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The British Journal of Ophthalmology|September 1, 1995
Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19qK Evans, M al-Maghtheh, F W Fitzke, et al.
Eye (London, England)|February 9, 2010
A preliminary trial to determine whether prevention of dark adaptation affects the course of early diabetic retinopathyG B Arden, M K Gündüz, A Kurtenbach, et al.
Ophthalmology|February 28, 1998
Incidence of idiopathic full-thickness macular holes in fellow eyes. A 5-year prospective natural history studyE Ezra, J A Wells, R H Gray, et al.
The British Journal of Ophthalmology|August 1, 1993
Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic studyA T Moore, F Fitzke, M Jay, et al.
The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.
The British Journal of Ophthalmology|May 1, 1985
A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosaA L Lyness, W Ernst, M P Quinlan, et al.
The British Journal of Ophthalmology|May 1, 1994
Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding siteS L Owens, F W Fitzke, C F Inglehearn, et al.
Ophthalmology|January 1, 1994
Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow geneJ J Wroblewski, J A Wells, A Eckstein, et al.
The British Journal of Ophthalmology|July 1, 1983
Rod and cone activity in patients with dominantly inherited retinitis pigmentosa: comparisons between psychophysical and electroretinographic measurementsG B Arden, R M Carter, C R Hogg, et al.
The British Journal of Ophthalmology|July 1, 1983
A modified ERG technique and the results obtained in X-linked retinitis pigmentosaG B Arden, R M Carter, C R Hogg, et al.
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