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Multiple Endocrine Neoplasia Type 1: The Potential Role of microRNAs in the Management of the Syndrome
Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited tumor syndrome, characterized by the development of multiple neuroendocrine tumors (NETs) in a single patient. Major manifestations include primary hyperparathyroidism, gastro-entero-pancreatic neuroendocrine tumors, and pituitary adenom...
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| Vydáno v: | Int J Mol Sci |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7589704/ https://ncbi.nlm.nih.gov/pubmed/33066578 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21207592 |
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