Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Adriana Maria Alves DE TOMMASO"'
Autor:
Bruna Caseri Marino, Sabrina Sayuri Suzuki, Lucas Rocha Alvarenga, Gabriel Hessel, Antonio Fernando Ribeiro, Elizete Aparecida Lomazi, Adriana Maria Alves de Tommaso, Roberta Vacari de Alcântara, Maria Angela Bellomo Brandão
Publikováno v:
Residência Pediátrica, Vol 13, Iss 4 (2023)
Biliary atresia is a rare condition, of undefined etiology and with a potentially fatal evolution. The cat eye syndrome is a rare chromosomal disease that is associated with several malformations, biliary atresia being among the most rarely described
Externí odkaz:
https://doaj.org/article/979f6697c01a41719f1692e009950f63
Autor:
Lucas Rocha ALVARENGA, Natascha Silva SANDY, Gabriela Souza GOMEZ, Gabriel HESSEL, Adriana Maria Alves DE TOMMASO, Maria Ângela BELLOMO-BRANDÃO
Publikováno v:
Arquivos de Gastroenterologia, Vol 58, Iss 2, Pp 227-233 (2021)
ABSTRACT BACKGROUND: Primary sclerosing cholangitis (PSC) is a rare hepatobiliary disorder, whose etiology remains not fully elucidated. Given how rare PSC is in childhood, until the recent publication of a multicenter international collaboration, ev
Externí odkaz:
https://doaj.org/article/d6607b8815f64b329e3fe80a2b758f40
Autor:
Marina Mayumi Vendrame TAKAO, Natascha Silva SANDY, Adriana Gut Lopes RICCETTO, Adriana Maria Alves DE TOMMASO
Publikováno v:
Arquivos de Gastroenterologia, Vol 58, Iss 1, Pp 87-92 (2021)
ABSTRACT BACKGROUND Glycogen storage disease (GSD) type 1b is a multisystemic disease in which immune and infectious complications are present, in addition to the well-known metabolic manifestations of GSD. Treatment with granulocyte-colony stimulati
Externí odkaz:
https://doaj.org/article/6b1427d47e2e48d2b53472d7ca5668bc
Publikováno v:
Revista Paulista de Pediatria, Vol 39 (2021)
ABSTRACT Objective: To perform anthropometric and dietary evaluation of patients with glycogenosis type Ia and Ib. Methods: This cross-sectional study is composed of a sample of 11 patients with glycogenosis divided into two subgroups according to th
Externí odkaz:
https://doaj.org/article/ded550660dce4d828e7476131cda4b7c
Autor:
Adriana Maria Alves De Tommaso, Flávia Fonseca de Carvalho Barra, Gabriel Hessel, Carolina Araújo Moreno, Roberto Giugliani, Cecília Amélia Fazzio Escanhoela
Publikováno v:
Revista Paulista de Pediatria, Iss 0 (2017)
RESUMO Objetivo: Descrever a doença de depósito de ésteres de colesterol (DDEC) e a importância da biópsia hepática na realização do diagnóstico. Descrição do caso: Paciente feminina, dois anos e dez meses de idade, com queixa de aumento d
Externí odkaz:
https://doaj.org/article/ff80c9167a2b487096ebb84debf61318
Autor:
Marcelo Paschoalete Carlin, Daniel Zanetti Scherrer, Adriana Maria Alves De Tommaso, Carmen Silvia Bertuzzo, Carlos Eduardo Steiner
Publikováno v:
Genetics and Molecular Biology, Vol 36, Iss 4, Pp 502-506 (2013)
Glycogen storage disease (GSD) comprises a group of autosomal recessive disorders characterized by deficiency of the enzymes that regulate the synthesis or degradation of glycogen. Types Ia and Ib are the most prevalent; while the former is caused by
Externí odkaz:
https://doaj.org/article/36e107e6ce8b4cd39e88db908bcd5212
Autor:
Elisa de Carvalho, Jorge Luiz dos Santos, Themis Reverbel da Silveira, Carlos Oscar Kieling, Luciana Rodrigues Silva, Gilda Porta, Irene Kazue Miura, Adriana Maria Alves De Tommaso, Maria Ângela Bellomo Brandão, Alexandre Rodrigues Ferreira, José Roberto de Deus Macêdo, José Tenório de Almeida Neto
Publikováno v:
Jornal de Pediatria, Vol 86, Iss 6, Pp 473-479 (2010)
OBJETIVO: Avaliar as características epidemiológicas, clínicas e prognósticas de crianças com atresia biliar. MÉTODOS: Dados sobre portoenterostomia, transplante hepático (TxH), idade no último seguimento e sobrevida foram coletados dos pront
Externí odkaz:
https://doaj.org/article/a566874e929a4c94998f3cba468c1788
Autor:
Maria Angela Bellomo-Brandão, Elizete Aparecida Lomazi da Costa-Pinto, Adriana Maria Alves De Tommaso, Gabriel Hessel
Publikováno v:
Arquivos de Gastroenterologia, Vol 43, Iss 1, Pp 45-49 (2006)
BACKGROUND: Few studies on autoimmune hepatitis have enrolled non-Caucasian groups. AIMS: To evaluate Brazilian children with type 1 and 2 autoimmune hepatitis regarding outcome and clinical and biochemical parameters. PATIENTS AND METHODS: Thirty-si
Externí odkaz:
https://doaj.org/article/1e67ca87ad89434e95c263817c29b2e6
Publikováno v:
Arquivos de Gastroenterologia, Vol 41, Iss 3, Pp 190-192 (2004)
BACKGROUND: Intrahepatic cholestasis secondary to paucity of bile duct is an alteration of the anatomic integrity of the biliary tract. Can be defined only histologically and, clinically, two categories are recognized: syndromic and non-syndromic, wh
Externí odkaz:
https://doaj.org/article/23ad0db36dd44f3d9b069c15335efc30
Autor:
Adriana Maria Alves de Tommaso, Gabriel Hessel, Adriana Gut Riccetto, Graziela de Oliveira Semenzati, Reinaldo Jordão Gusmão
Publikováno v:
Revista Paulista de Pediatria
ABSTRACT Objective: To discuss aspects of pre and post-operative otorhinolaryngology surgery in patients with glycogen storage disease type 1b. Case description: Description of three clinical cases with probable glycogen storage disease type 1b who u
Externí odkaz:
https://doaj.org/article/a18207bc27524954831b06e6a693c7bc