Imen Habibi - Search Results

Year	Number of Results
2010	1
2011	1
2014	1
2016	1
2017	3
2018	1
2019	4
2020	3
2021	4
2022	1

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. Genes (Basel). 2020 May 3;11(5):503. doi: 10.3390/genes11050503. Genes (Basel). 2020. PMID: 32375275 Free PMC article.

2

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. 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.

3

Genetic spectrum of retinal dystrophies in Tunisia.

Habibi I, Falfoul Y, Turki A, Hassairi A, El Matri K, Chebil A, Schorderet DF, El Matri L. Habibi I, et al. Sci Rep. 2020 Jul 8;10(1):11199. doi: 10.1038/s41598-020-67792-y. Sci Rep. 2020. PMID: 32641690 Free PMC article.

4

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: habibi i. Int Ophthalmol. 2020 Sep;40(9):2159-2168. doi: 10.1007/s10792-020-01396-3. Epub 2020 May 2. Int Ophthalmol. 2020. PMID: 32358734

5

Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB).

Habibi I, Falfoul Y, Todorova MG, Wyrsch S, Vaclavik V, Helfenstein M, Turki A, Matri KE, Matri LE, Schorderet DF. Habibi I, et al. Genes (Basel). 2019 Nov 21;10(12):953. doi: 10.3390/genes10120953. Genes (Basel). 2019. PMID: 31766397 Free PMC article.

6

Homozygous mutation in ABCA4 associated with cone rod dystrophy in a patient with Turner syndrome.

Falfoul Y, Habibi I, Turki A, Ben Yakhlef A, El Matri K, Chebil A, Chaker N, Schorderet D, El Matri L. Falfoul Y, et al. Among authors: habibi i. Tunis Med. 2021 Feb;99(2):302-305. Tunis Med. 2021. PMID: 33899203 Free PMC article.

7

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. Sci Rep. 2016 Nov 22;6:37455. doi: 10.1038/srep37455. Sci Rep. 2016. PMID: 27874104 Free PMC article.

8

Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia.

Habibi I, Youssef M, Marzouk E, El Shakankiri N, Gawdat G, El Sada M, F Schorderet D, Abou Zeid H. Habibi I, et al. Adv Exp Med Biol. 2019;1185:221-226. doi: 10.1007/978-3-030-27378-1_36. Adv Exp Med Biol. 2019. PMID: 31884615

9

Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography.

El Matri K, Falfoul Y, Habibi I, Chebil A, Schorderet D, El Matri L. El Matri K, et al. Among authors: habibi i. Genes (Basel). 2021 Nov 15;12(11):1795. doi: 10.3390/genes12111795. Genes (Basel). 2021. PMID: 34828401 Free PMC article.

10

Corrigendum: Identifying mutations in Tunisian families with retinal dystrophy.

Habibi I, Chebil A, Falfoul Y, Allaman-Pillet N, Kort F, Schorderet DF, Matri LE. Habibi I, et al. Sci Rep. 2017 May 4;7:46776. doi: 10.1038/srep46776. Sci Rep. 2017. PMID: 28471455 Free PMC article. No abstract available.

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