Ola Sandgren

Ophthalmology

Publications

Author

Title

Year sorteringsordning

Fulltext

Jonsson, Frida
Byström, Berit
Davidson, Alice E.; et al.

Mutations in Collagen, Type XVII, Alpha 1 (COL17A1) Cause Epithelial Recurrent Erosion Dystrophy (ERED)
Human Mutation, 36(4): 463-473

2015

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Jonsson, Frida
Burstedt, Marie S
Sandgren, Ola; et al.

Genetic heterogeneity and clinical outcome in a Swedish family with retinal degeneration caused by mutations in CRB1 and ABCA4 genes
Retinal Degenerative Diseases: 177-183

2014

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Jonsson, Frida
Burstedt, Marie S
Sandgren, Ola; et al.

Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family
European Journal of Human Genetics, 21(11): 1266-1271

2013

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Reinis, Ainars
Golovleva, Irina
Köhn, Linda; et al.

Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation
Acta Ophthalmologica, 91(3): 259-266

2013

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Kawaji, Takahiro
Ando, Yukio
Ando, Eiko; et al.

Transthyretin-related vitreous amyloidosis in different endemic areas.
Amyloid, 17(3-4): 105-108

2010

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Golovleva, Irina
Köhn, Linda
Burstedt, Marie; et al.

Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern sweden.
Advances in Experimental Medicine and Biology, 664: 255-262

2010

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Köhn, Linda
Kohl, Susanne
Bowne, Sara J; et al.

PITPNM3 is an uncommon cause of cone and cone-rod dystrophies.
Ophthalmic Genetics, 31(3): 139-140

2010

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Köhn, Linda
Bowne, Sara J
S Sullivan, Lori; et al.

Breakpoint characterization of a novel approximately 59 kb genomic deletion on 19q13.42 in autosomal-dominant retinitis pigmentosa with incomplete penetrance.
European Journal of Human Genetics, 17(5): 651-655

2009

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Köhn, Linda
Bowne, Sara J
Daiger, Stephen P; et al.

Breakpoint characterization of a novel ~59 kb genomic deletion on 19q13.42 in autosomal dominant retinitis pigmentosa with reduced penetrance
European Journal of Human Genetics, 17(5): 651-655

2009

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Burstedt, Marie S I
Sandgren, Ola
Golovleva, Irina; et al.

Effects of prolonged dark adaptation in patients with retinitis pigmentosa of Bothnia type: an electrophysiological study.
Doc Ophthalmol, 116(3): 193-205

2008

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