Phenotypes and survival in Erdheim‐Chester disease: Results from a 165‐patient cohort
Erdheim-Chester disease (ECD) is a multi-systemic non-Langerhans cell histiocytosis that is characterized by tissue infiltration of foamy histiocytes.1-3 Following the discovery that 60 to 100% of ECD patients carry the BRAFV600E mutation, ECD was recently re-classified as an inflammatory myeloid ne...
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| Hlavní autoři: | , , , , , , , , , , , |
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| Médium: | Carta |
| Jazyk: | angličtina |
| Vydáno: |
2018
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| On-line přístup: | https://doi.org/10.1002/ajh.25055 https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajh.25055 |
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