טוען...
A complementary component to atypical haemolytic uraemic syndrome
We describe a case of a 22-year-old man who presented with clinical features of atypical haemolytic uraemic syndrome and in whom genetic analysis of complement regulatory proteins demonstrated a CD46 mutation. He was treated with plasma exchange, intermittent haemodialysis and blood transfusions. At...
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| Main Authors: | , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMJ Publishing Group
2013
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3702985/ https://ncbi.nlm.nih.gov/pubmed/23780777 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2013-010214 |
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