Two cases of carbonic anhydrase VA deficiency—An ultrarare metabolic decompensation syndrome presenting with hyperammonemia, lactic acidosis, ketonuria, and good clinical outcome

por Marwaha, Ashish, Ibrahim, Judy, Rice, Taylor, Hamwi, Nadia, Rupar, Charles Anthony, Cresswell, David, Prasad, Chitra, Schulze, Andreas
Publicado 2020

Rapid and Efficient Stable Gene Transfer to Mesenchymal Stromal Cells Using a Modified Foamy Virus Vector

por Sweeney, Nathan Paul, Regan, Cathy, Liu, Jiahui, Galleu, Antonio, Dazzi, Francesco, Lindemann, Dirk, Rupar, Charles Anthony, McClure, Myra Olga
Publicado 2016