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Clinical Ophthalmology (Auckland, N.Z.)|April 15, 2010
Self-reported quality of life in patients with retinitis pigmentosa and maculopathy of Bothnia typeMarie S I Burstedt, Eva Mönestam
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 11, 2010
Central retinal findings in Bothnia dystrophy caused by RLBP1 sequence variationMarie S I Burstedt, Irina Golovleva
Ophthalmology|December 30, 2008
Rod-cone dystrophy with maculopathy in genetic glutathione synthetase deficiency: a morphologic and electrophysiologic studyMarie S I Burstedt, Ellinor Ristoff, Agne Larsson, 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|March 23, 2007
Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish familiesLinda Köhn, Konstantin Kadzhaev, Marie S I Burstedt, et al.
Investigative Ophthalmology & Visual Science|March 18, 2008
Carrier of R14W in carbonic anhydrase IV presents Bothnia dystrophy phenotype caused by two allelic mutations in RLBP1Linda Köhn, Marie S I Burstedt, Frida Jonsson, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
Breakpoint characterization of a novel approximately 59 kb genomic deletion on 19q13.42 in autosomal-dominant retinitis pigmentosa with incomplete penetranceLinda Köhn, Sara J Bowne, Lori S Sullivan, et al.
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