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Acute Hepatic Porphyrias: Recommendations for Evaluation and Long Term Management

The acute hepatic porphyrias (AHPs) are a group of four inherited disorders, each resulting from the deficient activity of a specific enzyme in the heme biosynthetic pathway. They present clinically with acute neurovisceral symptoms which may be sporadic or recurrent, and which, when severe, can be...

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Bibliografski detalji
Izdano u:Hepatology
Glavni autori: Balwani, Manisha, Wang, Bruce, Anderson, Karl E., Bloomer, Joseph R., Bissell, D. Montgomery, Bonkovsky, Herbert L., Phillips, John D., Desnick, Robert J.
Format: Artigo
Jezik:Inglês
Izdano: 2017
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5605422/
https://ncbi.nlm.nih.gov/pubmed/28605040
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hep.29313
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