Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Najoua Gandoura"'
Autor:
Sondess Hadj Fredj, Sihem Barsaoui, Lamia Boughamoura, Taieb Messaoud, Ahmed Mehrezi, Sonia Hilioui, Jihene Bouguila, S. Hamouda, Salma Ben Ameur, Khadija Boussetta, H. Ajmi, Mohamed Taher Sfar, N. Mattoussi, Saida Ben Becheur, Saoussen Abroug, Neji Tebib, Habib Besbes, Raoudha Boussoffara, F. Khalsi, Najoua Gandoura, N. Gueddiche, Faten Tinsa, A. Samoud, Mongia Hachicha
Publikováno v:
African Health Sciences
Aim: To establish a preliminary national report on clinical and genetic features of cystic fibrosis (CF) in Tunisian children as a first measure for a better health care organization. Methods: All children with CF diagnosed by positive sweat tests be
Publikováno v:
Chemosphere. 89:369-377
Thirty persistent organohalogen compounds including organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs) were determined in breast milk samples (n=36) of primipara and multipara mothers from B
Autor:
S Trabelsi, L. Ben Jemaa, S Barsaoui, R. M’rad, Lilia Kraoua, Yves Morel, Najoua Gandoura, Faouzi Maazoul, H. Chaabouni, Maher Kharrat, M. Chaabouni
Publikováno v:
Clinical Genetics. 78:398-401
Steroid 11β-hydroxylase deficiency is the second most common cause of congenital adrenal hyperplasia, resulting in virilization, glucocorticoid deficiency and hypertension. The 11β-hydroxylase enzyme is encoded by the CYP11B1 gene and mutations in
Autor:
Myriam, Chaabouni, Mounir, Fersi, Neila, Belghith, Faouzi, Maazoul, Ridha, M'rad, Lamia, Ben Jemaa, Najoua, Gandoura, Habiba, Chaabouni
Publikováno v:
La Tunisie medicale. 85(10)
Treacher Collins syndrome was first mentioned by Thompson in 1847, and described by Treacher Collins in 1900, then it was called mandibulo-facial dysostosis and well defined by Franceschetti in 1949. It is a very rare affection occurring lin 50.000 l
Autor:
Shouling Li, Habiba Chaabouni, Ezzedine Nouiri, Ridha Mrad, Asma Bouaziz, M. Chaabouni, Najoua Gandoura, Neila Mahfoudh, Yuri V. Sergeev, J. Fielding Hejtmancik, N. Smaoui, Faouzi Maazoul, Habib Kallel, Hassen Kammoun
Publikováno v:
Investigative Opthalmology & Visual Science. 47:3487
PURPOSE. To study Bardet-Biedl syndrome (BBS) in the Tunisian population and determine the presence of triallelism in the eight identified BBS genes. METHODS. DNA samples were collected from 19 consanguineous Tunisian families with BBS. Genome-wide s