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14. Diagnosis of familial hypercholesterolemia in general practice using clinical diagnostic criteria or genetic testing as part of cascade genetic screening. Leren TP; Finborud TH; Manshaus TE; Ose L; Berge KE Community Genet; 2008; 11(1):26-35. PubMed ID: 18196915 [TBL] [Abstract][Full Text] [Related]
16. Familial hypercholesterolemia and health information systems. Rocha E Rev Port Cardiol; 2006 Nov; 25(11):1017-23. PubMed ID: 17274458 [No Abstract] [Full Text] [Related]
17. Identification of gene mutations allows for the molecular diagnosis of familial hypercholesterolemia. Retief AE; Kotze MJ; Oosthuizen CJ S Afr Med J; 1989 Aug; 76(3):121. PubMed ID: 2762943 [No Abstract] [Full Text] [Related]
18. [How common is familial hypercholesterolemia?]. Svare A Tidsskr Nor Laegeforen; 2002 Sep; 122(21):2134. PubMed ID: 12555654 [No Abstract] [Full Text] [Related]
19. [Application of DNA analysis for differential diagnosis of familial hypercholesterolemia and familial defect of apolipoprotein b-100]. Krapivner SR; Malyshev PP; Rozhkova TA; Potaraus AB; Kukharchuk VV; Bochkov VN Ter Arkh; 2000; 72(4):9-12. PubMed ID: 10833789 [TBL] [Abstract][Full Text] [Related]
20. Screening for familial hypercholesterolemia: what is the most effective strategy? Daniels SR Nat Clin Pract Cardiovasc Med; 2008 Mar; 5(3):130-1. PubMed ID: 18059381 [No Abstract] [Full Text] [Related] [Next] [New Search]