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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: Mar 28, 2024
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Records 1 - 21 (of 21 Records)
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Arteriosclerosis[original query]>>Original Studies[Product Type]
Screening and clinical characteristics analysis of familial hypercholesterolemia in a tertiary public hospital.
Tianzhou Shen et al. Front Cardiovasc Med 2023 101237261
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Maternal Inheritance of Familial Hypercholesterolemia Gene Mutation Predisposes to Coronary Atherosclerosis as Assessed by Calcium Score in Adulthood.
Mourre Florian et al. Arteriosclerosis, thrombosis, and vascular biology 2022
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Situation in 2020 of the requirements for the use of PCSK9 inhibitors in Spain: Results of a national survey.
Guijarro Carlos et al. Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis 2021
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Familial Hypercholesterolemia-Risk-Score: A New Score Predicting Cardiovascular Events and Cardiovascular Mortality in Familial Hypercholesterolemia.
Paquette Martine et al. Arteriosclerosis, thrombosis, and vascular biology 2021 ATVBAHA121316106
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Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland.
Björnsson Eythór et al. Arteriosclerosis, thrombosis, and vascular biology 2021 ATVBAHA120315904
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Implantation of a biochemical and genetic screening programme for family hypercholesterolaemia. Collaboration between the clinical laboratory and lipid units: Design of the ARIAN Project.
Arrobas Velilla Teresa et al. Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis 2021
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Impact of statin therapy on LDL and non-HDL cholesterol levels in subjects with heterozygous familial hypercholesterolaemia.
Climent Elisenda et al. Nutrition, metabolism, and cardiovascular diseases : NMCD 2021
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Massive data screening is a second opportunity to improve the management of patients with familial hypercholesterolemia phenotype.
Zamora Alberto et al. Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis 2021
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Novel PCSK9 (Proprotein Convertase Subtilisin Kexin Type 9) Variants in Patients With Familial Hypercholesterolemia From Cape Town.
Huijgen Roeland et al. Arteriosclerosis, thrombosis, and vascular biology 2020 Nov ATVBAHA120314482
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Genetics and biochemistry of familial hypercholesterolemia in Southwest of the Iberian Peninsula.
Roa Garrido Jessica et al. Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis 2020 Oct
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Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease.
Hindy George et al. Arteriosclerosis, thrombosis, and vascular biology 2020 Sep ATVBAHA120314856
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Cascade Screening for Familial Hypercholesterolemia in South Africa: The Wits FIND-FH Program.
Raal Frederick J et al. Arteriosclerosis, thrombosis, and vascular biology 2020 Sep ATVBAHA120315040
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Lifestyle Moderates Genetic Risk of Venous Thromboembolism: The ARIC Study.
Evans Christina et al. Arteriosclerosis, thrombosis, and vascular biology 2020 Sep ATVBAHA120314668
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Efficacy of Hwangryunhaedok-tang (Huang-lian-jie-du-tang, Oren-gedoku-to) for patients with hyperlipidemia: a study protocol for a randomized, double-blind, placebo-controlled, parallel, investigator-initiated clinical trial.
Lee Boram et al. Trials 2020 Aug 21(1) 750
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Phenotypical, Clinical, and Molecular Aspects of Adults and Children With Homozygous Familial Hypercholesterolemia in Iberoamerica.
Alves Ana Catarina et al. Arteriosclerosis, thrombosis, and vascular biology 2020 Aug ATVBAHA120313722
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Efficacy of therapeutic lifestyle changes on lipid profiles assessed by NMR in children with familial and non-familial hypercholesterolemia.
Rodríguez-Borjabad Cèlia et al. Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis 2020 Jan
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Clinical and genetic differences between heterozygous familial hypercholesterolemia patients with and without type 2 diabetes.
Climent Elisenda et al. Revista espanola de cardiologia (English ed.) 2019 Oct
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Molecular basis of the familial chylomicronemia syndrome in patients from the National Dyslipidemia Registry of the Spanish Atherosclerosis Society.
Ariza María José et al. Journal of clinical lipidology 2018 Aug
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Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically.
Wang Jian et al. Arteriosclerosis, thrombosis, and vascular biology 2016 Dec 36(12) 2439-2445
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How many familial hypercholesterolemia patients are eligible for PCSK9 inhibition?
Masana Luis et al. Atherosclerosis 2017 May 262107-112
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Genomic medicine for improved prediction and primordial prevention of cardiovascular disease.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Mar 28, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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