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Journal of the Neurological Sciences|September 1, 1988
Oculomotor defects in patients with Huntington's disease and their offspringH Collewijn, L N Went, E P Tamminga, et al.Hemoglobin|January 1, 1977
Binding of Protoporphyrin to hemoglobin in red blood cells of patients with erythropoietic protoporphyriaJ van Steveninck, T M Dubbelman, A F de Goeij, et al.Annals of Human Genetics|July 1, 1983
Huntington's Chorea in the Netherlands. The problem of genetic heterogeneityL N Went, M Vegter-van der Vlis, G W Bruyn, et al.Seminars in Vascular Medicine|June 17, 2004
Changes of hemostatic variables during hormone replacement therapyAbel Thijs, Coen D A StehouwerSeminars in Vascular Medicine|October 14, 2005
Hormone replacement therapy in postmenopausal women with diabetes mellitusAbel Thijs, Coen D A StehouwerHuman Genetics|September 1, 1988
Further evidence for localization of the gene of erythrokeratodermia variabilisJ G van der Schroeff, I van Leeuwen-Cornelisse, A van Haeringen, et al.Journal of the Neurological Sciences|July 1, 1988
Hereditary cerebral haemorrhage caused by cortical amyloid angiopathyW Luyendijk, G T Bots, M Vegter-van der Vlis, et al.Clinical Chemistry and Laboratory Medicine|December 6, 2003
Homocysteine metabolism in renal diseaseCoen van Guldener, Coen D A StehouwerJournal of the American Society of Nephrology : JASN|July 11, 2006
Microalbuminuria and risk for cardiovascular disease: Analysis of potential mechanismsCoen D A Stehouwer, Yvo M SmuldersAmerican Journal of Human Genetics|March 1, 1992
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsinC J Weitz, Y Miyake, K Shinzato, et al.Pageof 87