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Missed clinical clues in patients with pheochromocytoma/paraganglioma discovered by imaging
BACKGROUND: Pheochromocytomas and paragangliomas (PPGLs) are rare but potentially harmful tumors that can vary in their clinical presentation. Tumors may be found due to signs and symptoms, as part of a hereditary syndrome or following an imaging procedure. OBJECTIVE: To investigate potential differ...
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| Vydáno v: | Endocr Connect |
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| Hlavní autoři: | , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Bioscientifica Ltd
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6215794/ https://ncbi.nlm.nih.gov/pubmed/30352425 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EC-18-0318 |
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