Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Marianne, Abifadel"'
Publikováno v:
Nutrition Journal, Vol 21, Iss 1, Pp 1-13 (2022)
Abstract Background Food frequency questionnaires (FFQ) is an easy and inexpensive tool that can be used to evaluate nutrient and dietary trends of groups and individuals. Few studies in the East Mediterranean region tailored FFQs to describe dietary
Externí odkaz:
https://doaj.org/article/1f9c71b5758040289ae004e53498a16e
Autor:
Carine Ayoub, Yara Azar, Dina Maddah, Youmna Ghaleb, Sandy Elbitar, Yara Abou-Khalil, Selim Jambart, Mathilde Varret, Catherine Boileau, Petra El Khoury, Marianne Abifadel
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Familial chylomicronemia syndrome is a rare autosomal recessive disorder of lipoprotein metabolism characterized by the presence of chylomicrons in fasting plasma and an important increase in plasma triglycerides (TG) levels that can exceed 22.58 mmo
Externí odkaz:
https://doaj.org/article/2c5b759b04c84417a55ba4080719ce9f
Autor:
Marie-Hélène Gannagé-Yared, Elie Naous, Anis Al Achkar, Wadih Issa, Ghassan Sleilaty, Vanda Barakett-Hamade, Marianne Abifadel
Publikováno v:
Metabolites, Vol 12, Iss 8, p 690 (2022)
Background: High levels of non-HDL cholesterol (non-HDL-C), triglycerides (TG), lipoprotein (a) (Lp(a)), and Proprotein convertase subtilisin/kexin type 9 (PCSK9) as well as low levels of HDL-C are strongly associated with cardiovascular disease (CVD
Externí odkaz:
https://doaj.org/article/41681ba5a41f496b9a4a1183e21e4b07
Autor:
Yara Azar, Marie-Hélène Gannagé-Yared, Elie Naous, Carine Ayoub, Yara Abou Khalil, Elise Chahine, Sandy Elbitar, Youmna Ghaleb, Catherine Boileau, Mathilde Varret, Petra El Khoury, Marianne Abifadel
Publikováno v:
Metabolites, Vol 12, Iss 6, p 504 (2022)
In adults, elevated levels of circulating Proprotein Convertase Subtilisin/Kexin type 9 (PCSK9) have been associated with increased Low-density lipoprotein cholesterol (LDL-C), triglycerides (TG), and worse cardiovascular outcomes. However, few studi
Externí odkaz:
https://doaj.org/article/863452b8f430462b935cb03d26cf1270
Autor:
Youmna Ghaleb, Sandy Elbitar, Anne Philippi, Petra El Khoury, Yara Azar, Miangaly Andrianirina, Alexia Loste, Yara Abou-Khalil, Gaël Nicolas, Marie Le Borgne, Philippe Moulin, Mathilde Di-Filippo, Sybil Charrière, Michel Farnier, Cécile Yelnick, Valérie Carreau, Jean Ferrières, Jean-Michel Lecerf, Alexa Derksen, Geneviève Bernard, Marie-Soleil Gauthier, Benoit Coulombe, Dieter Lütjohann, Bertrand Fin, Anne Boland, Robert Olaso, Jean-François Deleuze, Jean-Pierre Rabès, Catherine Boileau, Marianne Abifadel, Mathilde Varret
Publikováno v:
Metabolites, Vol 12, Iss 3, p 262 (2022)
Autosomal Dominant Hypercholesterolemia (ADH) is a genetic disorder caused by pathogenic variants in LDLR, APOB, PCSK9 and APOE genes. We sought to identify new candidate genes responsible for the ADH phenotype in patients without pathogenic variants
Externí odkaz:
https://doaj.org/article/f9db9bc7f55448e3aec7fcf601e7ab99
Autor:
Carine Ayoub, Yara Azar, Yara Abou-Khalil, Youmna Ghaleb, Sandy Elbitar, Georges Halaby, Selim Jambart, Marie-Hélène Gannagé-Yared, Cesar Yaghi, Carole Saade Riachy, Ralph El Khoury, Jean-Pierre Rabès, Mathilde Varret, Catherine Boileau, Petra El Khoury, Marianne Abifadel
Publikováno v:
Metabolites, Vol 11, Iss 9, p 564 (2021)
Familial hypobetalipoproteinemia (FHBL) is a codominant genetic disorder characterized by reduced plasma levels of low-density lipoprotein cholesterol and apolipoprotein B. To our knowledge, no study on FHBL in Lebanon and the Middle East region has
Externí odkaz:
https://doaj.org/article/a413722aeb3948ee9c005e48ce5d49b6
Autor:
Marianne ABIFADEL, Catherine Boileau
Publikováno v:
Journal of internal medicineReferences.
Atherosclerotic cardiovascular disease is the leading cause of death globally. Despite its important risk of premature atherosclerosis and cardiovascular disease, familial hypercholesterolemia (FH) is still largely underdiagnosed worldwide. It is one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::162c62c3208205d5154570a8209ac7ad
https://pubmed.ncbi.nlm.nih.gov/36196022
https://pubmed.ncbi.nlm.nih.gov/36196022
Autor:
Feng Ma, Maryam Darabi, Marie Lhomme, Emilie Tubeuf, Aurélie Canicio, Jean Brerault, Narcisse Medadje, Fabiana Rached, Sandrine Lebreton, Eric Frisdal, Fernando Brites, Carlos Serrano, Raul Santos, Emmanuel Gautier, Thierry Huby, Petra El Khoury, Alain Carrié, Marianne Abifadel, Eric Bruckert, Maryse Guerin, Philippe Couvert, Philippe Giral, Philippe Lesnik, Wilfried Le Goff, Isabelle Guillas, Anatol Kontush
Publikováno v:
Atherosclerosis. 372:57
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47997bb659a709cad26f798f3c145a70
https://doi.org/10.1016/j.atherosclerosis.2023.03.018
https://doi.org/10.1016/j.atherosclerosis.2023.03.018
Publikováno v:
JACC: Basic to Translational Science
Corresponding author
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b661471d3e858aa7544376767472568
https://doi.org/10.1016/j.jacbts.2021.10.004
https://doi.org/10.1016/j.jacbts.2021.10.004
Autor:
Olivier Milleron, Marie Paule Jacob, Benoît Ho-Tin-Noé, Marjolijn Renard, Nadine Hanna, Guillaume Jondeau, Laurent Gouya, Marie Sylvie Gross, Sebastien Dupont, Sandy Elbitar, Sébastien Gaertner, Marianne Abifadel, Jeremie Jonquet, Ketty Kessler, Bertrand Isidor, Catherine Boileau, Yves Alembik, Kiyotoshi Sekiguchi, Dianna M. Milewicz, Laurent Tosolini, Mathilde Varret, Mélodie Aubart, Yara Abou Khalil, Youmna Ghaleb, Dongchuan Guo, Jean-Baptiste Michel, Maud Langeois, Louise Benarroch, Ko Tsutsui, Vincenzo Dattilo, Pauline Arnaud, Julie De Backer, Carine Le Goff, Lynn Y. Sakai, Petra El Khoury
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
GENETICS IN MEDICINE
GENETICS IN MEDICINE
Purpose: Thoracic aortic aneurysm and dissection (TAAD) is a life-threatening disease with often unrecognized inherited forms. We sought to identify novel pathogenic variants associated with autosomal dominant inheritance of TAAD. Methods: We analyze
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d04cc9ec2bf0fbf625acf60866281fa2
https://doi.org/10.1038/s41436-020-00947-4
https://doi.org/10.1038/s41436-020-00947-4