El Matri L - Search Results

1

Correction: Habibi I. et al. "Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)" Genes, 2019, 10, 953.

Habibi I, Falfoul Y, Todorova MG, Wyrsch S, Vaclavik V, Helfenstein M, Turki A, El Matri K, El Matri L, Schorderet DF. Habibi I, et al. Among authors: el matri l, el matri k. Genes (Basel). 2020 May 3;11(5):503. doi: 10.3390/genes11050503. Genes (Basel). 2020. PMID: 32375275 Free PMC article.

2

Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy.

Ren Z, Lin PY, Klintworth GK, Iwata F, Munier FL, Schorderet DF, El Matri L, Theendakara V, Basti S, Reddy M, Hejtmancik JF. Ren Z, et al. Among authors: el matri l. Hum Genet. 2002 Jun;110(6):568-77. doi: 10.1007/s00439-002-0729-z. Epub 2002 Apr 20. Hum Genet. 2002. PMID: 12107443

3

Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene.

El Matri L, Ambresin A, Schorderet DF, Kawasaki A, Seeliger MW, Wenzel A, Arsenijevic Y, Borruat FX, Munier FL. El Matri L, et al. Graefes Arch Clin Exp Ophthalmol. 2006 Sep;244(9):1104-12. doi: 10.1007/s00417-005-0096-2. Epub 2006 Feb 28. Graefes Arch Clin Exp Ophthalmol. 2006. PMID: 16518657

4

Granulomatous uveitis and reactive arthritis as manifestations of post-streptococcal syndrome.

Abderrahim K, Chebil A, Falfoul Y, Bouladi M, El Matri L. Abderrahim K, et al. Among authors: el matri l. Int Ophthalmol. 2015 Oct;35(5):641-3. doi: 10.1007/s10792-012-9626-1. Epub 2012 Sep 18. Int Ophthalmol. 2015. PMID: 22986580

5

A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa.

Tiab L, Largueche L, Chouchane I, Derouiche K, Munier FL, El Matri L, Schorderet DF. Tiab L, et al. Among authors: el matri l. Mol Vis. 2013 Apr 5;19:829-34. Print 2013. Mol Vis. 2013. PMID: 23592920 Free PMC article.

6

[Clinical characterization of the Stargardt disease and molecular exploration of the c.2041C>T mutation (ABCA4 gene) in Tunisian patients].

Chouchene I, Largueche L, Ouechtati F, Derouiche K, Turki A, Abdelhak S, El Matri L. Chouchene I, et al. Among authors: el matri l. Ann Biol Clin (Paris). 2013 Nov-Dec;71(6):645-51. doi: 10.1684/abc.2013.0912. Ann Biol Clin (Paris). 2013. PMID: 24342785 Free article. French.

7

Vascular endothelial growth factor genetic polymorphisms and susceptibility to age-related macular degeneration in Tunisian population.

Habibi I, Sfar I, Chebil A, Kort F, Bouraoui R, Jendoubi-Ayed S, Makhlouf M, Abdallah TB, El Matri L, Gorgi Y. Habibi I, et al. Among authors: el matri l. Biomark Res. 2014 Aug 18;2:15. doi: 10.1186/2050-7771-2-15. eCollection 2014. Biomark Res. 2014. PMID: 25165559 Free PMC article.

8

[Genotype-phenotype correlation in ten Tunisian families with non-syndromic retinitis pigmentosa].

Chebil A, Falfoul Y, Habibi I, Munier F, Schorderet D, El Matri L. Chebil A, et al. Among authors: el matri l. J Fr Ophtalmol. 2016 Mar;39(3):277-86. doi: 10.1016/j.jfo.2015.08.013. Epub 2016 Feb 9. J Fr Ophtalmol. 2016. PMID: 26868535 French.

9

Effect of Risk Alleles in CFH, C3, and VEGFA on the Response to Intravitreal Bevacizumab in Tunisian Patients with Neovascular Age-related Macular Degeneration.

Habibi I, Kort F, Sfar I, Chebil A, Bouraoui R, Ben Abdallah T, Gorgi Y, El Matri L. Habibi I, et al. Among authors: el matri l. Klin Monbl Augenheilkd. 2016 Apr;233(4):465-70. doi: 10.1055/s-0041-111801. Epub 2016 Apr 26. Klin Monbl Augenheilkd. 2016. PMID: 27116510 Clinical Trial. English.

10

Identifying mutations in Tunisian families with retinal dystrophy.

Habibi I, Chebil A, Falfoul Y, Allaman-Pillet N, Kort F, Schorderet DF, El Matri L. Habibi I, et al. Among authors: el matri l. Sci Rep. 2016 Nov 22;6:37455. doi: 10.1038/srep37455. Sci Rep. 2016. PMID: 27874104 Free PMC article.

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