H Langrová

Myopia

The epidemics of myopia: Aetiology and prevention

Screening for Myopia and Refractive Errors Using LogMAR Visual Acuity by Optometrists and a Simplified Visual Acuity Chart by Nurses

The molecular basis of human retinal and vitreoretinal diseases

Nature and nurture: the complex genetics of myopia and refractive error

Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

Diabetic Retinopathy

Vascular endothelial growth factor in eye disease

Retinal function in relation to improved glycaemic control in type 1 diabetes

Leber congenital amaurosis: Genes, proteins and disease mechanisms

Myasthenia gravis

Specific removal of autoantibodies by extracorporeal immunoadsorption ameliorates experimental autoimmune myasthenia gravis

Local Multifocal Oscillatory Potential Abnormalities in Diabetes and Early Diabetic Retinopathy

Multifocal Electroretinogram and Short-Wavelength Automated PerimetryMeasures in Diabetic Eyes With Little or No Retinopathy

Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

Clinical Practice Guideline: Sudden Hearing Loss (Update)

Molecular genetics and protein function involved in nocturnal vision

Rheopheresis in treatment of idiopathic sensorineural sudden hearing loss

Mutations inGRM6Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram

Changes of the complement system and rheological indicators after therapy with rheohemapheresis

Rheohaemapheresis in the treatment of nonvascular age-related macular degeneration

Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene

Haemorheopheresis could block the progression of the dry form of age-related macular degeneration with soft drusen to the neovascular form

Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert–Bornschein type

Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.

[How should visual acuity be measured?].

Multifocal oscillatory potentials in type 1 diabetes without retinopathy.

Extracorporeal Immunoglobulin Elimination for the Treatment of Severe Myasthenia Gravis

Long-Term Outcomes of Rheohaemapheresis in the Treatment of Dry Form of Age-Related Macular Degeneration

Dynamics of Blood Count after Rheohemapheresis in Age-Related Macular Degeneration: Possible Association with Clinical Changes