Search Results - "Peeters, A.V."

MammaPrint risk score distribution in South African breast cancer patients with the pathogenic BRCA2 c.7934delG founder variant: towards application of genomic medicine at the point-of-care by Mampunye, I., Grant, K.A., Peeters, A.V., Torrorey-Sawe, R., French, D.J., Moremi, K.E., Kidd, M., van Eeden, P.C., Pienaar, F.M., van der Merwe, N.C., Kotze, M.J.

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P032 - MammaPrint risk score distribution in South African breast cancer patients with the pathogenic BRCA2 c.7934delG founder variant: towards application of genomic medicine at the point-of-care by Mampunye, I., Grant, K.A., Peeters, A.V., Torrorey-Sawe, R., French, D.J., Moremi, K.E., Kidd, M., van Eeden, P.C., Pienaar, F.M., van der Merwe, N.C., Kotze, M.J.

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1.P.306 Cardiovascular risk in patients with familial hypercholesterolemia by Peeters, A.V., Scholtz, C.L., Kotze, M.J.

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Analysis of low density lipoprotein receptor gene mutations in Belgians with type IIA hyperlipidemia by Peeters, A.V., Kotze, M.J., Van Gaal, L.F.

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Low-density lipoprotein receptor gene mutation analysis and clinical correlation in Belgian hypercholesterolaemics by Van Gaal, L.F., Peeters, A.V., De Block, C.E.M., de Leeuw, I.H., Thiart, R., Kotze, M.J.

“…It is generally believed that patients with familial hypercholesterolaemia (FH) have a higher cardiovascular risk than hypercholesterolaemics without a defect…”
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Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics by Kotze, M J, Peeters, A V, Langenhoven, E, Wauters, J G, Van Gaal, L F

“…DNA screening for apolipoprotein (apo) B mutations causing familial defective apolipoprotein B-100 (FDB) was performed in 87 hyperlipidemic Belgian individuals…”
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