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Brahim Nsiri
Observed names:
B Nsiri,
B N’Siri,
B. N'siri,
B. Nsiri,
Brahim N'siri,
Brahim N’Siri
show all 6
Institution:
Military Hospital of Tunis
Observed institutions:
University of Monastir,
Military Hospital of Tunis
OpenAlex ID:
A5110187158
Abnormalities of coagulation and fibrinolysis in homozygous sickle cell disease
1996
·
B. Nsiri
, N. Gritli
, et al.
·
Hematology and Cell Therapy
·
73
Association of MTHFR A1298C polymorphism (but not of MTHFR C677T) with elevated homocysteine levels and placental vasculopathies
2011
·
Sarra Klai
, Najiba Fekih-Mrissa
, et al.
·
Blood Coagulation & Fibrinolysis
·
67
The Effect of ACE I/D Polymorphisms Alone and With Concomitant Risk Factors on Coronary Artery Disease
2016
·
Ahmed Amara
, Meriem Mrad
, et al.
·
Clinical and Applied Thrombosis/Hemostasis
·
53
PDF
Methylenetetrahydrofolate Reductase (C677T and A1298C) Polymorphisms, Hyperhomocysteinemia, and Ischemic Stroke in Tunisian Patients
2013
·
Najiba Fekih-Mrissa
, Meriem Mrad
, et al.
·
Journal of Stroke and Cerebrovascular Diseases
·
52
Prevalence of antiphospholipid antibodies, factor V G1691A (Leiden) and prothrombin G20210A mutations in early and late recurrent pregnancy loss
2004
·
Nabil Mtiraoui
, Lobna Borgi
, et al.
·
European Journal of Obstetrics & Gynecology and Reproductive Biology
·
38
Association between adverse pregnancy outcomes and maternal factor V G1691A (Leiden) and prothrombin G20210A genotypes in women with a history of recurrent idiopathic miscarriages
2005
·
Touhami Mahjoub
, Nabil Mtiraoui
, et al.
·
American Journal of Hematology
·
35
Association of methylenetetrahydrofolate reductase A1298C polymorphism but not of C677T with multiple sclerosis in Tunisian patients
2013
·
Najiba Fekih Mrissa
, Meriem Mrad
, et al.
·
Clinical Neurology and Neurosurgery
·
29
-174G>C Interleukin-6 Gene Polymorphism in Tunisian Patients with Coronary Artery Disease
2011
·
Lakhdar Ghazouani
, Nesrine Abboud
, et al.
·
Annals of Saudi Medicine
·
29
Distinct association of factor V-Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisia and Lebanon
2006
·
Lobna Bouaziz-Borgi
, Wassim Y. Almawi
, et al.
·
American Journal of Hematology
·
28
PDF
Association of HLA-DR-DQ polymorphisms with diabetes in Tunisian patients
2013
·
Najiba Fekih Mrissa
, Meriem Mrad
, et al.
·
Transfusion and Apheresis Science
·
26
Fibrinolytic response to venous occlusion in patients with homozygous sickle cell disease
1997
·
B. Nsiri
, N. Gritli
, et al.
·
Hematology and Cell Therapy
·
20
Thrombophilic polymorphisms – factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T – in Tunisian patients with cerebral venous thrombosis
2012
·
Olfa Ben Salem-Berrabah
, Nejiba Fekih-Mrissa
, et al.
·
Journal of Clinical Neuroscience
·
18
Polymorphisme ABO dans une population de donneurs de sang tunisiens
2003
·
N Said
, F Ben Ahmed
, et al.
·
Transfusion Clinique et Biologique
·
17
Hyperhomocysteinemia, C677T MTHFR polymorphism and ischemic stroke in Tunisian patients.
2010
·
Olfa Ben Salem-Berrabah
, Ridha Mrissa
, et al.
·
PubMed
·
16
Human platelet alloantigens HPA-1, HPA-2, and HPA-3 polymorphisms associated with extent of severe coronary artery disease
2009
·
Nesrine Abboud
, Lakdhar Ghazouani
, et al.
·
Journal of Thrombosis and Thrombolysis
·
16
Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction
2012
·
Dhouha Berredjeb Ben Slama
, Najiba Fekih-Mrissa
, et al.
·
Cardiovascular Pathology
·
15
Association between an angiotensin-converting enzyme gene polymorphism and Alzheimer’s disease in a Tunisian population
2017
·
Najiba Fekih-Mrissa
, Ines Bedoui
, et al.
·
Annals of General Psychiatry
·
14
PDF
Antiphospholipid antibodies: lupus anticoagulants, anticardiolipin and antiphospholipid isotypes in patients with sickle cell disease.
1998
·
B Nsiri
, E Ghazouani
, et al.
·
PubMed
·
14
Association of FV G1691A Polymorphism but not A4070G With Coronary Artery Disease
2017
·
Ahmed Amara
, Meriem Mrad
, et al.
·
Clinical and Applied Thrombosis/Hemostasis
·
11
PDF
The Plasminogen Activator Inhibitor 1 4G/5G Polymorphism and the Risk of Alzheimer’s Disease
2017
·
Najiba Fekih-Mrissa
, Malek Mansour
, et al.
·
American Journal of Alzheimer s Disease & Other Dementias®
·
10
Association Between Thrombophilic Gene Mutations and the Risk of Vascular Access Thrombosis in Hemodialysis Patients
2016
·
Najiba Fekih‐Mrissa
, Aycha Sayeh
, et al.
·
Therapeutic Apheresis and Dialysis
·
10
Role of methylenetetrahydrofolate reductase A1298C polymorphism in cerebral venous thrombosis
2013
·
Najiba Fekih-Mrissa
, Sarra Klai
, et al.
·
Blood Coagulation & Fibrinolysis
·
9
Contribution of JAK2 and STAT3 variants to the genetic susceptibility of recurrent miscarriage among Bahraini and Tunisian Arabs
2012
·
Safia Messoudi
, Manar A. Al-Sulaiti
, et al.
·
Molecular Biology Reports
·
9
La thrombose veineuse cérébrale : étude étiologique prospective de 26 patients tunisiens
2010
·
O. Ben Salem-Berrabah
, N. Fekih-Mrissa
, et al.
·
Revue Neurologique
·
8
Role of the Apolipoprotein E Polymorphisms in the Development of Retinal Vein Occlusion in a Tunisian Population: A Case–Control Study
2016
·
Meriem Mrad
, Najiba Fekih-Mrissa
, et al.
·
Clinical and Applied Thrombosis/Hemostasis
·
6
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Works count:
40
Citation count:
653
H-index:
15
I10-index:
21
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