Mieke M. C. Bijveld

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

Maria M. van Genderen, Mieke M. C. Bijveld, Y. Claassen et al. · The American Journal of Human Genetics · 2009 · 237 citations · Full text

Developmental Biology, Ophthalmology, Genetic Disorder +3

Genotype and Phenotype of 101 Dutch Patients with Congenital Stationary Night Blindness

Mieke M. C. Bijveld, Ralph J. Florijn, Arthur A. Bergen et al. · Ophthalmology · 2013 · 147 citations

Sleep, Ocular Disease, Ophthalmology +4

Assessment of Night Vision Problems in Patients with Congenital Stationary Night Blindness

Mieke M. C. Bijveld, Maria M. van Genderen, Frank P. Hoeben et al. · PLoS ONE · 2013 · 47 citations · Full text

Night Vision Problems, Ophthalmology, Physiological Optic +13

An extended 15 Hz ERG protocol (1): the contributions of primary and secondary rod pathways and the cone pathway

Mieke M. C. Bijveld, Astrid M. L. Kappers, Frans C. C. Riemslag et al. · Documenta Ophthalmologica · 2011 · 10 citations

Signal Transduction, Neurophysiology, Extended 15 +8