Pages that link to "Q33641154"

The following pages link to The dark choroid in posterior retinal dystrophies (Q33641154):

Displaying 33 items.

• A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease (Q28141384) (← links)
• Cone Photoreceptor Abnormalities Correlate with Vision Loss in Patients with Stargardt Disease (Q30500872) (← links)
• Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease (Q30742275) (← links)
• Defective lipid transport and biosynthesis in recessive and dominant Stargardt macular degeneration (Q34157723) (← 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)
• Evaluation of phenotypic similarities between Stargardt flavimaculatus and retinal pigment epithelial pattern dystrophies. (Q34165112) (← links)
• A new locus for autosomal dominant stargardt-like disease maps to chromosome 4. (Q34389589) (← links)
• The genetics of inherited macular dystrophies (Q35213761) (← links)
• Inherited multifocal RPE-diseases: mechanisms for local dysfunction in global retinoid cycle gene defects (Q35581414) (← links)
• Treatment of Stargardt disease with dobesilate (Q35979853) (← links)
• Lipofuscin-associated photo-oxidative stress during fundus autofluorescence imaging (Q36290158) (← links)
• Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers (Q36531483) (← links)
• Autosomal dominant cone-rod dystrophy with negative electroretinogram (Q37315772) (← 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)
• Long-term follow-up of Stargardt's disease and fundus flavimaculatus (Q41719920) (← links)
• Stargardt's disease is not allelic to the genes for neuronal ceroid lipofuscinoses (Q42657783) (← links)
• Kjellin's syndrome: fundus autofluorescence, angiographic, and electrophysiologic findings (Q44086798) (← links)
• Autosomal-dominant fundus flavimaculatus. Clinicopathologic correlation (Q46453340) (← links)
• Annular fundus autofluorescence abnormality in a case of macular dystrophy (Q46896383) (← links)
• Optical coherence tomography angiography. (Q52755315) (← links)
• A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1 (Q55670938) (← links)
• Pattern Dystrophy of the Retinal Pigment Epithelium (Q58397659) (← links)
• Histopathology of Incipient Fundus Flavimaculatus (Q67935526) (← links)
• Delayed rod dark adaptation in patients with Stargardt's disease (Q67935531) (← links)
• Fundus flavimaculatus and subretinal neovascularization (Q68040431) (← links)
• Visual acuity loss in patients with Stargardt's macular dystrophy (Q69407310) (← links)
• The dark choroid in posterior retinal dystrophies (Q69454559) (← links)
• Indocyanine Green Angiography in Stargardt's Flavimaculatus (Q71969631) (← links)
• Stargardt's disease/fundus flavimaculatus: psychophysical and electrophysiologic results (Q72566834) (← links)
• Transplantation of human embryonic stem cell-derived retinal pigment epithelial cells (MA09-hRPE) in macular degeneration (Q93088606) (← links)