Pages that link to "Q69625653"
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The following pages link to Standard for clinical electroretinography. International Standardization Committee (Q69625653):
Displaying 50 items.
- The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness (Q24312225) (← links)
- Mutations in NYX of individuals with high myopia, but without night blindness (Q24653288) (← links)
- Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin (Q24676020) (← links)
- Clinical features of a Japanese family with autosomal dominant retinitis pigmentosa associated with a Thr494Met mutation in the HPRP3 gene (Q28256664) (← links)
- Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy (Q28268707) (← links)
- X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60 (Q28291575) (← links)
- Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy). (Q30827994) (← links)
- Episodic acute hypotonia after Nd:YAG laser capsulotomy—retinal function and choroidal swelling (Q32162638) (← links)
- Electrophysiological findings in Stargardt's-fundus flavimaculatus disease (Q33634255) (← links)
- Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness (Q33676559) (← links)
- The electroretinogram in diabetic retinopathy (Q33722276) (← links)
- Clinical applications of photopic negative response (PhNR) for the treatment of glaucoma and diabetic retinopathy (Q33774806) (← links)
- Photopic ON- and OFF-pathway abnormalities in retinal dystrophies (Q34164016) (← links)
- Retrospective study of hyperabnormal (supranormal) electroretinographic responses in 104 patients (Q34164076) (← links)
- Abnormal electroretinogram associated with developmental brain anomalies (Q34211157) (← links)
- Sorsby's fundus dystrophy in a family with a Ser-181-CVS mutation in the TIMP-3 gene: poor outcome after laser photocoagulation. (Q34211400) (← links)
- Pattern electroretinography (PERG) and an integrated approach to visual pathway diagnosis (Q34272310) (← links)
- Linkage analysis of two families with X-linked recessive congenital motor nystagmus (Q34461621) (← links)
- Severe course of cutaneous melanoma associated paraneoplastic retinopathy (Q34719757) (← links)
- Empirical mode decomposition and neural network for the classification of electroretinographic data (Q35187000) (← links)
- Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness (Q35299420) (← links)
- Helicoidal peripapillary chorioretinal degeneration: electrophysiology and psychophysics in 17 patients. (Q35304239) (← links)
- Electrophysiological evaluation of visual loss in Müller cell sheen dystrophy (Q35305428) (← links)
- Lens epithelial changes and mutated gene expression in patients with myotonic dystrophy (Q35309394) (← links)
- A controlled study comparing visual function in patients treated with vigabatrin and tiagabine (Q35472173) (← links)
- Visual field defects in pediatric patients on vigabatrin monotherapy (Q35602594) (← links)
- New COL6A6 variant detected by whole-exome sequencing is linked to break points in intron 4 and 3'-UTR, deleting exon 5 of RHO, and causing adRP. (Q35962525) (← links)
- Visual and brain function measurements in studies of n-3 fatty acid requirements of infants (Q35986342) (← links)
- Comparing DTL microfiber and Neuroline skin electrode in the Mini Ganzfeld ERG. (Q36095294) (← links)
- The care and fitting of Naka-Rushton functions to electroretinographic intensity-response data (Q36675966) (← links)
- In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier (Q37110827) (← links)
- Cone dystrophies with negative photopic electroretinogram (Q37302028) (← links)
- Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsin. (Q37302751) (← links)
- Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosa (Q37309065) (← links)
- A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family. (Q37343523) (← links)
- AIPL1 implicated in the pathogenesis of two cases of autosomal recessive retinal degeneration (Q37465006) (← links)
- A novel mutation (967-970+2)delAAAGGT in the choroideremia gene found in a Japanese family and related clinical findings (Q38287737) (← links)
- Longitudinal study of the early electroretinographic changes in Alström's syndrome. (Q38532977) (← links)
- Electroretinogram measures in a septuagenarian population. (Q39300304) (← links)
- Effect of shorter dark adaptation on ISCEV standard DA 0.01 and DA 3 skin ERGs in healthy adults (Q39618648) (← links)
- Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype. (Q39704029) (← links)
- Infantile presentation of X linked retinoschisis (Q39710597) (← links)
- Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway (Q40336962) (← links)
- Multi-centre variability of ISCEV standard ERGs in two normal adults. (Q41346515) (← links)
- Dystrophin in the retina (Q41676990) (← links)
- Effect of DA-8159, a selective phosphodiesterase type 5 inhibitor, on electroretinogram and retinal histology in rabbits (Q42138525) (← links)
- The evolving role of visual electrodiagnostics (Q42346342) (← links)
- The b-wave of the dark adapted flash electroretinogram in patients with advanced asymmetrical glaucoma and normal subjects (Q43092358) (← links)
- Absence of ocular interaction in flicker ERG responses reflecting cone opponent and luminance signals. (Q43112470) (← links)
- Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1. (Q43168499) (← links)