Kharrat M - Search Results

1

Response to clopidogrel and of the cytochrome CYP2C19 gene polymorphism.

Charfi R, Mzoughi K, Boughalleb M, Hosni H, Kouidhi S, Sfar I, Hammami N, Zaïri I, Limam M, Zedini C, Mrabet A, Klouz A, Gorgi Y, Kharrat M, Baccar H, Trabelsi S. Charfi R, et al. Among authors: kharrat m. Tunis Med. 2018 Mar;96(3):209-218. Tunis Med. 2018. PMID: 30325490

2

Impact of toll-like receptor 4 variations on nasopharyngeal carcinoma risk and survival in tunisian population.

Ben Chaaben A, Ayadi I, Abaza H, Baroudi O, Douik H, Harzallah L, Bouassida J, Bouckouaci W, Guemira F, Mankai A, Kharrat M, Tamouza R. Ben Chaaben A, et al. Among authors: kharrat m. Tunis Med. 2024 Feb 5;102(2):100-106. doi: 10.62438/tunismed.v102i2.4270. Tunis Med. 2024. PMID: 38567476

3

Crohn's disease and polymorphism of heat shock protein gene HSP70-2 in the Tunisian population.

Zouiten-Mekki L, Karoui S, Kharrat M, Fekih M, Matri S, Boubaker J, Filali A, Chaabouni H. Zouiten-Mekki L, et al. Among authors: kharrat m. Eur J Gastroenterol Hepatol. 2007 Mar;19(3):225-8. doi: 10.1097/01.meg.0000252625.65549.29. Eur J Gastroenterol Hepatol. 2007. PMID: 17301649

4

Non-syndromic autosomal recessive mental retardation in Tunisian families : exclusion of GRIK2 and TUSC3 genes.

Mhamdi O, Kharrat M, Mrad R, Maazoul F, Chaabouni Bouhamed H. Mhamdi O, et al. Among authors: kharrat m. Tunis Med. 2011 May;89(5):479-84. Tunis Med. 2011. PMID: 21557188

5

Prognostic values of detecting MSI phenotypes in colorectal carcinoma by immunohistochemical method compared to molecular investigation.

Trabelsi M, Farah F, Blel A, Jaafoura MH, Kharrat M, Rammeh S. Trabelsi M, et al. Among authors: kharrat m. Tunis Med. 2017 Dec;95(12):229-236. Tunis Med. 2017. PMID: 29878286

6

Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation.

Kharrat M, Tardy V, M'Rad R, Maazoul F, Jemaa LB, Refaï M, Morel Y, Chaabouni H. Kharrat M, et al. Among authors: m rad r. J Clin Endocrinol Metab. 2004 Jan;89(1):368-74. doi: 10.1210/jc.2003-031056. J Clin Endocrinol Metab. 2004. PMID: 14715874

7

A novel 13-bp deletion in exon 1 of CYP21 gene causing severe congenital adrenal hyperplasia.

Kharrat M, Tardy V, M'rad R, Maazoul F, Morel Y, Chaabouni H. Kharrat M, et al. Among authors: m rad r. Diagn Mol Pathol. 2005 Dec;14(4):250-2. doi: 10.1097/01.pas.0000177797.81206.eb. Diagn Mol Pathol. 2005. PMID: 16319697

8

MEFV mutations in Tunisian patients suffering from familial Mediterranean fever.

Chaabouni HB, Ksantini M, M'rad R, Kharrat M, Chaabouni M, Maazoul F, Bahloul Z, Ben Jemaa L, Ben Moussa F, Ben Chaabane T, Mrad S, Touitou I, Smaoui N. Chaabouni HB, et al. Among authors: m rad r, kharrat m. Semin Arthritis Rheum. 2007 Jun;36(6):397-401. doi: 10.1016/j.semarthrit.2006.12.004. Epub 2007 Feb 5. Semin Arthritis Rheum. 2007. PMID: 17276496

9

Tolllike receptor 4 (TLR4) polymorphisms in Tunisian patients with Crohn's disease: genotype-phenotype correlation.

Zouiten-Mekki L, Kharrat M, Karoui S, Serghimi M, Fekih M, Matri S, Kallel L, Boubaker J, Filali A, Chaabouni H. Zouiten-Mekki L, et al. Among authors: kharrat m. BMC Gastroenterol. 2009 Aug 7;9:62. doi: 10.1186/1471-230X-9-62. BMC Gastroenterol. 2009. PMID: 19664207 Free PMC article.

10

A novel UBE3A truncating mutation in large Tunisian Angelman syndrome pedigree.

Abaied L, Trabelsi M, Chaabouni M, Kharrat M, Kraoua L, M'rad R, Tebib N, Maazoul F, Chaabouni H. Abaied L, et al. Among authors: m rad r, kharrat m. Am J Med Genet A. 2010 Jan;152A(1):141-6. doi: 10.1002/ajmg.a.33179. Am J Med Genet A. 2010. PMID: 20034088

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