Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Afef Achouri-Rassas"'
Publikováno v:
Journal of genetics. 101
In this study, we investigate the impact of apolipoprotein E epsilon 4 (APOE ε4) as a major risk factor of Alzheimer's disease (AD), based on the clinical presentation of the disease in our population on the one hand, and comparison of the results w
Publikováno v:
Journal of Genetics. 101
Autor:
Saloua Fray, Afef Achouri-Rassas, Mariem Safia Ben Mahmoud, Hela Jamoussi, Nouria Oudia, Nadia Ben Ali, Mohamed Fredj
Publikováno v:
Revue Neurologique. 179:S10
Autor:
Faten Alaya, Afef Achouri-Rassas, Hela Jamoussi, Nadia Ben Ali, Amel Salhi Hannachi, Fradj Mohamed, Ghada Baraket
Publikováno v:
Revue Neurologique. 178:S133-S134
Autor:
Saloua Fray, Afef Achouri-Rassas, Nadia Ben Ali, Hela Jamoussi, Cherif Aroua, Taieb Messaoud, Fradj Mohamed
Publikováno v:
Revue Neurologique. 178:S4
Autor:
Afef Achouri-Rassas, Mohamed Zakaria Saied, Fray Saloua, Taieb Messaoud, Samir Blel, Samia Ben Sassi
Publikováno v:
Revue Neurologique. 178:S5
Publikováno v:
Revue Neurologique. 177:S5-S6
Introduction L’allele e4 du gene APOE est etabli principal facteur de risque genetique de la maladie d’Alzheimer, mais son association avec d’autres types de demence et avec le « Mild cognitive impairment » (MCI) n’est pas evidente. Objecti
Publikováno v:
Neurocase. 26(3)
Mutations in the presenilin-1 gene (PSEN1) on chromosome 14 are the most common cause of autosomal dominant Alzheimer's disease (ADAD), which has a broad clinical phenotype, encompassing not only dementia but a variety of other neurological features.
Autor:
Aroua Cherif, Samir Belal, Nadia Ben Ali, Nadia Anane, Saloua Fray, Sondes Hadj-Fredj, Mariem Kechaou, Nouria Oudiaa Zakraoui, Slim Echebi, Afef Achouri-Rassas, Taieb Messaoud, Hajer Siala
Publikováno v:
Journal of Neural Transmission. 123:317-321
Angiotensin-converting enzyme (ACE) has shown altered activity in patients with neurological diseases. An insertion/deletion (I/D) polymorphism of the ACE gene encoding angiotensin-converting enzyme has been reported to be associated with the risk fo
Autor:
Aroua Cherif, Samir Belal, S. Echebbi, Afef Achouri Rassas, Nouria Oudiaa, Meriem Kechaou, Saloua Fray, Nadia Ben Ali, Taieb Messaoud
Publikováno v:
Journal of Neural Transmission. 123:451-453
Several clinical phenotypes were associated with presenilin 1 (PSEN1) mutation in early-onset familial Alzheimer's disease (EOFAD). We report the clinical phenotype of two members of a familial dementia kindred who presented with EOFAD and early psyc