Charif M - Search Results

1

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: charif m. Mol Vis. 2021 Jan 15;27:17-25. eCollection 2021. Mol Vis. 2021. PMID: 33633436 Free PMC article.

2

Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss.

Li Y, Pohl E, Boulouiz R, Schraders M, Nürnberg G, Charif M, Admiraal RJ, von Ameln S, Baessmann I, Kandil M, Veltman JA, Nürnberg P, Kubisch C, Barakat A, Kremer H, Wollnik B. Li Y, et al. Among authors: charif m. Am J Hum Genet. 2010 Mar 12;86(3):479-84. doi: 10.1016/j.ajhg.2010.02.003. Epub 2010 Feb 18. Am J Hum Genet. 2010. PMID: 20170898 Free PMC article.

3

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: charif 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

4

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

5

Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.

Abidi O, Knari S, Sefri H, Charif M, Senechal A, Hamel C, Rouba H, Zaghloul K, El Kettani A, Lenaers G, Barakat A. Abidi O, et al. Among authors: charif m. Mol Vis. 2011;17:3541-7. Epub 2011 Dec 30. Mol Vis. 2011. PMID: 22219649 Free PMC article.

6

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. 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.

7

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. 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

8

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. 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.

9

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. 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.

10

Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability.

Angebault C, Charif M, Guegen N, Piro-Megy C, Mousson de Camaret B, Procaccio V, Guichet PO, Hebrard M, Manes G, Leboucq N, Rivier F, Hamel CP, Lenaers G, Roubertie A. Angebault C, et al. Among authors: charif m. Hum Mol Genet. 2015 Jul 15;24(14):3948-55. doi: 10.1093/hmg/ddv133. Epub 2015 Apr 21. Hum Mol Genet. 2015. PMID: 25901006

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