Kamoun H - Search Results

1

Chromosomal defects in infertile men with poor semen quality.

Ghorbel M, Gargouri Baklouti S, Ben Abdallah F, Zribi N, Cherif M, Keskes R, Chakroun N, Sellami A, Belguith N, Kamoun H, Fakhfakh F, Ammar-Keskes L. Ghorbel M, et al. Among authors: kamoun h. J Assist Reprod Genet. 2012 May;29(5):451-6. doi: 10.1007/s10815-012-9737-7. Epub 2012 Mar 11. J Assist Reprod Genet. 2012. PMID: 22406877 Free PMC article.

2

Ganglioneuroma of adrenal gland in a patient with Turner syndrome.

Kamoun M, Mnif MF, Rekik N, Belguith N, Charfi N, Mnif L, Elleuch M, Mnif F, Kamoun T, Mnif Z, Kamoun H, Sellami-Boudawara T, Hachicha M, Abid M. Kamoun M, et al. Among authors: kamoun h, kamoun t. Ann Diagn Pathol. 2010 Apr;14(2):133-6. doi: 10.1016/j.anndiagpath.2009.06.007. Epub 2009 Sep 8. Ann Diagn Pathol. 2010. PMID: 20227019

3

Sister chromatid exchange (SCE) and high-frequency cells (HFC) in peripheral blood lymphocytes of healthy Tunisian smokers.

Ben Salah G, Kamoun H, Rebai A, Ben Youssef A, Ayadi H, Belghith-Mahfoudh N, Fourati A, Ayadi H, Fakhfakh F. Ben Salah G, et al. Among authors: kamoun h. Mutat Res. 2011 Feb 3;719(1-2):1-6. doi: 10.1016/j.mrgentox.2010.09.003. Epub 2010 Sep 29. Mutat Res. 2011. PMID: 20869462

4

Polymorphisms of glutathione S-transferases M1, T1, P1 and A1 genes in the Tunisian population: an intra and interethnic comparative approach.

Ben Salah G, Kallabi F, Maatoug S, Mkaouar-Rebai E, Fourati A, Fakhfakh F, Ayadi H, Kamoun H. Ben Salah G, et al. Among authors: kamoun h. Gene. 2012 May 1;498(2):317-22. doi: 10.1016/j.gene.2012.01.054. Epub 2012 Jan 31. Gene. 2012. PMID: 22313526

5

Hematotoxicity and genotoxicity of mercuric chloride following subchronic exposure through drinking water in male rats.

Boujbiha MA, Ben Salah G, Ben Feleh A, Saoudi M, Kamoun H, Bousslema A, Ommezzine A, Said K, Fakhfakh F, El Feki A. Boujbiha MA, et al. Among authors: kamoun h. Biol Trace Elem Res. 2012 Jul;148(1):76-82. doi: 10.1007/s12011-012-9342-8. Epub 2012 Feb 15. Biol Trace Elem Res. 2012. PMID: 22351102

6

Clinical and laboratory findings in 8 patients with Bloom's syndrome.

Masmoudi A, Marrakchi S, Kamoun H, Chaaben H, Ben Salah G, Ben Salah R, Fakhfakh F, Zahaf A, Turki H. Masmoudi A, et al. Among authors: kamoun h. J Dermatol Case Rep. 2012 Mar 27;6(1):29-33. doi: 10.3315/jdcr.2012.1086. J Dermatol Case Rep. 2012. PMID: 22514588 Free PMC article.

7

A novel nonsense mutation in HSD17B3 gene in a Tunisian patient with sexual ambiguity.

Ben Rhouma B, Belguith N, Mnif MF, Kamoun T, Charfi N, Kamoun M, Abdelhedi F, Hachicha M, Kamoun H, Abid M, Fakhfakh F. Ben Rhouma B, et al. Among authors: kamoun m, kamoun h, kamoun t. J Sex Med. 2013 Oct;10(10):2586-9. doi: 10.1111/j.1743-6109.2012.02763.x. Epub 2012 May 17. J Sex Med. 2013. PMID: 22594312

8

An interethnic variability and a functional prediction of DNA repair gene polymorphisms: the example of XRCC3 (p.Thr241>Met) and XPD (p.Lys751>Gln) in a healthy Tunisian population.

Ben Salah G, Fendri-Kriaa N, Kamoun H, Kallabi F, Mkaouar-Rebai E, Fourati A, Ayadi H, Fakhfakh F. Ben Salah G, et al. Among authors: kamoun h. Mol Biol Rep. 2012 Oct;39(10):9639-47. doi: 10.1007/s11033-012-1829-z. Epub 2012 Jun 28. Mol Biol Rep. 2012. PMID: 22740138

9

DNA repair gene polymorphisms at XRCC1 (Arg194Trp, Arg280His, and Arg399Gln) in a healthy Tunisian population: interethnic variation and functional prediction.

Salah GB, Ayadi I, Fendri-Kriaa N, Kallabi F, Mkaouar-Rebai E, Fourati A, Fakhfakh F, Ayadi H, Kamoun H. Salah GB, et al. Among authors: kamoun h. Genet Test Mol Biomarkers. 2012 Oct;16(10):1218-25. doi: 10.1089/gtmb.2012.0035. Genet Test Mol Biomarkers. 2012. PMID: 23057594

10

Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease.

Kammoun Jellouli N, Salem IH, Ellouz E, Louhichi N, tlili A, Kammoun F, Triki C, Fakhfakh F; Tunisian Network on Mental Retardation Study. Kammoun Jellouli N, et al. Gene. 2013 Jan 25;513(2):233-8. doi: 10.1016/j.gene.2012.10.070. Epub 2012 Nov 7. Gene. 2013. PMID: 23142375

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