Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Eleonora Druve Tavares FAGUNDES"'
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:
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:
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
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
Autor:
Francislaine Veiga da Silva, Priscila Menezes Ferri, Thaís Costa Nascentes Queiroz, Pamela de Souza Haueisen Barbosa, Maria Cristina Cassiano de Oliveira, Laura Jácome de Melo Pereira, Ana Cristina Simões e Silva, Francisco José Penna, Eleonora Druve Tavares Fagundes, Alexandre Rodrigues Ferreira
Publikováno v:
Jornal de Pediatria, Vol 92, Iss 2, Pp 197-205 (2016)
Abstract Objective: To evaluate the nutritional status of children with persistent cholestasis and to compare the anthropometric indices between children with and without liver cirrhosis and children with and without jaundice. Methods: Children with
Externí odkaz:
https://doaj.org/article/3c3d7699ea1940b4b8e308cea5e86635
Autor:
Eleonora Druve Tavares FAGUNDES, Alexandre Rodrigues FERREIRA, Caroline Caldeira HOSKEN, Thaís Costa Nascentes QUEIROZ
Publikováno v:
Arquivos de Gastroenterologia, Iss 0 (2017)
ABSTRACT BACKGROUND: Primary sclerosing cholangitis is a rare disease, but its prevalence has been underestimated in children and adolescents due to broad variation in clinical presentation as well as diagnostic challenges in this life period. OBJECT
Externí odkaz:
https://doaj.org/article/cee5a68add6748caa8abfb58dcbe22bc
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
Autor:
Priscila Menezes Ferri, Ana Cristina Simões e Silva, Soraya Luiza Campos Silva, Diego Junior Queiroga de Aquino, Eleonora Druve Tavares Fagundes, Débora Marques de Miranda, Alexandre Rodrigues Ferreira
Publikováno v:
Gastroenterology Research and Practice, Vol 2016 (2016)
Primary sclerosing cholangitis (PSC) is a rare cholestatic liver disease characterized by chronic inflammation of the biliary tree resulting in liver fibrosis. PSC is more common in male less than 40 years of age. The diagnosis of PSC is based on cli
Externí odkaz:
https://doaj.org/article/a567421b2b9c4bd99b39adce33f25347