Fekih-Mrissa N - Search Results

1

Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction.

Berredjeb Ben Slama D, Fekih-Mrissa N, Haggui A, Nsiri B, Baraket N, Haouala H, Gritli N. Berredjeb Ben Slama D, et al. Cardiovasc Pathol. 2013 Jan-Feb;22(1):39-41. doi: 10.1016/j.carpath.2012.03.002. Epub 2012 Apr 5. Cardiovasc Pathol. 2013. PMID: 22483732

2

Combination of factor V Leiden and MTHFR mutations in myocardial infarction.

Fekih-Mrissa N, Berredjeb-Benslama D, Haggui A, Haouala H, Gritli N. Fekih-Mrissa N, et al. Ann Saudi Med. 2013 Mar-Apr;33(2):192-3. doi: 10.5144/0256-4947.2012.01.7.1520. Epub 2012 Jul 1. Ann Saudi Med. 2013. PMID: 22750768 Free PMC article.

3

Methylenetetrahydrofolate reductase (C677T and A1298C) polymorphisms, hyperhomocysteinemia, and ischemic stroke in Tunisian patients.

Fekih-Mrissa N, Mrad M, Klai S, Mansour M, Nsiri B, Gritli N, Mrissa R. Fekih-Mrissa N, et al. J Stroke Cerebrovasc Dis. 2013 May;22(4):465-9. doi: 10.1016/j.jstrokecerebrovasdis.2013.03.011. J Stroke Cerebrovasc Dis. 2013. PMID: 23642756

4

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

Fekih-Mrissa N, Klai S, Zaouali J, Gritli N, Mrissa R. Fekih-Mrissa N, et al. Clin Neurol Neurosurg. 2013 Jan;115(1):32-6. doi: 10.1016/j.clineuro.2012.04.001. Epub 2012 Apr 18. Clin Neurol Neurosurg. 2013. PMID: 22521184

5

Role of methylenetetrahydrofolate reductase A1298C polymorphism in cerebral venous thrombosis.

Fekih-Mrissa N, Klai S, Mrad M, Zaouali J, Sayeh A, Nsiri B, Gritli N, Mrissa R. Fekih-Mrissa N, et al. Blood Coagul Fibrinolysis. 2013 Mar;24(2):118-9. doi: 10.1097/MBC.0b013e32835707cd. Blood Coagul Fibrinolysis. 2013. PMID: 23314385

6

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

Fekih Mrissa N, Mrad M, Ouertani H, Baatour M, Sayeh A, Nsiri B, Lamine K, Zidi B, Gritli N. Fekih Mrissa N, et al. Transfus Apher Sci. 2013 Oct;49(2):200-4. doi: 10.1016/j.transci.2013.01.012. Epub 2013 Feb 9. Transfus Apher Sci. 2013. PMID: 23402837 Clinical Trial.

7

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

Fekih Mrissa N, Mrad M, Klai S, Zaouali J, Sayeh A, Mazigh C, Nsiri B, Machgoul S, Gritli N, Mrissa R. Fekih Mrissa N, et al. Clin Neurol Neurosurg. 2013 Sep;115(9):1657-60. doi: 10.1016/j.clineuro.2013.02.025. Epub 2013 Mar 21. Clin Neurol Neurosurg. 2013. PMID: 23523621

8

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

Mansouri L, Fekih-Mrissa N, Klai S, Mansour M, Gritli N, Mrissa R. Mansouri L, et al. Clin Neurol Neurosurg. 2013 Sep;115(9):1693-6. doi: 10.1016/j.clineuro.2013.03.015. Epub 2013 May 6. Clin Neurol Neurosurg. 2013. PMID: 23659764

9

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

Sayeh A, Cheikh CB, Mrad M, Lakhal N, Gritli N, Galelli S, Oumaya A, Fekih-Mrissa N. Sayeh A, et al. Ann Saudi Med. 2014 Nov-Dec;34(6):503-7. doi: 10.5144/0256-4947.2014.503. Ann Saudi Med. 2014. PMID: 25971824 Free PMC article.

10

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

Wathek C, Mrad M, Abdessalem NB, Maalej A, Gritli N, Gabsi S, Rannen R, Fekih-Mrissa N. Wathek C, et al. Blood Coagul Fibrinolysis. 2015 Sep;26(6):682-4. doi: 10.1097/MBC.0000000000000311. Blood Coagul Fibrinolysis. 2015. PMID: 26083981

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