Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marwa Haddaji-Mastouri"'
Autor:
Dorra H'mida-Ben Brahim, Marwa Haddaji Mastouri, Aicha Zaghabani, Paul Coucke, Ali Saad, Amina Ben Salem, Frej Jammali, Peter De Coster, Nabiha Raouahi
Publikováno v:
European journal of oral sciences. 126(1)
Non-syndromic tooth agenesis (NSTA) is the most common developmental anomaly in humans. Several studies have been conducted on dental agenesis and numerous genes have been identified. However, the pathogenic mechanisms responsible for NSTA are not cl
Autor:
Saoussen Trabelsi, Imed Harrabi, Sihem Sassi, Dorra H'mida-Ben Brahim, Moez Gribaa, Sana Ben Amor, Marwa Haddaji-Mastouri, Fatma Ezzahra Gahbiche, Ali Saad, Marwa Chourabi, Soumaya Mougou-Zereli, Sofiane Ben Ammou, Turkia Lamouchi
Publikováno v:
Genetics Research International, Vol 2014 (2014)
Genetics Research International
Genetics Research International
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder. The causative mutation is an expansion of more than 36 CAG repeats in the first exon of IT15 gene. Many studies have shown that the IT15 interacts with several modifier
Autor:
Dorra H'mida Ben-Brahim, Sihem Sassi, Saoussen Trabelsi, Mohamed Neji Guediche, Ali Saad, Abdelfattah Zakhama, Marwa Haddaji Mastouri, Moez Gribaa, Soumaya Mougou, S. Hammami, Maroua Chourabi
Publikováno v:
Applied & Translational Genomics
Applied and Translational Genomics, Vol 4, Iss C, Pp 1-3 (2015)
Applied and Translational Genomics, Vol 4, Iss C, Pp 1-3 (2015)
Beckwith–Wiedemann syndrome has a wide spectrum of complications such as embryonal tumors, namely adrenocortical tumor. Tumor predisposition is one of the most challenging manifestations of this syndrome. A 45-day old female with a family history o
Autor:
Paul Coucke, Dorra H'mida-Ben Brahim, Marwa Haddaji Mastouri, Aicha Zaghabani, Peter De Coster, Saoussen Trabelsi, Ali Saad, Yosra May
Publikováno v:
Archives of oral biology. 71
Background Dental agenesis is the most common developmental anomaly in man and may present either as an isolated trait or as part of a syndrome, such as ectodermal dysplasia. Until now, the underlying molecular pathogenic mechanisms responsible for d
Autor:
Haddaji Mastouri, Marwa, De Coster, Peter, Zaghabani, Aicha, Jammali, Frej, Raouahi, Nabiha, Ben Salem, Amina, Saad, Ali, Coucke, Paul, H'mida Ben Brahim, Dorra
Publikováno v:
European Journal of Oral Sciences; Feb2018, Vol. 126 Issue 1, p24-32, 9p, 1 Color Photograph, 3 Charts