Quality of life in Italian patients with Multiple endocrine neoplasia type 1 (MEN 1): results of an extensive survey

BACKGROUND: MEN1 is a complex, rare, syndrome inherited in an autosomal dominant tract and characterized by the development of multiple neuroendocrine tumors, requiring lifelong surveillance and multiple medical and surgical therapies throughout the patient’s life. For all these reasons, a diagnosis...

Descripción completa

Detalles Bibliográficos
Autores principales: Giusti, Francesca, Cioppi, Federica, Fossi, Caterina, Marini, Francesca, Masi, Laura, Tonelli, Francesco, Brandi, Maria Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788910/
https://www.ncbi.nlm.nih.gov/pubmed/33407684
http://dx.doi.org/10.1186/s13023-020-01650-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788910/
https://www.ncbi.nlm.nih.gov/pubmed/33407684
http://dx.doi.org/10.1186/s13023-020-01650-y

Ejemplares similares