Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine

por Mohammed, Fawziah, Elshafey, Alaa, Al-balool, Haya, Alaboud, Hayat, Al Ben Ali, Mohammed, Baqer, Adel, Bastaki, Laila
Publicado 2018

NOD2/CARD15 polymorphisms (P268S, IVS8(+158), G908R, L1007fs, R702W) among Kuwaiti patients with Crohn's disease: A case-control study

por Abdelnaby, Hassan, Ndiaye, Ndeye Coumba, D'Amico, Ferdinando, Fouad, Ahmed Mahmoud, Hassan, Sameh, Elshafey, Alaa, Al Hashash, Wafaa, Faisal, Mohammed, Alshamali, Yousef, Al-Taweel, Talal, Peyrin-Biroulet, Laurent
Publicado 2021