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Late‐onset hemophagocytic lymphohistiocytosis with neurological presentation
Missense mutations in genes involved in familial hemophagocytic lymphohistiocytosis can delay the onset of this life‐threatening disease. In children and adults, early recognition of aspecific features as neurological symptoms is crucial as urgent treatment is required.
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Clin Case Rep |
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| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
John Wiley and Sons Inc.
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5676276/ https://ncbi.nlm.nih.gov/pubmed/29152263 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1135 |
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