Erratum: Is optic never fibre mis-routing a feature of congenital stationary night blindness? (In Documenta Ophthalmologica (2005) vol. 111 (169-178) 10.1007/s10633-005-5503-9);Is optic nerve fibre mis-routing a feature of congenital stationary night blindness?

Documenta Ophthalmologica

Volumn 111, Issue 3, 2005, Pages 169-178

  Ung, T ^a   Allen, L E ^a   Moore, A T ^a,b   Trump, D ^a,c   Yates, J ^a   Bradshaw, Keith ^a  

^a ADDENBROOKE S HOSPITAL   (United Kingdom)

^b MOORFIELDS EYE HOSPITAL   (United Kingdom)

^c UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

Albinism; CSNB; Pattern Onset VEP

Indexed keywords

ADOLESCENT; ADULT; AGED; AMPLITUDE MODULATION; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL PROTOCOL; CONTROLLED STUDY; ELECTRORETINOGRAPHY; EVOKED VISUAL RESPONSE; GENE IDENTIFICATION; GENE MUTATION; HUMAN; LATENT PERIOD; MUTATIONAL ANALYSIS; NERVE MALFORMATION; NIGHT BLINDNESS; OCULAR ALBINISM; OPTIC NERVE FIBER; PEDIGREE; PHENOTYPE; SIGNAL DETECTION; STATISTICAL SIGNIFICANCE; VISUAL STIMULATION; X CHROMOSOME LINKED DISORDER;

EID: 33644802584     PISSN: 00124486     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10633-006-9014-0     Document Type: Erratum

References (22)

1. F Tremblay I Becker De C Cheung 1996 Visual evoked potentials with crossed asymmetry in incomplete congenital stationary night blindness Invest Ophthalmol Vis Sci 37 1783-92 1:STN:280:BymA3srgvVc%3D 8759345
2. D Creel H Spekreijse D Reits 1981 Evoked potentials in albinos: Efficacy of pattern stimuli in detecting misrouted optic fibers Electroencephalogr Clin Neurophysiol 52 595-603 1:STN:280:Bi2D1MvpsVY%3D 6172258
3. P Apkarian D Reits H Spekreijse 1983 A decisive electrophysiological test for human albinism Electroencephalogr Clin Neurophysiol 55 513-31 1:STN:280:BiyC2MjjtF0%3D 6187545
4. Mason C, Erskine L. The development of retinal decussation. In: Chalupa LM, Werner JS eds. The Visual Neurosciences. 2004: 94-108.
5. RW Guillery 1971 An abnormal retinogeniculate projection in the albino ferret (Mustela furo) Brain Res 33 482-5 10.1016/0006-8993(71)90121-1 1:STN:280:CS2D1cvpsVA%3D 5134931
6. K Huang RW Guillery 1985 A demonstration of two distinct geniculocortical projection patterns in albino ferrets Brain Res 352 213-20 1:STN:280:BiqB1c7ltVM%3D 4027667
7. RW Guillery G Jeffery N Saunders 1999 Visual abnormalities in albino wallabies: A brief note J Comp Neurol 403 33-8 10.1002/ (SICI)1096-9861(19990105)403:1<33::AID-CNE3>3.0.CO;2-W 1:STN:280:DyaK1M7ntlOlsQ%3D%3D 10075441
8. RW Guillery AN Okoro CJ Witkop Jr. 1975 Abnormal visual pathways in the brain of a human albino Brain Res 96 373-7 10.1016/0006-8993(75)90750-7 1:STN:280:CSmD38%2FivFA%3D 1175020
9. P Apkarian J Shallo-Hoffmann 1991 VEP projections in congenital nystagmus; VEP asymmetry in albinism: A comparison study Invest Ophthalmol Vis Sci 32 2653-61 1:STN:280:By6A3s7otFU%3D 1651299
10. J Shallo-Hoffmann P Apkarian 1993 Visual evoked response asymmetry only in the albino member of a family with congenital nystagmus Invest Ophthalmol Vis Sci 34 682-9 1:STN:280:ByyC1MvltFI%3D 8449686
11. P Apkarian D Reits H Spekreijse 1984 Component specificity in albino VEP asymmetry: Maturation of the visual pathway anomaly Exp Brain Res 53 285-94 10.1007/BF00238157 1:STN:280:BiuC2Mfot1w%3D 6705864
12. I Zito LE Allen RJ Patel 2003 Mutations in the CACNA1F and NYX genes in British CSNBX families Hum Mutat 21 16910.1002/humu.9106 12552565
13. LE Allen I Zito K Bradshaw 2003 Genotype-phenotype correlation in British families with X linked congenital stationary night blindness Br J Ophthalmol 87 1413-20 10.1136/bjo.87.11.1413 1:STN:280:DC%2BD3srjtF2qtA%3D%3D 14609846
14. K Bradshaw L Allen D Trump 2004 A comparison of ERG abnormalities in XLRS and XLCSNB Doc Ophthalmol 108 135-45 10.1023/ B:DOOP.0000036786.22179.44 15455796
15. TM Strom G Nyakatura E Apfelstedt-Sylla 1998 An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness Nat Genet 19 160-3
16. NT Bech-Hansen MU Naylor TA Matbaum 2000 Mutations in NYX, encoding the leucine-rich proteogycan nyctalopin, cause X-linked complete congenital stationary night blindness Nat Genet 26 319-23 10.1038/81619 1:CAS:528:DC%2BD3cXotVWhsb8%3D 11062471
17. CM Pusch C Zeitz O Brandou 2000 The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein Nat Genet 26 324-7 1:CAS:528:DC%2BD3cXotVWhsbw%3D 11062472
18. SE Dorey MM Neveu LC Burton 2003 The clinical features of albinism and their correlation with visual evoked potentials Br J Ophthalmol 87 767-72 10.1136/bjo.87.6.767 1:STN:280:DC%2BD3s3ks12ksw%3D%3D 12770978
19. F Soong AV Levin CA Westall 2000 Comparison of techniques for detecting visually evoked potential asymmetry in albinism J Aapos 4 302-10 1:STN:280:DC%2BD3M%2Fkt1equw%3D%3D 11040481
20. JW Pott NM Jansonius AC Kooijman 2003 Chiasmal coefficient of flash and pattern visual evoked potentials for detection of chiasmal misrouting in albinism Doc Ophthalmol 106 137-43 10.1023/A:1022526409674 1:STN:280:DC%2BD3s7mtFSnug%3D%3D 12678278
21. A Kriss I Russell-Eggitt D Taylor 1990 Childhood albinism. Visual electrophysiological features Ophthalmic Paediatr Genet 11 185-92 1:STN:280:By6C38rotlI%3D 2280976
22. P Apkarian 1992 A practical approach to albino diagnosis. VEP misrouting across the age span Ophthalmic Paediatr Genet 13 77-88 1:STN:280:By2A2MjktF0%3D 1495770