El Matri L - Search Results

1

Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies.

Habibi I, Falfoul Y, Tran HV, El Matri K, Chebil A, El Matri L, Schorderet DF. Habibi I, et al. Among authors: el matri l, el matri k. Front Cell Dev Biol. 2021 Feb 5;9:625560. doi: 10.3389/fcell.2021.625560. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33634125 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

Intravitreal injection of triamcinolone combined with bevacizumab for choroidal neovascularization associated with large retinal pigment epithelial detachment in age-related macular degeneration.

el Matri L, Chebil A, Kort F, Bouraoui R, Baklouti K, Mghaieth F. el Matri L, et al. Graefes Arch Clin Exp Ophthalmol. 2010 Jun;248(6):779-84. doi: 10.1007/s00417-010-1302-4. Epub 2010 Feb 19. Graefes Arch Clin Exp Ophthalmol. 2010. PMID: 20169357

5

[Vogt-Koyanagi-Harada disease associated with interferon-alpha and ribavirin therapy for chronic hepatitis C infection].

Chebil A, Kort F, Bouraoui R, Youssef NB, El Matri L. Chebil A, et al. Among authors: el matri l. J Fr Ophtalmol. 2010 Mar;33(3):185-8. doi: 10.1016/j.jfo.2010.01.009. Epub 2010 Feb 20. J Fr Ophtalmol. 2010. PMID: 20172621 French.

6

Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene.

Ouechtati F, Merdassi A, Bouyacoub Y, Largueche L, Derouiche K, Ouragini H, Nouira S, Tiab L, Baklouti K, Rebai A, Schorderet DF, Munier FL, Zografos L, Abdelhak S, El Matri L. Ouechtati F, et al. Among authors: el matri l. J Hum Genet. 2011 Jan;56(1):22-8. doi: 10.1038/jhg.2010.128. Epub 2010 Nov 25. J Hum Genet. 2011. PMID: 21107338

7

Intravitreal bevacizumab for the treatment of choroidal neovascularization secondary to angioid streaks: one year of follow-up.

El Matri L, Kort F, Bouraoui R, Karim B, Chebil A, Chaker N. El Matri L, et al. Acta Ophthalmol. 2011 Nov;89(7):641-6. doi: 10.1111/j.1755-3768.2009.01836.x. Epub 2010 Dec 14. Acta Ophthalmol. 2011. PMID: 21155980 Free article.

8

Pediatric penetrating keratoplasty: indications and outcomes.

Limaiem R, Chebil A, Baba A, Ben Youssef N, Mghaieth F, El Matri L. Limaiem R, et al. Among authors: el matri l. Transplant Proc. 2011 Mar;43(2):649-51. doi: 10.1016/j.transproceed.2011.01.055. Transplant Proc. 2011. PMID: 21440785

9

Intravitreal bevacizumab versus photodynamic therapy for myopic choroidal neovascularization in a North-African population.

El Matri L, Kort F, Chebil A, Bouraoui R, Merdassi A, Bouladi M. El Matri L, et al. Graefes Arch Clin Exp Ophthalmol. 2011 Sep;249(9):1287-93. doi: 10.1007/s00417-011-1654-4. Epub 2011 Apr 12. Graefes Arch Clin Exp Ophthalmol. 2011. PMID: 21484465

10

[Epidemiologic study of pediatric uveitis: a series of 49 cases].

Chebil A, Chaabani L, Kort F, Ben Youssef N, Turki F, El Matri L. Chebil A, et al. Among authors: el matri l. J Fr Ophtalmol. 2012 Jan;35(1):30-4. doi: 10.1016/j.jfo.2011.02.019. Epub 2011 Sep 1. J Fr Ophtalmol. 2012. PMID: 21889818 French.

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