Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Farah Korchi"'
Autor:
Wiam Hmimech, Hind Hassani Idrissi, Brehima Diakite, Farah Korchi, Dalila Baghdadi, Hind Tahri Joutey Hassani Idrissi, Meriem Haboub, Rachida Habbal, Sellama Nadifi
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
Abstract Objective Our case–control study aimed to access the potential association of insertion/deletion (I/D) ACE (angiotensin converting enzyme) gene polymorphism with myocardial infarction (MI) risk of occurrence among a sample of Moroccan pati
Externí odkaz:
https://doaj.org/article/a90a35209af243f4afc623c2a55461f1
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Hind Hassani Idrissi, Sellama Nadifi, Brehima Diakite, Wiam Hmimech, Farah Korchi, Rachida Habbal
Publikováno v:
Gene Reports. 11:165-169
Background Association studies around the world have investigated the influence of one Single Nucleotide Polymorphism (SNP) or many SNPs in one gene, which usually resulted in limited and inconclusive information that is difficult to replicate in cas
Autor:
Meriem Haboub, Sellama Nadifi, Brehima Diakite, Wiam Hmimech, Farah Korchi, Dalila Baghdadi, Hind Tahri Joutey Hassani Idrissi, Hind Hassani Idrissi, Rachida Habbal
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
BMC Research Notes
BMC Research Notes
Objective Our case–control study aimed to access the potential association of insertion/deletion (I/D) ACE (angiotensin converting enzyme) gene polymorphism with myocardial infarction (MI) risk of occurrence among a sample of Moroccan patients, esp
Autor:
Sellama Nadifi, Wiam Hmimech, Dalila Baghdadi, Brehima Diakite, Farah Korchi, Hind Hassani Idrissi, Rachida Habbal
Myocardial infarction (MI) is a common complex pathology, localized in the main leading causes of mortality worldwide. It is the result of the interaction of genetic and environmental factors. The aim of the present study was to investigate the poten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30d3e89c3144a999a7ebb5e813cf9384
https://europepmc.org/articles/PMC4998085/
https://europepmc.org/articles/PMC4998085/
G2691A and C2491T mutations of factor V gene and pre-disposition to myocardial infarction in Morocco
Autor:
Wiam Hmimech, Brehima Diakite, Khalil Hamzi, Farah Korchi, Dalila Baghdadi, Hind Hassani Idrissi, Sellama Nadifi, Rachida Habbal
Publikováno v:
Biomedical reports. 5(5)
Coagulation factor Leiden mutation has been described as a common genetic risk factor for venous thrombosis; however, this mutation was reported to be practically absent in an African population. Recently, a novel non-sense mutation in the gene encod
Autor:
Wiam Hmimech, Farah Korchi, H. Hassani Idrissi, Brehima Diakite, S. Nadifi, Dalila Baghdadi, Rachida Habbal
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 9:19-20
Autor:
Brehima Diakite, Farah Korchi, Rachida Habbal, Sellama Nadifi, H. Hassani Idrissi, Dalila Baghdadi, Wiam Hmimech
Publikováno v:
Meta Gene
Background Myocardial infarction (MI) is a common multifactorial disease. Numerous studies have found that genetic plays an essential role in MI occurrence. The main objective of our case–control study is to explore the association of G894T eNOS (r
Autor:
S. Nadifi, H. Hassani Idrissi, Farah Korchi, Brehima Diakite, Khalil Hamzi, Dalila Baghdadi, Wiam Hmimech, Rachida Habbal
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 9:20