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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587527/
https://www.ncbi.nlm.nih.gov/pubmed/30394579
http://dx.doi.org/10.1002/ajh.25343

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587527/
https://www.ncbi.nlm.nih.gov/pubmed/30394579
http://dx.doi.org/10.1002/ajh.25343

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