Literature DB >> 12044753

Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.

Hana Langrová1, Daphne Gamer, Christoph Friedburg, Dorothea Besch, Eberhart Zrenner, Eckart Apfelstedt-Sylla.   

Abstract

We investigated abnormalities of the retinal cone ON- and OFF-pathways in 24 males with Schubert-Bornschein congenital stationary night blindness (CSNB). Substantial differences were found between both CSNB types. In incomplete type, a-, b- and d-waves were reduced and delayed, whereas in complete type only the b-wave showed significant changes. Oscillatory potentials (OPs) were not discernible from noise in incomplete CSNB and showed significant peak alterations of the ON-OPs only in complete CSNB. In the complete CSNB type, the ON pathway appeared to be mainly affected. In the incomplete CSNB form marked involvement of both the ON and the OFF pathways was noted.

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Year:  2002        PMID: 12044753     DOI: 10.1016/s0042-6989(02)00068-8

Source DB:  PubMed          Journal:  Vision Res        ISSN: 0042-6989            Impact factor:   1.886


  13 in total

1.  Genotype-phenotype correlation in British families with X linked congenital stationary night blindness.

Authors:  L E Allen; I Zito; K Bradshaw; R J Patel; A C Bird; F Fitzke; J R Yates; D Trump; A J Hardcastle; A T Moore
Journal:  Br J Ophthalmol       Date:  2003-11       Impact factor: 4.638

2.  Asymmetrical growth of the photopic hill during the light adaptation effect.

Authors:  Marie-Lou Garon; Marianne Rufiange; Ruth Hamilton; Daphne L McCulloch; Pierre Lachapelle
Journal:  Doc Ophthalmol       Date:  2010-08-15       Impact factor: 2.379

3.  Negative electroretinograms in the pediatric and adult population.

Authors:  Johnstone M Kim; John F Payne; Jiong Yan; Claire S Barnes
Journal:  Doc Ophthalmol       Date:  2012-01-13       Impact factor: 2.379

4.  LED-generated multifocal ERG on- and off-responses in complete congenital stationary night blindness -- a case report.

Authors:  Dorothee Leifert; Margarita G Todorova; Chrisitan Prünte; Anja M Palmowski-Wolfe
Journal:  Doc Ophthalmol       Date:  2006-02-25       Impact factor: 2.379

5.  X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.

Authors:  R Jalkanen; M Mäntyjärvi; R Tobias; J Isosomppi; E-M Sankila; T Alitalo; N T Bech-Hansen
Journal:  J Med Genet       Date:  2006-02-27       Impact factor: 6.318

6.  CSNB1 in Chinese families associated with novel mutations in NYX.

Authors:  Xueshan Xiao; Xiaoyun Jia; Xiangming Guo; Shiqiang Li; Zhikuan Yang; Qingjiong Zhang
Journal:  J Hum Genet       Date:  2006-05-03       Impact factor: 3.172

7.  A comparison of ERG abnormalities in XLRS and XLCSNB.

Authors:  Keith Bradshaw; Louise Allen; Dorothy Trump; Alison Hardcastle; Nicolas George; Anthony Moore
Journal:  Doc Ophthalmol       Date:  2004-03       Impact factor: 2.379

8.  Photopic ON- and OFF-responses in complete type of congenital stationary night blindness in relation to stimulus intensity.

Authors:  Maja Sustar; Branka Stirn-Kranjc; Marko Hawlina; Jelka Brecelj
Journal:  Doc Ophthalmol       Date:  2007-11-18       Impact factor: 2.379

9.  Estimating ON and OFF contributions to the photopic hill: normative data and clinical applications.

Authors:  M-L Garon; A L Dorfman; J Racine; R K Koenekoop; J M Little; P Lachapelle
Journal:  Doc Ophthalmol       Date:  2014-06-04       Impact factor: 2.379

10.  Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease.

Authors:  Pooja Godara; Robert F Cooper; Panagiotis I Sergouniotis; Melissa A Diederichs; Megan R Streb; Mohamed A Genead; J Jason McAnany; Andrew R Webster; Anthony T Moore; Adam M Dubis; Maureen Neitz; Alfredo Dubra; Edwin M Stone; Gerald A Fishman; Dennis P Han; Michel Michaelides; Joseph Carroll
Journal:  Am J Ophthalmol       Date:  2012-09-07       Impact factor: 5.258

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