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Journal of Clinical Lipidology
|
September 15, 2024
Utilizing innovative implementation strategies for familial hypercholesterolemia: Implementation outcomes from the IMPACT-FH study
Gemme Campbell-Salome, Kelly M Morgan, Jazmine Gabriel, et al.
Circulation. Genomic and Precision Medicine
|
March 27, 2023
Interpreting Incidentally Identified Variants in Genes Associated With Heritable Cardiovascular Disease: A Scientific Statement From the American Heart Association
Andrew P Landstrom, Anwar A Chahal, Michael J Ackerman, et al.
Circulation. Genomic and Precision Medicine
|
October 26, 2018
Healthcare Utilization and Patients' Perspectives After Receiving a Positive Genetic Test for Familial Hypercholesterolemia
Laney K Jones, Alanna Kulchak Rahm, Kandamurugu Manickam, et al.
JACC. Cardiooncology
|
November 8, 2021
Genomic Screening for Pathogenic Transthyretin Variants Finds Evidence of Underdiagnosed Amyloid Cardiomyopathy From Health Records
Brendan J Carry, Katelyn Young, Samuel Fielden, et al.
Journal of the American Heart Association
|
August 25, 2021
Racial Disparities in Modifiable Risk Factors and Statin Usage in Black Patients With Familial Hypercholesterolemia
Anandita Agarwala, Nathan Bekele, Elena Deych, et al.
Journal of Genetic Counseling
|
December 7, 2016
Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study
Kevin Sweet, Shelly Hovick, Amy C Sturm, et al.
Implementation Science Communications
|
March 20, 2021
Evaluation of a multidisciplinary lipid clinic to improve the care of individuals with severe lipid conditions: a RE-AIM framework analysis
Laney K Jones, Megan McMinn, David Kann, et al.
JAMA Cardiology
|
May 26, 2021
Limited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis
Amy C Sturm, Rebecca Truty, Thomas E Callis, et al.
Circulation. Genomic and Precision Medicine
|
July 13, 2018
Managing Secondary Genomic Findings Associated With Arrhythmogenic Right Ventricular Cardiomyopathy: Case Studies and Proposal for Clinical Surveillance
Christopher M Haggerty, Brittney Murray, Crystal Tichnell, et al.
Journal of Personalized Medicine
|
July 2, 2021
Acceptability, Appropriateness, and Feasibility of Automated Screening Approaches and Family Communication Methods for Identification of Familial Hypercholesterolemia: Stakeholder Engagement Results from the IMPACT-FH Study
Laney K Jones, Nicole Walters, Andrew Brangan, et al.
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of 12
Search research articles
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Showing results (51-60 of 114) with videos related to
Sort By:
Page
of 12
Journal of Clinical Lipidology
|
September 15, 2024
Utilizing innovative implementation strategies for familial hypercholesterolemia: Implementation outcomes from the IMPACT-FH study
Gemme Campbell-Salome, Kelly M Morgan, Jazmine Gabriel, et al.
Circulation. Genomic and Precision Medicine
|
March 27, 2023
Interpreting Incidentally Identified Variants in Genes Associated With Heritable Cardiovascular Disease: A Scientific Statement From the American Heart Association
Andrew P Landstrom, Anwar A Chahal, Michael J Ackerman, et al.
Circulation. Genomic and Precision Medicine
|
October 26, 2018
Healthcare Utilization and Patients' Perspectives After Receiving a Positive Genetic Test for Familial Hypercholesterolemia
Laney K Jones, Alanna Kulchak Rahm, Kandamurugu Manickam, et al.
JACC. Cardiooncology
|
November 8, 2021
Genomic Screening for Pathogenic Transthyretin Variants Finds Evidence of Underdiagnosed Amyloid Cardiomyopathy From Health Records
Brendan J Carry, Katelyn Young, Samuel Fielden, et al.
Journal of the American Heart Association
|
August 25, 2021
Racial Disparities in Modifiable Risk Factors and Statin Usage in Black Patients With Familial Hypercholesterolemia
Anandita Agarwala, Nathan Bekele, Elena Deych, et al.
Journal of Genetic Counseling
|
December 7, 2016
Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study
Kevin Sweet, Shelly Hovick, Amy C Sturm, et al.
Implementation Science Communications
|
March 20, 2021
Evaluation of a multidisciplinary lipid clinic to improve the care of individuals with severe lipid conditions: a RE-AIM framework analysis
Laney K Jones, Megan McMinn, David Kann, et al.
JAMA Cardiology
|
May 26, 2021
Limited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis
Amy C Sturm, Rebecca Truty, Thomas E Callis, et al.
Circulation. Genomic and Precision Medicine
|
July 13, 2018
Managing Secondary Genomic Findings Associated With Arrhythmogenic Right Ventricular Cardiomyopathy: Case Studies and Proposal for Clinical Surveillance
Christopher M Haggerty, Brittney Murray, Crystal Tichnell, et al.
Journal of Personalized Medicine
|
July 2, 2021
Acceptability, Appropriateness, and Feasibility of Automated Screening Approaches and Family Communication Methods for Identification of Familial Hypercholesterolemia: Stakeholder Engagement Results from the IMPACT-FH Study
Laney K Jones, Nicole Walters, Andrew Brangan, et al.
Page
of 12