Works matching DE "RETINAL degeneration"
Results: 5000
Causes of visual impairment and blindness among Yemenis with diabetes: a hospital-based study.
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- Eastern Mediterranean Health Journal, 2011, v. 17, n. 11, p. 831, doi. 10.26719/2011.17.11.831
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- Article
Causes of blindness in people aged 50 years and over: community-based versus hospital-based study.
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- Eastern Mediterranean Health Journal, 2010, v. 16, n. 9, p. 942, doi. 10.26719/2010.16.9.942
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- Article
Severe Visual Impairment in Older Women.
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- Western Journal of Nursing Research, 2000, v. 22, n. 5, p. 571, doi. 10.1177/01939450022044601
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- Article
Eye on RNA unwinding.
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- Nature Structural & Molecular Biology, 2009, v. 16, n. 1, p. 7, doi. 10.1038/nsmb0109-7
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- Publication type:
- Article
Avacincaptad pegol in geographic atrophy secondary to age-related macular degeneration: a profile of its use.
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- Drugs & Therapy Perspectives, 2024, v. 40, n. 8, p. 293, doi. 10.1007/s40267-024-01097-2
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- Article
Risk factors for diabetic retinopathy in rural India.
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- 2009
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- Publication type:
- Editorial
Seeing the unseen: Charles Bonnet syndrome revisited.
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- Psychogeriatrics, 2015, v. 15, n. 3, p. 204, doi. 10.1111/psyg.12091
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- Publication type:
- Article
AOCT-NET: a convolutional network automated classification of multiclass retinal diseases using spectral-domain optical coherence tomography images.
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- 2020
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- Publication type:
- journal article
A new and effective method for human retina optic disc segmentation with fuzzy clustering method based on active contour model.
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- 2020
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- Publication type:
- journal article
Application of higher-order spectra for automated grading of diabetic maculopathy.
- Published in:
- 2015
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- Publication type:
- journal article
When smoke gets in your eyes.
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- Public Health Reports, 1997, v. 112, n. 2, p. 91
- Publication type:
- Article
Colourful Health Diet.
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- Innovation, 2006, v. 6, n. 2, p. 30
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- Publication type:
- Article
Guanylate cyclases and associated activator proteins in retinal disease.
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- Molecular & Cellular Biochemistry, 2010, v. 334, n. 1/2, p. 157, doi. 10.1007/s11010-009-0331-y
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- Publication type:
- Article
Novel functions of photoreceptor guanylate cyclases revealed by targeted deletion.
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- Molecular & Cellular Biochemistry, 2010, v. 334, n. 1/2, p. 141
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- Publication type:
- Article
Partial rescue of the full-field electroretinogram in patients with RPE65-related retinal dystrophy following gene augmentation therapy with voretigene neparvovec-rzyl.
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- Documenta Ophthalmologica, 2024, v. 149, n. 2, p. 63, doi. 10.1007/s10633-024-09987-6
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- Publication type:
- Article
Rod-sparing in a bardet-biedl syndrome patient with mutations in the ARL6 gene.
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- Documenta Ophthalmologica, 2024, v. 149, n. 2, p. 133, doi. 10.1007/s10633-024-09985-8
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- Publication type:
- Article
Crossed VEP asymmetry in a patient with AHR-linked infantile nystagmus and foveal hypoplasia.
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- 2024
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- Publication type:
- Case Study
An incipient late-onset retinal degeneration with a C1QTNF5 mutation: a case report with an 11-year follow-up.
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- 2024
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- Publication type:
- Case Study
A natural history study of autosomal dominant GUCY2D-associated cone–rod dystrophy.
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- Documenta Ophthalmologica, 2023, v. 147, n. 3, p. 189, doi. 10.1007/s10633-023-09954-7
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- Publication type:
- Article
Bilateral macular hole in a patient with CAPN5-related neovascular inflammatory vitreoretinopathy.
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- 2023
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- Publication type:
- Case Study
An early onset cone dystrophy due to CEP290 mutation: a case report.
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- Documenta Ophthalmologica, 2023, v. 147, n. 3, p. 203, doi. 10.1007/s10633-023-09940-z
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- Publication type:
- Article
A mild form of POC1B-associated retinal dystrophy with relatively preserved cone system function.
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- Documenta Ophthalmologica, 2023, v. 147, n. 1, p. 59, doi. 10.1007/s10633-023-09936-9
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- Publication type:
- Article
Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy.
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- Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 267, doi. 10.1007/s10633-022-09916-5
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- Publication type:
- Article
60th Annual Symposium of the International Society for Clinical Electrophysiology of Vision (ISCEV 2023 Kyoto).
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- Documenta Ophthalmologica, 2023, v. 146, p. 3, doi. 10.1007/s10633-023-09928-9
- Publication type:
- Article
Response to: No strong evidence to date for an association between RIMS1 and retinal dystrophy: Mahrood O, et al.
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- Documenta Ophthalmologica, 2023, v. 146, n. 1, p. 95, doi. 10.1007/s10633-022-09906-7
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- Publication type:
- Article
No strong evidence to date for an association between RIMS1 and retinal dystrophy.
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- Documenta Ophthalmologica, 2023, v. 146, n. 1, p. 93, doi. 10.1007/s10633-022-09905-8
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- Publication type:
- Article
Two cases of unilateral cone–rod dysfunction presenting in adult females.
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- Documenta Ophthalmologica, 2022, v. 145, n. 3, p. 271, doi. 10.1007/s10633-022-09893-9
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- Publication type:
- Article
A clinical and electrophysiological case study of a child with a novel frame shift mutation in the CACNA1F and missense variation of RIMS1 genes.
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- Documenta Ophthalmologica, 2022, v. 145, n. 2, p. 163, doi. 10.1007/s10633-022-09892-w
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- Publication type:
- Article
Electrophysiological evaluation and 18-month follow-up of two regimens with aflibercept for neovascular age-related macular degeneration.
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- Documenta Ophthalmologica, 2022, v. 144, n. 2, p. 99, doi. 10.1007/s10633-021-09863-7
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- Publication type:
- Article
Clinical characterization of autosomal dominant retinitis pigmentosa with NRL mutation in a three-generation Japanese family.
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- Documenta Ophthalmologica, 2022, v. 144, n. 3, p. 227, doi. 10.1007/s10633-022-09874-y
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- Publication type:
- Article
The second Japanese family with Malattia Leventinese/Doyne honeycomb retinal dystrophy.
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- Documenta Ophthalmologica, 2022, v. 144, n. 1, p. 67, doi. 10.1007/s10633-021-09859-3
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- Publication type:
- Article
Long-term follow-up of a patient with JAG1-associated retinopathy.
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- Documenta Ophthalmologica, 2021, v. 143, n. 2, p. 237, doi. 10.1007/s10633-021-09836-w
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- Publication type:
- Article
Evolution of the retinal function by flash-ERG in one child suffering from neuronal ceroid lipofuscinosis CLN2 treated with cerliponase alpha: case report.
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- Documenta Ophthalmologica, 2021, v. 143, n. 1, p. 99, doi. 10.1007/s10633-021-09825-z
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- Publication type:
- Article
A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430A > G in retinoid isomerohydrolase (RPE65) and c.37C > T in bestrophin 1 (BEST1).
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- Documenta Ophthalmologica, 2021, v. 143, n. 1, p. 61, doi. 10.1007/s10633-021-09819-x
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- Publication type:
- Article
Changes in cone-driven functions after intravitreal aflibercept injections in patients with age-related macular degeneration.
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- Documenta Ophthalmologica, 2020, v. 141, n. 2, p. 137, doi. 10.1007/s10633-020-09758-z
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- Publication type:
- Article
Novel biallelic splice-site BBS1 variants in Bardet–Biedle syndrome: a case report of the first Japanese patient.
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- Documenta Ophthalmologica, 2020, v. 141, n. 1, p. 77, doi. 10.1007/s10633-020-09752-5
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- Article
Late presentation of RPE65 retinopathy in three siblings.
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- Documenta Ophthalmologica, 2020, v. 140, n. 3, p. 289, doi. 10.1007/s10633-019-09745-z
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- Article
ISCEV extended protocol for the S-cone ERG.
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- Documenta Ophthalmologica, 2020, v. 140, n. 2, p. 95, doi. 10.1007/s10633-019-09730-6
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- Publication type:
- Article
Late-onset night blindness with peripheral flecks accompanied by progressive trickle-like macular degeneration.
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- Documenta Ophthalmologica, 2019, v. 139, n. 3, p. 171, doi. 10.1007/s10633-019-09705-7
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- Publication type:
- Article
A case of X-linked retinoschisis with atypical fundus appearance.
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- Documenta Ophthalmologica, 2019, v. 139, n. 1, p. 75, doi. 10.1007/s10633-019-09698-3
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- Publication type:
- Article
Retinal dystrophies with bull's-eye maculopathy along with negative ERGs.
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- Documenta Ophthalmologica, 2019, v. 139, n. 1, p. 45, doi. 10.1007/s10633-019-09694-7
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- Publication type:
- Article
ISCEV extended protocol for the stimulus–response series for light-adapted full-field ERG.
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- Documenta Ophthalmologica, 2019, v. 138, n. 3, p. 205, doi. 10.1007/s10633-019-09685-8
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- Publication type:
- Article
Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3).
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- Documenta Ophthalmologica, 2019, v. 138, n. 1, p. 55, doi. 10.1007/s10633-018-9665-7
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- Publication type:
- Article
Macular staphyloma in patients affected by Joubert syndrome with retinal dystrophy: a new finding detected by SD-OCT.
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- Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 25, doi. 10.1007/s10633-018-9646-x
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- Publication type:
- Article
Phenotypic expansion and progression of <italic>SPATA7</italic>-associated retinitis pigmentosa.
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- 2018
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- Publication type:
- Case Study
Response to risk of hydroxychloroquine retinopathy is not related to systemic lupus erythematosus or rheumatoid arthritis.
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- 2018
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- Publication type:
- Letter to the Editor
Retinopathy from hydroxychloroquine is not related to lupus or rheumatoid arthritis.
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- 2018
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- Publication type:
- Letter to the Editor
Perifoveal interdigitation zone loss in hydroxychloroquine toxicity leads to subclinical bull’s eye lesion appearance on near-infrared reflectance imaging.
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- Documenta Ophthalmologica, 2018, v. 136, n. 1, p. 57, doi. 10.1007/s10633-017-9615-9
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- Publication type:
- Article
Detailed electroretinographic findings in rd8 mice.
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- Documenta Ophthalmologica, 2017, v. 134, n. 3, p. 195, doi. 10.1007/s10633-017-9585-y
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- Publication type:
- Article
Progressive retinal degeneration in a girl with Knobloch syndrome who presented with signs of ocular albinism.
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- Documenta Ophthalmologica, 2017, v. 134, n. 2, p. 135, doi. 10.1007/s10633-017-9574-1
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- Publication type:
- Article