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Homozygous familial hypercholesterolemia: modern aspects of pathogenesis, diagnostics and treatment
Homozygous familial hypercholesterolemia is a rare genetic disease featuring extremely high of low-density lipoprotein blood level, cutaneous and tendon xanthomas and accelerated atherosclerosis with often manifestions in the first 2 decades of life, resulting to premature death due to atheroscleros...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Russo |
| Julkaistu: |
Remedium Group LLC
2018-10-01
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| Sarja: | Медицинский совет |
| Aiheet: | |
| Linkit: | https://www.med-sovet.pro/jour/article/view/2728 |
| Tagit: |
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