Identification of usher syndrome subtypes by ERG implicit time

Investigative Ophthalmology and Visual Science

Volumn 42, Issue 12, 2001, Pages 3066-3071

  Seeliger, M W ^a   Zrenner, E ^a   Apfelstedt Sylla, E ^a   Jaissle, G B ^a  

^a UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUDIOGRAPHY; CLINICAL ARTICLE; CONTROLLED STUDY; CRITICAL FLICKER FUSION; DIAGNOSTIC ACCURACY; DIAGNOSTIC TEST; ELECTRORETINOGRAPHY; HUMAN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RECESSIVE INHERITANCE; RETINA DISEASE; RETINITIS PIGMENTOSA; SENSITIVITY AND SPECIFICITY; SIGNAL PROCESSING; USHER SYNDROME;

ADOLESCENT; ADULT; CHILD; ELECTRORETINOGRAPHY; HEARING LOSS, SENSORINEURAL; HUMANS; MIDDLE AGED; RETINA; RETINITIS PIGMENTOSA; RETROSPECTIVE STUDIES; SENSITIVITY AND SPECIFICITY; SYNDROME; TIME FACTORS;

EID: 0034761079     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (34)

1. Usher's syndrome
2. Usher syndrome: Clinical findings and gene localization studies
3. Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q
4. Defective myosin VIIa gene responsible for Usher syndrome type IB
5. Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32
6. A gene for Usher syndrome type I (USH 1A) maps to chromosome 14q
7. Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
8. Localization of two genes for Usher syndrome type I to chromosome 11
9. Evidence for a fourth locus in Usher syndrome type I
10. A newly identified locus for Usher syndrome type I, USH 1E, maps to chromosome 21q21
11. Localization of Usher syndrome type II to chromosome 1q
12. Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa
13. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type ID
14. Myosin VIIa participates in opsin transport through the photoreceptor cilium
15. Comparative study of visual, auditory, and olfactory function in Usher syndrome
16. Clinical diagnosis of the Usher syndromes
17. The electroretinogram in retinitis pigmentosa
18. Electroretinographic findings in retinitis pigmentosa
19. Usher's Syndrome: Electrophysiological tests of the visual and auditory systems
20. Assessing retinal function with the multifocal technique
21. Clinical evaluation of multifocal electroretinogram
22. Multifocal electroretinography in retinitis pigmentosa
23. Assessment of local retinal function in patients with retinitis pigmentosa using the multi-focal ERG technique
24. Investigation of retinitis pigmentosa using the multifocal electroretinogram
25. Implicit time topography of multifocal electroretinograms
26. Photopic temporal processing in retinitis pigmentosa
27. Eine graphische Oberfläche zur Generierung von Datenbankanfragen basierend auf einem objektorientierten Datenmodell
28. Standard for clinical electroretinography
29. Narrow-band filtering for monitoring low-amplitude cone electroretinograms in retinitis pigmentosa
30. The field topography of ERG components in man. I: The photopic luminance response
31. Improved electrode for electroretinography
32. Evaluation of the Myosin VIIA gene and visual function in patients with Usher syndrome type I
33. A surprising property of electrical spread in the network of rods in the turtle's retina
34. Electrical coupling between cones in turtle retina