Yacoub-Youssef H - Search Results

1

Combining Gene Mutation with Expression of Candidate Genes to Improve Diagnosis of Escobar Syndrome.

Najjar D, Chikhaoui A, Zarrouk S, Azouz S, Kamoun W, Nassib N, Bouchoucha S, Yacoub-Youssef H. Najjar D, et al. Among authors: yacoub youssef h. Genes (Basel). 2022 Sep 27;13(10):1748. doi: 10.3390/genes13101748. Genes (Basel). 2022. PMID: 36292632 Free PMC article.

2

Chronic vascular rejection: histologic comparison between two murine experimental models.

Yacoub-Youssef H, Marcheix B, Calise D, Thiers JC, Benoist H, Blaes N, Ségui B, Dambrin C, Thomsen M. Yacoub-Youssef H, et al. Transplant Proc. 2005 Jul-Aug;37(6):2886-7. doi: 10.1016/j.transproceed.2005.05.030. Transplant Proc. 2005. PMID: 16182843

3

Human immune reconstitution with spleen cells in SCID/Beige mice.

Marcheix B, Yacoub-Youssef H, Calise D, Thiers JC, Benoist H, Blaes N, Ségui B, Thomsen M, Dambrin C. Marcheix B, et al. Transplant Proc. 2005 Jul-Aug;37(6):2888-9. doi: 10.1016/j.transproceed.2005.05.031. Transplant Proc. 2005. PMID: 16182844

4

Proinflammatory macrophages enhance the regenerative capacity of human myoblasts by modifying their kinetics of proliferation and differentiation.

Bencze M, Negroni E, Vallese D, Yacoub-Youssef H, Chaouch S, Wolff A, Aamiri A, Di Santo JP, Chazaud B, Butler-Browne G, Savino W, Mouly V, Riederer I. Bencze M, et al. Mol Ther. 2012 Nov;20(11):2168-79. doi: 10.1038/mt.2012.189. Epub 2012 Oct 16. Mol Ther. 2012. PMID: 23070116 Free PMC article.

5

Differentially activated macrophages orchestrate myogenic precursor cell fate during human skeletal muscle regeneration.

Saclier M, Yacoub-Youssef H, Mackey AL, Arnold L, Ardjoune H, Magnan M, Sailhan F, Chelly J, Pavlath GK, Mounier R, Kjaer M, Chazaud B. Saclier M, et al. Stem Cells. 2013 Feb;31(2):384-96. doi: 10.1002/stem.1288. Stem Cells. 2013. PMID: 23169615 Free article.

6

Identification of a ERCC5 c.2333T>C (L778P) Variant in Two Tunisian Siblings With Mild Xeroderma Pigmentosum Phenotype.

Chikhaoui A, Elouej S, Nabouli I, Jones M, Lagarde A, Ben Rekaya M, Messaoud O, Hamdi Y, Zghal M, Delague V, Levy N, De Sandre-Giovannoli A, Abdelhak S, Yacoub-Youssef H. Chikhaoui A, et al. Front Genet. 2019 Feb 14;10:111. doi: 10.3389/fgene.2019.00111. eCollection 2019. Front Genet. 2019. PMID: 30838033 Free PMC article.

7

Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 Cases.

Bouchoucha S, Chikhaoui A, Najjar D, Dallali H, Khammessi M, Abdelhak S, Nessibe N, Shboul M, Kircher SG, Al Kaissi A, Yacoub-Youssef H. Bouchoucha S, et al. Front Pediatr. 2020 Apr 16;8:172. doi: 10.3389/fped.2020.00172. eCollection 2020. Front Pediatr. 2020. PMID: 32373565 Free PMC article.

8

Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype.

Nabouli I, Chikhaoui A, Othman H, Elouej S, Jones M, Lagarde A, Rekaya MB, Messaoud O, Zghal M, Delague V, Levy N, De Sandre-Giovannoli A, Abdelhak S, Yacoub-Youssef H. Nabouli I, et al. Front Genet. 2021 May 31;12:650639. doi: 10.3389/fgene.2021.650639. eCollection 2021. Front Genet. 2021. PMID: 34135938 Free PMC article.

9

Identification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome B.

Zayoud K, Kraoua I, Chikhaoui A, Calmels N, Bouchoucha S, Obringer C, Crochemore C, Najjar D, Zarrouk S, Miladi N, Laugel V, Ricchetti M, Turki I, Yacoub-Youssef H. Zayoud K, et al. Among authors: yacoub youssef h. Genes (Basel). 2021 Nov 29;12(12):1922. doi: 10.3390/genes12121922. Genes (Basel). 2021. PMID: 34946871 Free PMC article.

10

Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations.

Chikhaoui A, Kraoua I, Calmels N, Bouchoucha S, Obringer C, Zayoud K, Montagne B, M'rad R, Abdelhak S, Laugel V, Ricchetti M, Turki I, Yacoub-Youssef H. Chikhaoui A, et al. Among authors: yacoub youssef h. Orphanet J Rare Dis. 2022 Mar 5;17(1):121. doi: 10.1186/s13023-022-02257-1. Orphanet J Rare Dis. 2022. PMID: 35248096 Free PMC article.

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