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(1 - 24 of 34)

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Association of bronchial steroid inducible methylation quantitative trait loci with asthma and chronic obstructive pulmonary disease treatment response
Associations of polymorphisms in the peroxisome proliferator-activated receptor gamma coactivator-1 alpha gene with subsequent coronary heart disease
Pharmacogenomic testing in paediatrics
Imatinib in patients with severe COVID-19
Imatinib in patients with severe COVID-19
Treatment eligibility of real-life mepolizumab-treated severe asthma patients
Characteristics and treatment regimens across ERS SHARP severe asthma registries
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events A GENIUS-CHD Study of Individual Participant Data
Subsequent Event Risk in Individuals With Established Coronary Heart Disease Design and Rationale of the GENIUS-CHD Consortium
Effects of age and genetic variations in VKORC1, CYP2C9 and CYP3A4 on the phenprocoumon dose in pediatric patients
The pediatric acenocoumarol dosing algorithm: the Children Anticoagulation and Pharmacogenetics Study
Characteristics and quality of oral anticoagulation treatment in pediatric patients in the Netherlands based on the CAPS cohort
Age-stratified outcome of a genotype-guided dosing algorithm for acenocoumarol and phenprocoumon
Dosing algorithms for vitamin K antagonists across VKORC1 and CYP2C9 genotypes
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
Comparison of dosing algorithms for acenocoumarol and phenprocoumon using clinical factors with the standard care in the Netherlands
HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data
A Randomized Trial of Genotype-Guided Dosing of Acenocoumarol and Phenprocoumon
Secretory Phospholipase A(2)-IIA and Cardiovascular Disease
Evaluation of the Effect of SNPs in CYP3A4 and CYP4F2 on the Stable Phenprocoumon and Acenocoumarol Maintenance Dose
Added value of pharmacogenetic testing in predicting statin response: results from the REGRESS trial
Evaluation of the effects of single-nucleotide polymorphisms in CYP3A4 and CYP4F2 on stable phenprocoumon and acenocoumarol maintenance doses

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