Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Renata, Pugliese"'
Autor:
Karina M.O. Roda, Rodrigo Vincenzi, Eduardo A. Fonseca, Paulo Chapchap, Renata Pugliese, Marcel Benavides, Rodrigo L. Azambuja, Fabio Payao Pereira, Joao Seda Neto
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 72, Iss , Pp 101957- (2021)
EBV-associated post-transplant smooth muscle tumors (EBV-PTSMTs) is a rare complication following solid organ transplantation and has been observed more frequently in pediatric and young adult populations. This manuscript reports a 10-month-old femal
Externí odkaz:
https://doaj.org/article/4367f0433d6845328ca7b26f0142b10d
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
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.
Autor:
Rodolpho Truffa Kleine, Renata Mendes, Renata Pugliese, Irene Miura, Vera Danesi, Gilda Porta
Publikováno v:
Clinics, Vol 67, Iss 3, Pp 231-235 (2012)
OBJECTIVES: Clinical-laboratory and evolutionary analysis of twenty-eight patients with Wilson's disease. METHODS: Twenty-eight children (twelve females and sixteen males) with Wilson's disease were evaluated retrospectively between 1987 and 2009, wi
Externí odkaz:
https://doaj.org/article/1939cbbcf73c435a948266b4ec1b2f9a
Autor:
Irene K. Miura, Renata Pugliese, Adriana Porta, C. M. F. Ribeiro, Paula S M Rigo, Vera B. Danesi, Gilda Porta, Cristian C V Borges, Eliene Oliveira
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 72:674-676
A case of low-γ-glutamyltranspetidase cholestasis associated with ubiquitin-specific peptidase 53 (USP53) gene mutation in a Brazilian child is described. Transient jaundice and hypocholia started at the age of 10 days. Liver enzymes, total bilirubi
Autor:
Helry L. Candido, Eduardo A. da Fonseca, Flávia H. Feier, Renata Pugliese, Marcel A. Benavides, Enis D. Silva, Karina Gordon, Marcelo Gama de Abreu, Jaume Canet, Paulo Chapchap, Joao Seda Neto
Publikováno v:
Journal of Transplantation, Vol 2015 (2015)
Living donor liver donation (LDLD) is an alternative to cadaveric liver donation. We aimed at identifying risk factors and developing a score for prediction of postoperative complications (POCs) after LDLD in donors. This is a retrospective cohort st
Externí odkaz:
https://doaj.org/article/8db3d9e234da451aa8ee1440469e2919
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
Autor:
Rodrigo Vincenzi, Flavia H. Feier, Joao Seda-Neto, Renata Pugliese, Paulo Chapchap, Mario Kondo, Karina M. O. Roda, Vera Baggio, Caio V Oliveira, Irene Miura, Eduardo A. Fonseca, Gilda Porta, Marcel Benavides, Aline F Freitas
Publikováno v:
Pediatric Transplantation
Background The impact of the COVID pandemic on liver transplant (LT) programs varied among countries. Few data are available about that impact in pediatric liver transplant (PLT) programs. This study aimed at comparing the data of our program in Braz
Autor:
Irene Kazue Miura, Natalia Canale Person, Fabiana Roberto Lima, Vera B. Danesi, Gabriel Nuncio Benevides, Renata Pugliese, Gilda Porta
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 95, Iss 5, Pp 552-558 (2019)
Jornal de Pediatria, Vol 95, Iss 5, Pp 552-558 (2019)
Jornal de Pediatria v.95 n.5 2019
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Vol 95, Iss 5, Pp 552-558 (2019)
Jornal de Pediatria v.95 n.5 2019
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Objective: To describe the demographic, clinical, laboratory and molecular characteristics of patients with lysosomal acid lipase deficiency. Methods: A retrospective review of the medical records of children with the disease. Results: Seven children
Autor:
Alexandre Rodrigues Ferreira, Sandra M. Vieira, Daniela G. Menezes, Adriana Maria Alves De Tommaso, Cristina Helena Targa Ferreira, Regina Sawamura, Carlos Oscar Kieling, Gabriel Hessel, Marcia A. Valladares, Maria Angela Bellomo-Brandão, Jorge Gama, Renata B.P.M. Seixas, Nilza Perin, Renata Pugliese, Eleonora Druve Tavares Fagundes, Leonardo Rodrigues Resende, Irene K. Miura, Mariana N. de Paula, Cristian V. Borges, Themis Reverbel da Silveira, Cibele Dantas Ferreira Marques, Vera L. Danesi, Adriana Porta, Jussara Maia, Luciana Rodrigues Silva, Elisa de Carvalho, Marise E. Marsillac, Gilda Porta, Juliana R. Vasconcelos, Jorge Luiz dos Santos, Melina Utz Melere
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Jornal de Pediatria, Vol 95, Iss 4, Pp 419-427 (2019)
Jornal de Pediatria v.95 n.4 2019
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Volume: 95, Issue: 4, Pages: 419-427, Published: 12 SEP 2019
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Jornal de Pediatria (Versão em Português), Vol 95, Iss 4, Pp 419-427 (2019)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Jornal de Pediatria, Vol 95, Iss 4, Pp 419-427 (2019)
Jornal de Pediatria v.95 n.4 2019
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Volume: 95, Issue: 4, Pages: 419-427, Published: 12 SEP 2019
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Jornal de Pediatria (Versão em Português), Vol 95, Iss 4, Pp 419-427 (2019)
In this large clinical series of Brazilian children and adolescents, autoimmunehepatitis-1 was more frequent, and patients with autoimmune hepatitis-2 exhibited higherdisease remission rates with earlier response to treatment. Patients with autoimmun