Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Wiam Hmimech"'
Autor:
Hind Hassani Idrissi, Wiam Hmimech, Nada El Khorb, Hafid Akoudad, Rachida Habbal, Sellama Nadifi
Publikováno v:
BMC Research Notes, Vol 11, Iss 1, Pp 1-6 (2018)
Abstract Objective The main objective of our study was to investigate the association of CYP2C19*2 and CYP2C19*3 loss-of-function and CYP2C19*17 gain-of-function variants of CYP2C19 gene with Clopidogrel resistance in a sample of Moroccan Acute Coron
Externí odkaz:
https://doaj.org/article/aed1aee0a6e544bfb85dd251ef65a1ba
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
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:
Wiam Hmimech, Hafid Akoudad, Rachida Habbal, Sellama Nadifi, Hind Hassani Idrissi, Nada El Khorb
Publikováno v:
Genetics Research International
Genetics Research International, Vol 2017 (2017)
Genetics Research International, Vol 2017 (2017)
Background. An interindividual variability in response to Clopidogrel has been widely described in patients with acute coronary syndromes (ACS). The contribution of genetics on modulating this response was widely discussed. The objective of our study
Autor:
Sellama Nadifi, Hind Hassani Idrissi, Hafid Akoudad, Nada El Khorb, Rachida Habbal, Wiam Hmimech
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 11, Iss 1, Pp 1-6 (2018)
BMC Research Notes, Vol 11, Iss 1, Pp 1-6 (2018)
Objective The main objective of our study was to investigate the association of CYP2C19*2 and CYP2C19*3 loss-of-function and CYP2C19*17 gain-of-function variants of CYP2C19 gene with Clopidogrel resistance in a sample of Moroccan Acute Coronary Syndr
Autor:
Idrissi, Hind Hassani, Wiam Hmimech, Khorb, Nada, Akoudad, Hafid, Habbal, Rachida, Sellama Nadifi
Additional file 1: Table S1. Demographic data of the 75 ACS patients.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3479da0c31cee1a5e22aecef8b42de
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:
Wiam Hmimech, Idrissi, Hind, Brehima Diakite, Korchi, Farah, Baghdadi, Dalila, Idrissi, Hind Tahri Joutey Hassani, Meriem Haboub, Habbal, Rachida, Sellama Nadifi
Additional file 1: Table S1. Hardy–Weinberg equilibrium (HWE) among cases and control. Table 2. Traditional risk factors vs I/D ACE genotypes distribution among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34101ef966d75cfcb9a5542476f401ed
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/
Publikováno v:
Journal of genetics. 95(2)
Ischaemic stroke is a multifactorial disease. Genetic polymorphisms involved in lipid, inflammatory and thrombotic metabolisms play an important role in the development of ischaemic stroke. The present study aimed to assess the relationship between T