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

par Bouchoucha, Sami, Chikhaoui, Asma, Najjar, Dorra, Dallali, Hamza, Khammessi, Maleke, Abdelhak, Sonia, Nessibe, Nabil, Shboul, Mohammad, Kircher, Susanne G., Al Kaissi, Ali, Yacoub-Youssef, Houda
Publié dans Front Pediatr (2020)

Identification of a Novel Mutation of LAMB3 Gene in a Lybian Patient with Hereditary Epidermolysis Bullosa by Whole Exome Sequencing

par Laroussi, Nadia, Messaoud, Olfa, Chargui, Mariem, Ben Fayala, Chaima, Elahlafi, Abdelaziz, Mokni, Mourad, Bashamboo, Anu, McElreavey, Kenneth, Boubaker, Mohamed Samir, Yacoub Youssef, Houda, Abdelhak, Sonia
Publié dans Ann Dermatol (2017)

Proinflammatory Macrophages Enhance the Regenerative Capacity of Human Myoblasts by Modifying Their Kinetics of Proliferation and Differentiation

par Bencze, Maximilien, Negroni, Elisa, Vallese, Denis, Yacoub–Youssef, Houda, Chaouch, Soraya, Wolff, Annie, Aamiri, Ahmed, Di Santo, James P, Chazaud, Bénédicte, Butler-Browne, Gillian, Savino, Wilson, Mouly, Vincent, Riederer, Ingo
Publié 2012

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

par Chikhaoui, Asma, Elouej, Sahar, Nabouli, Imen, Jones, Meriem, Lagarde, Arnaud, Ben Rekaya, Meriem, Messaoud, Olfa, Hamdi, Yosr, Zghal, Mohamed, Delague, Valerie, Levy, Nicolas, De Sandre-Giovannoli, Annachiara, Abdelhak, Sonia, Yacoub-Youssef, Houda
Publié dans Front Genet (2019)

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

par Nabouli, Imen, Chikhaoui, Asma, Othman, Houcemeddine, Elouej, Sahar, Jones, Meriem, Lagarde, Arnaud, Rekaya, Meriem Ben, Messaoud, Olfa, Zghal, Mohamed, Delague, Valerie, Levy, Nicolas, De Sandre-Giovannoli, Annachiara, Abdelhak, Sonia, Yacoub-Youssef, Houda
Publié dans Front Genet (2021)

Further Evidence of Mutational Heterogeneity of the XPC Gene in Tunisian Families: A Spectrum of Private and Ethnic Specific Mutations

par Ben Rekaya, Mariem, Jerbi, Manel, Messaoud, Olfa, Ben Brick, Ahlem Sabrine, Zghal, Mohamed, Mbarek, Chiraz, Chadli-Debbiche, Ashraf, Jones, Meriem, Mokni, Mourad, Boussen, Hamouda, Boubaker, Mohamed Samir, Fazaa, Becima, Yacoub-Youssef, Houda, Abdelhak, Sonia
Publié 2013

A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy

par Ben Rekaya, Mariem, Laroussi, Nadia, Messaoud, Olfa, Jones, Mariem, Jerbi, Manel, Naouali, Chokri, Bouyacoub, Yosra, Chargui, Mariem, Kefi, Rym, Fazaa, Becima, Boubaker, Mohamed Samir, Boussen, Hamouda, Mokni, Mourad, Abdelhak, Sonia, Zghal, Mohamed, Khaled, Aida, Yacoub-Youssef, Houda
Publié 2014