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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...
Sparad:
| Huvudupphovsmän: | , , , , |
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| Materialtyp: | Artigo |
| Språk: | Russo |
| Publicerad: |
Remedium Group LLC
2018-10-01
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| Serie: | Медицинский совет |
| Ämnen: | |
| Länkar: | https://www.med-sovet.pro/jour/article/view/2728 |
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