Chouchene I - Search Results

1

Coexistence of mal de Meleda and congenital cataract in a consanguineous Tunisian family: two case reports.

Bchetnia M, Merdassi A, Charfeddine C, Mgaieth F, Kassar S, Ouechtati F, Chouchene I, Boussen H, Mokni M, Osman AD, Boubaker MS, Abdelhak S, Elmatri L. Bchetnia M, et al. Among authors: chouchene i. J Med Case Rep. 2010 Apr 20;4:108. doi: 10.1186/1752-1947-4-108. J Med Case Rep. 2010. PMID: 20406438 Free PMC article.

2

Central areolar choroidal dystrophy associated with inherited drusen in a multigeneration Tunisian family: exclusion of the PRPH2 gene and the 17p13 locus.

Ouechtati F, Belhadj Tahar O, Mhenni A, Chakroun S, Chouchene I, Oueslati S, Rebai A, Abdelhak S, Jeddi-Blouza A. Ouechtati F, et al. Among authors: chouchene i. J Hum Genet. 2009 Oct;54(10):589-94. doi: 10.1038/jhg.2009.82. Epub 2009 Aug 21. J Hum Genet. 2009. PMID: 19696794

3

[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. 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.

4

Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia.

Ben Halim N, Hsouna S, Lasram K, Rejeb I, Walha A, Talmoudi F, Messai H, Sabrine Ben Brick A, Ouragini H, Cherif W, Nagara M, Ben Rhouma F, Chouchene I, Ouechtati F, Bouyacoub Y, Ben Rekaya M, Messaoud O, Ben Ammar S, El Matri L, Tebib N, Ben Dridi MF, Mokni M, Amouri A, Kefi R, Abdelhak S. Ben Halim N, et al. Among authors: chouchene i. Am J Hum Biol. 2016 Mar-Apr;28(2):171-80. doi: 10.1002/ajhb.22764. Epub 2015 Jul 16. Am J Hum Biol. 2016. PMID: 26179682

5

Retinal dystrophy and congenital glaucoma as major causes of vision loss in students attending two institutions for the visually disabled in Tunis city, Tunisia.

Chouchene I, Derouiche K, Ben Halim N, Merdassi A, Limaiem R, Abdelhak S, El Matri L. Chouchene I, et al. J Fr Ophtalmol. 2014 Nov;37(9):695-701. doi: 10.1016/j.jfo.2014.03.010. Epub 2014 Sep 8. J Fr Ophtalmol. 2014. PMID: 25199482

6

Identification of a novel mutation in FOXL2 gene that leads to blepharophimosis ptosis epicanthus inversus and telecanthus syndrome in a Tunisian consanguineous family.

Chouchene I, Derouiche K, Chaabouni A, Cherif L, Amouri A, Largueche L, Abdelhak S, El Matri L. Chouchene I, et al. Genet Test Mol Biomarkers. 2010 Feb;14(1):145-8. doi: 10.1089/gtmb.2009.0091. Genet Test Mol Biomarkers. 2010. PMID: 19929410

7

[Molecular exploration of the R91W (RPE65 gene) in Tunisian patients with early onset retinal dystrophy and early onset retinitis pigmentosa].

Chouchene I, Largueche L, Derouiche K, Mabrouk S, Abdelhak S, El Matri L. Chouchene I, et al. Tunis Med. 2015 Jul;93(7):445-8. Tunis Med. 2015. PMID: 26757501 Free article. French.

8

Y402H polymorphism in complement factor H and age-related macular degeneration in the Tunisian population.

Habibi I, Sfar I, Kort F, Aounallah-Skhiri H, Chebil A, Chouchene I, Bouraoui R, Limaiem R, Largheche L, Jendoubi-Ayed S, Makhlouf M, Ben Abdallah T, Ayed K, El Matri L, Gorgi Y. Habibi I, et al. Among authors: chouchene i. Ophthalmic Res. 2013;49(4):177-84. doi: 10.1159/000345068. Epub 2013 Jan 10. Ophthalmic Res. 2013. PMID: 23306536

9

Mechanical ventilation in patients with cardiogenic pulmonary edema: a sub-analysis of the LUNG SAFE study.

Amado-Rodríguez L, Rodríguez-Garcia R, Bellani G, Pham T, Fan E, Madotto F, Laffey JG, Albaiceta GM; LUNG SAFE investigators. Amado-Rodríguez L, et al. J Intensive Care. 2022 Dec 25;10(1):55. doi: 10.1186/s40560-022-00648-x. J Intensive Care. 2022. PMID: 36567347 Free PMC article.

10

Validation and utility of ARDS subphenotypes identified by machine-learning models using clinical data: an observational, multicohort, retrospective analysis.

Maddali MV, Churpek M, Pham T, Rezoagli E, Zhuo H, Zhao W, He J, Delucchi KL, Wang C, Wickersham N, McNeil JB, Jauregui A, Ke S, Vessel K, Gomez A, Hendrickson CM, Kangelaris KN, Sarma A, Leligdowicz A, Liu KD, Matthay MA, Ware LB, Laffey JG, Bellani G, Calfee CS, Sinha P; LUNG SAFE Investigators and the ESICM Trials Group. Maddali MV, et al. Lancet Respir Med. 2022 Apr;10(4):367-377. doi: 10.1016/S2213-2600(21)00461-6. Epub 2022 Jan 10. Lancet Respir Med. 2022. PMID: 35026177 Free PMC article.

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