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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...
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| 出版年: | Orphanet J Rare Dis |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7788910/ https://ncbi.nlm.nih.gov/pubmed/33407684 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-01650-y |
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