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Plos One
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December 28, 2020
Barriers, facilitators, and solutions to familial hypercholesterolemia treatment
Laney K Jones, Amy C Sturm, Terry L Seaton, et al.
Advances in Experimental Medicine and Biology
|
June 17, 2024
Molecular Pathways and Animal Models of Arrhythmias
Tyler L Stevens, Sara Coles, Amy C Sturm, et al.
Journal of Clinical Lipidology
|
December 5, 2022
Sex-related differences in premature cardiovascular disease in familial hypercholesterolemia
Anandita Agarwala, Elena Deych, Laney K Jones, et al.
Journal of Personalized Medicine
|
July 27, 2018
Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health
Amy C Sturm, Tara Schmidlen, Laura Scheinfeldt, et al.
Orphanet Journal of Rare Diseases
|
November 15, 2011
Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities
Cameron M Beech, Sandya Liyanarachchi, Nidhi P Shah, et al.
Journal of Personalized Medicine
|
December 23, 2022
Investigating Psychological Impact after Receiving Genetic Risk Results-A Survey of Participants in a Population Genomic Screening Program
Cara Zayac McCormick, Kristen Dilzell Yu, Alicia Johns, et al.
British Journal of Haematology
|
November 28, 2008
Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF
Andrea E Ament, Zhongyuan Li, Amy C Sturm, et al.
JIMD Reports
|
February 23, 2013
Hereditary intrinsic factor deficiency in chaldeans
Amy C Sturm, Elizabeth C Baack, Michael B Armstrong, et al.
Journal of Clinical Lipidology
|
June 9, 2020
Genetic testing in dyslipidemia: A scientific statement from the National Lipid Association
Emily E Brown, Amy C Sturm, Marina Cuchel, et al.
Public Health Genomics
|
April 21, 2025
Reporting Modifications from the IMPACT-FH Study using the FRAME-IS
Christie Gilbert Klaczko, Nicole L Walters, Andrew Brangan, et al.
Page
of 12
Search research articles
Search
Showing results (31-40 of 114) with videos related to
Sort By:
Page
of 12
Plos One
|
December 28, 2020
Barriers, facilitators, and solutions to familial hypercholesterolemia treatment
Laney K Jones, Amy C Sturm, Terry L Seaton, et al.
Advances in Experimental Medicine and Biology
|
June 17, 2024
Molecular Pathways and Animal Models of Arrhythmias
Tyler L Stevens, Sara Coles, Amy C Sturm, et al.
Journal of Clinical Lipidology
|
December 5, 2022
Sex-related differences in premature cardiovascular disease in familial hypercholesterolemia
Anandita Agarwala, Elena Deych, Laney K Jones, et al.
Journal of Personalized Medicine
|
July 27, 2018
Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health
Amy C Sturm, Tara Schmidlen, Laura Scheinfeldt, et al.
Orphanet Journal of Rare Diseases
|
November 15, 2011
Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities
Cameron M Beech, Sandya Liyanarachchi, Nidhi P Shah, et al.
Journal of Personalized Medicine
|
December 23, 2022
Investigating Psychological Impact after Receiving Genetic Risk Results-A Survey of Participants in a Population Genomic Screening Program
Cara Zayac McCormick, Kristen Dilzell Yu, Alicia Johns, et al.
British Journal of Haematology
|
November 28, 2008
Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF
Andrea E Ament, Zhongyuan Li, Amy C Sturm, et al.
JIMD Reports
|
February 23, 2013
Hereditary intrinsic factor deficiency in chaldeans
Amy C Sturm, Elizabeth C Baack, Michael B Armstrong, et al.
Journal of Clinical Lipidology
|
June 9, 2020
Genetic testing in dyslipidemia: A scientific statement from the National Lipid Association
Emily E Brown, Amy C Sturm, Marina Cuchel, et al.
Public Health Genomics
|
April 21, 2025
Reporting Modifications from the IMPACT-FH Study using the FRAME-IS
Christie Gilbert Klaczko, Nicole L Walters, Andrew Brangan, et al.
Page
of 12