ロード中...
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.
保存先:
| 出版年: | Clin Case Rep |
|---|---|
| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2017
|
| 主題: | |
| オンライン･アクセス: | 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 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|