Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Sales Craveiro Sarmento A"'
Autor:
Ana Clara Gomes Lima, Geissiane Felizardo Vivian, José Cleyton de Oliveira Santos, Aquiles Sales Craveiro-Sarmento, Ricardo Barbosa-Lima, Glebson Moura Silva
Publikováno v:
HSJ, Vol 14, Iss 1 (2024)
Objective: To evaluate health promotion and prevention in the Brazilian Unified Health System (SUS) between 2008 and 2022. Method: An epidemiological study was conducted, with an ecological approach, as a time series. APPS-related data available in t
Externí odkaz:
https://doaj.org/article/4c0e48919c4041b7a1b1a851b2430909
Autor:
Jorge Luiz Dantas de Medeiros, Bruno Carneiro Bezerra, Helen Rainara Araújo Cruz, Katarina Azevedo de Medeiros, Maria Eduarda Cardoso de Melo, Aquiles Sales Craveiro Sarmento, Marcela Abbott Galvão Ururahy, Lucymara Fassarella Agnez Lima, Alcebíades José dos Santos Neto, Josivan Gomes Lima, Vanessa Resqueti, Lucien Peroni Gualdi, Guilherme Fregonezi, Julliane Tamara Araújo de Melo Campos
Publikováno v:
BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-14 (2022)
Abstract Background Congenital Generalized Lipodystrophy (CGL) is an ultra-rare disease characterized by metabolic disorders. However, the evaluation of functional exercise capacity, cardiovascular (CV) response to exercise, and peripheral arterial d
Externí odkaz:
https://doaj.org/article/d159033567974215a1d75ed58a0b351c
Autor:
Araújo de Melo Campos, Julliane Tamara, Dantas de Medeiros, Jorge Luiz, Cardoso de Melo, Maria Eduarda, Alvares da Silva, Monique, Oliveira de Sena, Matheus, Sales Craveiro Sarmento, Aquiles, Fassarella Agnez Lima, Lucymara, de Freitas Fregonezi, Guilherme Augusto, Gomes Lima, Josivan
Publikováno v:
In BBA - Molecular Basis of Disease 1 June 2021 1867(6)
Autor:
Ricardo Barbosa Lima, Taigor Alves Azevedo, Amanda Lopes, Aquiles Sales Craveiro Sarmento, Carlos Eduardo Palanch Repeke
Publikováno v:
Revista da Faculdade de Odontologia de Porto Alegre, Vol 61, Iss 1, Pp 105-110 (2020)
Introduction: Tricho-dento-osseous syndrome is a ultra-rare ectodermal dysplasia related to genetic alterations in the DLX3 gene of interest to the health sciences due to its clinical manifestations. Aim: To synthesize the scientific evidence about t
Externí odkaz:
https://doaj.org/article/bbe175bfdf414c16a785a4d5cf2e6d9e
Autor:
Jorge Luiz Dantas de Medeiros, Bruno Carneiro Bezerra, Thiago Anderson Brito de Araújo, Aquiles Sales Craveiro Sarmento, Lázaro Batista de Azevedo Medeiros, Lucien Peroni Gualdi, Maria do Socorro Luna Cruz, Thaiza Teixeira Xavier Nobre, Josivan Gomes Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
Respiratory Research, Vol 19, Iss 1, Pp 1-11 (2018)
Abstract Background Berardinelli-Seip Congenital Generalized Lipodystrophy (BSCL) is an ultra-rare metabolic disease characterized by hypertriglyceridemia, hyperinsulinemia, hyperglycemia, hypoleptinemia, and diabetes mellitus. Although cardiovascula
Externí odkaz:
https://doaj.org/article/f2d814d5ef1d44e7880b225b27c456e7
Autor:
João Vitor Silva, Bruno Henrique E Silva Bezerra, Rayssa Maria Do Nascimento, Jocellem Alves de Medeiros, Virgínia Thalita Da Silva, Lázaro Batista De Azevedo Medeiros, Aquiles Sales Craveiro Sarmento, Jane Carla De Souza, Julliane Tamara Araújo de Melo Campos
Publikováno v:
Revista Extensão em Ação. 23:70-79
Os Cursos de Férias de Morfofisiologia Humana têm sido realizados desde 2012 para estudantes do ensino médio das escolas públicas do Trairi, no estado do Rio Grande do Norte. O presente trabalho objetivou demonstrar os seus resultados positivos n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c93ebe57c4246c1ec4aed0fee857939
https://doi.org/10.32356/exta.v23.n1.41683
https://doi.org/10.32356/exta.v23.n1.41683
Autor:
Lázaro Batista de Azevedo Medeiros, Verônica Kristina Cândido Dantas, Aquiles Sales Craveiro Sarmento, Lucymara Fassarella Agnez-Lima, Adriana Lúcia Meireles, Thaiza Teixeira Xavier Nobre, Josivan Gomes de Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 9, Iss 1, Pp 1-6 (2017)
Abstract Background Berardinelli-Seip Congenital Lipodystrophy (BSCL) is a rare disease characterized by the almost complete absence of adipose tissue. Although a large number of BSCL cases was previously identified in Rio Grande do Norte (RN), a sta
Externí odkaz:
https://doaj.org/article/bd469e6262c245ff8cc9f66b09ca263b
Autor:
Geissiane Felizardo Vivian, Aline da Silva Frajuca, Kaisa Silva Nascimento de Gois, Davi Moreira Santana, Ricardo Barbosa Lima, Taíssa Cássia de Souza Furtado, Paula Iáddia Zarpellon Barbosa, Mariana Ferreira Ramos, Aquiles Sales Craveiro Sarmento, Roberto dos Santos Lacerda, Simone Yuriko Kameo
Publikováno v:
Science, Society and Emerging Technologies ISBN: 9786553811058
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69831d3a0cbccc3c6fd0678b46c2527c
https://doi.org/10.51859/amplla.sset.1123-5
https://doi.org/10.51859/amplla.sset.1123-5
Autor:
Verônica Kristina Cândido Dantas, Joice da Silva Soares, Lázaro Batista de Azevedo Medeiros, Aquiles Sales Craveiro Sarmento, Thaiza Teixeira Xavier Nobre, Fábia Barbosa de Andrade, Josivan Gomes de Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0197784 (2018)
Berardinelli-Seip Congenital Lipodystrophy (BSCL) is a rare autosomal recessive disease characterized by the almost complete absence of adipose tissue. Due to a strong founder effect that resulted in a higher prevalence of BSCL in Rio Grande do Norte
Externí odkaz:
https://doaj.org/article/969b9eee78494548a3f7c0021a75dac2
Autor:
Aquiles Sales Craveiro Sarmento, Lázaro Batista de Azevedo Medeiros, Lucymara Fassarella Agnez-Lima, Josivan Gomes Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
International Journal of Cell Biology, Vol 2018 (2018)
Seipin is a nonenzymatic protein encoded by the BSCL2 gene. It is involved in lipodystrophy and seipinopathy diseases. Named in 2001, all seipin functions are still far from being understood. Therefore, we reviewed much of the research, trying to fin
Externí odkaz:
https://doaj.org/article/d2a440ecee854ee8b36efd6a0a56b2f2