Abnormalities of coagulation and fibrinolysis in homozygous sickle cell disease

Brahim Nsiri, Nasreddine Gritli, Fethi Bayoudh, +3

Hematology and Cell Therapy

ImmunohematologyLaboratory HematologyPathogenesisHematologyImmunology +7

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, +4

Blood Coagulation & Fibrinolysis

GeneticsGenetic EpidemiologyHuman PolymorphismPathologyGynecology +19

Methylenetetrahydrofolate Reductase (C677T and A1298C) Polymorphisms, Hyperhomocysteinemia, and Ischemic Stroke in Tunisian Patients

Najiba Fekih‐Mrissa, Meriem Mrad, Sarra Klai, +4

Journal of Stroke and Cerebrovascular Diseases

Metabolic SyndromeCardiovascular DiseaseIschemic StrokeMedicineMethylenetetrahydrofolate Reductase +13

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

Ahmed Amara, Meriem Mrad, Aicha Sayeh, +6

Clinical and Applied Thrombosis/Hemostasis

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

Nabil Mtiraoui, Lobna Borgi, Sondes Hizem, +5

European Journal of Obstetrics & Gynecology and Reproductive Biology

InfertilityGenetic DisorderGeneticsGenetic EpidemiologyHematology +8

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

Touhami Mahjoub, Nabil Mtiraoui, Hala Tamim, +4

American Journal of Hematology

Recurrent Pregnancy LossesGeneticsReproductive HealthGenetic EpidemiologyGynecology +25

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, +6

American Journal of Hematology

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

Lakhdar Ghazouani, Nesrine Abboud, S. Ben Khalifa, +5

Annals of Saudi Medicine

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

Najiba Fekih Mrissa, Meriem Mrad, Sarra Klai, +7

Clinical Neurology and Neurosurgery

Genetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenetic Epidemiology +8

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

Najiba Fekih Mrissa, Meriem Mrad, H. Ouertani, +6

Transfusion and Apheresis Science

Autoimmune DiseaseHla-dr-dq PolymorphismsDiabetesGenetic EpidemiologyHla Typing +4