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Screening of ABCG5 and ABCG8 Genes for Sitosterolemia in a Familial Hypercholesterolemia Cascade Screening Program.
Circ Genom Precis Med. 2022 Jun;15(3):e003390. doi: 10.1161/CIRCGEN.121.003390. Epub 2022 May 12.
Circ Genom Precis Med. 2022.
PMID: 35549507
A novel GPIHBP1 mutation related to familial chylomicronemia syndrome: A series of cases.
Lima JG, Helena C Nobrega L, Moura Bandeira FT, Pires Sousa AG, Medeiros de Araujo Macedo TB, Cavalcante Nogueira AC, Fernandes de Oliveira Filho A, Alves RJ, Costa Gurgel Castelo MH, Silva Coelho FM, Maia RE, Lima DN, Timoteo ARS, de Melo Campos JTA.
Lima JG, et al. Among authors: costa gurgel castelo mh.
Atherosclerosis. 2021 Apr;322:31-38. doi: 10.1016/j.atherosclerosis.2021.02.020. Epub 2021 Feb 23.
Atherosclerosis. 2021.
PMID: 33706081
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Evolocumab in Pediatric Heterozygous Familial Hypercholesterolemia.
Santos RD, Ruzza A, Hovingh GK, Wiegman A, Mach F, Kurtz CE, Hamer A, Bridges I, Bartuli A, Bergeron J, Szamosi T, Santra S, Stefanutti C, Descamps OS, Greber-Platzer S, Luirink I, Kastelein JJP, Gaudet D; HAUSER-RCT Investigators.
Santos RD, et al.
N Engl J Med. 2020 Oct 1;383(14):1317-1327. doi: 10.1056/NEJMoa2019910. Epub 2020 Aug 29.
N Engl J Med. 2020.
PMID: 32865373
Clinical Trial.
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