Lenaers G - Search Results

1

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: lenaers g. 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.

2

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: lenaers g. Mol Vis. 2011;17:3541-7. Epub 2011 Dec 30. Mol Vis. 2011. PMID: 22219649 Free PMC article.

3

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: lenaers g. 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.

4

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: lenaers g. 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.

5

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: lenaers g. 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

6

Optic neuropathy, cardiomyopathy, cognitive disability in patients with a homozygous mutation in the nuclear MTO1 and a mitochondrial MT-TF variant.

Charif M, Titah SM, Roubertie A, Desquiret-Dumas V, Gueguen N, Meunier I, Leid J, Massal F, Zanlonghi X, Mercier J, Raynaud de Mauverger E, Procaccio V, Mousson de Camaret B, Lenaers G, Hamel CP. Charif M, et al. Among authors: lenaers g. Am J Med Genet A. 2015 Oct;167A(10):2366-74. doi: 10.1002/ajmg.a.37188. Epub 2015 Jun 10. Am J Med Genet A. 2015. PMID: 26061759

7

Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.

Charoute H, Bakhchane A, Benrahma H, Romdhane L, Gabi K, Rouba H, Fakiri M, Abdelhak S, Lenaers G, Barakat A. Charoute H, et al. Among authors: lenaers g. Hum Mutat. 2015 Nov;36(11):E2441-53. doi: 10.1002/humu.22835. Epub 2015 Jul 30. Hum Mutat. 2015. PMID: 26173767

8

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: lenaers g. Gene. 2015 Dec 10;574(1):28-33. doi: 10.1016/j.gene.2015.07.075. Epub 2015 Jul 28. Gene. 2015. PMID: 26226225

9

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees.

Bakhchane A, Charif M, Salime S, Boulouiz R, Nahili H, Roky R, Lenaers G, Barakat A. Bakhchane A, et al. Among authors: lenaers g. PLoS One. 2015 Sep 15;10(9):e0138072. doi: 10.1371/journal.pone.0138072. eCollection 2015. PLoS One. 2015. PMID: 26371875 Free PMC article.

10

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability.

Charif M, Roubertie A, Salime S, Mamouni S, Goizet C, Hamel CP, Lenaers G. Charif M, et al. Among authors: lenaers g. Front Genet. 2015 Oct 19;6:311. doi: 10.3389/fgene.2015.00311. eCollection 2015. Front Genet. 2015. PMID: 26539208 Free PMC article.

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