Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII

Amyloidosis is characterized by extracellular deposition of misfolded proteins as insoluble fibrils. Most renal amyloidosis cases are Ig light chain, AA, or leukocyte chemotactic factor 2 amyloidosis, but rare hereditary forms can also involve the kidneys. Here, we describe the case of a 61-year-old...

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Detalhes bibliográficos
Publicado no:J Am Soc Nephrol
Main Authors: Nasr, Samih H., Dasari, Surendra, Hasadsri, Linda, Theis, Jason D., Vrana, Julie A., Gertz, Morie A., Muppa, Prasuna, Zimmermann, Michael T., Grogg, Karen L., Dispenzieri, Angela, Sethi, Sanjeev, Highsmith, W. Edward, Merlini, Giampaolo, Leung, Nelson, Kurtin, Paul J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2017
Assuntos:
Brief Communications
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5280007/
https://ncbi.nlm.nih.gov/pubmed/27297947
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2015111228
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