Disease: Sosby syndrome
- 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