Barakat A - Search Results

1

A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.

Salime S, Riahi Z, Elrharchi S, Elkhattabi L, Charoute H, Nahili H, Rouba H, Kabine M, Bonnet C, Petit C, Barakat A. Salime S, et al. Among authors: barakat a. Gene. 2018 Jun 15;659:89-92. doi: 10.1016/j.gene.2018.03.042. Epub 2018 Mar 15. Gene. 2018. PMID: 29551497

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: barakat a. 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

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: barakat a. 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.

4

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

Bakhchane A, Charoute H, Nahili H, Roky R, Rouba H, Charif M, Lenaers G, Barakat A. Bakhchane A, et al. Among authors: barakat a. Gene. 2015 Dec 10;574(1):28-33. doi: 10.1016/j.gene.2015.07.075. Epub 2015 Jul 28. Gene. 2015. PMID: 26226225

5

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.

Bakhchane A, Bousfiha A, Charoute H, Salime S, Detsouli M, Snoussi K, Nadifi S, Kabine M, Rouba H, Dehbi H, Roky R, Charif M, Barakat A. Bakhchane A, et al. Among authors: barakat a. Eur J Med Genet. 2016 Jun;59(6-7):325-9. doi: 10.1016/j.ejmg.2016.05.002. Epub 2016 May 8. Eur J Med Genet. 2016. PMID: 27169813

6

A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.

Bousfiha A, Bakhchane A, Charoute H, Riahi Z, Snoussi K, Rouba H, Bonnet C, Petit C, Barakat A. Bousfiha A, et al. Among authors: barakat a. Hum Genome Var. 2017 Apr 13;4:17009. doi: 10.1038/hgv.2017.9. eCollection 2017. Hum Genome Var. 2017. PMID: 28446956 Free PMC article.

7

Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.

Salime S, Charif M, Bousfiha A, Elrharchi S, Bakhchane A, Charoute H, Kabine M, Snoussi K, Lenaers G, Barakat A. Salime S, et al. Among authors: barakat a. Int J Pediatr Otorhinolaryngol. 2017 Oct;101:25-29. doi: 10.1016/j.ijporl.2017.07.024. Epub 2017 Jul 21. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28964305

8

Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome.

Elrharchi S, Riahi Z, Salime S, Nahili H, Rouba H, Kabine M, Bonnet C, Petit C, Barakat A. Elrharchi S, et al. Among authors: barakat a. Int J Pediatr Otorhinolaryngol. 2018 Oct;113:46-50. doi: 10.1016/j.ijporl.2018.07.010. Epub 2018 Jul 10. Int J Pediatr Otorhinolaryngol. 2018. PMID: 30174009

9

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.

Bousfiha A, Riahi Z, Elkhattabi L, Bakhchane A, Charoute H, Snoussi K, Bonnet C, Petit C, Barakat A. Bousfiha A, et al. Among authors: barakat a. Hum Hered. 2019;84(3):109-116. doi: 10.1159/000503450. Epub 2019 Dec 4. Hum Hered. 2019. PMID: 31801140

10

A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family.

Amalou G, Bonnet C, Riahi Z, Bouzidi A, Elrharchi S, Bousfiha A, Charif M, Kandil M, Lenaers G, Petit C, Barakat A. Amalou G, et al. Among authors: barakat a. Int J Pediatr Otorhinolaryngol. 2021 Jan;140:110481. doi: 10.1016/j.ijporl.2020.110481. Epub 2020 Nov 2. Int J Pediatr Otorhinolaryngol. 2021. PMID: 33234333

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