F C Riemslag

Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family.

P T de Jong, L I van den Born, M J van Schooneveld, 1994, Ophthalmic genetics.

The luminance origin of the pattern electroretinogram in man.

H Spekreijse, F C Riemslag, J L Ringo, 1985, The Journal of physiology.

The laplacian analysis of the pattern onset response in man.

H Spekreijse, F C Riemslag, H. Spekreijse, 1992, Electroencephalography and clinical neurophysiology.