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Acta Ophthalmologica|April 26, 2008
Ocular manifestations in liver transplant recipients with familial amyloid polyneuropathyOla Sandgren, Daniel Kjellgren, Ole B Suhr
Acta Ophthalmologica|March 13, 2012
Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutationAinars Reinis, Irina Golovleva, Linda Köhn, et al.
Advances in Experimental Medicine and Biology|March 19, 2010
Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern SwedenIrina Golovleva, Linda Köhn, Marie Burstedt, et al.
Vision Research|September 18, 2003
Retinal function in Bothnia dystrophy. An electrophysiological studyMarie S I Burstedt, Ola Sandgren, Irina Golovleva, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 9, 2007
Effects of prolonged dark adaptation in patients with retinitis pigmentosa of Bothnia type: an electrophysiological studyMarie S I Burstedt, Ola Sandgren, Irina Golovleva, et al.
Acta Ophthalmologica Scandinavica|March 23, 2007
Tinted contact lenses in Bothnia dystrophyAsa C Jonsson, Marie S I Burstedt, Irina Golovleva, et al.
European Journal of Human Genetics : EJHG|February 28, 2013
Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish familyFrida Jonsson, Marie S Burstedt, Ola Sandgren, et al.
Advances in Experimental Medicine and Biology|March 26, 2014
Genetic heterogeneity and clinical outcome in a Swedish family with retinal degeneration caused by mutations in CRB1 and ABCA4 genesFrida Jonsson, Marie S Burstedt, Ola Sandgren, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|November 17, 2010
Transthyretin-related vitreous amyloidosis in different endemic areasTakahiro Kawaji, Yukio Ando, Eiko Ando, et al.
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