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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.Journal of Advanced Nursing|August 1, 1996
Breaking the boundaries between nursing and sociology: a critical realist ethnography of the theory-practice gapS Porter, S RyanJournal of Clinical Microbiology|February 1, 1987
Improved method for recovery of peritonitis-causing microorganisms from peritoneal dialysateS Ryan, S FessiaRedox Report : Communications in Free Radical Research|March 24, 2000
Substrate-dependent effect of phenolic antioxidants on Ca2+ accumulation by rat liver mitochondriaS Ryan, V GogvadzeHealthcare (Basel, Switzerland)|November 9, 2024
Young Children Benefit from Intensive, Group-Based Pediatric Constraint-Induced Movement TherapyKatherine S Ryan-BloomerExperimental and Toxicologic Pathology : Official Journal of the Gesellschaft Fur Toxikologische Pathologie|February 1, 1997
The nephrotoxicity of fractionated components of Aipysurus laevis venomS Ryan, J YongOphthalmology|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.Pageof 128