Benrahma H - Search Results

1

Association of the MTHFR A1298C variant with unexplained severe male infertility.

Eloualid A, Abidi O, Charif M, El Houate B, Benrahma H, Louanjli N, Chadli E, Ajjemami M, Barakat A, Bashamboo A, McElreavey K, Rhaissi H, Rouba H. Eloualid A, et al. Among authors: benrahma h. PLoS One. 2012;7(3):e34111. doi: 10.1371/journal.pone.0034111. Epub 2012 Mar 23. PLoS One. 2012. PMID: 22457816 Free PMC article.

2

Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a Moroccan population.

Benrahma H, Abidi O, Melouk L, Ajjemami M, Rouba H, Chadli A, Oudghiri M, Farouqui A, Barakat A. Benrahma H, et al. Genet Test Mol Biomarkers. 2012 May;16(5):383-7. doi: 10.1089/gtmb.2011.0179. Epub 2011 Nov 21. Genet Test Mol Biomarkers. 2012. PMID: 22103601

3

Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.

Nahili H, Charif M, Boulouiz R, Bounaceur S, Benrahma H, Abidi O, Chafik A, Rouba H, Kandil M, Barakat A. Nahili H, et al. Among authors: benrahma h. Int J Pediatr Otorhinolaryngol. 2010 Sep;74(9):1071-4. doi: 10.1016/j.ijporl.2010.06.008. Epub 2010 Jul 15. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20637512

4

TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis.

Sefri H, Benrahma H, Charoute H, Lakbakbi el Yaagoubi F, Rouba H, Lyoussi B, Nourlil J, Abidi O, Barakat A. Sefri H, et al. Among authors: benrahma h. Mol Biol Rep. 2014 Sep;41(9):5805-11. doi: 10.1007/s11033-014-3454-5. Epub 2014 Jun 22. Mol Biol Rep. 2014. PMID: 24952604

5

Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients.

Lakbakbi El Yaagoubi F, Charoute H, Bakhchane A, Ajjemami M, Benrahma H, Errouagui A, Kandil M, Rouba H, Barakat A. Lakbakbi El Yaagoubi F, et al. Among authors: benrahma h. Pathol Biol (Paris). 2015 Dec;63(6):243-7. doi: 10.1016/j.patbio.2015.09.002. Pathol Biol (Paris). 2015. PMID: 26524954

6

Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.

Ouatou S, Ajjemami M, Charoute H, Sefri H, Ghalim N, Rhaissi H, Benrahma H, Barakat A, Rouba H. Ouatou S, et al. Among authors: benrahma h. Lipids Health Dis. 2014 Apr 1;13:60. doi: 10.1186/1476-511X-13-60. Lipids Health Dis. 2014. PMID: 24684850 Free PMC article.

7

Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.

Benrahma H, Charoute H, Lasram K, Boulouiz R, Atig RK, Fakiri M, Rouba H, Abdelhak S, Barakat A. Benrahma H, et al. Biochem Genet. 2014 Oct;52(9-10):430-42. doi: 10.1007/s10528-014-9658-5. Epub 2014 Jun 5. Biochem Genet. 2014. PMID: 24898818

8

Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome.

Ajjemami M, Ouatou S, Charoute H, Fakiri M, Rhaissi H, Benrahma H, Rouba H, Barakat A. Ajjemami M, et al. Among authors: benrahma h. J Diabetes Metab Disord. 2015 Apr 16;14:29. doi: 10.1186/s40200-015-0160-3. eCollection 2015. J Diabetes Metab Disord. 2015. PMID: 25909077 Free PMC article.

9

Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.

Benrahma H, Arfa I, Charif M, Bounaceur S, Eloualid A, Boulouiz R, Nahili H, Abidi O, Rouba H, Chadli A, Oudghiri M, Farouqui A, Abdelhak S, Barakat A. Benrahma H, et al. J Community Health. 2011 Dec;36(6):943-8. doi: 10.1007/s10900-011-9393-3. J Community Health. 2011. PMID: 21442339

10

Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.

Charif M, Boulouiz R, Bakhechane A, Benrahma H, Nahili H, Eloualid A, Rouba H, Kandil M, Abidi O, Lenaers G, Barakat A. Charif M, et al. Among authors: benrahma h. Indian J Hum Genet. 2013 Jul;19(3):331-6. doi: 10.4103/0971-6866.120828. Indian J Hum Genet. 2013. PMID: 24339547 Free PMC article.

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