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1. Full Text Question and Answer Sessions with Prof. Eberhart Zrenner
by Tamai, Makoto and Miyake, Yozo and Fujikado, Takashi and Zrenner, Zrenner
Ophthalmologica, ISSN 0030-3755, 2002, Volume 216, Issue 1, pp. 52 - 53
  The 14th CIBA Vision Symposium. October 25, 2001, Osaka; October 27, 2001, Tokyo. Proceedings. Guest Editors: Yoshihisa Oguchi, Tokyo; Yoshihito Honda, Osaka 
Question and Answer | OPHTHALMOLOGY
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2. Full Text Fighting blindness with microelectronics
by Zrenner, Eberhart
Science Translational Medicine, ISSN 1946-6234, 11/2013, Volume 5, Issue 210, pp. 210ps16 - 210ps16
There is no approved cure for blindness caused by degeneration of the photoreceptor cells of the retina. However, there has been encouraging progress with... 
RETINAL DEGENERATION | MEDICINE, RESEARCH & EXPERIMENTAL | VISION LOSS | THERAPY | TRANSCORNEAL ELECTRICAL-STIMULATION | CONGENITAL-AMAUROSIS | EFFICACY | GENE-TRANSFER | IMPLANTS | RETINITIS-PIGMENTOSA | PROSTHESIS | CELL BIOLOGY | Electronics - instrumentation | Animals | Blindness - therapy | Visual Prosthesis | Humans | Miniaturization - instrumentation | Index Medicus
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3. Neurophysiological aspects of color vision in primates
: comparative studies on simian retinal ganglion cells and the human visual system
by Zrenner, Eberhart, 1945
1983, Studies of brain function, ISBN 0387116532, Volume 9, xvi, 218
Color vision | Physiology, Comparative | Neurons | Cytology | Primates | Retina | Physiology | Color perception | Neurophysiology
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4. Full Text Artificial vision: Solar cells for the blind
by Zrenner, Eberhart
Nature Photonics, ISSN 1749-4885, 06/2012, Volume 6, Issue 6, pp. 344 - 345
PHYSICS, APPLIED | RETINA | STIMULATION | OPTICS | FEASIBILITY | VISUAL PROSTHESIS
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5. Full Text Solar cells for the blind
by Zrenner, Eberhart
Nature Photonics, ISSN 1749-4885, 06/2012, Volume 6, Issue 6, pp. 344 - 345
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6. Full Text Beiträge zu Behandlungsmöglichkeiten für Patienten mit erblichen Netzhautdystrophien
by Zrenner, Eberhart
Karger Kompass Ophthalmologie, ISSN 2297-0118, 2017, Volume 3, Issue 2, pp. 72 - 74
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7. Full Text Emmetropes and myopes differ little in their accommodation dynamics but strongly in their ciliary muscle morphology
Vision research, 08/2019
Index Medicus
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8. Full Text Subretinal electronic chips allow blind patients to read letters and combine them to words
by Eberhart Zrenner and Karl Ulrich Bartz-Schmidt and Heval Benav and Dorothea Besch and Anna Bruckmann and Veit-Peter Gabel and Florian Gekeler and Udo Greppmaier and Alex Harscher and Steffen Kibbel and Johannes Koch and Akos Kusnyerik and Tobias Peters and Katarina Stingl and Helmut Sachs and Alfred Stett and Peter Szurman and Barbara Wilhelm and Robert Wilke
Proceedings: Biological Sciences, ISSN 0962-8452, 5/2011, Volume 278, Issue 1711, pp. 1489 - 1497
A light-sensitive, externally powered microchip was surgically implanted subretinally near the macular region of volunteers blind from hereditary retinal... 
Electrodes | Retinal images | Geometric shapes | Materials | Retina | Implanted electrodes | Electric fields | Pixels | Visual perception | Perceptual localization | Subretinal neuro-prosthetics | Bionic vision | Retinal implant | Retinitis pigmentosa | Artificial vision | Blindness | retinal implant | ARRAY | VISION | blindness | INFORMATION | VISUAL PERFORMANCE | subretinal neuro-prosthetics | PIGMENTOSA | artificial vision | IMPLANTS | bionic vision | RESPONSES | EVOLUTIONARY BIOLOGY | ISOLATED CHICKEN RETINA | ELECTRICAL-STIMULATION | BIOLOGY | retinitis pigmentosa | ECOLOGY | PROSTHESIS | Reading | Visual Perception - physiology | Implants, Experimental | Retina - surgery | Humans | Light | Adult | Female | Male | Electrodes, Implanted | Sensory Aids | Retinal Dystrophies - surgery | Index Medicus | 133 | 1001
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9. Full Text Electrical activation of degenerated photoreceptors in blind mouse retina elicited network-mediated responses in different types of ganglion cells
by Haq, Wadood and Dietter, Johannes and Zrenner, Eberhart
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 16998 - 11
Electrical (e-) stimulation is explored in schemes to rescue the vision of blind people, e.g. those affected by Retinitis Pigmentosa (RP). We e-activated... 
GAP-JUNCTIONS | STIMULATION | CONE PHOTORECEPTORS | HORIZONTAL CELLS | ABNORMALITIES | MULTIDISCIPLINARY SCIENCES | ADAPTATION | CLASSIFICATION | CHANNELS | RD/RD | RECEPTORS | Calcium channels | Retinitis pigmentosa | Gap junctions | Calcium channels (voltage-gated) | Spatial discrimination | Calcium imaging | Retina | Retinal ganglion cells | γ-Aminobutyric acid | Platinum | Vision | Blindness | Photoreceptors | Retinitis | Ganglion cells
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10. Full Text Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies
by Glöckle, Nicola and Kohl, Susanne and Mohr, Julia and Scheurenbrand, Tim and Sprecher, Andrea and Weisschuh, Nicole and Bernd, Antje and Rudolph, Günther and Schubach, Max and Poloschek, Charlotte and Zrenner, Eberhart and Biskup, Saskia and Berger, Wolfgang and Wissinger, Bernd and Neidhardt, John
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 1, pp. 99 - 104
Hereditary retinal dystrophies (RD) constitute a group of blinding diseases that are characterized by clinical variability and pronounced genetic... 
next generation sequencing | BIOCHEMISTRY & MOLECULAR BIOLOGY | ABCA4 | RECESSIVE RETINITIS-PIGMENTOSA | GENOTYPING MICROARRAY | genetic modifiers | gene diagnostics | CHIP | GENE | GENETICS & HEREDITY | hereditary retinal dystrophy | de-novo mutations | PARADIGM | Genetic Predisposition to Disease | Exons | Extracellular Matrix Proteins - genetics | Humans | Retinal Dystrophies - pathology | Retinitis Pigmentosa - genetics | Retinal Dystrophies - etiology | Sequence Analysis, DNA | ATP-Binding Cassette Transporters - genetics | Usher Syndromes - genetics | Pedigree | Usher Syndromes - etiology | Usher Syndromes - pathology | High-Throughput Nucleotide Sequencing | Eye Proteins - genetics | Mutation | Retinitis Pigmentosa - etiology | Pathology, Molecular | Retinal Dystrophies - genetics | USH2A protein | Congenital diseases | Disease | Retinitis pigmentosa | Retina | Gene expression | Genetic counseling | Respiratory distress syndrome | Genetics | Photoreceptors | Retinitis | Diagnosis | Index Medicus
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11. Full Text Ciliary muscle thickness profiles derived from optical coherence tomography images: Erratum
by Wagner, Sandra and Zrenner, Eberhart and Strasser, Torsten
Biomedical Optics Express, ISSN 2156-7085, 2019, Volume 10, Issue 1, p. 119
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12. Full Text Erratum: Ciliary muscle thickness profiles derived from optical coherence tomography images: erratum
by Wagner, Sandra and Zrenner, Eberhart and Strasser, Torsten
Biomedical optics express, ISSN 2156-7085, 01/2019, Volume 10, Issue 1, pp. 119 - 119
[This corrects the article on p. 5100 in vol. 9, PMID: 30319924.]. 
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13. Full Text Prolonged nearwork affects the ciliary muscle morphology
by Wagner, Sandra and Schaeffel, Frank and Zrenner, Eberhart and Straßer, Torsten
Experimental Eye Research, ISSN 0014-4835, 09/2019, Volume 186, pp. 107741 - 107741
There is evidence for a possible link between myopia development and near vision. We investigated the effect of prolonged nearwork on ciliary muscle (CM)... 
Autonomous nervous system | Accommodation | Optical coherence tomography | Nearwork | Ciliary muscle | Myopia | Index Medicus
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14. Full Text Poly ADP ribosylation and extracellular vesicle activity in rod photoreceptor degeneration
by Vidal-Gil, L and Sancho-Pelluz, J and Zrenner, E and Oltra, M and Sahaboglu, A
SCIENTIFIC REPORTS, ISSN 2045-2322, 03/2019, Volume 9, Issue 1, pp. 3758 - 10
Retinitis Pigmentosa is a group of inherited neurodegenerative diseases that result in selective cell death of photoreceptors. In the developed world, RP is... 
POLY(ADP-RIBOSE) POLYMERASE | NUCLEAR | ANGIOGENESIS | MITOCHONDRIAL | MULTIDISCIPLINARY SCIENCES | MOUSE | EXOSOMES | PHOSPHODIESTERASE | MUTATIONS | CELL-DEATH | SUBUNIT | Neuroprotection | Animal models | Neurodegenerative diseases | Retinitis pigmentosa | Poly(ADP-ribose) polymerase | Lipids | Retina | Cell interactions | Poly(ADP-ribose) Polymerase 1 | Cell death | Ribose | Neurodegeneration | Blindness | Retinal degeneration | Photoreceptors | Retinitis | Mutation | Ribosylation | Age | Phosphodiesterase | Apoptosis
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15. Full Text Identification of a common non-apoptotic cell death mechanism in hereditary retinal degeneration
by Arango-Gonzalez, Blanca and Trifunović, Dragana and Sahaboglu, Ayse and Kranz, Katharina and Michalakis, Stylianos and Farinelli, Pietro and Koch, Susanne and Koch, Fred and Cottet, Sandra and Janssen-Bienhold, Ulrike and Dedek, Karin and Biel, Martin and Zrenner, Eberhart and Euler, Thomas and Ekström, Per and Ueffing, Marius and Paquet-Durand, Franҫois and Oftalmologi, Lund and Lund University and Ophthalmology, Lund and Lunds universitet
PLoS ONE, ISSN 1932-6203, 11/2014, Volume 9, Issue 11, pp. e112142 - e112142
Cell death in neurodegenerative diseases is often thought to be governed by apoptosis; however, an increasing body of evidence suggests the involvement of... 
POLY(ADP-RIBOSE) POLYMERASE | MUTANT MICE | MODELS | MULTIDISCIPLINARY SCIENCES | INHERITED PHOTORECEPTOR DEGENERATION | MOUSE RETINA | RETINITIS-PIGMENTOSA | GUANOSINE-MONOPHOSPHATE | CONGENITAL AMAUROSIS | RD1 MOUSE | IN-SITU | Cyclic GMP - physiology | Poly Adenosine Diphosphate Ribose - physiology | Animals, Genetically Modified | Retinal Degeneration - genetics | Rats | Light Signal Transduction - genetics | Retinal Degeneration - physiopathology | Poly(ADP-ribose) Polymerases - physiology | Calpain - physiology | Animals | Cell Death - genetics | Cell Death - physiology | Mice | Histone Deacetylases - physiology | Mutation | Disease Models, Animal | Histone deacetylase | Neurosciences | Animal models | Neurodegenerative diseases | Mortality | Guanosine | Science | Retina | Calpain | ADP | Mutants | Neurological diseases | Polymerase | Ribose | Cell death | Neurodegeneration | Rodents | Cyclic GMP | Blindness | Retinal degeneration | Degeneration | Apoptosis | Index Medicus | Clinical Medicine | Ophthalmology | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Oftalmologi
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16. Full Text Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia
by Kohl, S and Zobor, D and Chiang, W.C and Weisschuh, N and Staller, J and Menendez, I.G and Chang, S and Beck, S.C and Garrido, M. Garcia and Sothilingam, V and Seeliger, M.W and Stanzial, F and Benedicenti, F and Inzana, F and Heon, E and Vincent, A and Beis, J and Strom, T.M and Rudolph, G and Roosing, S and Hollander, A.I. den and Cremers, F.P.M and Lopez, I and Ren, H and Moore, A.T and Webster, A.R and Michaelides, M and Koenekoop, R.K and Zrenner, E and Kaufman, R.J and Tsang, S.H and Wissinger, B and Lin, J.H
Nature Genetics, ISSN 1061-4036, 2015, Volume 47, Issue 7, pp. 757 - 765
Achromatopsia (ACHM) is an autosomal recessive disorder characterized by color blindness, photophobia, nystagmus and severely reduced visual acuity. Using... 
LONG-TERM | RETINAL STRUCTURE | ALPHA-SUBUNIT | CONGENITAL ACHROMATOPSIA | OPTICAL COHERENCE TOMOGRAPHY | MOUSE MODEL | GENETICS & HEREDITY | GENE-THERAPY | ENDOPLASMIC-RETICULUM STRESS | TRANSCRIPTION FACTOR | TOTAL COLOURBLINDNESS | Genetic Association Studies | Humans | Mice, Inbred C57BL | Middle Aged | Male | Mutation, Missense | Unfolded Protein Response | Activating Transcription Factor 6 - genetics | Color Vision Defects - genetics | Mice, Knockout | Young Adult | Animals | Pedigree | Retinal Cone Photoreceptor Cells - pathology | Adolescent | HEK293 Cells | Aged, 80 and over | Adult | Female | Transcription, Genetic | Child | Gene mutations | Genetic susceptibility | Genetic research | Genetic aspects | Research | Color blindness | Health aspects | Risk factors | Haplotypes | Medical research | Biomedical research | Laboratories | Genes | Grants | Patients | Proteins | Hospitals | Photoreceptors | Software | Mutation | Chromosomes | Index Medicus
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17. Full Text PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome
by Ebermann, Inga and Phillips, Jennifer B and Liebau, Max C and Koenekoop, Robert K and Schermer, Bernhard and Lopez, Irma and Schäfer, Ellen and Roux, Anne-Francoise and Dafinger, Claudia and Bernd, Antje and Zrenner, Eberhart and Claustres, Mireille and Blanco, Bernardo and Nürnberg, Gudrun and Nürnberg, Peter and Ruland, Rebecca and Westerfield, Monte and Benzing, Thomas and Bolz, Hanno J
Journal of Clinical Investigation, ISSN 0021-9738, 06/2010, Volume 120, Issue 6, pp. 1812 - 1823
Usher syndrome is a genetically heterogeneous recessive disease characterized by hearing loss and retinitis pigmentosa (RP). It frequently presents with... 
MEDICINE, RESEARCH & EXPERIMENTAL | HEARING-LOSS | SENSORY HAIR-CELLS | PROTEIN NETWORK | GENE-PRODUCTS | MYOSIN XVA | SYNDROME-TYPE-II | LINKAGE ANALYSIS | DEAFNESS | MUTATIONS | RETINITIS-PIGMENTOSA | Frameshift Mutation | Humans | Retinitis Pigmentosa - genetics | Genotype | Male | Syndrome | Hearing Loss - genetics | Homozygote | Phenotype | Usher Syndromes - genetics | Receptors, G-Protein-Coupled - genetics | Mutation | Usher Syndromes - metabolism | Siblings | Usher's syndrome | Care and treatment | Gene mutations | Development and progression | Genetic aspects | Properties | Retinal diseases | Identification and classification | Membrane proteins | Index Medicus | Abridged Index Medicus
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18. Full Text The Spatial Extent of Epiretinal Electrical Stimulation in the Healthy Mouse Retina
by Hosseinzadeh, Zohreh and Jalligampala, Archana and Zrenner, Eberhart and Rathbun, Daniel Lleweylln
Neurosignals, ISSN 1424-862X, 01/2018, Volume 25, Issue 1, pp. 15 - 25
Background/Aims: Retinal prostheses use electrical stimulation to restore functional vision to patients blinded by retinitis pigmentosa. A key detail is the... 
Original Paper | Bionic vision | Retinal implant | Electrical point spread function | Electrical response function | Hysteresis | Index Medicus
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19. Full Text Disinhibition of intrinsic photosensitive retinal ganglion cells in patients with X-linked congenital stationary night blindness
by Schatz, A and Kelbsch, C and Zeitz, C and Kohl, S and Zrenner, E and Gekeler, F and Wilhelm, H and Wilhelm, B and Willmann, G
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, ISSN 0721-832X, 06/2019, Volume 257, Issue 6, pp. 1207 - 1215
PurposeTo assess the pupil light response (PLR) to chromatic stimulation in patients with different types of X-linked congenital stationary night blindness... 
PUPILLARY CONSTRICTION | RESPONSES DRIVEN | LIGHT RESPONSES | Pupillography | MELANOPSIN | MOUSE | Night blindness | NYCTALOPIN | CACNA1F | NYX | CHANNEL | GENE | Retinal degeneration | OPHTHALMOLOGY | CSNB | MUTATIONS | Pupil - physiology | Retinal Ganglion Cells - physiology | Eye Diseases, Hereditary - physiopathology | Humans | Middle Aged | Night Blindness - diagnosis | Dark Adaptation - physiology | Eye Diseases, Hereditary - diagnosis | Male | Genetic Diseases, X-Linked - diagnosis | Reflex, Pupillary - physiology | Myopia - physiopathology | Night Blindness - physiopathology | Rod Opsins - metabolism | Myopia - diagnosis | Female | Photic Stimulation | Genetic Diseases, X-Linked - physiopathology | Diagnostic Techniques, Ophthalmological | Care and treatment | Genetic disorders | Ophthalmology | Ganglion | Analysis | Retinal ganglion cells | Blindness | Bipolar cells | Retina | Nyctalopia | Ganglion cells | Stationary night blindness
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