Catharina J.M. Frijns

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

Alison Brashear, William B. Dobyns, Patrícia de Carvalho Aguiar et al. · Brain · 2007 · 277 citations

Medicine, Genetics, Neurology +17

The Origin of P-selectin as a Circulating Plasma Protein

Rob Fijnheer, Catharina J.M. Frijns, J Korteweg et al. · Thrombosis and Haemostasis · 1997 · 253 citations

Medicine, Cell Biology, Hematology +15

Brain areas involved in spatial working memory

Marieke van Asselen, Roy P. C. Kessels, Sebastiaan F.W. Neggers et al. · Neuropsychologia · 2005 · 217 citations · Full text

Social Sciences, Neuroscience, Psychology +14

Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy

Kornelia Neveling, Lilian A. Martinez-Carrera, Irmgard Hölker et al. · The American Journal of Human Genetics · 2013 · 177 citations · Full text

Medicine, Genetics, Molecular Genetics +12

Soluble Adhesion Molecules Reflect Endothelial Cell Activation in Ischemic Stroke and in Carotid Atherosclerosis

Catharina J.M. Frijns, L. Jaap Kappelle, J. van Gijn et al. · Stroke · 1997 · 163 citations

Life Sciences, Cell Biology, Hematology +17