Cascade Screening in Familial Hypercholesterolemia: Advancing Forward
Author:
Affiliation:
1. Lipid Clinic, Heart Institute (InCor), University of São Paulo Medical School Hospital
2. Laboratory of Immungenetic, Arthur de Siqueira Cavalcanti Hematology Institute (HEMORIO)
Publisher
Japan Atherosclerosis Society
Subject
Biochemistry, medical,Cardiology and Cardiovascular Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/jat/22/9/22_31237/_pdf
Reference103 articles.
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2. 2) Austin MA, Hutter CM, Zimmern RL, Humphries SE: Genetic causes of monogenic heterozygous familial hypercholesterolaemia: a HuGE prevalence review. Am J Epidemiol, 2004; 160: 407-420
3. 3) Benn M, Watts GF, Tybjaerg-Hansen A, Nordestgaard BG: Familial hypercholesterolemia in the Danish general population: prevalence, coronary artery disease, and cholesterol-lowering medication. J Clin Endocrinol Metab, 2012; 97: 3956-3964
4. 4) Nordestgaard BG, Chapman MJ, Humphries SE, Ginsberg HN, Masana L, Descamps OS, Wiklund O, Hegele RA, Raal FJ, Defesche JC, Wiegman A, Santos RD, Watts GF, Parhofer KG, Hovingh GK, Kovanen PT, Boileau C, Averna M, Borén J, Bruckert E, Catapano AL, Kuivenhoven JA, Pajukanta P, Ray K, Stalenhoef AF, Stroes E, Taskinen MR, Tybjærg-Hansen A; European Atherosclerosis Society Consensus Panel: Familial hypercholesterolaemia is under diagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease Consensus Statement of the European Atherosclerosis Society. Eur Heart J, 2013; 34, 3478-3490
5. 5) Modell SM, Kardia SL, Citrin: Stakeholder consultation insights on the future of genomics at the clinical-public health interface. Transl Res, 2014; 163: 466-477
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