Elisabeth Wittström

发表

Clinical, optical coherence tomography, and fundus autofluorescence findings in patients with intraocular tumors

K. Engelsberg, Danielle Samuelsson, Monika Sznage, 2016, Clinical ophthalmology.

Anterior Segment Abnormalities and Angle-Closure Glaucoma in a Family with a Mutation in the BEST1 Gene and Best Vitelliform Macular Dystrophy

M. Bondeson, V. Ponjavic, Elisabeth Wittström, 2011, Ophthalmic genetics.

Genotype-phenotype Correlations, and Retinal Function and Structure in von Hippel-Lindau Disease

M. Nordling, Elisabeth Wittström, S. Andreasson, 2014, Ophthalmic genetics.

Central Retinal Vein Occlusion in Younger Swedish Adults: Case Reports and Review of the Literature

Elisabeth Wittström, 2017, The open ophthalmology journal.

Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1

S. Ekvall, M. Bondeson, V. Ponjavic, 2011, Ophthalmic genetics.

Electrophysiology, Optical Coherence Tomography and Molecular Genetic Analysis in Patients with Glaucoma and/or Best Vitelliform Macular Dystrophy as Part of Clinical Care

Elisabeth Wittström, 2011 .

Biallelic Mutations in the BEST1 Gene: Additional Families with Autosomal Recessive Bestrophinopathy

S. Berland, D. Austeng, C. Bredrup, 2016, Ophthalmic genetics.

Electrophysiological evaluation and visual outcome in patients with central retinal vein occlusion, primary open‐angle glaucoma and neovascular glaucoma

M. Lövestam-Adrian, J. Larsson, V. Ponjavic, 2010, Acta ophthalmologica.

Improved retinal function after trabeculectomy in glaucoma patients

M. Lövestam-Adrian, V. Ponjavic, Patrik Schatz, 2009, Graefe's Archive for Clinical and Experimental Ophthalmology.

Clinical and Electrophysiologic Outcome in Patients with Neovascular Glaucoma Treated with and without Bevacizumab

H. Holmberg, C. Hvarfner, Elisabeth Wittström, 2012, European journal of ophthalmology.

Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a de novo novel mosaic mutation in the LAMP2 gene

E. Englund, A. Oldfors, Monika Meinert, 2019, Ophthalmic genetics.