Najiba Fekih-Mrissa

Summary

Country: France

Publications

  1. ncbi request reprint Association of HLA-DR/DQ polymorphisms with Guillain-Barré syndrome in Tunisian patients
    Najiba Fekih-Mrissa
    hôpital militaire principal d instruction de Tunis, Service d Hematologie, Laboratoire de Biologie Moleculaire, 1008 Montfleury, Tunis, Tunisie Académie Militaire Fondouk Jédid, 8012 Nabeul, Tunisie Electronic address
    Clin Neurol Neurosurg 121:19-22. 2014
  2. ncbi request reprint Apolipoprotein E genotypes associated with Alzheimer disease and concomitant stroke
    Najiba Fekih-Mrissa
    Laboratoire de Biologie Moleculaire, Service d Hematologie, hôpital militaire principal d instruction de Tunis, Montfleury, Tunis, Tunisie Académie Militaire Fondouk Jédid, Nabeul, Tunisie Electronic address
    J Stroke Cerebrovasc Dis 23:681-5. 2014
  3. doi request reprint Association of HLA-DR-DQ polymorphisms with diabetes in Tunisian patients
    Najiba Fekih Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital of Tunisia, Tunisia Electronic address
    Transfus Apher Sci 49:200-4. 2013
  4. doi request reprint Association of methylenetetrahydrofolate reductase A1298C polymorphism but not of C677T with multiple sclerosis in Tunisian patients
    Najiba Fekih Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital of Tunisia, Tunis, Tunisia
    Clin Neurol Neurosurg 115:1657-60. 2013
  5. doi request reprint Role of methylenetetrahydrofolate reductase A1298C polymorphism in cerebral venous thrombosis
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunis, Tunisia
    Blood Coagul Fibrinolysis 24:118-9. 2013
  6. doi request reprint Combination of factor V Leiden and MTHFR mutations in myocardial infarction
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, 1008 Mont Fleury, Tunis, Tunisia
    Ann Saudi Med 33:192-3. 2013
  7. doi request reprint Methylenetetrahydrofolate reductase (C677T and A1298C) polymorphisms, hyperhomocysteinemia, and ischemic stroke in Tunisian patients
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunisia
    J Stroke Cerebrovasc Dis 22:465-9. 2013
  8. doi request reprint Association of HLA-DR/DQ polymorphism with myasthenia gravis in Tunisian patients
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunis, Tunisia
    Clin Neurol Neurosurg 115:32-6. 2013
  9. doi request reprint Role of thrombophilia in vascular access thrombosis among chronic hemodialysis patients in Tunisia
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunis, Tunisia
    Ther Apher Dial 15:40-3. 2011
  10. doi request reprint Maternal cerebral venous thrombosis, uncommon but serious disorder, pathologic predictors and contribution of prothrombotic abnormalities
    Sarra Klai
    Department of Hematology, Unit of Molecular Biology, Military Hospital, Tunis, Tunisia
    Blood Coagul Fibrinolysis 24:269-72. 2013

Collaborators

  • Chakib Mazigh
  • Sarra Klai
  • Meriem Mrad
  • Nasreddine Gritli
  • Ridha Mrissa
  • Najiba Fekih Mrissa
  • Brahim Nsiri
  • Radhouen Rachdi
  • Nasredine Gritli
  • Riadh Rannen
  • Cheima Wathek
  • Salem Gabsi
  • Khaled Lamine
  • Makrem Baatour
  • Issam Jalouli
  • Leila Mansouri
  • Malek Mansour
  • Dhouha Berredjeb Ben Slama
  • Aycha Sayeh
  • Mekki Ben Saleh
  • Iheb Labbene
  • Borni Zidi
  • Abdeddayem Haggui
  • Jamel Zaouali
  • Nadia Baraket
  • Anis Lebbi
  • Zied Hajjej
  • Mustapha Ferjani
  • Haroun Ouertani
  • Anis Riahi
  • Salem Machgoul
  • Aicha Seyah
  • Habib Haouala
  • Anis Baffoun
  • Brahim Nciri
  • Jalel Hmida
  • Raja B Sassi
  • Anouer Ghachem
  • Sonia El Housaini
  • Naziha Kaabechi

Detail Information

Publications20

  1. ncbi request reprint Association of HLA-DR/DQ polymorphisms with Guillain-Barré syndrome in Tunisian patients
    Najiba Fekih-Mrissa
    hôpital militaire principal d instruction de Tunis, Service d Hematologie, Laboratoire de Biologie Moleculaire, 1008 Montfleury, Tunis, Tunisie Académie Militaire Fondouk Jédid, 8012 Nabeul, Tunisie Electronic address
    Clin Neurol Neurosurg 121:19-22. 2014
    ..Human leukocyte antigen (HLA) alleles have been implicated in many autoimmune diseases. The aim of this study is to assess whether HLA-DR/DQ alleles confer susceptibility to Guillain-Barré syndrome (GBS) in a Tunisian population...
  2. ncbi request reprint Apolipoprotein E genotypes associated with Alzheimer disease and concomitant stroke
    Najiba Fekih-Mrissa
    Laboratoire de Biologie Moleculaire, Service d Hematologie, hôpital militaire principal d instruction de Tunis, Montfleury, Tunis, Tunisie Académie Militaire Fondouk Jédid, Nabeul, Tunisie Electronic address
    J Stroke Cerebrovasc Dis 23:681-5. 2014
    ..The association between stroke and a higher risk for AD has also been reported. Our study sought to determine the relationship between the APOE gene and AD and the comorbid risk of stroke...
  3. doi request reprint Association of HLA-DR-DQ polymorphisms with diabetes in Tunisian patients
    Najiba Fekih Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital of Tunisia, Tunisia Electronic address
    Transfus Apher Sci 49:200-4. 2013
    ..The aim of this study was to evaluate HLA DR-DQ alleles and to asses them as risk factors for type 1 diabetes in the Tunisian population...
  4. doi request reprint Association of methylenetetrahydrofolate reductase A1298C polymorphism but not of C677T with multiple sclerosis in Tunisian patients
    Najiba Fekih Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital of Tunisia, Tunis, Tunisia
    Clin Neurol Neurosurg 115:1657-60. 2013
    ..The aim of this study was to investigate a possible association between the methylenetetrahydrofolate reductase (MTHFR) gene and multiple sclerosis in Tunisian patients...
  5. doi request reprint Role of methylenetetrahydrofolate reductase A1298C polymorphism in cerebral venous thrombosis
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunis, Tunisia
    Blood Coagul Fibrinolysis 24:118-9. 2013
    ..To our knowledge, there are no previous reports assessing the correlation between the MTHFR A1298C variant and CVT. Large study populations would be required to understand the contribution of this marker in the risk of CVT...
  6. doi request reprint Combination of factor V Leiden and MTHFR mutations in myocardial infarction
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, 1008 Mont Fleury, Tunis, Tunisia
    Ann Saudi Med 33:192-3. 2013
    ..Genetic screening for inherited thrombophilia in young patients, especially in the presence of a common risk factor, may be useful for primary thrombopro.phylaxis and in asymptomatic relatives of patients...
  7. doi request reprint Methylenetetrahydrofolate reductase (C677T and A1298C) polymorphisms, hyperhomocysteinemia, and ischemic stroke in Tunisian patients
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunisia
    J Stroke Cerebrovasc Dis 22:465-9. 2013
    ..The present study evaluated the role of the methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C gene polymorphisms and correlated these results with plasma homocysteine (Hcy) levels in Tunisian ischemic stroke (IS) patients...
  8. doi request reprint Association of HLA-DR/DQ polymorphism with myasthenia gravis in Tunisian patients
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunis, Tunisia
    Clin Neurol Neurosurg 115:32-6. 2013
    ..MG has been shown to be associated with many human leukocyte antigens (HLA) in different populations. The aim of this study was to investigate the probable association between HLA-DR/DQ alleles and MG in Tunisian patients...
  9. doi request reprint Role of thrombophilia in vascular access thrombosis among chronic hemodialysis patients in Tunisia
    Najiba Fekih-Mrissa
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunis, Tunisia
    Ther Apher Dial 15:40-3. 2011
    ..005). Our data demonstrated a significantly increased risk of vascular access thrombosis in carriers of the C677T methylene tetrahydrofolate reductase mutation...
  10. doi request reprint Maternal cerebral venous thrombosis, uncommon but serious disorder, pathologic predictors and contribution of prothrombotic abnormalities
    Sarra Klai
    Department of Hematology, Unit of Molecular Biology, Military Hospital, Tunis, Tunisia
    Blood Coagul Fibrinolysis 24:269-72. 2013
    ..Maternal CVT has been associated with factor V Leiden, the prothrombin G20210A mutation, protein C deficiency and hyperhomocysteinemia. We also speculate that non-O blood groups and preeclampsia could be independent risk factors for CVT...
  11. doi request reprint Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction
    Dhouha Berredjeb Ben Slama
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital of Tunis, Tunis, Tunisia
    Cardiovasc Pathol 22:39-41. 2013
    ..Myocardial infarction is a multifactorial disease. It is provoked by occlusions in the coronary arteries resulting from exposure to multiple risk factors...
  12. doi request reprint Association of methylenetetrahydrofolate reductase polymorphisms with susceptibility to Alzheimer's disease
    Leila Mansouri
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunis, Tunisia
    Clin Neurol Neurosurg 115:1693-6. 2013
    ..In this case-control study, we examined the C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene and their correlation with this pathology...
  13. doi request reprint Thrombophilic disorders: a real threat to patients with end-stage renal disease on hemodialysis and at the time of renal transplantation
    Sarra Klai
    Unit of Molecular Biology, Department of Hematology, Military Hospital of Tunis, Tunis, Tunisia
    Blood Coagul Fibrinolysis 23:406-10. 2012
    ..These results will serve as a basis for anticoagulant prophylaxis aimed at preventing kidney rejection and renal allograft thrombosis...
  14. ncbi request reprint Effects of prothrombotic markers and non-O blood group in maternal venous thromboembolism during pregnancy and postpartum
    Sarra Klai
    Unit of Molecular Biology, Department of Hematology, Military Hospital, Tunis, Tunisia
    Blood Coagul Fibrinolysis 23:649-52. 2012
    ..The non-O blood group could also have an important influence, especially when concomitant with another prothrombotic risk factor mainly pregnancy and thrombophilia...
  15. doi request reprint Association of MTHFR A1298C polymorphism (but not of MTHFR C677T) with elevated homocysteine levels and placental vasculopathies
    Sarra Klai
    Laboratory of Molecular Biology, Department of Hematology, Rabta University Hospital, Tunis, Tunisia
    Blood Coagul Fibrinolysis 22:374-8. 2011
    ..The MTHFR A1298C mutation also had a positive impact on elevated homocysteine levels. The lack of association between the MTHFR C677T polymorphism and pregnancy morbidities needs further studies...
  16. ncbi request reprint Thrombophilic risk factors in different types of retinal vein occlusion in tunisian patients
    Meriem Mrad
    Faculté des Science de Tunis, Universite Tunis El Manar, El Manar, Tunisie Laboratoire de Biologie Moléculaire, Service d Hematologie, hôpital militaire principal d instruction de Tunis, Montfleury, Tunisie
    J Stroke Cerebrovasc Dis 23:1592-8. 2014
    ..The pathogenesis of RVO is multifactorial. The role of factor V Leiden (FVL) and prothrombin mutations was examined in patients with CRVO and BRVO...
  17. doi request reprint Association of HLA-DR/DQ polymorphism with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in Tunisian patients
    Meriem Mrad
    Universite Tunis El Manar, Faculté des Science de Tunis, El Manar, Tunisia Hôpital Militaire Principal d Instruction de Tunis, Service d Hematologie, Laboratoire de Biologie Moleculaire, 1008 Montfleury, Tunisia
    Transfus Apher Sci 49:623-6. 2013
    ..The aim of this study was to investigate associations between HLA-DR/DQ alleles and CIDP in Tunisian patients...
  18. ncbi request reprint Association of methylenetetrahydrofolate reductase (A1298C and C677T) polymorphisms with retinal vein occlusion in Tunisian patients
    Meriem Mrad
    Universite Tunis El Manar, Faculté des Science de Tunis, El Manar, Tunisia Hôpital Militaire Principal d Instruction de Tunis, Service d Hematologie, Laboratoire de Biologie Moleculaire, 1008 Montfleury, Tunisia
    Transfus Apher Sci 50:283-7. 2014
    ..This suggests an association between this polymorphism and RVO. Large study populations would be required to understand more completely the contribution of these markers in the risk of RVO. ..
  19. doi request reprint Inherited thrombophilia-related complications in the treatment of a biatrial thrombus
    Issam Jalouli
    Department of Anesthesia and Intensive Care, Military Hospital of Tunisia, Tunis, Tunisia
    Blood Coagul Fibrinolysis 24:205-7. 2013
    ..The combination of these thrombophilic factors can probably explain the poor anticoagulant response, embolic events, and the failure of resolution of the biatrial masses...
  20. doi request reprint The status of thrombophilic defects and non-O blood group as risk factors for gestational vascular complications among Tunisian women
    Sarra Klai
    Laboratory of Molecular Biology, Department of Hematology, Military Hospital, Tunis, Tunisia
    Acta Haematol 125:115-20. 2011
    ..Our objectives were to assess inherited thrombophilia and non-O blood group for the risk of gestational vascular complications among the Tunisian population...