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Clinical Syndromes and Genetic Screening Strategies of Pheochromocytoma and Paraganglioma
Pheochromocytomas (PCCs) are rare neuroendocrine tumors that originate from chromaffin cells of the adrenal medulla, and paragangliomas (PGLs) are extra-adrenal pheochromocytomas. These can be mainly found in clinical syndromes including multiple endocrine neoplasia (MEN), von Hippel–Lindau (VHL) sy...
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| Publicado no: | J Kidney Cancer VHL |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Codon Publications
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6308242/ https://ncbi.nlm.nih.gov/pubmed/30613466 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15586/jkcvhl.2018.113 |
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