Lin M, Paik E, Mishra B, et al. Re-creating hereditary persistence of fetal hemoglobin (PHFH) with CRISPR/CAS9 to treat sickle cell disease (SCD) and beta-thalassemia (beta-thal). EHA 2017, abstract S147.
Langetermijnfollow-up van MGUS
apr 2018
jun 2024 | Niertransplantatie, Stamceltransplantatie, Virale infecties
okt 2020
apr 2020 | Transplantatie
apr 2020
jan 2020 | Leukemie