In silico analysis of alpha1-antitrypsin variants: The effects of a novel mutation

por Denden, Sabri, Leban, Nadia, Hayek, Donia, Knani, Jalel, Chibani, Jemni Ben, Khelil, Amel Haj
Publicado 2010

Alpha-1 antitrypsin gene polymorphism in Chronic Obstructive Pulmonary Disease (COPD)

por Denden, Sabri, Khelil, Amel Haj, Knani, Jalel, Lakhdar, Ramzi, Perrin, Pascale, Lefranc, Gérard, Chibani, Jemni Ben
Publicado 2010

Combined Analysis of EPHX1, GSTP1, GSTM1 and GSTT1 Gene Polymorphisms in Relation to Chronic Obstructive Pulmonary Disease Risk and Lung Function Impairment

por Lakhdar, Ramzi, Denden, Sabri, Knani, Jalel, Leban, Nadia, Daimi, Houria, Hassine, Mohsen, Lefranc, Gérard, Chibani, Jemni Ben, Khelil, Amel Haj
Publicado 2011

Screening for Alpha 1 antitrypsin deficiency in Tunisian subjects with obstructive lung disease: a feasibility report

por Denden, Sabri, Zorzetto, Michele, Amri, Fethi, Knani, Jalel, Ottaviani, Stefania, Scabini, Roberta, Gorrini, Marina, Ferrarotti, Ilaria, Campo, Ilaria, Chibani, Jemni Ben, Khelil, Amel Haj, Luisetti, Maurizio
Publicado 2009

Polymorphism of C3 complement in association with myocardial infarction in a sample of central Tunisia

por Leban, Nadia, Jraba, Karim, Chalghoum, Abdelkader, Hassine, Selma, Elhayek, Donia, Denden, Sabri, Lakhdhar, Ramzi, Maatoug, Faouzi, Gamra, Habib, Braham, Hammadi, Chibani, Jemni Ben, Khelil, Amel Haj
Publicado 2013