Zobrazeno 1 - 3
of 3
pro vyhledávání: '"M H Muhmad Hamidi"'
Publikováno v:
The Malaysian journal of pathology. 44(3)
Homozygous familial hypercholesterolaemia (FH) is a rare genetic disorder with aberrantly high level of low-density lipoprotein cholesterol (LDL-C) requiring multiple combined aggressive lipidlowering therapy to reduce the progression of atherosclero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e0b264b330bc71cb324040ba25e5f402
https://pubmed.ncbi.nlm.nih.gov/36591721
https://pubmed.ncbi.nlm.nih.gov/36591721
Autor:
R Raja Shariff, K S Ibrahim, H A Zainal Abidin, A B Md Radzi, M H Muhmad Hamidi, H Sani, S Kasim
Publikováno v:
European Heart Journal. 43
Funding Acknowledgements Type of funding sources: None. Background With advancement in valvular interventions, outcomes of valvular heart disease (VHD) patients have improved dramatically. However, very little is known regarding levels of knowledge a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1108737fe98ce131b1154feaef5c3ad7
https://doi.org/10.1093/eurheartj/ehab849.106
https://doi.org/10.1093/eurheartj/ehab849.106
