Výsledky vyhledávání - "Adriana Maria Alves DE TOMMASO"

Akademický článek

Atresia de vias biliares em paciente com síndrome do olho do gato - relato de caso

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

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Akademický článek

SYMPTOMATIC CHOLELITHIASIS AS THE PRESENTATION OF PEDIATRIC PRIMARY SCLEROSING CHOLANGITIS - CASE SERIES AND LITERATURE REVIEW

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

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Akademický článek

LONG TERM MANAGEMENT OF GLYCOGEN STORAGE DISEASE TYPE 1B: A BRAZILIAN TERTIARY CENTER EXPERIENCE

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

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Akademický článek

ANTHROPOMETRIC AND DIETARY ASSESSMENT OF PATIENTS WITH GLYCOGENOSIS TYPE I

Autor: Natália Bauab Jorge, Adriana Maria Alves de Tommaso, Gabriel Hessel

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

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Akademický článek

IMPORTÂNCIA DA BIÓPSIA HEPÁTICA NO DIAGNÓSTICO DA DEFICIÊNCIA DE LIPASE ÁCIDA LISOSSOMAL: RELATO DE CASO

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

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Akademický článek

Determining mutations in G6PC and SLC37A4 genes in a sample of Brazilian patients with glycogen storage disease types Ia and Ib

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

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Akademický článek

Atresia biliar: a experiência Brasileira

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

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Akademický článek

Clinical and biochemical features of autoimmune hepatitis in 36 pediatric patients Características clínicas e bioquímicas da hepatite autoimune em 36 pacientes pediátricos

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

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Colelitíase sintomática como apresentação de colangite esclerosante primária na infância - série de casos e revisão de literatura

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, Issue: ahead, Published: 16 JUL 2021
Arquivos de Gastroenterologia v.58 n.2 2021
Arquivos de gastroenterologia
Instituto Brasileiro de Estudos e Pesquisas de Gastroenterologia
instacron:IBEPEGE
Arquivos de Gastroenterologia, Vol 58, Iss 2, Pp 227-233 (2021)
Arquivos de Gastroenterologia, Volume: 58, Issue: 2, Pages: 227-233, Published: 16 JUL 2021

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, even data o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d227fbab996c493477b08f7c025dcdbc
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032021005005205&lng=en&tlng=en

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