Zobrazeno 1 - 10
of 14
pro vyhledávání: '"João Seda-Neto"'
Autor:
Eduardo A. Fonseca, Flavia Feier, Rodrigo Vincenzi, Helry L. L. Candido, Rodrigo L. Azambuja, Fabio Payao, Marcel R. Benavides, Karina M. O. Roda, Katia M. R. Leite, Cristiane M. F. Ribeiro, Maria D. Begnami, Charles E. Zurstrassen, Francisco C. Carnevale, Paulo Chapchap, João Seda-Neto
Publikováno v:
Case Reports in Surgery, Vol 2022 (2022)
Background & Aims. The most dangerous complications of hepatocellular adenomas are hemorrhage and malignant transformation, both of which require surgical treatment. The surgical treatment strategy for patients with benign large or central tumors is
Externí odkaz:
https://doaj.org/article/cc5a18be89ed4f4c8d4f8dc02ee4baac
Autor:
Aline F. Freitas, Renata P. S. Pugliese, Flavia Feier, Irene K. Miura, Vera Lúcia B. Danesi, Eliene N. Oliveira, Adriana P. M. Hirschfeld, Cristian B. V. Borges, Juliana V. Lobato, Gilda Porta, João Seda-Neto, Eduardo A. Fonseca
Publikováno v:
Microorganisms, Vol 10, Iss 5, p 1030 (2022)
Background: The COVID-19 infection has received the attention of the scientific community due to its respiratory manifestations and association with evolution to severe acute respiratory syndrome (SARS-CoV-2). There are few studies characterizing SAR
Externí odkaz:
https://doaj.org/article/06e52f468898432ba36cb8912fee410d
Autor:
Ana Vitoria Barban Margutti, Wilson Araújo Silva, Daniel Fantozzi Garcia, Greice Andreotti de Molfetta, Adriana Aparecida Marques, Tatiana Amorim, Vânia Mesquita Gadelha Prazeres, Raquel Tavares Boy da Silva, Irene Kazue Miura, João Seda Neto, Emerson de Santana Santos, Mara Lúcia Schmitz Ferreira Santos, Charles Marques Lourenço, Tássia Tonon, Fernanda Sperb-Ludwig, Carolina Fischinger Moura de Souza, Ida Vanessa Döederlein Schwartz, José Simon Camelo
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Maple syrup urine disease (MSUD) is an autosomal recessive inherited metabolic disease caused by deficient activity of the branched-chain α-keto acid dehydrogenase (BCKD) enzymatic complex. BCKD is a mitochondrial complex encoded
Externí odkaz:
https://doaj.org/article/2039cf41956a41fdbfad39b064da9a4f
Autor:
João Seda Neto, Paulo Chapchap, Flavia H. Feier, Renata Pugliese, Rodrigo Vincenzi, Marcel R Benavides, Karina Roda, Mário Kondo, Eduardo A. Fonseca
Publikováno v:
Journal of Pediatric Surgery. 57:955-961
infants who require liver transplantation represent a treatment challenge because chronic liver disease at this early age affects the child's growth and development during a critical phase. The aim is to compare demographics, operative data, and long
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e267564e3f427e570da871aaa35acee
https://doi.org/10.1016/j.jpedsurg.2022.05.014
https://doi.org/10.1016/j.jpedsurg.2022.05.014
Autor:
João Seda Neto, Carolina Magalhães Costa, Fabio Payão Pereira, Renata Pugliese, Nathalia P. Travassos, Caio M. Oliveira, Rodrigo Vincenzi, Marcel R. Benavides, Karina Roda, Mário Kondo, Eduardo A. Fonseca
Publikováno v:
Pediatric Transplantation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3047b7cc468675ca16b63a8dae6e985c
https://doi.org/10.1111/petr.14518
https://doi.org/10.1111/petr.14518
Autor:
Eduardo Antunes da Fonseca, Flavia Heinz Feier, Carolina Magalhães Costa, Marcel Albeiro Ruiz Benavides, Rodrigo Vincenzi, Karina Moreira de Oliveira Roda Vincenzi, Renata Pereira Sustovich Pugliese, Gilda Porta, Irene Kazuo Miura, Caio Marcio Vieira de Oliveira, Paulo Chapchap, João Seda Neto
Publikováno v:
Liver Transplantation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1b1bd41181a01f462f7bbb8e38929de
https://doi.org/10.1097/lvt.0000000000000108
https://doi.org/10.1097/lvt.0000000000000108
Autor:
Carolina Magalhães Costa, João Seda Neto, Marcel R. Benavidez, Rodrigo Vincenzi, Karina Roda, Caio Márcio V. Oliveira, Nathália Porto R. Travassos, Luiz Guilherme C. A. de Lima, Fabio Payão Pereira, Eduardo A. Fonseca
Publikováno v:
Pediatric Transplantation. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc870163589bbe726ec6aae9be4baa03
https://doi.org/10.1111/petr.14445
https://doi.org/10.1111/petr.14445
Autor:
João Seda Neto, Carolina M. Costa, Eduardo A. Fonseca, Rodrigo Vincenzi, Renata Pugliese, João Ivo X. Rocha, Karina Roda, Marcel R. Benavidez, Caio Márcio V. Oliveira, Fabio Payão Pereira, André Moreira Assis, Flavia H. Feier, Paulo Chapchap
Publikováno v:
Pediatric transplantationREFERENCES. 26(3)
Acquired diaphragmatic hernia (DH) following liver transplantation (LT) is usually considered a surgical emergency. Interplay of contributing elements determines its occurrence but, in children, LT with partial liver grafts seems to be the most impor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8ed5d669369987d1b3befb7641649da
https://pubmed.ncbi.nlm.nih.gov/34881487
https://pubmed.ncbi.nlm.nih.gov/34881487
Autor:
Flávia H, Feier, Paulo, Chapchap, Renata, Pugliese, Eduardo A, da Fonseca, Francisco C, Carnevale, Airton M, Moreira, Charles, Zurstrassen, Aline C, Santos, Irene K, Miura, Vera, Baggio, Adriana, Porta, Teresa, Guimarães, Helry, Cândido, Marcel, Benavides, Andre, Godoy, Katia M R, Leite, Gilda, Porta, Mario, Kondo, João, Seda-Neto
Publikováno v:
Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society. 20(8)
The incidence of biliary complications (BCs) after living donor liver transplantation (LDLT) can reach 40%. Published data on the pediatric population are limited, and treatment protocols vary. Our aim was to describe the clinical scenario for BCs an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c85615311a60c83d2f90fe0ff3a22154
https://pubmed.ncbi.nlm.nih.gov/24943482
https://pubmed.ncbi.nlm.nih.gov/24943482
Autor:
Francisco C, Carnevale, Aline C B, Santos, João, Seda-Neto, Charles E, Zurstrassen, Airton M, Moreira, Eduardo, Carone, Antonio S Z, Marcelino, Gilda, Porta, Renata, Pugliese, Irene, Miura, Vera D, Baggio, Teresa, Guimarães, Giovanni G, Cerri, Paulo, Chapchap
Publikováno v:
Pediatric transplantation. 15(1)
Portal vein thrombosis is a complication that occurs anytime after liver transplantation and can compromise the patient and graft survival. We describe a combined technique for PV recanalization in cases of PV obstruction after liver transplantation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b07b406343df82227584ce4747487571
https://pubmed.ncbi.nlm.nih.gov/21241438
https://pubmed.ncbi.nlm.nih.gov/21241438