Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Thais Costa Nascentes Queiroz"'
Autor:
Mariana Pena COSTA, Alexandre Rodrigues FERREIRA, Adriana Teixeira RODRIGUES, Eleonora Druve Tavares FAGUNDES, Thais Costa Nascentes QUEIROZ
Publikováno v:
Arquivos de Gastroenterologia, Vol 60, Iss 4, Pp 438-449 (2023)
ABSTRACT Background: Alpha 1-antitrypsin deficiency (AATD) is a hereditary codominant autosomal disease. This liver disease ranges from asymptomatic cases to terminal illness, which makes early recognition and diagnosis challenging. It is the main ca
Externí odkaz:
https://doaj.org/article/c6720c65449c4120b396748ca199983e
Autor:
José Andrade FRANCO NETO, Priscila Menezes Ferri LIU, Thais Costa Nascentes QUEIROZ, Paulo Fernando Souto BITTENCOURT, Simone Diniz CARVALHO, Alexandre Rodrigues FERREIRA
Publikováno v:
Arquivos de Gastroenterologia, Vol 58, Iss 3, Pp 281-288 (2021)
ABSTRACT BACKGROUND: Percutaneous endoscopic gastrostomy (PEG) is an important option for enteral nutrition for both children and adults. It is considered a safe, effective, and advantageous technique in comparison to other complementary feeding rout
Externí odkaz:
https://doaj.org/article/10a10deaf689481fbde894a8f1566928
Autor:
Thais Costa Nascentes QUEIROZ, Alexandre Rodrigues FERREIRA, Eleonora Druve Tavares FAGUNDES, Mariza Leitão Valadares ROQUETE, Francisco José PENNA
Publikováno v:
Arquivos de Gastroenterologia, Vol 51, Iss 1, Pp 53-58 (2014)
Context Biliary atresia is a progressive, idiopathic, fibro-obliterative disease of the extrahepatic biliary tree that presents with biliary obstruction exclusively in the neonatal period. Objectives To assess the differences regarding age at refer
Externí odkaz:
https://doaj.org/article/a00b199777824b3bbbb2bdb6a4e8abf4
Publikováno v:
Biblioteca Digital de Teses e Dissertações da UFMGUniversidade Federal de Minas GeraisUFMG.
A atresia biliar (AB) é uma doença exclusiva da infância1, sendo a principal causa de transplante hepático em crianças (responsável por 50% das indicações) 2,3, com uma incidência que varia de 1:5000 a 1:18000 nascidos vivos 4-8, com pequeno
Externí odkaz:
http://hdl.handle.net/1843/BUOS-97RH4Q
Autor:
Letícia Drumond ALBERTO, Eleonora Druve Tavares FAGUNDES, Adriana Teixeira RODRIGUES, Thaís Costa Nascentes QUEIROZ, Gustavo Valverde de CASTRO, Alexandre Rodrigues FERREIRA
Publikováno v:
Arquivos de Gastroenterologia, Vol 61 (2024)
ABSTRACT Background: Hepatopulmonary syndrome (HPS) is characterized by the triad of abnormal arterial oxygenation caused by intrapulmonary vascular dilatations (IPVD) in the setting of advanced liver disease or portal hypertension, impacting the pat
Externí odkaz:
https://doaj.org/article/c20a4927e5de4ceab10538ce7d87b3c4
Autor:
Maria Carolina Feres de Lima Rocha GAMA, Eleonora Druve Tavares FAGUNDES, Thaís Costa Nascentes QUEIROZ, Adriana Teixeira RODRIGUES, Luiza Caroline VIEIRA, Alexandre Rodrigues FERREIRA
Publikováno v:
Arquivos de Gastroenterologia, Vol 60, Iss 2, Pp 247-256 (2023)
ABSTRACT Background: Most data on the natural history of portal hypertension come from studies in adults. The morbidity rate of upper gastrointestinal bleeding (UGIB) in children with portal hypertension has not been systematically characterized. Obj
Externí odkaz:
https://doaj.org/article/7713acb0ccc0484cb860835489c9c3de
Publikováno v:
Repositório Institucional da UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
Introdução: A atresia biliar (AB) é a principal causa de icterícia obstrutiva nos primeiros três meses de vida e a indicação mais frequente de transplante hepático pediátrico. A portoenterostomia de Kasai é uma alternativa terapêutica e co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::0f4f687900fd7219909f5a8cd504eec3
Autor:
Ana Paula Pereira de Oliveira, Alexandre Rodrigues Ferreira, Eleonora Druve Tavares Fagundes, Thaís Costa Nascentes Queiroz, Simone Diniz Carvalho, José Andrade Franco Neto, Paulo Fernando Souto Bittencourt
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 96, Iss 6, Pp 755-762 (2020)
Objectives: This study aimed to evaluate factors associated with upper digestive hemorrhage and primary and secondary endoscopic prophylaxis outcomes in children with extrahepatic portal vein obstruction. Methods: This observational and prospective s
Externí odkaz:
https://doaj.org/article/dadcf90a687c4d7faec35565f06f0858
Autor:
Natália Duarte Linhares, Eleonora Druve Tavares Fagundes, Alexandre Rodrigues Ferreira, Thaís Costa Nascentes Queiroz, Luiz Roberto da Silva, Sergio D. J. Pena
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
The arthrogryposis, renal dysfunction, and cholestasis syndrome (ARCS) is an autosomal recessive multisystem disease caused by variants in VPS33B or VIPAS39. The classical presentation includes congenital joint contractures, renal tubular dysfunction
Externí odkaz:
https://doaj.org/article/df7833407f724c688d217ef611eb91e3
Autor:
Alexandre Rodrigues FERREIRA, Thaís Costa Nascentes QUEIROZ, Paula Vieira Teixeira VIDIGAL, Raquel di Paula FERREIRA, David Campos WANDERLEY, Eleonora Druve Tavares FAGUNDES
Publikováno v:
Arquivos de Gastroenterologia, Vol 56, Iss 1, Pp 71-78 (2019)
ABSTRACT BACKGROUND: Biliary atresia represents the most common surgically treatable cause of cholestasis in newborns. If not corrected, secondary biliary cirrhosis invariably results. OBJECTIVE: To evaluate, through multivariate analysis, the progno
Externí odkaz:
https://doaj.org/article/b099675d92f043f3b84f38909cbcd03c