Marie Burstedt

Ophthalmology

Publications

Author

Title

Year sorteringsordning

Fulltext

Golovleva, Irina
Jonsson, Frida
Burstedt, Marie

Heterogeneity and complexity of EYS mutations in autosomal recessive retinitis pigmentosa in northern Sweden
Investigative Ophthalmology and Visual Science, 57(12)

2016

-

Wang, Ling
el Azazi, Mildred
Eklund, Anders; et al.

The response of the neuronal adaptive system to background illumination and readaptation to dark in the immature retina
Acta Ophthalmologica, 93(2): 146-153

2015

-

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

-

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

-

Burstedt, Marie
Jonsson, Frida
Köhn, Linda; et al.

Genotype-phenotype correlations in Bothnia dystrophy caused by RLBP1 gene sequence variations
Acta Ophthalmologica, 91(5): 437-444

2013

-

Burstedt, Marie Si
Mönestam, Eva

Self-reported quality of life in patients with retinitis pigmentosa and maculopathy of Bothnia type.
Clinical ophthalmology (Auckland, N.Z.), 4: 147-154

2010

-

Burstedt, Marie
Golovleva, Irina

Central Retinal Findings in Bothnia Dystrophy Caused by RLBP1 Sequence Variation
Archives of ophthalmology (1960), 128(8): 989-995

2010

-

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

-

Burstedt, Marie S I
Ristoff, Ellinor
Larsson, Agne; et al.

Rod-cone dystrophy with maculopathy in genetic glutathione synthetase deficiency: a morphologic and electrophysiologic study.
Ophthalmology, 116(2): 324-331

2009

-

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

-