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Complements Spurned: Our Experience with Atypical Hemolytic Uremic Syndrome
Atypical hemolytic uremic syndrome (aHUS) is a rare disorder resulting from a dysregulated activation of the alternative pathway of the complement system. It results in significant morbidity and mortality if not diagnosed and treated promptly. It lends itself to myriad renal and extrarenal manifesta...
Tallennettuna:
| Julkaisussa: | Indian J Crit Care Med |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications & Media Pvt Ltd
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5330049/ https://ncbi.nlm.nih.gov/pubmed/28250608 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijccm.IJCCM_341_16 |
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