Search Results - "Farah, Korchi"

Analysis of the influence of glutathione S-transferase (GSTM1 and GSTT1) genes on the risk of essential hypertension by Nassereddine, Sanaa, Habbal, Rachida, Kassogue, Yaya, Kaltoum, Ait Boujmia Oum, Farah, Korchi, Majda, Haraka, Rhizlane, Abou Elfath, Nadifi, Sellama, Dehbi, Hind

“…Essential hypertension (EH) results from a complex interaction between environmental factors and an individual's genetic background. To assess the relationship…”
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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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Association of methylenetetrahydrofolate reductase gene (C677T) with the risk of hypertension in Morocco by Nassereddine, Sanaa, Kassogue, Yaya, Korchi, Farah, Habbal, Rachida, Nadifi, Sellama

“…Hypertension is a multifactorial disease caused by the interaction between genetic and environmental factors. Mutations in the methylenetetrahydrofolate…”
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TCT-712 Immediate and mid-term impact of successful percutaneous transvenous mitral commissurotomy on right ventricular systolic function by El hammiri, Ayoub, Amina, Asadi, Benhaourech, Sanaa, Korchi, Farah, Allouch, Marouane, Azzouzi, Leila, Habbal, Rachida

“…Methods Twelve patients with severe symptomatic mitral stenosis who underwent PTMC were included, all patients were subjected to transthoracic echocardiography…”
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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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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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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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326: Pulmonary embolysm and thrombolysis by Baaddy, Naima, El Honsali, Zineb, Korchi, Farah

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280 Variability affecting autonomic nervous system of the upgrading of the morning blood pressure in Moroccan patients (about 100 cases) by Elhonsali, Zannouba, Korchi, Farah, Alj, Meryem

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0032 : Genetics of hypertension by Korchi, Farah, Asadi, Amina, Benchaouia, Zineb, Habbal, Rachida, Nadifi, S., Nasserreddine, N.

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150 Immediate results of percutaneous mitral commissurotomy (Experience of Center of cardiology-University Hospital Ibn Rochd-Casablanca-Morocco) by Wadrahmane, Fatima, Kongo Minga, Roger, Korchi, Farah

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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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