Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mauricio Teruo, Tada"'
Autor:
Isabella Ramos Lima, Mauricio Teruo Tada, Theo G.M. Oliveira, Cinthia Elim Jannes, Isabela Bensenor, Paulo A. Lotufo, Raul D. Santos, Jose E. Krieger, Alexandre C. Pereira
Publikováno v:
Atherosclerosis Plus, Vol 49, Iss , Pp 47-55 (2022)
Background and aims: Familial hypercholesterolemia (FH) is a genetic disorder characterized by high levels of LDL-C leading to premature cardiovascular disease (CAD). Only about 40% of individuals with a clinical diagnosis of FH have a causative gene
Externí odkaz:
https://doaj.org/article/91bd4a9f5d294aae81f1d9573bdd8f2f
Autor:
Cinthia Elim Jannes, Júnea Paolucci Paiva Silvino, Pãmela Rodrigues de Souza Silva, Isabella Ramos Lima, Mauricio Teruo Tada, Theo Gremen Mimary Oliveira, Raul D. Santos, José Eduardo Krieger, Alexandre da Costa Pereira
Publikováno v:
Arquivos Brasileiros de Cardiologia (2022)
Resumo Fundamento A hipercolesterolemia familiar (HF) é uma doença genética dominante que se caracteriza por níveis sanguíneos elevados de colesterol de lipoproteína de baixa densidade (LDL-C), e está associada à ocorrência de doença cardio
Externí odkaz:
https://doaj.org/article/c5e03c2829484bf785ba733811c95a26
Autor:
Viviane Zorzanelli Rocha, Mauricio Teruo Tada, Ana Paula Marte Chacra, Marcio Hiroshi Miname, Marjorie H. Mizuta
Publikováno v:
Current Atherosclerosis Reports. 25:181-187
Autor:
Mauricio Teruo Tada
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Introdução: A Hipercolesterolemia Familiar (HF) é uma doença autossômica dominante que resulta no aumento da concentração do colesterol total e LDL colesterol no plasma, aumentando o risco do desenvolvimento de doença cardiovascular em idade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48920d32cf57a9d795398ad23d4ac15c
https://doi.org/10.11606/d.5.2022.tde-19012023-111803
https://doi.org/10.11606/d.5.2022.tde-19012023-111803
Autor:
Erika Macedo da silva, MAURICIO TERUO TADA, NATALIA CRUZ E MELO, ANDREA SANTOS LIMA, RENATA DE ALMEIDA COUDRY
Publikováno v:
Anais do III Congresso Brasileiro de Biologia Molecular On-line.
Autor:
Erika Macedo da silva, MAURICIO TERUO TADA, SIBELE INACIO MEIRELES, KATHARYNA CARDOSO DE GOIS, JAINE SOARES LIMA DA SILVA
Publikováno v:
Anais do III Congresso Brasileiro de Biologia Molecular On-line.
Autor:
NATALIA CRUZ E MELO, MAURICIO TERUO TADA, ROXANNE HATANAKA, ROSELAINE SILVA BARROSO, ERIKA MACEDO DA SILVA
Publikováno v:
Anais do II Congresso Brasileiro de Doenças Infectocontagiosas On-line.
Autor:
José Eduardo Krieger, Mauricio Teruo Tada, Alexandre C. Pereira, Raquel Arroyo-Olivares, Ovidio Muñiz-Grijalvo, Luiza Antoniazzi, Márcio Sommer Bittencourt, Pedro Mata, José Luis Díaz-Díaz, Cinthia E. Jannes, Isabella Ramos Lima, Gracia M. Quintana-Navarro, Rodrigo Alonso, Raul D. Santos
Publikováno v:
Nutrition, Metabolism and Cardiovascular Diseases. 31:2014-2022
Familial Hypercholesterolemia (FH) is characterized by elevated LDL-cholesterol (LDL-C) and high atherosclerosis risk. The impact of different dietary patterns on atherosclerosis biomarkers has been poorly studied in FH. This study verified the assoc
Autor:
Mauricio Teruo Tada, Viviane Zorzanelli Rocha, Isabella Ramos Lima, Théo Gremen Mimary Oliveira, Ana Paula Chacra, Marcio Hiroshi Miname, Valéria Sutti Nunes, Edna Regina Nakandakare, Maria Helane Costa Gurgel Castelo, Cinthia Elim Jannes, Raul D. Santos, José Eduardo Krieger, Alexandre Costa Pereira
Publikováno v:
Circulation: Genomic and Precision Medicine. 15
Background: Sitosterolemia is a rare autosomal recessive disorder caused by homozygous or compound heterozygous variants in ABCG5/ABCG8 . The disease is characterized by increased plasma plant sterols. Small case series suggest that patients with sit
Autor:
Mauricio Teruo, Tada, Viviane Zorzanelli, Rocha, Isabella Ramos, Lima, Théo Gremen Mimary, Oliveira, Ana Paula, Chacra, Marcio Hiroshi, Miname, Valéria Sutti, Nunes, Edna Regina, Nakandakare, Maria Helane, Costa Gurgel Castelo, Cinthia Elim, Jannes, Raul D, Santos, José Eduardo, Krieger, Alexandre Costa, Pereira
Publikováno v:
Circulation. Genomic and precision medicine. 15(3)
Sitosterolemia is a rare autosomal recessive disorder caused by homozygous or compound heterozygous variants inFrom 443 familial hypercholesterolemia index cases, 260 were negative for familial hypercholesterolemia genes and were sequenced for theEig