Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Fatma Ezzahra Gahbiche"'
Autor:
Matthias Welsner, Sarah Dietz-Terjung, Florian Stehling, Tim Schulte, Ute Niehammer, Fatma-Ezzahra Gahbiche, Christian Taube, Svenja Strassburg, Christoph Schoebel, Gerhard Weinreich, Sivagurunathan Sutharsan
Publikováno v:
BMC Pulmonary Medicine, Vol 22, Iss 1, Pp 1-12 (2022)
Abstract Background Obstructive sleep apnea (OSA), nocturnal hypoxemia and excessive daytime sleepiness (EDS) are common comorbidities in people with cystic fibrosis (pwCF). Most of the data showing this originates from children and adolescents. The
Externí odkaz:
https://doaj.org/article/0343ef958efc494e9fcf795bec7b0f74
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