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Familial hypercholesterolemia: the lipids or the genes?

author

Georges Nemer

published in: Nutrition and Metabolism

date of publication: 2011-04-22

main subject: hypercholesterolemia, familial hypercholesterolemia

Cites articles 76

Date

Title

Authors

2011-01-05

PCSK9: an emerging target for treatment of hypercholesterolemia

Nigel Mark Hooper
2011-02-17

Commentary: Lipoprotein(a) and atherosclerosis
2010-11-26

Preventing cardiovascular disease: a review of the effectiveness of identifying the people with familial hypercholesterolaemia in New Zealand

Peter George
2010-11-11

Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlation

Georges Nemer
2010-09-01

Defining the challenges of FH screening for familial hypercholesterolemia
2010-06-01

Molecular diagnosis of familial hypercholesterolemia: an important tool for cardiovascular risk stratification
2010-07-07

Statins for children with familial hypercholesterolemia

Stephen E Humphries, Alpo Vuorio, Petri T Kovanen, Jaana Kuoppala, Serena Tonstad, Timo Strandberg, Helena Gylling
2010-08-01

Integrating provision of specialist lipid services with cascade testing for familial hypercholesterolaemia
2010-02-06

Moderate phenotypic expression of familial hypercholesterolemia in Tunisia

Mathilde Varret
2010-02-03

A novel Thr56Met mutation of the autosomal recessive hypercholesterolemia gene associated with hypercholesterolemia

Yoshihiro Kokubo
2010-03-13

Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project

Matthew J. Farrer, Stephen E Humphries
2010-05-01

PCSK9 as a therapeutic target in atherosclerosis
2009-07-03

LXR regulates cholesterol uptake through Idol-dependent ubiquitination of the LDL receptor

Peter Tontonoz
2009-04-01

Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease

Jean-Pierre Rabès, Mathilde Varret, Catherine Boileau, Marianne Abifadel, Claudine Junien, Martine Devillers, Danièle Erlich
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The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier gene

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2008-07-30

PCSK9 and LDL cholesterol: unravelling the target to design the bullet
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2008-01-15

Diagnosis of familial hypercholesterolemia in general practice using clinical diagnostic criteria or genetic testing as part of cascade genetic screening
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Comparison of genetic versus clinical diagnosis in familial hypercholesterolemia

Emilio Ros, Luís Masana, Núria Plana
2008-12-11

Evaluation of high-resolution melting analysis for screening the LDL receptor gene.

Peter George
2008-11-21

PCSK9 as a therapeutic target of dyslipidemia

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2007-09-25

No certain predictors for mutation status in a Danish cohort with familial hypercholesterolemia: a descriptive study

Klaus Brusgaard
2007-09-01

Apolipoprotein polymorphisms and familial hypercholesterolemia
2007-09-22

Child-parent screening for familial hypercholesterolaemia: screening strategy based on a meta-analysis
2006-11-01

Genetic susceptibility to heart disease in Canada: lessons from patients with familial hypercholesterolemia

Robert A. Hegele
2006-12-08

ApoB-100 R3500Q mutation in the Lebanese population: prevalence and historical review of the literature

Ghazi Zaatari, Rami Mahfouz, Zaher K Otrock, Amira S Sabbagh, Rabab N Abdel Khalek
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Molecular genetic testing for familial hypercholesterolemia in the Netherlands: a stepwise screening strategy enhances the mutation detection rate.
2006-03-01

Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia.

Klaus Brusgaard
2005-11-01

Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia

Jean-Pierre Rabès, Mathilde Varret, Michel Krempf, Catherine Boileau, Marianne Abifadel, Delphine Allard, Claudine Junien, Martine Devillers, Mélanie Trillard, Gérald Luc
2005-01-01

Familial hypercholesterolemia and response to statin therapy according to LDLR genetic background
2005-09-23

Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia

Davide Noto, Patrizia Tarugi, Maurizio Averna
2005-08-01

Implementation of cascade testing for the detection of familial hypercholesterolaemia

Article - wd:Q35014525

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