Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maria Eduarda Cardoso de Melo"'
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:
Maria Eduarda Cardoso de Melo, Aquiles Sales Craveiro Sarmento, Josivan Gomes de Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
Genética na Escola. 15:72-79
O gene AGPAT2 codifica para a proteína 1-acil-sn-glicerol-3- fosfato aciltransferase 2. Mutações na sequência nucleotídica do gene AGPAT2 resultam na rara síndrome de Berardinelli-Seip do tipo 1, também conhecida como Lipodistrofia Congênita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2647f0b7490f97272413e895ae3ede0
https://doi.org/10.55838/1980-3540.ge.2020.328
https://doi.org/10.55838/1980-3540.ge.2020.328
Autor:
Lucymara Fassarella Agnez Lima, Maria Eduarda Cardoso de Melo, Julliane Tamara Araújo de Melo Campos, Guilherme Fregonezi, Aquiles Sales Craveiro Sarmento, Matheus Oliveira de Sena, Jorge Luiz Dantas De Medeiros, Monique Alvares da Silva, Josivan Gomes de Lima
Publikováno v:
Biochimica et biophysica acta. Molecular basis of disease. 1867(6)
Lipodystrophy syndromes are a group of rare diseases related to the pathological impairment of adipose tissue and metabolic comorbidities, including dyslipidemia, diabetes, insulin resistance, hypoleptinemia, and hypoadiponectinemia. They can be cate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7558a5d4c9c9c3e4b63ee89c4ff6422
https://pubmed.ncbi.nlm.nih.gov/33713793
https://pubmed.ncbi.nlm.nih.gov/33713793