E Hoogendoorn

Two Patients with Cryptococcal Meningitis and Idiopathic CD4 Lymphopenia: Defective Cytokine Production and Reversal by Recombinant Interferon-  Therapy

M. G. Netea, Annemarie E. Brouwer, E Hoogendoorn et al. · Clinical Infectious Diseases · 2004 · 98 citations

Proliferation and cytogenetic analysis of hairy cell leukemia upon stimulation via the CD40 antigen

Hanneke C. Kluin‐Nelemans, G.C. Beverstock, P. Mollevanger et al. · Blood · 1994 · 67 citations · Full text

Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.

Monique Losekoot, E Hoogendoorn, Renske Olmer et al. · Journal of Medical Genetics · 1997 · 62 citations · Full text

Mental Retardation Syndrome, Fragile X Syndrome, Fmr1 Gene +15

Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities

A T Helderman-van den Enden, P. D. Maaswinkel‐Mooij, E Hoogendoorn et al. · Journal of Medical Genetics · 1999 · 46 citations

Domain Organization and Evolution of the Highly Divergent 5′ Coding Region of Genomes of Arteriviruses, Including the Novel Possum Nidovirus

Anastasia Gulyaeva, Magdalena Dunowska, E Hoogendoorn et al. · Journal of Virology · 2017 · 30 citations · Full text