Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fernanda Canova Denardi"'
Autor:
Denise Engelbrecht Zantut-Wittmann, Marcos Antonio Tambascia, Arnaldo Moura Neto, José Vassallo, Roberto Caldato, Marcia Torresan Delamain, Fernanda Canova Denardi
Publikováno v:
The American Journal of the Medical Sciences. 344:418-421
The objective of this case report is to present a rare association of a mucosa-associated lymphoid tissue lymphoma masquerading as Graves' orbitopathy in a patient with autoimmune hyperthyroidism, without evidence of Graves' ophthalmopathy. A 66-year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6228deab7a1c9d501a267a2520a38755
https://doi.org/10.1097/maj.0b013e3182582330
https://doi.org/10.1097/maj.0b013e3182582330
Autor:
Lília D'Souza-Li, Arnaldo Moura-Neto, Maricilda Palandi de Mello, Heraldo Mendes Garmes, Adriana Mangue Esquiaveto-Aun, Sofia Helena Valente de Lemos-Marini, Fernanda Canova Denardi, Maria Tereza Matias Baptista, Gil Guerra-Júnior, Daniel Minutti de Oliveira, Fernanda Caroline Soardi, Patrícia Sabino de Matos, Helena Campos Fabbri
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia. 54:754-760
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant hereditary cancer syndrome characterized mostly by parathyroid, enteropancreatic, and anterior pituitary tumors. We present a case of an 8-year-old boy referred because of hypoglycem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2252da8019bad6d4198fde8a91ea974
https://doi.org/10.1590/s0004-27302010000800016
https://doi.org/10.1590/s0004-27302010000800016
Autor:
Antonia Paula Marques-de-Faria, Daiane R.B. Belgini, Fernanda Canova Denardi, Heraldo Mendes Garmes, Maricilda Palandi de Mello, C.L.B. Pinto, Maria Tereza Matias Baptista, Daniel Minutti de Oliveira, Oswaldo da Rocha Grassiotto, Andréa Trevas Maciel-Guerra, Gil Guerra-Júnior
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 54(8)
In 2004, Costa-Santos and cols. reported 24 patients from 19 Brazilian families with 17α-hydroxylase deficiency and showed that p.W406R and p.R362C corresponded to 50% and 32% of CYP17A1 mutant alleles, respectively. The present report describes cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a895b7ba3ff15a56cdf93b7fa37971a3
https://pubmed.ncbi.nlm.nih.gov/21340157
https://pubmed.ncbi.nlm.nih.gov/21340157