Cargando…
Low-dose Synachten test with measurement of salivary cortisol in adult patients with β-thalassemia major
PURPOSE: Beta-thalassemia major is a severe, congenital hematological disorder and, if untreated, leads to early mortality. Progress in therapeutical strategies improved clinical outcomes and life expectancy; however, increased survival led to the development of new disorders, including endocrinopat...
Autores principales: | Ambrogio, Alberto G., Danesi, Leila, Baldini, Marina, Radin, Raffaella, Cassinerio, Elena, Graziadei, Giovanna, Mirra, Nadia, D’Angelo, Emanuela, Marcon, Alessia, Mancarella, Marta, Orsatti, Alessandra, Bonetti, Federico, Scacchi, Massimo, Cappellini, Maria Domenica, Persani, Luca, Pecori Giraldi, Francesca |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893656/ https://www.ncbi.nlm.nih.gov/pubmed/29572711 http://dx.doi.org/10.1007/s12020-018-1562-z |
Ejemplares similares
-
Pregnant women affected by thalassemia major: a controlled study of traits and personality
por: Messina, Giuseppina, et al.
Publicado: (2010) -
Unexpected Genotype in a Non-Transfusion Dependent Thalassemia Family
por: Curcio, Cristina, et al.
Publicado: (2020) -
Coagulopathy in Beta-Thalassemia: Current Understanding and Future Perspectives
por: Cappellini, M. Domenica, et al.
Publicado: (2009) -
Cardiopulmonary testing in adult patients with β-thalassemia major in comparison to healthy subjects
por: Piatti, G., et al.
Publicado: (2022) -
Oocyte quality in women with thalassaemia major: insights from IVF cycles
por: Mensi, Laura, et al.
Publicado: (2019)