Publications by authors named "Brahim Nsiri"

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Neuro-meningeal cryptococcal infection revealing a multiple myeloma.
Sameh Sayhi, Sawsen Bouzidi, Imen Beji, Aman Allah Nasr, Souha Hannachi, Brahim Nsiri

Pan Afr Med J· January 2021

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[Disseminated intravascular coagulation: role of the International Society on Thrombosis and Haemostasis (ISTH) diagnostic scoring system].
Sawsen Bouzidi, Mayssa Daiki, Amen Allah Nasr, Kaouther Nsiri, Samy Layouni, Brahim Nsiri

Pan Afr Med J· December 2020

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Association of FV G1691A Polymorphism but not A4070G With Coronary Artery Disease.
Ahmed Amara, Meriem Mrad, Aicha Sayeh, Abdeddayem Haggui, Dhaker Lahideb, Brahim Nsiri

Clin Appl Thromb Hemost· March 2018

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The Effect of ACE I/D Polymorphisms Alone and With Concomitant Risk Factors on Coronary Artery Disease.
Ahmed Amara, Meriem Mrad, Aicha Sayeh, Dhaker Lahideb, Samy Layouni, Brahim Nsiri

Clin Appl Thromb Hemost· January 2018

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Association between an angiotensin-converting enzyme gene polymorphism and Alzheimer's disease in a Tunisian population.
Najiba Fekih-Mrissa, Ines Bedoui, Aycha Sayeh, Hajer Derbali, Meriem Mrad, Brahim Nsiri

Ann Gen Psychiatry· November 2017

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Role of the Apolipoprotein E Polymorphisms in the Development of Retinal Vein Occlusion in a Tunisian Population: A Case-Control Study.
Meriem Mrad, Najiba Fekih-Mrissa, Cheima Wathek, Aicha Sayeh, Afef Maalej, Brahim Nsiri

Clin Appl Thromb Hemost· September 2017

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The Plasminogen Activator Inhibitor 1 4G/5G Polymorphism and the Risk of Alzheimer's Disease.
Najiba Fekih-Mrissa, Malek Mansour, Aicha Sayeh, Ines Bedoui, Meriem Mrad, Brahim Nsiri

Am J Alzheimers Dis Other Demen· September 2017

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HLA DRB1*03 as a possible common etiology of schizophrenia, Graves' disease, and type 2 diabetes.
Aicha Sayeh, Cheker Ben Cheikh, Ali Mardessi, Meriem Mrad, Brahim Nsiri

Ann Gen Psychiatry· February 2017

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Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015.
Jerry W. Shay, Noriko Homma, Ruyun Zhou, Muhammad Imran Naseer, Adeel G. Chaudhary

BMC Genomics· July 2016

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Association Between Thrombophilic Gene Mutations and the Risk of Vascular Access Thrombosis in Hemodialysis Patients.
Najiba Fekih-Mrissa, Aycha Sayeh, Anis Baffoun, Maher Beji, Meriem Mrad, Brahim Nsiri

Ther Apher Dial· April 2016

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Association of HLA-DR-DQ polymorphisms with diabetes in Tunisian patients.
Najiba Fekih Mrissa, Meriem Mrad, Haroun Ouertani, Makrem Baatour, Aycha Sayeh, Brahim Nsiri

Transfus Apher Sci· October 2013

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Association of methylenetetrahydrofolate reductase A1298C polymorphism but not of C677T with multiple sclerosis in Tunisian patients.
Najiba Fekih Mrissa, Meriem Mrad, Sarra Klai, Jamel Zaouali, Aycha Sayeh, Brahim Nsiri

Clin Neurol Neurosurg· September 2013

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Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction.
Dhouha Berredjeb Ben Slama, Najiba Fekih-Mrissa, Abdeddayem Haggui, Brahim Nsiri, Nadia Baraket

Cardiovasc Pathol· May 2013

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Factor VII levels, R353Q and -323P0/10 Factor VII variants, and the risk of acute coronary syndrome among Arab-African Tunisians.
Sonia Ben-Hadj-Khalifa, Basma Lakhal, Brahim Nsiri, Touhami Mahjoub, Wassim Y Almawi

Mol Biol Rep· May 2013

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Methylenetetrahydrofolate reductase (C677T and A1298C) polymorphisms, hyperhomocysteinemia, and ischemic stroke in Tunisian patients.
Najiba Fekih-Mrissa, Meriem Mrad, Sarra Klai, Malek Mansour, Brahim Nsiri

J Stroke Cerebrovasc Dis· May 2013

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Role of methylenetetrahydrofolate reductase A1298C polymorphism in cerebral venous thrombosis.
Najiba Fekih-Mrissa, Sarra Klai, Meriem Mrad, Jamel Zaouali, Aycha Sayeh, Brahim Nsiri

Blood Coagul Fibrinolysis· March 2013

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Contribution of JAK2 and STAT3 variants to the genetic susceptibility of recurrent miscarriage among Bahraini and Tunisian Arabs.
Safia Messoudi, Manar A Al-Sulaiti, Amna S Al-Busaidi, Maryam Dendana, Brahim Nsiri

Mol Biol Rep· January 2013

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Thrombophilic polymorphisms - factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T - in Tunisian patients with cerebral venous thrombosis.
Olfa Ben Salem-Berrabah, Nejiba Fekih-Mrissa, Brahim N'siri, Abdelmajid Ben Hamida, Amel Benammar-Elgaaied

J Clin Neurosci· September 2012

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Association of MTHFR A1298C polymorphism (but not of MTHFR C677T) with elevated homocysteine levels and placental vasculopathies.
Sarra Klai, Najiba Fekih-Mrissa, Sonia El Housaini, Naziha Kaabechi, Brahim Nsiri

Blood Coagul Fibrinolysis· July 2011

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-174G>C interleukin-6 gene polymorphism in Tunisian patients with coronary artery disease.
Lakhdar Ghazouani, Nesrine Abboud, Sonia Ben Hadj Khalifa, Faouzi Added, Ali Ben Khalfallah, Brahim Nsiri

Ann Saudi Med· May 2011

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TNF-alpha -308G>A and IL-6 -174G>C polymorphisms in Tunisian patients with coronary artery disease.
Lakhdar Ghazouani, Sonia Ben Hadj Khalifa, Nesrine Abboud, Khaldoun Ben Hamda, Ali Ben Khalfallah, Nsiri Brahim

Clin Biochem· September 2010

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Hyperhomocysteinemia, C677T MTHFR polymorphism and ischemic stroke in Tunisian patients.
Olfa Ben Salem-Berrabah, Ridha Mrissa, Salem Machghoul, Abdelhamid Ben Hamida, Brahim N'siri

Tunis Med· September 2010

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Human platelet alloantigens HPA-1, HPA-2, and HPA-3 polymorphisms associated with extent of severe coronary artery disease.
Nesrine Abboud, Lakdhar Ghazouani, Sonia Ben-Hadj-Khalifa, Fatma Anabi, Faouzi Added, Brahim Nsiri

J Thromb Thrombolysis· May 2010

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-308G>A and -1031T>C tumor necrosis factor gene polymorphisms in Tunisian patients with coronary artery disease.
Lakhdar Ghazouani, Sonia-Ben-Hadj Khalifa, Nesrine Abboud, Faouzi Addad, Ali Ben Khalfallah, Nsiri Brahim

Clin Chem Lab Med· December 2009

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Distinct association of factor V-Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisia and Lebanon.
Lobna Bouaziz-Borgi, Wassim Y Almawi, Nabil Mtiraoui, Brahim Nsiri, Sose H Keleshian

Am J Hematol· August 2006

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