Nahili H - Search Results

1

The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.

Charoute H, Nahili H, Abidi O, Gabi K, Rouba H, Fakiri M, Barakat A. Charoute H, et al. Among authors: nahili h. Eur J Hum Genet. 2014 Mar;22(3):322-6. doi: 10.1038/ejhg.2013.151. Epub 2013 Jul 17. Eur J Hum Genet. 2014. PMID: 23860041 Free PMC article.

2

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: nahili h. 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

3

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.

Abidi O, Boulouiz R, Nahili H, Ridal M, Alami MN, Tlili A, Rouba H, Masmoudi S, Chafik A, Hassar M, Barakat A. Abidi O, et al. Among authors: nahili h. Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1239-45. doi: 10.1016/j.ijporl.2007.04.019. Epub 2007 Jun 5. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17553572

4

Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness.

Nahili H, Ridal M, Boulouiz R, Abidi O, Imken L, Rouba H, Alami MN, Chafik A, Hassar M, Barakat A. Nahili H, et al. Int J Pediatr Otorhinolaryngol. 2008 Nov;72(11):1633-6. doi: 10.1016/j.ijporl.2008.07.015. Epub 2008 Sep 21. Int J Pediatr Otorhinolaryngol. 2008. PMID: 18809214

5

The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population.

Abidi O, Boulouiz R, Nahili H, Imken L, Rouba H, Chafik A, Barakat A. Abidi O, et al. Among authors: nahili h. Biochem Biophys Res Commun. 2008 Dec 19;377(3):971-4. doi: 10.1016/j.bbrc.2008.10.086. Epub 2008 Oct 24. Biochem Biophys Res Commun. 2008. PMID: 18952066

6

Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.

Abidi O, Boulouiz R, Nahili H, Bakhouch K, Wakrim L, Rouba H, Chafik A, Hassar M, Barakat A. Abidi O, et al. Among authors: nahili h. Genet Test. 2008 Dec;12(4):569-74. doi: 10.1089/gte.2008.0063. Genet Test. 2008. PMID: 19072567

7

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. 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

8

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. Among authors: nahili h. J Community Health. 2011 Dec;36(6):943-8. doi: 10.1007/s10900-011-9393-3. J Community Health. 2011. PMID: 21442339

9

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: nahili h. 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.

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: nahili 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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