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Association of the MTHFR A1298C variant with unexplained severe male infertility.
PLoS One. 2012;7(3):e34111. doi: 10.1371/journal.pone.0034111. Epub 2012 Mar 23.
PLoS One. 2012.
PMID: 22457816
Free PMC article.
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. Among authors: ajjemami m.
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
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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: ajjemami m.
Pathol Biol (Paris). 2015 Dec;63(6):243-7. doi: 10.1016/j.patbio.2015.09.002.
Pathol Biol (Paris). 2015.
PMID: 26524954
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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: ajjemami m.
Lipids Health Dis. 2014 Apr 1;13:60. doi: 10.1186/1476-511X-13-60.
Lipids Health Dis. 2014.
PMID: 24684850
Free PMC article.
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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.
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.
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