Falfoul Y - Search Results

1

Posterior staphylomas in non-highly myopic eyes with retinitis pigmentosa.

El Matri L, Falfoul Y, El Matri K, El Euch I, Ghali H, Habibi I, Hassairi A, Chaker N, Schorderet D, Chebil A. El Matri L, et al. Among authors: falfoul y. Int Ophthalmol. 2020 Sep;40(9):2159-2168. doi: 10.1007/s10792-020-01396-3. Epub 2020 May 2. Int Ophthalmol. 2020. PMID: 32358734

2

[Ophthalmologic manifestations of congenital rubella].

Merdassi A, Limaiem R, Turki F, Chaker N, Falfoul Y, Mghaieth F, Korchane N, Matri LE. Merdassi A, et al. Among authors: falfoul y. Arch Pediatr. 2011 Aug;18(8):870-3. doi: 10.1016/j.arcped.2011.05.009. Epub 2011 Jun 12. Arch Pediatr. 2011. PMID: 21665443 French.

3

[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: falfoul y. 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.

4

[Contribution of multimodal imaging in the various stages of Stargardt disease].

El Matri L, Falfoul Y, Kortli M, Hassairi A, Charfi H, Turki A, Kort F, Chebil A. El Matri L, et al. Among authors: falfoul y. J Fr Ophtalmol. 2017 Oct;40(8):666-675. doi: 10.1016/j.jfo.2017.05.008. Epub 2017 Sep 15. J Fr Ophtalmol. 2017. PMID: 28919188 French.

5

Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations.

Falfoul Y, Habibi I, Turki A, Chebil A, Hassairi A, Schorderet DF, El Matri L. Falfoul Y, et al. J Ophthalmol. 2018 Mar 15;2018:1030184. doi: 10.1155/2018/1030184. eCollection 2018. J Ophthalmol. 2018. PMID: 29736279 Free PMC article.

6

Granular type I corneal dystrophy in a large consanguineous Tunisian family with homozygous p.R124S mutation in the TGFBI gene.

Bouyacoub Y, Falfoul Y, Ouederni M, Sayeb M, Chedli A, Chargui M, Sassi H, Chakroun Chenguel I, Munier FL, El Matri L, Abdelhak S, Cheour M. Bouyacoub Y, et al. Among authors: falfoul y. Ophthalmic Genet. 2019 Aug;40(4):329-337. doi: 10.1080/13816810.2019.1639202. Epub 2019 Jul 19. Ophthalmic Genet. 2019. PMID: 31322463

7

[Documented case of MELAS syndrome].

Falfoul Y, Hassairi A, Chebil A, Chaker N, Matri LE. Falfoul Y, et al. J Fr Ophtalmol. 2020 Apr;43(4):e143-e146. doi: 10.1016/j.jfo.2019.08.016. Epub 2020 Feb 24. J Fr Ophtalmol. 2020. PMID: 32107026 French. No abstract available.

8

[A case of pigmented paravenous retinochoroidal atrophy with cystoid macular edema].

Falfoul Y, Hassairi A, Chaker N, El Matri L. Falfoul Y, et al. J Fr Ophtalmol. 2020 Oct;43(8):834-836. doi: 10.1016/j.jfo.2019.11.021. Epub 2020 Jul 2. J Fr Ophtalmol. 2020. PMID: 32624322 French. No abstract available.

9

Multimodal Imaging in Retinitis Pigmentosa: Correlations among Microvascular Changes, Macular Function and Retinal Structure.

Falfoul Y, Elleuch I, El Matri K, Ghali H, Hassairi A, Chebil A, Chaker N, El Matri L. Falfoul Y, et al. J Curr Ophthalmol. 2020 Apr 30;32(2):170-177. doi: 10.4103/JOCO.JOCO_99_20. eCollection 2020 Apr-Jun. J Curr Ophthalmol. 2020. PMID: 32671301 Free PMC article.

10

[Retinal abnormalities in three genetic disorders involving the X chromosome].

Falfoul Y, El Leuch IE, El Matri K, Chaker N, El Matri L. Falfoul Y, et al. J Fr Ophtalmol. 2020 Dec;43(10):1107-1108. doi: 10.1016/j.jfo.2020.01.017. Epub 2020 Aug 20. J Fr Ophtalmol. 2020. PMID: 32829937 French. No abstract available.

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