• A new autosomal dominant eye and lung syndrome linked to mutations in TIMP3 gene
• Acoustic Tumour, ? Ménière's Syndrome: Case for Diagnosis
• Acoustic Tumour, ? Ménière's Syndrome: Case for Diagnosis
• Antivascular endothelial growth factor in hereditary dystrophies
• Birt-Hogg-Dubé syndrome associated with chorioretinopathy and nyctalopia: a case report and review of the literature
• Brachydactyly type B: case report and further evidence for clinical heterogeneity
• Clinical characteristics and current therapies for inherited retinal degenerations
• Colour vision in a family with Sorsby's dystrophy
• Evaluation of the gene encoding the tissue inhibitor of metalloproteinases-3 in various maculopathies
• Hereditary disorders of the retina and choroid
• Intravitreal anti-vascular endothelial growth factor therapy for choroidal neovascularization due to Sorsby macular dystrophy
• Macular neovascularisation in inherited retinal diseases: A review
• Methylation profile of the promoter CpG islands of 31 genes that may contribute to colorectal carcinogenesis
• On "Gronblad-Strandberg" and "Sorsby" syndrome
• PERIPHERAL RETINAL DRUSEN-LIKE DEPOSITS IN GUCY2C CONGENITAL SECRETORY DIARRHEA SYNDROME
• Ranibizumab for the management of Sorsby fundus dystrophy
• Reticular Pseudodrusen in Sorsby Fundus Dystrophy
• Retinal imaging in inherited retinal diseases
• ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome
• Some notes on publications of Professor Arnold Sorsby and on Aland eye disease (Forsius-Eriksson syndrome)
• Sorsby syndrome: a report on further generations of the original family
• Successful photodynamic therapy for subretinal neovascularisation due to Sorsby's fundus dystrophy: 1 year follow up
• The Abiotrophies of the Retina and Choroid: (Section of Ophthalmology)
• Two Familial Groups of the Laurence-Moon-Biedl Syndrome