Conny Dekker

Clinical and biochemical spectrum of D‐bifunctional protein deficiency

Sacha Ferdinandusse, Simone Denis, P. A. W. Mooyer et al. · Annals of Neurology · 2005 · 195 citations

Life Sciences, Biochemistry, Pediatrics +17

Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the <i>PEX16</i> gene

Merel S. Ebberink, W.K. Chong, S. Denis et al. · Journal of Medical Genetics · 2010 · 94 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

The interaction <i>in vivo</i> of transferrin and asialotransferrin with liver cells

Th.J.C. van Berkel, Conny Dekker, J. Kar Kruijt et al. · Biochemical Journal · 1987 · 55 citations · Full text

Pharmacy, Biochemistry, Cell Biology +16

Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40°C: Implications for other inborn errors of metabolism

Jeannette Gootjes, Frank Schmohl, Petra A.W. Mooijer et al. · Human Mutation · 2004 · 39 citations

Life Sciences, Genetics, Molecular Genetics +17

Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria

K. J. Van Acker, François Eyskens, Marc Espeel et al. · Kidney International · 1996 · 38 citations

Life Sciences, Biochemistry, Endocrinology +10