Sten Andréasson
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- 2011
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Mark
Electrophysiological evaluation of retinal function in children receiving vigabatrin medication
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- Contribution to journal › Article
- 2010
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Mark
Identification of Retinal Autoantigens in a Young Patient with Osteosarcoma and a Paraneoplastic Retinitis
2010) 39th Annual Meeting of the Scandinavian-Society-for-Immunology/Baltic-Immunological-Society Meeting In Scandinavian Journal of Immunology 71(6). p.479-479(
- Contribution to journal › Published meeting abstract
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Mark
Electrophysiological Assessment of Retinal Function During 6 Months of Bevacizumab Treatment in Neovascular Age-Related Macular Degeneration
(
- Contribution to journal › Article
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Mark
Evaluation of Macular Structure and Function by OCT and Electrophysiology in Patients with Vitelliform Macular Dystrophy Due to Mutations in BEST1
(
- Contribution to journal › Article
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Mark
Transcutaneous Oximetry But Not Arterial Toe Blood Pressure Predicts Macular Thickness In Patients With Chronic Diabetic Foot Ulcers
(
- Contribution to journal › Published meeting abstract
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Mark
Macular disorder in defined genotype in inherent retinal degeneration measured by OCT and mfERG
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- Contribution to journal › Published meeting abstract
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Mark
Treatments for all RP-patients?
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- Contribution to journal › Published meeting abstract
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Mark
RECOVERY OF RETINAL FUNCTION AFTER RECENT-ONSET RHEGMATOGENOUS RETINAL DETACHMENT IN RELATION TO TYPE OF SURGERY.
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- Contribution to journal › Article
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Mark
Multifocal electroretinogram for functional evaluation of retinal injury following ischemia-reperfusion in pigs.
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- Contribution to journal › Article
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Mark
Long-term 12 year follow-up of X-linked congenital retinoschisis.
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- Contribution to journal › Article
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Mark
Improved retinal function after trabeculectomy in glaucoma patients.
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- Contribution to journal › Article
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Mark
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.
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- Contribution to journal › Article
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Mark
Electrophysiological evaluation and visual outcome in patients with central retinal vein occlusion, primary open-angle glaucoma and neovascular glaucoma.
(
- Contribution to journal › Article
- 2009
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Mark
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene
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- Contribution to journal › Article
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Mark
Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
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- Contribution to journal › Article