Familial hypercholesterolemia in Brazil: Cascade screening program, clinical and genetic aspects (2015)
- Authors:
- USP affiliated authors: SANTOS FILHO, RAUL DIAS DOS - FM ; KRIEGER, JOSE EDUARDO - FM
- Unidade: FM
- DOI: 10.1016/j.atherosclerosis.2014.11.009
- Subjects: MUTAÇÃO GENÉTICA; APOLIPOPROTEÍNAS; LIPÍDEOS; HIPERCOLESTEROLEMIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Atherosclerosis
- ISSN: 0021-9150
- Volume/Número/Paginação/Ano: v. 238, n. 1, p. 101-107, 2015
- Status:
- Artigo possui versão em acesso aberto em repositório (Green Open Access)
- Versão do Documento:
- Versão submetida (Pré-print)
- Acessar versão aberta:
-
ABNT
JANNES, Cinthia E. et al. Familial hypercholesterolemia in Brazil: Cascade screening program, clinical and genetic aspects. Atherosclerosis, v. 238, n. 1, p. 101-107, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.atherosclerosis.2014.11.009. Acesso em: 07 maio 2026. -
APA
Jannes, C. E., Santos, R. D., Silva, P. R. de S., Turolla, L., Gagliardi, A. C. M., Marsiglia, J. D. C., et al. (2015). Familial hypercholesterolemia in Brazil: Cascade screening program, clinical and genetic aspects. Atherosclerosis, 238( 1), 101-107. doi:10.1016/j.atherosclerosis.2014.11.009 -
NLM
Jannes CE, Santos RD, Silva PR de S, Turolla L, Gagliardi ACM, Marsiglia JDC, Chacra AP, Miname MH, Rocha VZ, Salgado Filho W, Krieger JE, Pereira AC. Familial hypercholesterolemia in Brazil: Cascade screening program, clinical and genetic aspects [Internet]. Atherosclerosis. 2015 ; 238( 1): 101-107.[citado 2026 maio 07 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2014.11.009 -
Vancouver
Jannes CE, Santos RD, Silva PR de S, Turolla L, Gagliardi ACM, Marsiglia JDC, Chacra AP, Miname MH, Rocha VZ, Salgado Filho W, Krieger JE, Pereira AC. Familial hypercholesterolemia in Brazil: Cascade screening program, clinical and genetic aspects [Internet]. Atherosclerosis. 2015 ; 238( 1): 101-107.[citado 2026 maio 07 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2014.11.009 - Presence and type of low density lipoprotein receptor (LDLR) mutation influences the lipid profile and response to lipid-lowering therapy in Brazilian patients with heterozygous familial hypercholesterolemia
- Predictors of Family Enrollment in a Genetic Cascade Screening Program for Familial Hypercholesterolemia
- Evaluation of clinical and laboratory parameters used in the identification of index cases for genetic screening of familial hypercholesterolemia in Brazil
- Predictors of cardiovascular events after one year of molecular screening for Familial hypercholesterolemia
- Health related quality of life in individuals at high risk for familial hypercholesterolemia undergoing genetic cascade screening in Brazil
- Phenotypical, Clinical, and Molecular Aspects of Adults and Children With Homozygous Familial Hypercholesterolemia in Iberoamerica
- Clinical and molecular aspects of familial hypercholesterolemia in Ibero-American countries
- Cardiovascular disease onset in old people with severe hypercholesterolemia
- Cardiovascular disease and cholesterol lowering therapy in women and men with molecularly defined heterozygous familial hypercholesterolemia from Brazil
- Long-term efficacy and safety of mipomersen in patients with familial hypercholesterolaemia: 2-year interim results of an open-label extension
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