Search Results - "Hassani Idrissi, Hind"

Impact of I/D polymorphism of angiotensin-converting enzyme (ACE) gene on myocardial infarction susceptibility among young Moroccan patients by Hmimech, Wiam, Idrissi, Hind Hassani, Diakite, Brehima, Korchi, Farah, Baghdadi, Dalila, Tahri Joutey Hassani Idrissi, Hind, Haboub, Meriem, Habbal, Rachida, Nadifi, Sellama

“…Our case-control study aimed to access the potential association of insertion/deletion (I/D) ACE (angiotensin converting enzyme) gene polymorphism with…”
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Does i-T744C P2Y12 Polymorphism Modulate Clopidogrel Response among Moroccan Acute Coronary Syndromes Patients? by Hassani Idrissi, Hind, Hmimech, Wiam, El Khorb, Nada, Akoudad, Hafid, Habbal, Rachida, Nadifi, Sellama

“…Background. An interindividual variability in response to Clopidogrel has been widely described in patients with acute coronary syndromes (ACS). The…”
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Targeted methods for molecular characterization of EGFR mutational profile in lung cancer Moroccan cohort by Kaanane, Houda, El Attar, Hicham, Louahabi, Amal, Berradi, Hind, Idrissi, Hind Hassani, Khyatti, Meriem, Nadifi, Sellama

“…The study of EGFR gene mutational profile in NSCLC patients has a special clinical significance in the selection of patients for tyrosine-kinase inhibitors…”
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The polymorphism G894 T of endothelial nitric oxide synthase (eNOS) gene is associated with susceptibility to essential hypertension (EH) in Morocco by Nassereddine, Sanaa, Hassani Idrissi, Hind, Habbal, Rachida, Abouelfath, Rhizlane, Korch, Farah, Haraka, Majda, Karkar, Adnane, Nadifi, Sellama

“…Hypertension is a multifactorial disease involving both environmental and genetic Factros. G894 T eNOS polymorphism has been suggested to be responsible for…”
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A synergic effect between CYP2C192, CYP2C193 loss-of-function and CYP2C1917 gain-of-function alleles is associated with Clopidogrel resistance among Moroccan Acute Coronary Syndromes patients by Hassani Idrissi, Hind, Hmimech, Wiam, Khorb, Nada El, Akoudad, Hafid, Habbal, Rachida, Nadifi, Sellama

“…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…”
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Synergic predisposing effect of G894T (eNOS), 4G/5G (PAI) and T1131C (APOA5) polymorphisms to myocardial infarction by Hassani Idrissi, Hind, Hmimech, Wiam, Diakite, Brehima, Korchi, Farah, Habbal, Rachida, Nadifi, Sellama

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Association of G894T eNOS, 4G/5G PAI and T1131C APOA5 polymorphisms with susceptibility to myocardial infarction in Morocco by Hassani Idrissi, Hind, Hmimech, Wiam, Diakite, Brehima, Korchi, Farah, Baghdadi, Dalila, Habbal, Rachida, Nadifi, Sellama

“…Myocardial infarction (MI) is a common multifactorial disease. Numerous studies have found that genetic plays an essential role in MI occurrence. The main…”
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Association of CYP2C192/3 gene polymorphism with lung cancer in Moroccan population by Berradi, Hind, Kaanane, Houda, Hassani Idrissi, Hind, Elkadmiri, Nadia, Benchakroun, Nadia, Benider, Abdellatif, Izaabel, El Hassan, Nadifi, Sellama

“…As it is the case for all kinds of cancer; lung cancer is a multifactorial disease. The interaction between both Exposures to different carcinogens and…”
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The polymorphism G894 T of endothelial nitric oxide synthase in Morocco by Nassereddine, Sanaa, Hassani Idrissi, Hind, Habbal, Rachida, Abouelfath, Rhizlane, Korch, Farah, Haraka, Majda, Karkar, Adnane, Nadifi, Sellama

“…Hypertension is a multifactorial disease involving both environmental and genetic Factros. G894 T eNOS polymorphism has been suggested to be responsible for…”
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Association of C677T MTHFR and G20210A FII prothrombin polymorphisms with susceptibility to myocardial infarction by Hmimech, Wiam, Idrissi, Hind Hassani, Diakite, Brehima, Baghdadi, Dalila, Korchi, Farah, Habbal, Rachida, Nadifi, Sellama

“…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…”
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Association of CYP2B6 ( G15631T ) polymorphism with Clopidogrel resistance and genetic predisposition to Acute Coronary Syndromes (ACSs) in Morocco by Hassani Idrissi, Hind, El Khorb, Nada, Akoudad, Abdelhafid, Habbal, Rachida, Nadifi, Sellama

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G2691A and C2491T mutations of factor V gene and pre-disposition to myocardial infarction in Morocco by Hmimech, Wiam, Diakite, Brehima, Idrissi, Hind Hassani, Hamzi, Khalil, Korchi, Farah, Baghdadi, Dalila, Habbal, Rachida, Nadifi, Sellama

“…Coagulation factor Leiden mutation has been described as a common genetic risk factor for venous thrombosis; however, this mutation was reported to be…”
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