Methylenetetrahydrofolate Reductase (C677T and A1298C) Polymorphisms, Hyperhomocysteinemia, and Ischemic Stroke in Tunisian Patients von Fekih-Mrissa, Najiba, PhD, Mrad, Meriem, PhD, Klai, Sarra, PhD, Mansour, Malek, PhD, Nsiri, Brahim, PhD, Gritli, Nasreddine, PhD, Mrissa, Ridha, MD

Volltext

Association of HLA-DR/DQ Polymorphism With Alzheimer’s Disease von Mansouri, Leila, PhD, Klai, Sarra, PhD, Gritli, Nasreddine, PhD, Fekih-Mrissa, Najiba, PhD, Messalmani, Mariem, MD, Bedoui, Ines, MD, Derbali, Hajer, MD, Mrissa, Ridha, MD

Volltext

Thrombophilic Risk Factors in Different Types of Retinal Vein Occlusion in Tunisian Patients von Mrad, Meriem, PhD, Fekih-Mrissa, Najiba, PhD, Wathek, Cheima, MD, Rannen, Riadh, MD, Gabsi, Salem, MD, Gritli, Nasreddine, PhD

Volltext

Association of HLA-DR/DQ polymorphisms with schizophrenia in Tunisian patients von Sayeh, Aicha, Cheikh, Cheker Ben, Mrad, Meriem, Lakhal, Najwa, Gritli, Nasreddine, Galelli, Slaheddine, Oumaya, Abdelaziz, Fekih-Mrissa, Najiba

Volltext

Apolipoprotein E Genotypes Associated with Alzheimer Disease and Concomitant Stroke von Fekih-Mrissa, Najiba, PhD, Klai, Sarra, PhD, Mrad, Meriem, PhD, Mansour, Malek, MD, Zaouali, Jamel, MD, Gritli, Nasreddine, PhD, Mrissa, Ridha, MD

Volltext

Combination of factor V Leiden and MTHFR mutations in myocardial infarction von Fekih-Mrissa, Najiba, Berredjeb-Benslama, Dhouha, Haggui, Abdeddayem, Haouala, Habib, Gritli, Nasreddine

Volltext

Stroke and inherited thrombophilia in a Tunisian girl with sickle cell anemia von Nefissi, Rim Belhaj, Ouali, Faida, Massaoud, Taieb, Gritli, Nasreddine

Volltext

Association of methylenetetrahydrofolate reductase polymorphisms with susceptibility to Alzheimer's disease von Mansouri, Leila, Fekih-Mrissa, Najiba, Klai, Sarra, Mansour, Malek, Gritli, Nasreddine, Mrissa, Ridha

Volltext

Association of HLA-DR/DQ polymorphisms with Guillain–Barré syndrome in Tunisian patients von Fekih-Mrissa, Najiba, Mrad, Meriem, Riahi, Anis, Sayeh, Aicha, Zaouali, Jamel, Gritli, Nasreddine, Mrissa, Ridha

Volltext

Methylenetetrahydrofolate Reductase (MTHFR) (C677T and A1298C) Polymorphisms and Vascular Complications in Patients with Type 2 Diabetes von Fekih-Mrissa, Najiba, Mrad, Meriem, Ibrahim, Hazard, Akremi, Imen, Sayeh, Aicha, Jaidane, Amel, Ouertani, Haroun, Zidi, Borni, Gritli, Nasreddine

Volltext

Association of HLA-DR/DQ polymorphism with myasthenia gravis in Tunisian patients von Fekih-Mrissa, Najiba, Klai, Sarra, Zaouali, Jamel, Gritli, Nasreddine, Mrissa, Ridha

Volltext

Association of HLA-DR/DQ polymorphism with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in Tunisian patients von Mrad, Meriem, Fekih-Mrissa, Najiba, Mansour, Malek, Seyah, Aicha, Riahi, Anis, Gritli, Nasreddine, Mrissa, Ridha

Volltext

Association of HLA-DR-DQ polymorphisms with diabetes in Tunisian patients von Fekih Mrissa, Najiba, Mrad, Meriem, Ouertani, Haroun, Baatour, Makrem, Sayeh, Aycha, Nsiri, Brahim, Lamine, Khaled, Zidi, Borni, Gritli, Nasreddine

Volltext

Association of methylenetetrahydrofolate reductase A1298C polymorphism but not of C677T with multiple sclerosis in Tunisian patients von Fekih Mrissa, Najiba, Mrad, Meriem, Klai, Sarra, Zaouali, Jamel, Sayeh, Aycha, Mazigh, Chakib, Nsiri, Brahim, Machgoul, Salem, Gritli, Nasreddine, Mrissa, Ridha

Volltext

Association of methylenetetrahydrofolate reductase (A1298C and C677T) polymorphisms with retinal vein occlusion in Tunisian patients von Mrad, Meriem, Wathek, Cheima, Saleh, Mekki Ben, Baatour, Makrem, Rannen, Riadh, Lamine, Khaled, Gabsi, Salem, Gritli, Nasreddine, Fekih-Mrissa, Najiba

Volltext

Prothrombin G20210A and methylenetetrahydrofolate reductase C677T polymorphisms in peripheral capillary nonperfusion: a case report von Wathek, Chaima, Mrad, Meriem, Abdessalem, Nadia Ben, Maalej, Afef, Gritli, Nasreddine, Gabsi, Salem, Rannen, Riadh, Fekih-Mrissa, Najiba

Volltext

Role of methylenetetrahydrofolate reductase A1298C polymorphism in cerebral venous thrombosis von Fekih-Mrissa, Najiba, Klai, Sarra, Mrad, Meriem, Zaouali, Jamel, Sayeh, Aycha, Nsiri, Brahim, Gritli, Nasreddine, Mrissa, Ridha

Volltext

Thrombophilic disorders: a real threat to patients with end-stage renal disease on hemodialysis and at the time of renal transplantation von Klai, Sarra, Fekih-Mrissa, Najiba, Ghachem, Anouer, Baffoun, Anis, Nciri, Brahim, Hmida, Jalel, Gritli, Nasreddine

Volltext

Thrombophilic polymorphisms – factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T – in Tunisian patients with cerebral venous thrombosis von Ben Salem-Berrabah, Olfa, Fekih-Mrissa, Nejiba, N’Siri, Brahim, Ben Hamida, Abdelmajid, Benammar-Elgaaied, Amel, Gritli, Nasreddine, Mrissa, Ridha

Volltext

Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction von Berredjeb Ben Slama, Dhouha, Fekih-Mrissa, Najiba, Haggui, Abdeddayem, Nsiri, Brahim, Baraket, Nadia, Haouala, Habib, Gritli, Nasreddine

Volltext