Multiple phenotypes and epigenetic profiles in a three-generation family history with GATA2 deficiency
Damià Romero–Moya(Institut d'Investigació Biomédica de Bellvitge), Alessandra Giorgetti(Fondazione Pisa), Albert Català(Hospital Sant Joan de Déu Barcelona), Marcin W. Włodarski(St. Jude Children's Research Hospital), Alessandro Liquori(Instituto de Salud Carlos III), José Cervera(Instituto de Salud Carlos III), Javier Rodríguez‐Ubreva(Josep Carreras Leukaemia Research Institute), Oskar Marín-Béjar(Institut d'Investigació Biomédica de Bellvitge), Cristina Díaz de Heredia(Universitat Autònoma de Barcelona), Laura Murillo(Centro de Salud Casa del Barco), Joan Pera(Hospital Sant Joan de Déu Barcelona), Eric Torralba-Sales(Institut d'Investigació Biomédica de Bellvitge), María Julia Montoro(Vall d'Hebron Hospital Universitari)
Cited by 1
Related Papers
B cell–helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen
|Nature Immunology|2011|724
Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel
|Haematologica|2014|389
Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents
|Blood|2015|387
Total Body Irradiation or Chemotherapy Conditioning in Childhood ALL: A Multinational, Randomized, Noninferiority Phase III Study
|Journal of Clinical Oncology|2020|333
Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study
|Journal of Allergy and Clinical Immunology|2017|318