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SDH-related Pheochromocytoma and paraganglioma
Pheochromocytoma and paraganglioma are rare tumors of adrenals as well as the sympathetic and parasympathetic paraganglia. Clinical presentation of these tumors depends on localization, secretory profile and malignant potential. Four distinct syndromes - PGL1–4 - are related to mutations in the succ...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2939070/ https://ncbi.nlm.nih.gov/pubmed/20833333 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.beem.2010.04.001 |
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