N. Fekih-Mrissa

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.

Thrombophilic risk factors in different types of retinal vein occlusion in Tunisian patients.

N. Fekih-Mrissa, C. Wathek, R. Rannen, 2014, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

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.

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.

Maternal HLA DRB1*01 allele or closely linked genes and unexplained recurrent pregnancy losses

Sarra Klai, N. Fekih-Mrissa, Radhouen Rachdi, 2014, Comparative Clinical Pathology.

Association of HLA-DR/DQ polymorphisms with Guillain–Barré syndrome in Tunisian patients

N. Fekih-Mrissa, A. Riahi, M. Mrad, 2014, Clinical Neurology and Neurosurgery.

Role of Thrombophilia in Vascular Access Thrombosis Among Chronic Hemodialysis Patients in Tunisia

Sarra Klai, N. Fekih-Mrissa, N. Gritli, 2011, 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.

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.

Combination of factor V Leiden and MTHFR mutations in myocardial infarction

N. Fekih-Mrissa, A. Haggui, H. Haouala, 2013, Annals of Saudi medicine.

C677T and A1298C gene polymorphisms and sporadic early-onset Alzheimer's disease

Sarra Klai, N. Fekih-Mrissa, L. Mansouri, 2013 .

C 677 T and A 1298 C gene polymorphisms and sporadic early-onset Alzheimer ’ s disease

Sarra Klai, N. Fekih-Mrissa, L. Mansouri, 2013 .

Limbic encephalitis associated with leucine-rich glioma-inactivated 1 antibodies

N. Fekih-Mrissa, M. Messelmani, J. Zaouali, 2015, Annals of Saudi medicine.

Idiopathic Intracranial Hypertension: an Unusual Presentation of Neuromyelitis Optica—A Case Report

N. Fekih-Mrissa, M. Messelmani, H. Derbali, 2021, SN Comprehensive Clinical Medicine.

Maternal cerebral venous thrombosis, uncommon but serious disorder, pathologic predictors and contribution of prothrombotic abnormalities

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

Association of HLA-DR/DQ Polymorphism With Alzheimer's Disease

Sarra Klai, N. Fekih-Mrissa, L. Mansouri, 2015, The American journal of the medical sciences.

Association of HLA-DR/DQ polymorphism with myasthenia gravis in Tunisian patients

Sarra Klai, N. Fekih-Mrissa, N. Gritli, 2013, Clinical Neurology and Neurosurgery.

Methylenetetrahydrofolate Reductase (MTHFR) (C677T and A1298C) Polymorphisms and Vascular Complications in Patients with Type 2 Diabetes.

N. Fekih-Mrissa, M. Mrad, N. Gritli, 2017, Canadian journal of diabetes.

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.

Association of HLA-DR/DQ polymorphism with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in Tunisian patients.

N. Fekih-Mrissa, A. Riahi, M. Mrad, 2013, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

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.

Thrombophilic disorders: a real threat to patients with end-stage renal disease on hemodialysis and at the time of renal transplantation

Sarra Klai, N. Fekih-Mrissa, Anis Baffoun, 2012, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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.

Effects of prothrombotic markers and non-O blood group in maternal venous thromboembolism during pregnancy and postpartum

Sarra Klai, N. Fekih-Mrissa, Radhouen Rachdi, 2012, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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.

The signification of antiphospholipid antibodies in pregnancy-associated pathologies and venous thromboembolism

Sarra Klai, N. Fekih-Mrissa, Radhouen Rachdi, 2012, Comparative Clinical Pathology.

The Status of Thrombophilic Defects and Non-O Blood Group as Risk Factors for Gestational Vascular Complications among Tunisian Women

Sarra Klai, N. Fekih-Mrissa, Radhouen Rachdi, 2010, Acta Haematologica.

Lack of association between monocyte protein-1 (MCP-1) –2518 A>G chemoattractant and C–C chemokine receptor 2 (CCR2) Val64Ile polymorphisms and multiple sclerosis in a Tunisian population

N. Fekih-Mrissa, Y. Sédiri, R. Jemaa, 2010, Journal of Clinical Neuroscience.

Association of methylenetetrahydrofolate reductase polymorphisms with susceptibility to Alzheimer's disease

Leila Mansouri, Sarra Klai, N. Fekih-Mrissa, 2013, Clinical Neurology and Neurosurgery.

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.

Association of HLA-DR/DQ polymorphisms with schizophrenia in Tunisian patients

N. Fekih-Mrissa, A. Oumaya, M. Mrad, 2014, Annals of Saudi medicine.

Association of methylenetetrahydrofolate reductase (A1298C and C677T) polymorphisms with retinal vein occlusion in Tunisian patients.

N. Fekih-Mrissa, C. Wathek, R. Rannen, 2014, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Apolipoprotein E genotypes associated with Alzheimer disease and concomitant stroke.

Sarra Klai, N. Fekih-Mrissa, M. Mrad, 2014, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Genetic polymorphisms and their association with central retinal vein occlusion combined with cilioretinal artery occlusion

N. Fekih-Mrissa, R. Rannen, S. Gabsi, 2015, Comparative Clinical Pathology.

Prothrombin G20210A and methylenetetrahydrofolate reductase C677T polymorphisms in peripheral capillary nonperfusion: a case report

N. Fekih-Mrissa, A. Maalej, R. Rannen, 2015, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.