A Novel RUNX1 Genetic Variant Identified in a Young Male with Severe Osteoporosis

por Block, Tomasz J., Shore‐Lorenti, Cat, Zebaze, Roger, Kerr, Peter G., Kalff, Anna, Perkins, Andrew Charles, Ebeling, Peter R., Milat, Frances
Publicado 2023

Patient-reported Outcomes and Quality of Life in Anemic and Symptomatic Patients With Myelofibrosis: Results From the MOMENTUM Study

por Mesa, Ruben A., Harrison, Claire, Palmer, Jeanne M., Gupta, Vikas, McLornan, Donal P., McMullin, Mary Frances, Kiladjian, Jean-Jacques, Foltz, Lynda, Platzbecker, Uwe, Fox, Maria Laura, Mead, Adam J., Ross, David M., Oh, Stephen T., Perkins, Andrew Charles, Leahy, Michael F., Kawashima, Jun, Ro, Sunhee, Donahue, Rafe, Gorsh, Boris, Deheshi, Samineh, Verstovsek, Srdan
Publicado 2023