Familial hypercholesterolemia. The determination of phenotype - Contents

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Familial hypercholesterolemia. The determination of phenotype

Jansen, A.C.M.

Publication date

2003

Link to publication

Citation for published version (APA):

Jansen, A. C. M. (2003). Familial hypercholesterolemia. The determination of phenotype.

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Contents s

Chapterr 1. General introduction and outline of this thesis 7

Chapterr 2. Phenotypic variability in familial hypercholesterolemia: an update 17

Chapterr 3. The contribution of classical risk factors to cardiovascular disease 31 inn familial hypercholesterolemia. Data in 2400 patients

Chapterr 4. Diagnosing familial hypercholesterolemia. The need for genetic 45 testing.. A study in 2400 FH heterozygotes

Chapterr 5. Data collection from medical records: Guidelines for the 59 physician-scientist t

Chapterr 6. Cardiovascular disease risk and genetic variation. A study in 2000 71 familiall hypercholesterolemia heterozygotes

Chapterr 7. Susceptibility genes for all-cause mortality from familial 85 hypercholesterolemia:: a large parent-offspring study

Chapterr 8. Genetic determinants of plasma HDL-cholesterol in familial 97 hypercholesterolemia.. A study in 1000 FH heterozygotes

Chapterr 9. The risk of hyperhomocysteinemia in patients with familial 113 hypercholesterolemia a

Chapterr 10. PON-1 levels, PON-1 genotype and prevalence of symptomatic 125 cardiovascularr disease in subjects with familial

hypercholesterolemia. .

Chapterr 11. Summary

137 7

Samenvattingg 145 Listt of participating Lipid Clinics 155

Dankwoordd 159 Curriculumm Vitae 177