H. Brink

Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)

Janneke J.C. van Lith-Verhoeven, Saskia D. van der Velde-Visser, Melanie M. Sohocki et al. · Ophthalmic Genetics · 2002 · 31 citations

Life Sciences, Genetics, Ophthalmology +16

Echographic classification of intraocular tumours

A. M. Verbeek, J.M. Thijssen, M.H.M. Cuypers et al. · Acta Ophthalmologica · 1994 · 24 citations

Medicine, Oncology, Pathology +17

The electrooculogram in heterozygote carriers of Usher syndrome, retinitis pigmentosa, neuronal ceroid lipofuscinosis, Senior syndrome and choroideremia

A. Pinckers, A. van Aarem, H. Brink · Ophthalmic Genetics · 1994 · 18 citations

Medicine, Neurology, Ophthalmology +10

Unusual retinal pigment epitheliopathy and choroidopathy in carcinomatosis: A rare case of cancer-associated retinopathy

H. Brink, August F. Deutman, L.V.A.M. Beex · Graefe s Archive for Clinical and Experimental Ophthalmology · 1997 · 18 citations

Medicine, Oncology, Ophthalmology +16

Instantaneous measurement of glomerular filtration rate in the isolated perfused rat kidney

H. Brink, J. F. G. Slegers · Pflügers Archiv - European Journal of Physiology · 1979 · 12 citations

Pharmacy, Nephrology, Physiology +10