Pages that link to "Q36400102"

The following pages link to Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease (Q36400102):

Displaying 26 items.

• Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB) (Q28594570) (← links)
• Adaptive optics retinal imaging--clinical opportunities and challenges (Q33649997) (← links)
• Selective cone photoreceptor injury in acute macular neuroretinopathy (Q33787103) (← links)
• Outer retinal structure after closed-globe blunt ocular trauma. (Q34243600) (← links)
• Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health (Q34531205) (← links)
• Development of an MRI biomarker sensitive to tetrameric visual arrestin 1 and its reduction via light-evoked translocation in vivo (Q35039320) (← links)
• The fundus photo has met its match: optical coherence tomography and adaptive optics ophthalmoscopy are here to stay (Q35998541) (← links)
• Assessment of Different Sampling Methods for Measuring and Representing Macular Cone Density Using Flood-Illuminated Adaptive Optics (Q36024563) (← links)
• Variation in rod and cone density from the fovea to the mid-periphery in healthy human retinas using adaptive optics scanning laser ophthalmoscopy (Q36031304) (← links)
• Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness (Q36289008) (← links)
• Automatic detection of modal spacing (Yellott's ring) in adaptive optics scanning light ophthalmoscope images (Q36948227) (← links)
• Photoreceptor and postreceptor responses in congenital stationary night blindness (Q37012780) (← links)
• Understanding the changes of cone reflectance in adaptive optics flood illumination retinal images over three years. (Q37103211) (← links)
• cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindness (Q37137455) (← links)
• Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome. (Q37384216) (← links)
• The Effect of Retinal Melanin on Optical Coherence Tomography Images (Q37738325) (← links)
• Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer. (Q38880551) (← links)
• Photoreceptor-Based Biomarkers in AOSLO Retinal Imaging (Q41615277) (← links)
• CELLULAR IMAGING OF THE TAPETAL-LIKE REFLEX IN CARRIERS OF RPGR-ASSOCIATED RETINOPATHY. (Q46033100) (← links)
• Adaptive optics imaging of inherited retinal diseases. (Q46250842) (← links)
• Intraobserver Repeatability and Interobserver Reproducibility of Ellipsoid Zone Measurements in Retinitis Pigmentosa. (Q54968856) (← links)
• Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs? (Q60809499) (← links)
• Repeatability of Adaptive Optics Automated Cone Measurements in Subjects With Retinitis Pigmentosa and Novel Metrics for Assessment of Image Quality (Q64063069) (← links)
• Reduced expression of the nob8 gene does not normalize the distribution or function of mGluR6 in the mouse retina (Q89558179) (← links)
• Cellular imaging of inherited retinal diseases using adaptive optics (Q92525966) (← links)
• New variants and in silico analyses in GRK1 associated Oguchi disease (Q103737028) (← links)