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A luminous efficiency function, V<sub>D65</sub>* ( λ), for daylight adaptation: A correction.
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- Color Research & Application, 2011, v. 36, n. 1, p. 42, doi. 10.1002/col.20602
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- Publication type:
- Article
The importance of gene order in expression of the red and green visual pigment genes and in color vision.
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- Color Research & Application, 2001, v. 26, n. S1, p. S79, doi. 10.1002/1520-6378(2001)26:1+<::AID-COL18>3.0.CO;2-4
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- Publication type:
- Article
I used to be color blind.
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- Color Research & Application, 2001, v. 26, n. S1, p. S269, doi. 10.1002/1520-6378(2001)26:1+<::AID-COL58>3.0.CO;2-0
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- Publication type:
- Article
Manifestations of rod monochromacy.
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- Color Research & Application, 2001, v. 26, n. S1, p. S96, doi. 10.1002/1520-6378(2001)26:1+<::AID-COL22>3.0.CO;2-L
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- Publication type:
- Article
Makulopathie bei Sichelzellerkrankung.
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- Der Ophthalmologe, 2021, v. 118, n. 10, p. 1013, doi. 10.1007/s00347-020-01319-8
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- Article
Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration.
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- Human Molecular Genetics, 2014, v. 23, n. 19, p. 5197, doi. 10.1093/hmg/ddu242
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- Article
Clinical Heterogeneity in Autosomal Recessive Bestrophinopathy with Biallelic Mutations in the BEST1 Gene.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 24, p. 9353, doi. 10.3390/ijms21249353
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- Article
Transcorneal Electrical Stimulation for the Treatment of Retinitis Pigmentosa: A Multicenter Safety Study of the OkuStim® System (TESOLA-Study).
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- Ophthalmic Research, 2020, v. 63, n. 3, p. 234, doi. 10.1159/000505001
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- Article
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.
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- European Journal of Human Genetics, 2008, v. 16, n. 7, p. 812, doi. 10.1038/ejhg.2008.23
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- Article
CNGB3 mutations account for 50%of all cases with autosomal recessive achromatopsia.
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- European Journal of Human Genetics, 2005, v. 13, n. 3, p. 302, doi. 10.1038/sj.ejhg.5201269
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- Publication type:
- Article
The multifocal pattern electroretinogram (mfPERG) and cone-isolating stimuli.
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- Visual Neuroscience, 2007, v. 24, n. 6, p. 805, doi. 10.1017/S0952523807070733
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- Publication type:
- Article
Multifocal electroretinogram in trichromat and dichromat observers under cone isolating conditions.
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- Visual Neuroscience, 2004, v. 21, n. 3, p. 249, doi. 10.1017/S0952523804213347
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- Publication type:
- Article
Multifocal electroretinogram in trichromat and dichromat observers under cone isolating conditions.
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- Visual Neuroscience, 2004, v. 21, n. 3, p. 249, doi. 10.1017/s0952523804213347
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- Publication type:
- Article
TGF-β Signaling Protects Retinal Neurons from Programmed Cell Death during the Development of the Mammalian Eye.
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- Journal of Neuroscience, 2013, v. 33, n. 35, p. 14246, doi. 10.1523/JNEUROSCI.0991-13.2013
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- Publication type:
- Article
Management of strabismus with hemianopic visual field defects.
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- Graefe's Archive of Clinical & Experimental Ophthalmology, 2013, v. 251, n. 2, p. 575, doi. 10.1007/s00417-012-2045-1
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- Article
Angiotensin-Receptor-Associated Protein Modulates Ca2+ Signals in Photoreceptor and Mossy Fiber cells.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-55380-8
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- Article
Progressive Retinal Degeneration and Glial Activation in the CLN6<i><sup>nclf</sup></i> Mouse Model of Neuronal Ceroid Lipofuscinosis: A Beneficial Effect of DHA and Curcumin Supplementation.
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- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0075963
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- Article
Rod and Cone Function in Patients with KCNV2 Retinopathy.
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- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046762
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- Article
Cortical Thickness Related to Compensatory Viewing Strategies in Patients With Macular Degeneration.
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- Frontiers in Neuroscience, 2021, p. 1, doi. 10.3389/fnins.2021.718737
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- Article
Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel.
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- Nature Genetics, 1998, v. 19, n. 3, p. 257, doi. 10.1038/935
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- Publication type:
- Article
Suppression of SNARE-dependent exocytosis in retinal glial cells and its effect on ischemia-induced neurodegeneration.
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- Glia, 2017, v. 65, n. 7, p. 1059, doi. 10.1002/glia.23144
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- Article
Visual cortex organisation in a macaque monkey with macular degeneration.
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- European Journal of Neuroscience, 2013, v. 38, n. 10, p. 3456, doi. 10.1111/ejn.12349
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- Article
Dose-dependent regulation of horizontal cell fate by Onecut family of transcription factors.
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- PLoS ONE, 2020, v. 15, n. 8, p. 1, doi. 10.1371/journal.pone.0237403
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- Article
Retinal characteristics of the congenital disorder of glycosylation PMM2-CDG.
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- Journal of Inherited Metabolic Disease, 2013, v. 36, n. 6, p. 1039, doi. 10.1007/s10545-013-9594-2
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- Article
ElVisML: an open data format for the exchange and storage of electrophysiological data in ophthalmology.
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- Documenta Ophthalmologica, 2018, v. 136, n. 1, p. 75, doi. 10.1007/s10633-017-9618-6
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- Article
Full-field electroretinogram in autism spectrum disorder.
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- Documenta Ophthalmologica, 2016, v. 132, n. 2, p. 83, doi. 10.1007/s10633-016-9529-y
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- Article
Recurrent episodes of night blindness in a patient with short bowel syndrome.
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- Documenta Ophthalmologica, 2015, v. 131, n. 3, p. 221, doi. 10.1007/s10633-015-9516-8
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- Publication type:
- Article
Ten-year follow-up of two unrelated patients with Müller cell sheen dystrophy and first report of successful vitrectomy.
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- Documenta Ophthalmologica, 2014, v. 129, n. 3, p. 191, doi. 10.1007/s10633-014-9463-9
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- Article
Psychophysically determined full-field stimulus thresholds (FST) in retinitis pigmentosa: relationships with electroretinography and visual field outcomes.
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- Documenta Ophthalmologica, 2013, v. 127, n. 2, p. 123, doi. 10.1007/s10633-013-9393-y
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- Article
A comparison of the performance of three visual evoked potential-based methods to estimate visual acuity.
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- Documenta Ophthalmologica, 2013, v. 126, n. 1, p. 45, doi. 10.1007/s10633-012-9359-5
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- Article
Detailed functional and structural characterization of a macular lesion in a rhesus macaque.
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- Documenta Ophthalmologica, 2012, v. 125, n. 3, p. 179, doi. 10.1007/s10633-012-9340-3
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- Article
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.
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- Documenta Ophthalmologica, 2012, v. 125, n. 1, p. 81, doi. 10.1007/s10633-012-9335-0
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- Article
Accommodation limits induced optical defocus in defocus experiments.
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- Documenta Ophthalmologica, 2010, v. 121, n. 2, p. 103, doi. 10.1007/s10633-010-9237-y
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- Article
Molecular Basis of an Inherited Form of Incomplete Achromatopsia.
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- Journal of Neuroscience, 2004, v. 24, n. 1, p. 138, doi. 10.1523/JNEUROSCI.3883-03.2004
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- Article
Genetic targeting or pharmacological inhibition of galectin-3 dampens microglia reactivity and delays retinal degeneration.
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- 2022
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- Publication type:
- journal article
Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase.
- Published in:
- Human Mutation, 2009, v. 30, n. 8, p. E782, doi. 10.1002/humu.21055
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- Article
Gene Therapy with Voretigene Neparvovec Improves Vision and Partially Restores Electrophysiological Function in Pre-School Children with Leber Congenital Amaurosis.
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- Biomedicines, 2023, v. 11, n. 1, p. 103, doi. 10.3390/biomedicines11010103
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- Article
Common synonymous variants in ABCA4 are protective for chloroquine induced maculopathy (toxic maculopathy)
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- BMC Ophthalmology, 2015, v. 15, n. 1, p. 18, doi. 10.1186/s12886-015-0008-0
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- Article
Common synonymous variants in ABCA4 are protective for chloroquine induced maculopathy (toxic maculopathy).
- Published in:
- 2015
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- Publication type:
- journal article
Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.
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- Human Mutation, 2011, v. 32, n. 12, p. 1398, doi. 10.1002/humu.21580
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- Publication type:
- Article
Orbital compartment: effects of emergent canthotomy and cantholysis.
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- European Archives of Oto-Rhino-Laryngology, 2015, v. 272, n. 2, p. 479, doi. 10.1007/s00405-014-3238-5
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- Article
The agonistic TSPO ligand XBD173 attenuates the glial response thereby protecting inner retinal neurons in a murine model of retinal ischemia.
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- 2019
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- Publication type:
- journal article
Mutated olfactomedin 1 in the interphotoreceptor matrix of the mouse retina causes functional deficits and vulnerability to light damage.
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- Histochemistry & Cell Biology, 2017, v. 147, n. 4, p. 453, doi. 10.1007/s00418-016-1510-z
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- Article
Complement Factor H-Related 3 Enhanced Inflammation and Complement Activation in Human RPE Cells.
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- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.769242
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- Article
Reorganization of human cortical maps caused by inherited photoreceptor abnormalities.
- Published in:
- Nature Neuroscience, 2002, v. 5, n. 4, p. 364, doi. 10.1038/nn817
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- Article
The molecular basis of dichromatic color visionin males with multiple red and green visual pigment genes.
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- Human Molecular Genetics, 2002, v. 11, n. 1, p. 23, doi. 10.1093/hmg/11.1.23
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- Publication type:
- Article
Mutations in the CNGB3 gene encoding the β -subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3 ) linked to chromosome 8q21.
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- Human Molecular Genetics, 2000, v. 9, n. 14, p. 2107, doi. 10.1093/hmg/9.14.2107
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- Article
Orbital floor fracture repair: the endonasal approach.
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- Rhinology, 2017, v. 55, n. 4, p. 348, doi. 10.4193/rhino17.088
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- Article
Systemic therapy of necrobiotic xanthogranuloma: a systematic review.
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- 2022
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- Publication type:
- journal article