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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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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)
Heart, Lung, Blood and Sleep Disorders
Last data update: Apr 19, 2024
. (Total: 63627 Documents since 2012)
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Records 1 - 9 (of 9 Records)
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Stroke[original query]>>Guidelines Related[Product Type]
Screening for Lipid Disorders in Children and Adolescents: US Preventive Services Task Force Recommendation Statement.
et al. JAMA 2023 330(3) 253-260
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PCSK9 inhibitors and ezetimibe for the reduction of cardiovascular events: a clinical practice guideline with risk-stratified recommendations.
Hao Qiukui et al. BMJ (Clinical research ed.) 2022 377e069066
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Local Coverage Determination (LCD): CYP2C19, CYP2D6, CYP2C9, and VKORC1 Genetic Testing (L35698)
The U.S. Centers for Medicare & Medicaid Services
Local Coverage Determination (LCD): Biomarkers Overview (L35062)
The U.S. Centers for Medicare & Medicaid Services
Screening for Atrial Fibrillation With Electrocardiography: US Preventive Services Task Force Recommendation Statement.
et al. JAMA 2018 Aug 320(5) 478-484
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Biomarkers of stroke recovery: Consensus-based core recommendations from the Stroke Recovery and Rehabilitation Roundtable.
Boyd Lara A et al. International journal of stroke : official journal of the International Stroke Society 2017 Jul 12(5) 480-493
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Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association.
Mital Seema et al. Circulation. Cardiovascular genetics 2016 Sep
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Recommendations from the international stroke genetics consortium, part 1: standardized phenotypic data collection.
Majersik Jennifer J et al. Stroke 2015 Jan 46(1) 279-84
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Recommendations from the international stroke genetics consortium, part 2: biological sample collection and storage.
Battey Thomas W K et al. Stroke 2015 Jan 46(1) 285-90
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 19, 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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