Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Carolina S. V. Oliveira"'
Autor:
Valdecira M. Piveta, Fernando M. A. Giuffrida, Celia S. Bittencourt, Carolina S. V. Oliveira, Pedro Saddi-Rosa, Deyse M. Meira, André F. Reis
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 59, Iss 4, Pp 367-370
Introduction Undiagnosed hyperglycemia is common in high cardiovascular risk individuals, especially in those with coronary artery disease (CAD). There is no consensus about the optimal method for the screening of hyperglycemia in this population.Sub
Externí odkaz:
https://doaj.org/article/cfac3b2e91f648b68c29a36f02e1a80a
Autor:
Carolina S. V. Oliveira, Epole Ntungwe N, Amílcar Roberto, Joana Marçalo, Claudia Oliveira, Catarina Teodósio, Catarina Garcia, Catarina Pinto Reis
Publikováno v:
Journal Biomedical and Biopharmaceutical Research. 14:95-108
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba592df52364211b8be559026f079f52
https://doi.org/10.19277/bbr.14.1.153
https://doi.org/10.19277/bbr.14.1.153
Autor:
Pedro Saddi-Rosa, Carolina S. V. Oliveira, Felipe Crispim, André F. Reis, Fernando M. A. Giuffrida
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.55 n.7 2011
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Plasma adiponectin and the coding gene for adiponectin, ADIPOQ, are thought to explain part of the interaction between obesity, insulin resistance, type 2 diabetes (T2DM) and coronary artery disease (CAD). Here, we illustrate the role that adiponecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09dc1aeac1a7e1f6fe1d6d6afac06995
https://doi.org/10.1590/s0004-27302011000700003
https://doi.org/10.1590/s0004-27302011000700003
Autor:
Fernando Kok, Farida Jennane, André F. Reis, Thais Della Manna, Roberta Diaz Savoldelli, Bernard Grandchamp, Gilberto Velho, Carolina S. V. Oliveira, Caroline Kannengiesser, Nadir Cheurfa, Claire Oudin
Publikováno v:
Pediatric Diabetes. 12:187-191
Wolcott-Rallison syndrome (WRS, OMIM 226980) is a rare autosomal recessive disorder characterized by permanent neonatal diabetes mellitus, epiphyseal dysplasia, and other multisystemic clinical manifestations. We described two novel mutations in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad41df95fc6bdcfe0a5215c93cacaa33
https://doi.org/10.1111/j.1399-5448.2010.00679.x
https://doi.org/10.1111/j.1399-5448.2010.00679.x
Autor:
José Gilberto H. Vieira, Jorma Ilonen, Minna Sjöroos, André F. Reis, Carolina S. V. Oliveira, Omar M. Hauache
Publikováno v:
Disease Markers
Disease Markers, Vol 21, Iss 3, Pp 139-145 (2005)
Disease Markers, Vol 21, Iss 3, Pp 139-145 (2005)
The study aimed to further characterise HLA encoded risk factors of type 1 diabetes (T1D) in Brazilian population and test the capability of a low resolution full-house DR-DQ typing method to find subjects at diabetes risk. Insulin and CTLA-4 gene po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd63a4b0ce179dd7ad2304d434648f32
http://europepmc.org/articles/PMC3851392
http://europepmc.org/articles/PMC3851392
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 46, Issue: 2, Pages: 186-192, Published: APR 2002
Arquivos Brasileiros de Endocrinologia & Metabologia v.46 n.2 2002
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia v.46 n.2 2002
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Estima-se que perto de 5% dos indivíduos classificados como portadores de diabetes mellitus (DM) tipo 2 e 10% daqueles considerados como tipo 1 (anteriormente classificado como juvenil) sejam, na verdade, portadores de mutações MODY. Nesta forma d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed4c386a1ca680c01acc5e1d251693e6
https://doi.org/10.1590/s0004-27302002000200012
https://doi.org/10.1590/s0004-27302002000200012
Autor:
Antonio Roberto Chacra, Gilberto K. Furuzawa, Carolina S. V. Oliveira, Sergio Atala Dib, Fernando M. A. Giuffrida, André F. Reis
Publikováno v:
Diabetes Research and Clinical Practice. 81:e12-e14
Prevalence of MODY2 and MODY3 mutations has been assessed in 23 Brazilian families with MODY phenotype. Mutations in HNF-1alpha have been found in 3 families (13%) and 2 families (8.7%) had new glucokinase mutations. These genes do not explain the ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c8f0a2ba513ff2f569791bde78104f1
https://doi.org/10.1016/j.diabres.2008.06.011
https://doi.org/10.1016/j.diabres.2008.06.011
Autor:
Gilberto Velho, Pedro Saddi-Rosa, André F. Reis, José Gilberto H. Vieira, Fernando M. A. Giuffrida, Luis Henrique Santos Canani, Fernando Gerchman, Carolina S. V. Oliveira, Felipe Crispim
Publikováno v:
Journal of diabetes and its complications. 26(2)
Objective To investigate the association of ADIPOQ variants, total and high molecular weight adiponectin (HMW) adiponectin levels with the prevalence of diabetes mellitus and coronary artery disease (CAD) diagnosed by coronary angiography in Brazilia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc8a0276410bdda15513aacb178c364c
https://pubmed.ncbi.nlm.nih.gov/22459242
https://pubmed.ncbi.nlm.nih.gov/22459242
Autor:
Cláudia H.M.C. Oliveira, Omar M. Hauache, André F. Reis, Carolina S. V. Oliveira, Gilberto Velho, Rui M. B. Maciel, Cláudia M. Ferrer, Cristina Khawali, Maria Teresa Ghiringhello, Teresinha T. Tachibana, José Gilberto H. Vieira
Publikováno v:
Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Impaired fasting glucose (IFG) and impaired glucose tolerance (IGT) represent intermediate states between normal fasting glucose (NFG) or normal glucose tolerance (NGT), respectively, and diabetes (1). The regulation of fasting and glucose concentrat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c51479d0c021ee92e0435b7deacf0885
http://repositorio.unifesp.br/handle/11600/29899
http://repositorio.unifesp.br/handle/11600/29899
Autor:
Carolina S V, Oliveira, José Gilberto H, Vieira, Maria Teresa, Ghiringhello, Omar M, Hauache, Cláudia Helena M, Oliveira, Cristina, Khawali, Claúdia, Ferrer, Teresinha T, Tachibana, Rui M B, Maciel, Gilberto, Velho, André F, Reis
Publikováno v:
Diabetes care. 30(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::816ab1ceabe379f32968ca87be875015
https://pubmed.ncbi.nlm.nih.gov/17473058
https://pubmed.ncbi.nlm.nih.gov/17473058