Makrelouf M - Search Results

1

Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy.

Demir E, Sabatelli P, Allamand V, Ferreiro A, Moghadaszadeh B, Makrelouf M, Topaloglu H, Echenne B, Merlini L, Guicheney P. Demir E, et al. Among authors: makrelouf m. Am J Hum Genet. 2002 Jun;70(6):1446-58. doi: 10.1086/340608. Epub 2002 Apr 24. Am J Hum Genet. 2002. PMID: 11992252 Free PMC article.

2

A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family.

Behlouli A, Bonnet C, Abdi S, Hasbellaoui M, Boudjenah F, Hardelin JP, Louha M, Makrelouf M, Ammar-Khodja F, Zenati A, Petit C. Behlouli A, et al. Among authors: makrelouf m. Int J Pediatr Otorhinolaryngol. 2016 Aug;87:28-33. doi: 10.1016/j.ijporl.2016.04.040. Epub 2016 May 20. Int J Pediatr Otorhinolaryngol. 2016. PMID: 27368438

3

A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa.

Arredi B, Poloni ES, Paracchini S, Zerjal T, Fathallah DM, Makrelouf M, Pascali VL, Novelletto A, Tyler-Smith C. Arredi B, et al. Among authors: makrelouf m. Am J Hum Genet. 2004 Aug;75(2):338-45. doi: 10.1086/423147. Epub 2004 Jun 16. Am J Hum Genet. 2004. PMID: 15202071 Free PMC article.

4

EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness.

Behlouli A, Bonnet C, Abdi S, Bouaita A, Lelli A, Hardelin JP, Schietroma C, Rous Y, Louha M, Cheknane A, Lebdi H, Boudjelida K, Makrelouf M, Zenati A, Petit C. Behlouli A, et al. Among authors: makrelouf m. Orphanet J Rare Dis. 2014 Apr 17;9:55. doi: 10.1186/1750-1172-9-55. Orphanet J Rare Dis. 2014. PMID: 24741995 Free PMC article.

5

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome.

Abdi S, Bahloul A, Behlouli A, Hardelin JP, Makrelouf M, Boudjelida K, Louha M, Cheknene A, Belouni R, Rous Y, Merad Z, Selmane D, Hasbelaoui M, Bonnet C, Zenati A, Petit C. Abdi S, et al. Among authors: makrelouf m. PLoS One. 2016 Sep 1;11(9):e0161893. doi: 10.1371/journal.pone.0161893. eCollection 2016. PLoS One. 2016. PMID: 27583663 Free PMC article.

6

Molecular screening of deafness in Algeria: high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F.

Ammar-Khodja F, Faugère V, Baux D, Giannesini C, Léonard S, Makrelouf M, Malek R, Djennaoui D, Zenati A, Claustres M, Roux AF. Ammar-Khodja F, et al. Among authors: makrelouf m. Eur J Med Genet. 2009 Jul-Aug;52(4):174-9. doi: 10.1016/j.ejmg.2009.03.018. Epub 2009 Apr 16. Eur J Med Genet. 2009. PMID: 19375528

7

Frequency of the 35delG allele causing nonsyndromic recessive deafness in the Algerian patients.

Ammar-Khodja F, Makrelouf M, Malek R, Ibrahim H, Zenati A. Ammar-Khodja F, et al. Among authors: makrelouf m. Genet Couns. 2007;18(4):383-91. Genet Couns. 2007. PMID: 18286819

8

The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells.

Pepermans E, Michel V, Goodyear R, Bonnet C, Abdi S, Dupont T, Gherbi S, Holder M, Makrelouf M, Hardelin JP, Marlin S, Zenati A, Richardson G, Avan P, Bahloul A, Petit C. Pepermans E, et al. Among authors: makrelouf m. EMBO Mol Med. 2014 Jul;6(7):984-92. doi: 10.15252/emmm.201403976. EMBO Mol Med. 2014. PMID: 24940003 Free PMC article.

9

Polymorphisms in NAT2 gene and atherosclerosis in an Algerian population.

Khelil M, Zenati A, Makrelouf M, Otmane A, Tayebi B. Khelil M, et al. Among authors: makrelouf m. Arch Med Res. 2010 Apr;41(3):215-20. doi: 10.1016/j.arcmed.2010.03.008. Arch Med Res. 2010. PMID: 20682180

10

[No title available]

[No authors listed] [No authors listed] PMID: 36026943

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