Bousfiha A - Search Results

1

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. Hum Hered. 2019;84(3):109-116. doi: 10.1159/000503450. Epub 2019 Dec 4. Hum Hered. 2019. PMID: 31801140

2

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: bousfiha 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

3

Intra-familial phenotypic variability in a Moroccan family with hearing loss and palmoplantar keratoderma (PPK).

Bousfiha A, Bakhchane A, Elrharchi S, Dehbi H, Kabine M, Nadifi S, Charoute H, Barakat A. Bousfiha A, et al. Curr Res Transl Med. 2016 Apr-Jun;64(2):61-4. doi: 10.1016/j.retram.2016.01.011. Epub 2016 Mar 4. Curr Res Transl Med. 2016. PMID: 27316387

4

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. 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.

5

Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.

Bakhchane A, Charif M, Bousfiha A, Boulouiz R, Nahili H, Rouba H, Charoute H, Lenaers G, Barakat A. Bakhchane A, et al. Among authors: bousfiha a. PLoS One. 2017 May 4;12(5):e0176516. doi: 10.1371/journal.pone.0176516. eCollection 2017. PLoS One. 2017. PMID: 28472130 Free PMC article.

6

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.

Bousfiha A, Bakhchane A, Charoute H, Detsouli M, Rouba H, Charif M, Lenaers G, Barakat A. Bousfiha A, et al. Mol Biol Rep. 2017 Oct;44(5):429-434. doi: 10.1007/s11033-017-4129-9. Epub 2017 Sep 26. Mol Biol Rep. 2017. PMID: 28951997

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: bousfiha 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

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: bousfiha 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

9

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.

AitRaise I, Amalou G, Bousfiha A, Charoute H, Rouba H, Abdelghaffar H, Bonnet C, Petit C, Barakat A. AitRaise I, et al. Among authors: bousfiha a. Mol Biol Rep. 2022 May;49(5):3949-3954. doi: 10.1007/s11033-022-07245-z. Epub 2022 Mar 17. Mol Biol Rep. 2022. PMID: 35301649

10

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.

AitRaise I, Amalou G, Bakhchane A, Bousfiha A, Abdelghaffar H, Majida C, Bonnet C, Petit C, Barakat A. AitRaise I, et al. Among authors: bousfiha a. Biochem Genet. 2024 Jun;62(3):1914-1924. doi: 10.1007/s10528-023-10515-5. Epub 2023 Oct 1. Biochem Genet. 2024. PMID: 37777971

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