A 13-bp deletion in α(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia

Por ROSENBERG, N., HAUSCHNER, H., PERETZ, H., MOR-COHEN, R., LANDAU, M., SHENKMAN, B., KENET, G., COLLER, B. S., AWIDI, A. A., SELIGSOHN, U.
Publicado em 2005

Delayed Inflammatory Reactions to Hyaluronic Acid Fillers: A Literature Review and Proposed Treatment Algorithm

Por Artzi O, Cohen JL, Dover JS, Suwanchinda A, Pavicic T, Landau M, Goodman GJ, Ghannam S, Al Niaimi F, van Loghem JAJ, Goldie K, Sattler S, Cassuto D, Lim TS, Wanitphakdeedecha R, Verner I, Fischer TC, Bucay V, Sprecher E, Shalmon D
Publicado em 2020-05-01