothy A. Thompson, M. Marmor, Theodore Leng, 2012, Retina.

Hereditäre Makuladystrophien

U. Kellner, A. Renner, Renner Ab, 2016, Klinische Monatsblätter für Augenheilkunde.

Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation

H. Jägle, B. Fiebig, A. Renner, 2012, Documenta Ophthalmologica.

Hereditäre Makuladystrophien in der Differenzialdiagnose der AMD

H. Jägle, A. Renner, 2012, Klin Monatsbl Augenheilkd.

Clinical Heterogeneity in Autosomal Recessive Bestrophinopathy with Biallelic Mutations in the BEST1 Gene

H. Stöhr, H. Jägle, C. Framme, 2020, International journal of molecular sciences.

Late onset is common in best macular dystrophy associated with VMD2 gene mutations.

U. Kellner, H. Kraus, M. Foerster, 2005, Ophthalmology.

MORPHOLOGY AND FUNCTIONAL CHARACTERISTICS IN ADULT VITELLIFORM MACULAR DYSTROPHY

B. Wissinger, S. Kohl, U. Kellner, 2004, Retina.

Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscope

Jay Neitz, Maureen Neitz, John S Werner, 2004, Visual Neuroscience.

Photopigment optical density of the human foveola and a paradoxical senescent increase outside the fovea

J. Werner, J. Neitz, M. Neitz, 2004, Visual Neuroscience.

Gray matter alterations in visual cortex of patients with loss of central vision due to hereditary retinal dystrophies

Mark W. Greenlee, Tina Plank, Horst Helbig, 2011, NeuroImage.

Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.

F. Cremers, I. MacDonald, M. Preising, 2006, Ophthalmology.

Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa.

J. Corbo, E. Zrenner, Silvio Alessandro Di Gioia, 2010, American journal of human genetics.

Recording of Both VEP and Multifocal ERG for Evaluation of Unexplained Visual Loss

U. Kellner, H. Kraus, M. Foerster, 2005, Documenta Ophthalmologica.

[Hereditary retinochoroidal dystrophies. Part 2: differential diagnosis].

U. Kellner, A. Renner, H. Tillack, 2004, Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft.

Late onset is common in best macular dystrophy associated with VMD 2 gene mutations

A. Renner, 2005 .

Retinoschisis: Formen, Manifestation, Therapiemöglichkeiten (Retinoschisis: Types, Morphological Characteristics, Therapeutic Options)

A. Renner, H. Helbig, 2009 .

Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations.

B. Wissinger, B. Fiebig, S. Kohl, 2009, American journal of ophthalmology-glaucoma.