Lenaers G - Search Results

1

Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.

Bouzidi A, Charoute H, Charif M, Amalou G, Kandil M, Barakat A, Lenaers G. Bouzidi A, et al. Among authors: lenaers g. Orphanet J Rare Dis. 2022 May 12;17(1):197. doi: 10.1186/s13023-022-02340-7. Orphanet J Rare Dis. 2022. PMID: 35551639 Free PMC article. Review.

2

Homozygous deletion related to Alu repeats in RLBP1 causes retinitis punctata albescens.

Humbert G, Delettre C, Sénéchal A, Bazalgette C, Barakat A, Bazalgette C, Arnaud B, Lenaers G, Hamel CP. Humbert G, et al. Among authors: lenaers g. Invest Ophthalmol Vis Sci. 2006 Nov;47(11):4719-24. doi: 10.1167/iovs.05-1488. Invest Ophthalmol Vis Sci. 2006. PMID: 17065479

3

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.

4

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.

5

Dominant optic atrophy.

Lenaers G, Hamel C, Delettre C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P, Milea D. Lenaers G, et al. Orphanet J Rare Dis. 2012 Jul 9;7:46. doi: 10.1186/1750-1172-7-46. Orphanet J Rare Dis. 2012. PMID: 22776096 Free PMC article. Review.

6

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.

7

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.

8

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

9

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

10

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

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