Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Larissa G. Gomes"'
Autor:
Beatriz D. S. F. Bonamichi, Stella L. M. Santiago, Débora R. Bertola, Chong A. Kim, Nivaldo Alonso, Berenice B. Mendonca, Tania A. S. S. Bachega, Larissa G. Gomes
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 60, Iss 5, Pp 500-504 (2016)
SUMMARY P450 oxidoreductase deficiency (PORD) is a variant of congenital adrenal hyperplasia that is caused by POR gene mutations. The POR gene encodes a flavor protein that transfers electrons from nicotinamide adenine dinucleotide phosphate (NADPH)
Externí odkaz:
https://doaj.org/article/df86afc9d68f45c9ab37d97e9ef92f6a
Autor:
Gustavo A.Rosa Maciel, Ricardo P.P. Moreira, Diogo D.G. Bugano, Sylvia A.Y. Hayashida, José A.M. Marcondes, Larissa G. Gomes, Berenice B. Mendonça, Tânia A.S.S. Bachega, Edmund C. Baracat
Publikováno v:
Clinics, Vol 69, Iss 3, Pp 179-184 (2014)
OBJECTIVES: We aimed to investigate whether glucocorticoid receptor gene polymorphisms are associated with clinical and metabolic profiles in patients with polycystic ovary syndrome. Polycystic ovary syndrome is a complex endocrine disease that affec
Externí odkaz:
https://doaj.org/article/89500d4cee794351b84a3f9d62541254
Publikováno v:
Clinics, Vol 68, Iss 2, Pp 147-152 (2013)
OBJECTIVE: The protocols for glucocorticoid replacement in children with salt wasting 21-hydroxylase deficiency are well established; however, the current recommendation for mineralocorticoid replacement is general and suggests individualized dose ad
Externí odkaz:
https://doaj.org/article/1236edddf2244e67a552e7bb795ba8db
Autor:
Ricardo P. P. Moreira, Alexander A. L. Jorge, Larissa G. Gomes, Laura C. Kaupert, João Massud Filho, Berenice B. Mendonca, Tânia A. S. S. Bachega
Publikováno v:
Clinics, Vol 66, Iss 8, Pp 1361-1366 (2011)
INTRODUCTION: 21-hydroxylase deficiency is an autosomal recessive disorder that causes glucocorticoid deficiency and increased androgen production. Treatment is based on glucocorticoid replacement; however, interindividual variability in the glucocor
Externí odkaz:
https://doaj.org/article/3ce8e63f566f438699215588f1c13121
Autor:
Ricardo P. P. Moreira, Larissa G. Gomes, Guiomar Madureira, Berenice B. Mendonca, Tânia A. S. S. Bachega
Publikováno v:
International Journal of Endocrinology, Vol 2014 (2014)
Background. Pediatric CAH patients have an increased risk of cardiovascular disease, and it remains unknown if genetic predisposition is a contributing factor. Glucocorticoid receptor gene (NR3C1) polymorphisms are associated with an adverse metaboli
Externí odkaz:
https://doaj.org/article/1f0d9c6b937146ac8241255d69f4bd2d
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 62, Iss 3, Pp 352-361
ABSTRACT Polycystic ovary syndrome (PCOS) is a common and complex endocrine disorder that affects 5-20% of reproductive age women. PCOS clinical symptoms include hirsutism, menstrual dysfunction, infertility, obesity and metabolic syndrome. There is
Externí odkaz:
https://doaj.org/article/015f1cdf1efa485f809a03f58b75f472
Autor:
Viviani De-Marco, Luciani R. Carvalho, Mariana F. Guzzo, Paulo S.L. Oliveira, Larissa G. Gomes, Berenice B. Mendonca
Publikováno v:
Clinics, Vol 72, Iss 9, Pp 575-581
OBJECTIVES: Pituitary-dependent hyperadrenocorticism is the most common cause of naturally occurring hypercortisolism in dogs. CRHR1 expression in human and dog corticotrophinomas suggested that this gene affects pituitary tumorigenesis. The present
Externí odkaz:
https://doaj.org/article/87a01d35acb04e03ad2aa18cd3a8b456
Publikováno v:
Sociedade, Contabilidade e Gestão. 16:83-104
As universidades, por meio de suas pesquisas acadêmicas, passaram a atuar não apenas na geração do conhecimento, como instituições de ensino e pesquisa, mas também na difusão, uma vez que podem ser consideradas importantes agentes dentro da p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e048740bc3cce6386d164f7347680d1
https://doi.org/10.21446/scg_ufrj.v0i0.24002
https://doi.org/10.21446/scg_ufrj.v0i0.24002
Autor:
Raiane P Crespo, Thais P Rocha, Luciana R Montenegro, Mirian Y Nishi, Alexander A L Jorge, Gustavo A R Maciel, Edmund Baracat, Ana Claudia Latronico, Berenice B Mendonca, Larissa G Gomes
Publikováno v:
Journal of the Endocrine Society. 6(9)
Context Polycystic ovary syndrome (PCOS) etiology remains to be elucidated, but familial clustering and twin studies have shown a strong heritable component. Objective The purpose of this study was to identify rare genetic variants that are associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5de633c83d8163dd98b6d1d779d18c88
https://pubmed.ncbi.nlm.nih.gov/35898701
https://pubmed.ncbi.nlm.nih.gov/35898701
Autor:
João Renato Rebello Pinho, Gustavo Arantes Rosa Maciel, P. Oliveira Claudia, Amanda Medeiros Recuero, Flair José Carrilho, Sandra Tochetto, Maria Cristina Chammas, Fernanda de Mello Malta, Paula Salles Ana, Denise Cerqueira Paranaguá-Vezozzo, Edmund Chada Baracat, Larissa G. Gomes, Alex Jones Flores Cassenote, José Tadeu Stefano
Publikováno v:
Annals of Hepatology, Vol 24, Iss, Pp 100501-(2021)
Introduction: The patatin-like phospholipase 3 gene polymorphism (PNPLA3) has been consistently associated with non-alcoholic fatty liver disease (NAFLD) and its histological severity on different populations. In addition, increasing evidence demonst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1a77552c89a147a6a966ffc7a8158cb
http://www.sciencedirect.com/science/article/pii/S1665268121002003
http://www.sciencedirect.com/science/article/pii/S1665268121002003