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Akl C Fahed

Showing results (31-40 of 92) with videos related to

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Cell Metabolism|July 3, 2024
Association of genetic risk, lifestyle, and their interaction with obesity and obesity-related morbiditiesMin Seo Kim, Injeong Shim, Akl C Fahed, et al.
Journal of Dermatological Science|December 6, 2018
Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axisHadla Hariri, Mazen Kurban, Christiane Al-Haddad, et al.
Molecular Genetics and Metabolism|December 15, 2010
Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlationAkl C Fahed, Raya M Safa, Fadi F Haddad, et al.
Molecular Genetics & Genomic Medicine|April 12, 2016
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patientKameel Kassab, Hadla Hariri, Lara Gharibeh, et al.
Cardiovascular Revascularization Medicine : Including Molecular Interventions|April 23, 2026
Safe implementation of an expedited radial hemostatic compression device removal protocol in the cardiac catheterization labRoukoz Abou-Karam, Marc P Allard-Ratick, Caitlin M Hughes, et al.
European Journal of Preventive Cardiology|April 3, 2023
Genetic and clinical factors underlying a self-reported family history of heart diseaseAmanda R Jowell, Romit Bhattacharya, Christopher Marnell, et al.
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life CourseSarah M Urbut, So Mi Jemma Cho, Kaavya Paruchuri, et al.
Cardiac Electrophysiology Clinics|February 28, 2016
The Muscle-Bound HeartMarwan M Refaat, Akl C Fahed, Sylvana Hassanieh, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomyAkl C Fahed, Ruby Khalaf, Rony Salloum, et al.
Circulation. Genomic and Precision Medicine|January 24, 2025
Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life CourseSarah M Urbut, So Mi Jemma Cho, Kaavya Paruchuri, et al.
Pageof 10

Showing results (31-40 of 92) with videos related to

Sort By:
Pageof 10
Cell Metabolism|July 3, 2024
Association of genetic risk, lifestyle, and their interaction with obesity and obesity-related morbiditiesMin Seo Kim, Injeong Shim, Akl C Fahed, et al.
Journal of Dermatological Science|December 6, 2018
Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axisHadla Hariri, Mazen Kurban, Christiane Al-Haddad, et al.
Molecular Genetics and Metabolism|December 15, 2010
Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlationAkl C Fahed, Raya M Safa, Fadi F Haddad, et al.
Molecular Genetics & Genomic Medicine|April 12, 2016
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patientKameel Kassab, Hadla Hariri, Lara Gharibeh, et al.
Cardiovascular Revascularization Medicine : Including Molecular Interventions|April 23, 2026
Safe implementation of an expedited radial hemostatic compression device removal protocol in the cardiac catheterization labRoukoz Abou-Karam, Marc P Allard-Ratick, Caitlin M Hughes, et al.
European Journal of Preventive Cardiology|April 3, 2023
Genetic and clinical factors underlying a self-reported family history of heart diseaseAmanda R Jowell, Romit Bhattacharya, Christopher Marnell, et al.
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life CourseSarah M Urbut, So Mi Jemma Cho, Kaavya Paruchuri, et al.
Cardiac Electrophysiology Clinics|February 28, 2016
The Muscle-Bound HeartMarwan M Refaat, Akl C Fahed, Sylvana Hassanieh, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomyAkl C Fahed, Ruby Khalaf, Rony Salloum, et al.
Circulation. Genomic and Precision Medicine|January 24, 2025
Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life CourseSarah M Urbut, So Mi Jemma Cho, Kaavya Paruchuri, et al.
Pageof 10