MEFV gene mutations in Egyptian children with Henoch-Schonlein purpura

por Salah, Samia, Rizk, Samia, Lotfy, Hala M, EL Houchi, Salma, Marzouk, Huda, Farag, Yomna
Publicado 2014

Diagnostic Performance Analysis of the Point-of-Care Bilistick System in Identifying Severe Neonatal Hyperbilirubinemia by a Multi-Country Approach

por Greco, Chiara, Iskander, Iman F., El Houchi, Salma Z., Rohsiswatmo, Rinawati, Rundjan, Lily, Ogala, Williams N., Ofakunrin, Akinyemi O.D., Moccia, Luciano, Hoi, Nguyen Thi Xuan, Bedogni, Giorgio, Tiribelli, Claudio, Coda Zabetta, Carlos D.
Publicado 2018