Related references
Note: Only part of the references are listed.Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy
Stefano Bertolini et al.
ATHEROSCLEROSIS (2013)
Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease
Borge G. Nordestgaard et al.
EUROPEAN HEART JOURNAL (2013)
Homozygous familial hypercholesterolemia: Current perspectives on diagnosis and treatment
Frederick J. Raal et al.
ATHEROSCLEROSIS (2012)
Discriminative Ability of LDL-Cholesterol to Identify Patients With Familial Hypercholesterolemia
Roeland Huijgen et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2012)
Low Prevalence of Mutations in Known Loci for Autosomal Dominant Hypercholesterolemia in a Multiethnic Patient Cohort
Zahid Ahmad et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2012)
Genetic Variation in APOB, PCSK9, and ANGPTL3 in Carriers of Pathogenic Autosomal Dominant Hypercholesterolemic Mutations with Unexpected Low LDL-C Levels
Roeland Huijgen et al.
HUMAN MUTATION (2012)
Familial Hypercholesterolemia in the Danish General Population: Prevalence, Coronary Artery Disease, and Cholesterol-Lowering Medication
Marianne Benn et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
ESC/EAS Guidelines for the management of dyslipidaemias The Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS)
Alberico L. Catapano et al.
ATHEROSCLEROSIS (2011)
Molecular genetic epidemiology of homozygous familial hypercholesterolemia in the Hokuriku district of Japan
Hiroshi Mabuchi et al.
ATHEROSCLEROSIS (2011)
Reduction in Mortality in Subjects With Homozygous Familial Hypercholesterolemia Associated With Advances in Lipid-Lowering Therapy
Frederick J. Raal et al.
CIRCULATION (2011)
Molecular Basis of Autosomal Dominant Hypercholesterolemia Assessment in a Large Cohort of Hypercholesterolemic Children
Anouk van der Graaf et al.
CIRCULATION (2011)
Assessment of Carotid Atherosclerosis in Normocholesterolemic Individuals With Proven Mutations in the Low-Density Lipoprotein Receptor or Apolipoprotein B Genes
Roeland Huijgen et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2011)
Probabilistic cost-effectiveness analysis of cascade screening for familial hypercholesterolaemia using alternative diagnostic and identification strategies
L. Nherera et al.
HEART (2011)
Homozygous familial hypercholesterolemia in Lebanon: A genotype/phenotype correlation
Akl C. Fahed et al.
MOLECULAR GENETICS AND METABOLISM (2011)
Integrating provision of specialist lipid services with cascade testing for familial hypercholesterolaemia
Borunendra N. Datta et al.
CURRENT OPINION IN LIPIDOLOGY (2010)
Functionality of Sequence Variants in the Genes Coding for the Low-Density Lipoprotein Receptor and Apolipoprotein B in Individuals with Inherited Hypercholesterolemia
Roeland Huijgen et al.
HUMAN MUTATION (2010)
Guidelines on the Use of Therapeutic Apheresis in Clinical Practice Evidence-Based Approach from the Apheresis Applications Committee of the American Society for Apheresis
Zbigniew M. Szczepiorkowski et al.
JOURNAL OF CLINICAL APHERESIS (2010)
Longitudinal Evaluation and Assessment of Cardiovascular Disease in Patients With Homozygous Familial Hypercholesterolemia
Daniel M. Kolansky et al.
AMERICAN JOURNAL OF CARDIOLOGY (2008)
Efficacy of statins in familial hypercholesterolaemia: a long term cohort study
Jorie Versmissen et al.
BMJ-BRITISH MEDICAL JOURNAL (2008)
Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9
C Jonathan et al.
NATURE GENETICS (2005)