Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Safa Sahnoun"'
Publikováno v:
Annales de biologie clinique. 73:181-183
The identification of polymorphism A4059V associated with the 12276 AG at exon 45 of the PKD1 gene in a Tunisian polycystic patient.
Autor:
Safa Sahnoun, Amina Bibi, Sondess Hadj Fredj, Taieb Messaoud, K. Boussetta, Monia Boudaya, Sabrine Oueslati, Hajer Siala, Chaima Abdelhafidh Sahli
Publikováno v:
Journal of Genetics. 92:81-83
More than 1800 CFTR (cystic fibrosis transmembrane conductance regulator gene) sequence variations have been identified in the cystic fibrosis (CF) mutation database (http://www.genet.sickkids.on.ca/cftr/). For North African populations, however, the
Autor:
Afef Achouri Rassas, Hajer Siala, Safa Sahnoun, Amina Bibi, Hela Mrabet Khiari, Amel Mrabet, Taieb Messaoud, Sondess Hadj Fredj
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996). 120(9)
We examined the potential involvement of the polymorphism in intron 8 of the presenilin-1 (PSEN1) gene as a risk factor for Alzheimer disease (AD), both through independent effect and interaction with the apolipoprotein E (APOE) e4 allele risk, in 85
Autor:
Afef Achouri Rassas, Aroua Cherif, Amel Mrabet, Sondes Hadj Fredj, Nadia Anane, Hela Mrabet Khiari, Nouria Oudiaa Zakraoui, Safa Sahnoun, Taieb Messaoud, H. Batti, Nadia Ben Ali
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 33(1)
The goal of the study was to examine the Apolipoprotein E (APOE) genotypes in a Tunisian sample of patients with Alzheimer disease (AD) and normal controls, and to compare the results with the findings from the literature. A hospital-based case–con