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Journal of Cell Science|December 8, 1998
Inhibition of adhesion and induction of epithelial cell invasion by HAV-containing E-cadherin-specific peptidesV Noë, J Willems, J Vandekerckhove, et al.
Knee Surgery, Sports Traumatology, Arthroscopy : Official Journal of the ESSKA|April 11, 2006
Mid-term results of arthroscopic reconstruction in chronic posterior cruciate ligament instabilityJ M G T Jenner, C P van der Hart, W J Willems
International Journal of Cancer|November 15, 1987
Cellular immunity changes caused by LDH virus: analogy with observations of neuroblastoma-bearing miceG Leclercq, J Willems, H Heremans, et al.
American Journal of Preventive Medicine|December 21, 2013
Seasonal influenza vaccination at school: a randomized controlled trialSharon G Humiston, Stanley J Schaffer, Peter G Szilagyi, et al.
The Journal of Antibiotics|November 1, 1987
CP-54,883 a novel chlorine-containing polyether antibiotic produced by a new species of Actinomadura: taxonomy of the producing culture, fermentation, physico-chemical and biological properties of the antibioticW P Cullen, W D Celmer, L R Chappel, et al.
JAMA|January 27, 2011
Association between stroke center hospitalization for acute ischemic stroke and mortalityYing Xian, Robert G Holloway, Paul S Chan, et al.
Journal of Toxicology. Clinical Toxicology|January 1, 1992
Prolonged toxicity with intermediate syndrome after combined parathion and methyl parathion poisoningJ De Bleecker, J Willems, K Van Den Neucker, et al.
Acta Clinica Belgica|July 3, 2016
DNA Diagnosis of Cystic Fibrosis by Direct Detection of the Af508 MutationJ Hendrickx, J Wauters, P Coucke, et al.
Clinical Chemistry|March 1, 1981
Analysis for 1,25-dihydroxyvitamin D in human plasma, after a liquid-chromatographic purification procedure, with a modified competitive protein-binding assayM J Jongen, W J van der Vijgh, H J Willems, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1E Fransen, V Lemmon, G Van Camp, et al.
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