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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Rare Diseases
Last data update: May 03, 2024
. (Total: 63770 Documents since 2012)
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Prevalence of elevated lipoprotein(a) in cardiac rehabilitation patients - results from a large-scale multicentre registry in Germany.
Christoph Altmann et al. Clin Res Cardiol 2024
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Contemporary Homozygous Familial Hypercholesterolemia in the United States: Insights From the CASCADE FH Registry.
Marina Cuchel et al. J Am Heart Assoc 2023 e029175
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Lipoprotein(a) in atherosclerotic cardiovascular disease and aortic stenosis: a European Atherosclerosis Society consensus statement.
Kronenberg Florian et al. European heart journal 2022
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Lipoprotein(a) and its Significance in Cardiovascular Disease: A Review.
Duarte Lau Freddy et al. JAMA cardiology 2022
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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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Lipoprotein(a), LDL-cholesterol, and hypertension: predictors of the need for aortic valve replacement in familial hypercholesterolaemia.
Pérez de Isla Leopoldo et al. European heart journal 2021 Jan
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Autosomal recessive hypercholesterolemia: update for 2020.
D'Erasmo Laura et al. Current opinion in lipidology 2020 Jan
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Elevated Lipoprotein(a) and Risk of Ischemic Stroke.
Langsted Anne, et al. Journal of the American College of Cardiology 2019 7 0. (1) 54-66
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Genetic Variation in LPA, Calcific Aortic Valve Stenosis in Patients Undergoing Cardiac Surgery, and Familial Risk of Aortic Valve Microcalcification.
Perrot Nicolas et al. JAMA cardiology 2019 May
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Clinical and molecular characteristics of homozygous familial hypercholesterolemia patients: Insights from SAFEHEART registry.
Alonso Rodrigo et al. Journal of clinical lipidology 10(4) 953-61
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 03, 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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