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Identifying suspected familial chylomicronemia syndrome
Familial chylomicronemia syndrome (FCS) is a rare lipid disorder posing significant clinical burdens on patients. Due to its rarity, variety of presentations, and lack of universal diagnostic criteria, patients see an average of five physicians before diagnosis. We screened adults for a triglyceride...
Uloženo v:
| Vydáno v: | Proc (Bayl Univ Med Cent) |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Taylor & Francis
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5997083/ https://ncbi.nlm.nih.gov/pubmed/29904289 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/08998280.2018.1463784 |
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