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A case report of heterozygous familial hypercholesterolaemia with LDLR gene mutation complicated by premature coronary artery disease detected in primary care.
Eur Heart J Case Rep. 2024 Jan 29;8(2):ytae039. doi: 10.1093/ehjcr/ytae039. eCollection 2024 Feb.
Eur Heart J Case Rep. 2024.
PMID: 38425725
Free PMC article.
Factors associated with usability of the EMPOWER-SUSTAIN Global Cardiovascular Risks Self-Management Booklet© among individuals with metabolic syndrome in primary care: a cross-sectional study.
Abdul-Halim MAZ, Baharudin N, Abdul-Hamid H, Mohamed-Yassin MS, Daud MH, Badlishah-Sham SF, Abdul-Razak S, Ramli AS.
Abdul-Halim MAZ, et al.
BMC Prim Care. 2024 Feb 3;25(1):51. doi: 10.1186/s12875-024-02281-z.
BMC Prim Care. 2024.
PMID: 38310212
Free PMC article.
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