SLCO1B1 haplotypes are not associated with atorvastatin-induced myalgia in Brazilian patients with familial hypercholesterolemia.
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Genetic factors affecting statin concentrations and subsequent myopathy: a HuGENet systematic reviewNon-cardiovascular effects associated with statinsAssociation between SLCO1B1 -521T>C and -388A>G polymorphisms and risk of statin-induced adverse drug reactions: A meta-analysisACTN3 R577X polymorphism and long-term survival in patients with chronic heart failure.The clinical pharmacogenetics implementation consortium guideline for SLCO1B1 and simvastatin-induced myopathy: 2014 update.The MYLIP p.N342S polymorphism is associated with response to lipid-lowering therapy in Brazilian patients with familial hypercholesterolemia.SLCO1B1 polymorphism is not associated with risk of statin-induced myalgia/myopathy in a Czech population.Marked differences in frequencies of statin therapy relevant SLCO1B1 variants and haplotypes between Roma and Hungarian populations.A pharmacogenetic pilot study reveals MTHFR, DRD3, and MDR1 polymorphisms as biomarker candidates for slow atorvastatin metabolizers.MYLIP p.N342S polymorphism is not associated with lipid profile in the Brazilian populationAssociation Between SLCO1B1 Gene T521C Polymorphism and Statin-Related Myopathy Risk: A Meta-Analysis of Case-Control StudiesFrequencies of single-nucleotide polymorphisms and haplotypes of the SLCO1B1 gene in selected populations of the western balkans.Molecular mechanisms of statin intoleranceSLCO1B1 Polymorphisms and Statin-Induced Myopathy.Intolerance to statins: mechanisms and management.Pharmacogenomics of lipid-lowering therapies.Type of LDLR mutation and the pharmacogenetics of familial hypercholesterolemia treatment.Do MDR1 and SLCO1B1 polymorphisms influence the therapeutic response to atorvastatin? A study on a cohort of Egyptian patients with hypercholesterolemia.Statin-associated muscle symptoms and SLCO1B1 rs4149056 genotype in patients with familial hypercholesterolemia.Review of the Reported Measures of Clinical Validity and Clinical Utility as Arguments for the Implementation of Pharmacogenetic Testing: A Case Study of Statin-Induced Muscle Toxicity.Genetic and Clinical Factors Are Associated With Statin-Related Myotoxicity of Moderate Severity: A Case-Control Study.Association between statin-induced creatine kinase elevation and genetic polymorphisms in SLCO1B1, ABCB1 and ABCG2.
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P2860
SLCO1B1 haplotypes are not associated with atorvastatin-induced myalgia in Brazilian patients with familial hypercholesterolemia.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
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2011年学术文章
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2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
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2011年學術文章
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2011年學術文章
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name
SLCO1B1 haplotypes are not ass ...... familial hypercholesterolemia.
@en
SLCO1B1 haplotypes are not ass ...... familial hypercholesterolemia.
@nl
type
label
SLCO1B1 haplotypes are not ass ...... familial hypercholesterolemia.
@en
SLCO1B1 haplotypes are not ass ...... familial hypercholesterolemia.
@nl
prefLabel
SLCO1B1 haplotypes are not ass ...... familial hypercholesterolemia.
@en
SLCO1B1 haplotypes are not ass ...... familial hypercholesterolemia.
@nl
P2093
P2860
P1476
SLCO1B1 haplotypes are not ass ...... familial hypercholesterolemia.
@en
P2093
Alexandre Costa Pereira
Ana Carolina Moron Gagliardi
Ana Paula Chacra
Márcio Hiroshi Miname
Paulo Caleb Junior Lima Santos
Raul Dias Santos
P2860
P2888
P304
P356
10.1007/S00228-011-1125-1
P577
2011-09-18T00:00:00Z