Development of a patient‐reported outcomes symptom measure for patients with nontransfusion‐dependent thalassemia (NTDT‐PRO(©))

β‐Thalassemia, a hereditary blood disorder caused by reduced or absent synthesis of the β‐globin chain of hemoglobin, is characterized by ineffective erythropoiesis, and can manifest as nontransfusion‐dependent thalassemia (NTDT) or transfusion‐dependent thalassemia (TDT). Many patients with NTDT de...

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Detalhes bibliográficos
Publicado no:Am J Hematol
Main Authors: Taher, Ali, Viprakasit, Vip, Cappellini, Maria Domenica, Sutcharitchan, Pranee, Ward, Richard, Mahmoud, Dalia, Laadem, Abderrahmane, Khan, Anzalee, Gwaltney, Chad, Harding, Gale, Attie, Kenneth, Zhang, Xiaosha, Zou, Jun, Pariseau, Joseph, Hu, X. Henry, Kattamis, Antonis
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Inc. 2018
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6587527/
https://ncbi.nlm.nih.gov/pubmed/30394579
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajh.25343
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