B. Nsiri

发表

Association of MTHFR A1298C polymorphism (but not of MTHFR C677T) with elevated homocysteine levels and placental vasculopathies

Sarra Klai, N. Fekih-Mrissa, Sonia El Housaini, 2011, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

The Effect of ACE I/D Polymorphisms Alone and With Concomitant Risk Factors on Coronary Artery Disease

N. Fekih-Mrissa, B. Nsiri, A. Haggui, 2018, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Human platelet alloantigens HPA-1, HPA-2, and HPA-3 polymorphisms associated with extent of severe coronary artery disease

W. Almawi, T. Mahjoub, B. Nsiri, 2010, Journal of Thrombosis and Thrombolysis.

Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction.

N. Fekih-Mrissa, B. Nsiri, A. Haggui, 2013, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

[CRP and micro-albumin: new markers of cardiovascular risk in type 2 diabetes].

B. Nsiri, C. Mazigh, Z. Aouni, 2011, Annales de cardiologie et d'angeiologie.

Factor VII levels, R353Q and -323P0/10 Factor VII variants, and the risk of acute coronary syndrome among Arab-African Tunisians

W. Almawi, T. Mahjoub, B. Nsiri, 2013, Molecular Biology Reports.

Association Between Thrombophilic Gene Mutations and the Risk of Vascular Access Thrombosis in Hemodialysis Patients

N. Fekih-Mrissa, B. Nsiri, Anis Baffoun, 2016, Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy.

Role of methylenetetrahydrofolate reductase A1298C polymorphism in cerebral venous thrombosis

Sarra Klai, N. Fekih-Mrissa, B. Nsiri, 2013, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Prevalence of antiphospholipid antibodies, factor V G1691A (Leiden) and prothrombin G20210A mutations in early and late recurrent pregnancy loss.

J. Gris, W. Almawi, T. Mahjoub, 2005, European journal of obstetrics, gynecology, and reproductive biology.

Abnormalities of coagulation and fibrinolysis in homozygous sickle cell disease.

B. Nsiri, T. Messaoud, N. Gritli, 1996, Hematology and cell therapy.

Antiphospholipid antibodies: lupus anticoagulants, anticardiolipin and antiphospholipid isotypes in patients with sickle cell disease.

B. Nsiri, C. Mazigh, T. Messaoud, 1998, Hematology and cell therapy.

Association between adverse pregnancy outcomes and maternal factor V G1691A (Leiden) and prothrombin G20210A genotypes in women with a history of recurrent idiopathic miscarriages

W. Almawi, T. Mahjoub, B. Nsiri, 2005, American journal of hematology.

Association of methylenetetrahydrofolate reductase C677T and A1298C polymorphisms with myocardial infarction in Tunisian young patients

B. Nsiri, A. Haggui, H. Haouala, 2014, Comparative Clinical Pathology.

Association of FV G1691A Polymorphism but not A4070G With Coronary Artery Disease

N. Fekih-Mrissa, B. Nsiri, A. Haggui, 2017, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Distinct association of factor V‐Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisia and Lebanon

W. Almawi, T. Mahjoub, B. Nsiri, 2006, American journal of hematology.

Fibrinolytic response to venous occlusion in patients with homozygous sickle cell disease.

B. Nsiri, C. Mazigh, N. Gritli, 1997, Hematology and cell therapy.

NA antigen frequencies in the Tunisian population.

F. Jenhani, B. Nsiri, S. Abid, 2000, Pathologie-biologie.

Association of HLA-DR-DQ polymorphisms with diabetes in Tunisian patients.

B. Nsiri, Khaled Lamine, M. Mrad, 2013, Transfusion and Apheresis Science.

HLA DRB1*03 as a possible common etiology of schizophrenia, Graves’ disease, and type 2 diabetes

N. Fekih-Mrissa, B. Nsiri, A. Oumaya, 2017, Annals of General Psychiatry.

-174G>C interleukin-6 gene polymorphism in Tunisian patients with coronary artery disease

T. Mahjoub, B. Nsiri, N. Abboud, 2011, Annals of Saudi medicine.

Factor VII levels, R353Q and -323P0/10 Factor VII variants, and the risk of acute coronary syndrome among Arab-African Tunisians

W. Almawi, T. Mahjoub, B. Nsiri, 2013, Molecular Biology Reports.

The Plasminogen Activator Inhibitor 1 4G/5G Polymorphism and the Risk of Alzheimer’s Disease

N. Fekih-Mrissa, B. Nsiri, A. Riahi, 2017, American journal of Alzheimer's disease and other dementias.

Association between an angiotensin-converting enzyme gene polymorphism and Alzheimer’s disease in a Tunisian population

N. Fekih-Mrissa, B. Nsiri, M. Mrad, 2017, Annals of General Psychiatry.

Methylenetetrahydrofolate reductase (C677T and A1298C) polymorphisms, hyperhomocysteinemia, and ischemic stroke in Tunisian patients.

Sarra Klai, N. Fekih-Mrissa, B. Nsiri, 2013, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Role of the Apolipoprotein E Polymorphisms in the Development of Retinal Vein Occlusion in a Tunisian Population: A Case–Control Study

N. Fekih-Mrissa, B. Nsiri, A. Maalej, 2017, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Contribution of JAK2 and STAT3 variants to the genetic susceptibility of recurrent miscarriage among Bahraini and Tunisian Arabs

W. Almawi, T. Mahjoub, B. Nsiri, 2012, Molecular Biology Reports.

Association of methylenetetrahydrofolate reductase A1298C polymorphism but not of C677T with multiple sclerosis in Tunisian patients

Sarra Klai, B. Nsiri, C. Mazigh, 2013, Clinical Neurology and Neurosurgery.

[Cerebral venous thrombosis: Prospective etiological study of 26 Tunisian patients].

B. Nsiri, N. Gritli, S. Layouni, 2011, Revue neurologique.

Neuro-meningeal cryptococcal infection revealing a multiple myeloma

N. Fekih-Mrissa, B. Nsiri, S. Layouni, 2020, The Pan African medical journal.