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Apolipoprotein A-1-related amyloidosis 2 case reports and review of the literature
RATIONALE: Apolipoprotein A-1 (ApoA-1)-related amyloidosis is characterized by the deposition of ApoA-1 in various organs and can be either hereditary or nonhereditary. It is rare and easily misdiagnosed. Renal involvement is common in hereditary ApoA-1 amyloidosis, but rare in the nonhereditary for...
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| Vydáno v: | Medicine (Baltimore) |
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| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wolters Kluwer Health
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5626298/ https://ncbi.nlm.nih.gov/pubmed/28953655 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000008148 |
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