Pages that link to "Q67876698"
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The following pages link to Fundus flavimaculatus. A clinical classification (Q67876698):
Displaying 50 items.
- A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy (Q24324625) (← links)
- Assessment of estimated retinal atrophy progression in Stargardt macular dystrophy using spectral-domain optical coherence tomography (Q27320223) (← links)
- The photoreceptor rim protein is an ABC transporter encoded by the gene for recessive Stargardt's disease (ABCR) (Q28114964) (← links)
- Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease (Q30742275) (← links)
- Evaluation of macular abnormalities in Stargardt's disease using optical coherence tomography and scanning laser ophthalmoscope microperimetry (Q33378564) (← links)
- Electrophysiological findings in Stargardt's-fundus flavimaculatus disease (Q33634255) (← links)
- Refractive errors in patients with fundus flavimaculatus (Q33641811) (← links)
- Infrared scanning laser ophthalmoscope imaging of the macula and its correlation with functional loss and structural changes in patients with stargardt disease (Q33811640) (← links)
- The value of retinal imaging with infrared scanning laser ophthalmoscopy in patients with stargardt disease (Q33902976) (← links)
- Psychophysical measurement of rod and cone thresholds in stargardt disease with full-field stimuli (Q34090794) (← links)
- Photopic ON- and OFF-pathway abnormalities in retinal dystrophies (Q34164016) (← links)
- Stargardt's disease and fundus flavimaculatus: evaluation of morphologic progression and intrafamilial co-existence. (Q34165042) (← links)
- Funduscopically controlled scotometry. (Q34213037) (← links)
- Association of dark-adapted visual function with retinal structural changes in patients with Stargardt disease (Q34274994) (← links)
- A new locus for autosomal dominant stargardt-like disease maps to chromosome 4. (Q34389589) (← links)
- Structural and genetic assessment of the ABCA4-associated optical gap phenotype (Q34496041) (← links)
- Difficulty in performing everyday activities in patients with juvenile macular dystrophies: comparison with patients with retinitis pigmentosa (Q35303358) (← links)
- Multifocal electroretinography in patients with Stargardt's macular dystrophy (Q35303893) (← links)
- Disruption in Bruch membrane in patients with Stargardt disease (Q35532081) (← links)
- Inherited multifocal RPE-diseases: mechanisms for local dysfunction in global retinoid cycle gene defects (Q35581414) (← links)
- A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13. (Q35643142) (← links)
- A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p. (Q35644079) (← links)
- Clinical and molecular characteristics of childhood-onset Stargardt disease. (Q35694440) (← links)
- Clinical phenotypes and prognostic full-field electroretinographic findings in Stargardt disease (Q35826340) (← links)
- Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene. (Q36089243) (← links)
- Optical Coherence Tomography Angiography Findings in Stargardt Disease (Q36267441) (← links)
- Recessive Stargardt disease phenocopying hydroxychloroquine retinopathy (Q36627171) (← links)
- Spectral-domain OCT peripapillary retinal nerve fibre layer thickness measurements in patients with stargardt disease (Q36969143) (← links)
- Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin gene (Q37309913) (← links)
- Test-Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy Trial. (Q37320089) (← links)
- Functional Analysis of Retinal Flecks in Stargardt Disease (Q37440969) (← links)
- Clinical polymorphism of stargardt disease in a large consanguineous tunisian family; implications for nosology (Q37642285) (← links)
- Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations (Q37671070) (← links)
- Generalized choriocapillaris dystrophy, a distinct phenotype in the spectrum of ABCA4-associated retinopathies (Q37734290) (← links)
- Allelic and phenotypic heterogeneity in ABCA4 mutations (Q37867686) (← links)
- Juvenile-onset macular degeneration and allied disorders (Q38204635) (← links)
- Multimodal analysis of the Preferred Retinal Location and the Transition Zone in patients with Stargardt Disease. (Q38736594) (← links)
- ELLIPSOID ZONE MAPPING AND OUTER RETINAL ASSESSMENT IN STARGARDT DISEASE. (Q39371866) (← links)
- Electrophysiology and inherited retinal disorders (Q39829821) (← links)
- Historical evolution in the understanding of Stargardt macular dystrophy (Q39841882) (← links)
- A clinical review of Stargardt's disease and/or fundus flavimaculatus with follow-up (Q39865129) (← links)
- Histopathology and immunocytochemistry of the neurosensory retina in fundus flavimaculatus. (Q40674593) (← links)
- Long-term follow-up of Stargardt's disease and fundus flavimaculatus (Q41719920) (← links)
- A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence in Stargardt Disease (Q42378291) (← links)
- Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1). (Q43762306) (← links)
- The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene (Q45198203) (← links)
- Autosomal-dominant fundus flavimaculatus. Clinicopathologic correlation (Q46453340) (← links)
- Peripheral Visual Fields in ABCA4 Stargardt Disease and Correlation With Disease Extent on Ultra-widefield Fundus Autofluorescence (Q47241696) (← links)
- EDI OCT evaluation of choroidal thickness in Stargardt disease. (Q48302946) (← links)
- Asymmetric fundus flavimaculatus/Stargardt's disease, associated with unilateral myopia (Q49107499) (← links)