Publications by authors named "Khalil Hamzi"

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G2691A and C2491T mutations of factor V gene and pre-disposition to myocardial infarction in Morocco.
Wiam Hmimech, Brehima Diakite, Hind Hassani Idrissi, Khalil Hamzi, Farah Korchi

Biomed Rep· November 2016

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Genetic polymorphisms of T-1131C APOA5 and ALOX5AP SG13S114 with the susceptibility of ischaemic stroke in Morocco.
Brehima Diakite, Khalil Hamzi, Wiam Hmimech, Sellama Nadifi,

J Genet· June 2016

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First study of C2491T FV mutation with ischaemic stroke risk in Morocco.
Brehima Diakite, Khalil Hamzi, Wiam Hmimech, Sellama Nadifi,

J Genet· June 2015

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Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients.
Meryam El Khachibi, Brehima Diakite, Khalil Hamzi, Abdallah Badou, Mohamed Amine Senhaji

BMC Cancer· February 2015

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G894T endothelial nitric oxide synthase polymorphism and ischemic stroke in Morocco.
Brehima Diakite, Khalil Hamzi, Ilham Slassi, Mohammed El Yahyaoui, Moulay M F El Alaoui

Meta Gene· December 2014

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Novel mutations in the amyloid precursor protein gene within Moroccan patients with Alzheimer's disease.
Nadia El Kadmiri, Nabil Zaid, Ahmed Hachem, Younes Zaid, Marie-Pierre Dubé, Khalil Hamzi

J Mol Neurosci· June 2014

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Prenatal diagnosis of BMD in Morocco: evolution and limits.
Khalil Hamzi, Afaf Ben Itto, Mohammed Itri, Sellama Nadifi

J Mol Neurosci· April 2014

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Stem cells in cerebrovascular diseases.
Khalil Hamzi, Brehima Diakite, Sellama Nadifi,

J Mol Neurosci· October 2013

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Sickle cell disease with double stroke in a Moroccan family.
Khalil Hamzi, Afaf Ben Itto, Zineb Jouhadi, Ilham Slassi, Sellama Nadifi

J Mol Neurosci· June 2013

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Evolution of molecular diagnosis of Duchenne muscular dystrophy.
Afaf Ben Itto, Khalil Hamzi, Hanane Bellayou, Mohammed Itri, Ilham Slassi

J Mol Neurosci· June 2013

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Methylenetetrahydrofolate reductase C677T variant in Moroccan patients with inflammatory bowel disease.
Nezha Senhaji, Nadia Serbati, Brehima Diakité, Sofia Arazzakou, Khalil Hamzi

Gene· May 2013

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Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals.
Khalil Hamzi, Bréhima Diakité, Amal Tazzite, Sellama Nadifi

Indian J Hum Genet· April 2013

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Effect of the novel Moroccan BRCA1 and BRCA2 frameshift mutations.
Amal Tazzite, Hassan Jouhadi, Khalil Hamzi, Abdellatif Benider, Sellama Nadifi

Indian J Hum Genet· April 2013

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Duchenne muscular dystrophy: Advances in molecular appraoch.
Afaf Benitto, Khalil Hamzi, Mohammed Itri, Ilham Slassi, Sellama Nadifi

Indian J Hum Genet· January 2013

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Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals.
Khalil Hamzi, Amal Tazzite, Sellama Nadifi

Indian J Hum Genet· September 2011

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Prevalence of angiotensin-converting enzyme, methylenetetrahydrofolate reductase, Factor V Leiden, prothrombin and apolipoprotein E gene polymorphisms in Morocco.
Thierry Paluku They-They, Khalil Hamzi, Mohamed Taha Moutawafik, Hanane Bellayou, Mariame El Messal

Ann Hum Biol· November 2010

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Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?
Khalil Hamzi, Afaf Ben Itto, Sanaa Nassereddine, Sellama Nadifi

Indian J Hum Genet· September 2010

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A rapid polymerase chain reaction-based test for screening Steinert's disease (DM1).
Khalil Hamzi, Hanane Bellayou, Ilham Slassi, Sellama Nadifi

Neurol India· June 2010

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Duchenne and Becker muscular dystrophy: contribution of a molecular and immunohistochemical analysis in diagnosis in Morocco.
Hanane Bellayou, Khalil Hamzi, Mohamed Abdou Rafai, Mehdi Karkouri, Ilham Slassi

J Biomed Biotechnol· July 2009

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