Cargando…
Patient- and Caregiver-Reported Burden of Transfusion-Dependent β-Thalassemia Measured Using a Digital Application
BACKGROUND AND OBJECTIVE: Transfusion-dependent β-thalassemia (TDT) is a rare genetic disease characterized by a deficiency of functional β-globin, ultimately leading to lifelong dependence on blood transfusions. There is little patient- and caregiver-reported data with which to understand the holis...
Autores principales: | Paramore, Clark, Levine, Laurice, Bagshaw, Emma, Ouyang, Chengyu, Kudlac, Amber, Larkin, Mark |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884594/ https://www.ncbi.nlm.nih.gov/pubmed/33123986 http://dx.doi.org/10.1007/s40271-020-00473-0 |
Ejemplares similares
-
Health state utilities associated with treatment for transfusion-dependent β-thalassemia
por: Matza, Louis S., et al.
Publicado: (2019) -
Economic evaluation of betibeglogene autotemcel (Beti-cel) gene addition therapy in transfusion-dependent β-thalassemia
por: Kansal, Anuraag R., et al.
Publicado: (2021) -
Psychiatric disorders and caregiver burden in children with transfusion dependent β-thalassaemia and their caregivers
por: Sahu, Samiksha, et al.
Publicado: (2023) -
Hydroxyurea Treatment in Transfusion-Dependent β-Thalassemia Patients
por: Bordbar, Mohammad Reza, et al.
Publicado: (2014) -
β-Thalassemia Mutations among Transfusion-Dependent Thalassemia Major Patients in Northern Iraq
por: Al-Allawi, Nasir A. S., et al.
Publicado: (2010)