Kandil M - Search Results

1

Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population.

Charoute H, Kefi R, Bounaceur S, Benrahma H, Reguig A, Kandil M, Rouba H, Bakhchane A, Abdelhak S, Barakat A. Charoute H, et al. Among authors: kandil m. Mitochondrial DNA A DNA Mapp Seq Anal. 2018 Jan;29(1):9-13. doi: 10.1080/24701394.2016.1233530. Epub 2016 Oct 11. Mitochondrial DNA A DNA Mapp Seq Anal. 2018. PMID: 27728995

2

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: kandil m. Pathol Biol (Paris). 2015 Dec;63(6):243-7. doi: 10.1016/j.patbio.2015.09.002. Pathol Biol (Paris). 2015. PMID: 26524954

3

Association analysis of genetic variants with metabolic syndrome components in the Moroccan population.

Lakbakbi El Yaagoubi F, Charoute H, Morjane I, Sefri H, Rouba H, Ainahi A, Kandil M, Benrahma H, Barakat A. Lakbakbi El Yaagoubi F, et al. Among authors: kandil m. Curr Res Transl Med. 2017 Sep;65(3):121-125. doi: 10.1016/j.retram.2017.08.001. Epub 2017 Sep 12. Curr Res Transl Med. 2017. PMID: 28919193

4

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: kandil m. 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

5

The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.

Charif M, Bounaceur S, Abidi O, Nahili H, Rouba H, Kandil M, Boulouiz R, Barakat A. Charif M, et al. Among authors: kandil m. Mol Biol Rep. 2012 Dec;39(12):11011-6. doi: 10.1007/s11033-012-2003-3. Epub 2012 Oct 8. Mol Biol Rep. 2012. PMID: 23053991

6

Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.

Charif M, Bakhchane A, Abidi O, Boulouiz R, Eloualid A, Roky R, Rouba H, Kandil M, Lenaers G, Barakat A. Charif M, et al. Among authors: kandil m. Gene. 2013 Jul 1;523(1):103-5. doi: 10.1016/j.gene.2013.03.123. Epub 2013 Apr 13. Gene. 2013. PMID: 23590985 Free article.

7

Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss.

Charif M, Abidi O, Boulouiz R, Nahili H, Rouba H, Kandil M, Delprat B, Lenaers G, Barakat A. Charif M, et al. Among authors: kandil m. Biochem Biophys Res Commun. 2012 Mar 23;419(4):643-7. doi: 10.1016/j.bbrc.2012.02.066. Epub 2012 Feb 20. Biochem Biophys Res Commun. 2012. PMID: 22382023 Free article.

8

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: kandil m. 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.

9

Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes.

Bouzidi A, Charif M, Bouzidi A, Amalou G, Kandil M, Barakat A, Lenaers G. Bouzidi A, et al. Among authors: kandil m. Mol Vis. 2021 Jan 15;27:17-25. eCollection 2021. Mol Vis. 2021. PMID: 33633436 Free PMC article.

10

Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.

Bouzidi A, Charoute H, Charif M, Amalou G, Kandil M, Barakat A, Lenaers G. Bouzidi A, et al. Among authors: kandil m. Orphanet J Rare Dis. 2022 May 12;17(1):197. doi: 10.1186/s13023-022-02340-7. Orphanet J Rare Dis. 2022. PMID: 35551639 Free PMC article. Review.

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