Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Théo Gremen Mimary Oliveira"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1c32df3f92a41a01617fce073037e92
https://doi.org/10.1161/circgen.121.003390
https://doi.org/10.1161/circgen.121.003390
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ff5b49694709b5d672b6887bc56e8c76
https://pubmed.ncbi.nlm.nih.gov/35549507
https://pubmed.ncbi.nlm.nih.gov/35549507
Autor:
Luciana Rodrigues Carvalho Barros, Samuel Campanelli Freitas Couto, Daniela da Silva Santurio, Emanuelle Arantes Paixão, Fernanda Cardoso, Viviane Jennifer da Silva, Paulo Klinger, Paula do Amaral Costa Ribeiro, Felipe Augusto Rós, Théo Gremen Mimary Oliveira, Eduardo Magalhães Rego, Rodrigo Nalio Ramos, Vanderson Rocha
Publikováno v:
Cancers. 14:2667
In this systematic review, we foresee what could be the approved scenario in the next few years for CAR-T cell therapies directed against hematological and solid tumor malignancies. China and the USA are the leading regions in numbers of clinical stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e50d5044e2973f65cde9ab00638cddbb
https://doi.org/10.3390/cancers14112667
https://doi.org/10.3390/cancers14112667
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:
Luciana Sacilotto, Hindalis Ballesteros Epifanio, Francisco Carlos da Costa Darrieux, Fanny Wulkan, Theo Gremen Mimary Oliveira, Denise Tessariol Hachul, Alexandre da Costa Pereira, Mauricio Ibrahim Scanavacca
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 108, Iss 1, Pp 70-73
Abstract Compound heterozygosity has been described in inherited arrhythmias, and usually associated with a more severe phenotype. Reports of this occurrence in Brugada syndrome patients are still rare. We report a study of genotype-phenotype correla
Externí odkaz:
https://doaj.org/article/129e081ca20a41d589b335d86c574a78