Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Nana Miura"'
Autor:
Fabricio Marcondes Camargo, Maria de Lourdes Brizot, Rossana Pulcineli Vieira Francisco, Werther Brunow de Carvalho, Nana Miura Ikari, Stella Verzinhasse Peres, Marco Antônio Borges Lopes, Lilian Maria Lopes
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 121, Iss 1 (2024)
Resumo Fundamento: Seguimento de coorte retrospectiva de 30 anos que se aproxima da história natural dos tumores cardíacos diagnosticados no feto uma vez que nenhum caso foi submetido à interrupção da gestação. Objetivo: Avaliar a morbidade e
Externí odkaz:
https://doaj.org/article/0a3c60e9387f4c66a0fcc82421f2a928
Autor:
Marcília Sierro Grassi, Marília Montenegro, Evelin Aline Zanardo, Antonio Carlos Pastorino, Mayra Barros Dorna, Chong Kim, Marcelo Jatene, Nana Miura, Leslie Kulikowski, Magda Carneiro-Sampaio
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 118, Iss 1, Pp 61-67 (2022)
Resumo Fundamento Algumas síndromes têm características específicas e facilmente reconhecíveis, enquanto outras podem ser mais complexas de se identificar e podem apresentar diferentes manifestações fenotípicas, por exemplo. Um diagnóstico e
Externí odkaz:
https://doaj.org/article/08218b1bdaf54a3886500e21a7fffaf4
Autor:
Rachel Sayuri Honjo, Evelyn Cristina Nuñez Vaca, Gabriela Nunes Leal, Deipara Monteiro Abellan, Nana Miura Ikari, Marcelo Biscegli Jatene, Ana Maria Martins, Chong Ae Kim
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background The Mucopolysaccharidosis type VI (MPS VI), also known as Maroteaux-Lamy syndrome (OMIM 253200) is an autosomal recessive lysosomal disorder, caused by the deficiency of the enzyme N-acetylgalactosamine 4-sulfatase (also known as
Externí odkaz:
https://doaj.org/article/7cdb8dec43974bb7b44713da18cf9cd0
Autor:
Estela Azeka, Adam Arshad, Cristiane Martins, Anna Claudia Dominguez, Adailson Siqueira, Andre Silveira Loss, Marcelo Jatene, Nana Miura
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Objective: The objective of this study was to describe the clinical course of a newborn who developed dilated cardiomyopathy (DCM) after COVID-19 infection.Methods: We retrospectively assessed the clinical notes of a pediatric patient with decompensa
Externí odkaz:
https://doaj.org/article/22ce9f163e7740828ec72a4ef94c38a4
Autor:
Leonardo Augusto Miana, Luiz Fernando Canêo, Carla Tanamati, Juliano Gomes Penha, Vanessa Alves Guimarães, Nana Miura, Filomena Regina Barbosa Gomes Galas, Marcelo Biscegli Jatene
Publikováno v:
Brazilian Journal of Cardiovascular Surgery, Vol 30, Iss 4, Pp 409-416 (2015)
Abstract Introduction: Post-cardiotomy myocardial dysfunction requiring mechanical circulatory support occurs in about 0.5% of cases. In our environment, the use of extracorporeal membrane oxygenation has been increasing in recent years. Objective: T
Externí odkaz:
https://doaj.org/article/c0db126a081f45afbdd936a771ec24fa
Autor:
Luiz Fernando Canêo, Leonardo Augusto Miana, Carla Tanamati, Juliano Gomes Penha, Monica Satsuki Shimoda, Estela Azeka, Nana Miura, Filomena Regina Barbosa Gomes Galas, Vanessa Alves Guimarães, Marcelo Biscegli Jatene
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 104, Iss 1, Pp 78-84 (2015)
Background: Heart transplantation is considered the gold standard therapy for the advanced heart failure, but donor shortage, especially in pediatric patients, is the main limitation for this procedure, so most sick patients die while waiting for the
Externí odkaz:
https://doaj.org/article/23391744c12548f3ac710511a635f397
Autor:
Marcília S. Grassi, Cristina M. A. Jacob, Leslie D. Kulikowski, Antonio C. Pastorino, Roberta L. Dutra, Nana Miura, Marcelo B. Jatene, Stephanie P. Pegler, Chong A. Kim, Magda Carneiro-Sampaio
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 103, Iss 5, Pp 382-390 (2014)
Background: To alert for the diagnosis of the 22q11.2 deletion syndrome (22q11.2DS) in patients with congenital heart disease (CHD). Objective: To describe the main CHDs, as well as phenotypic, metabolic and immunological findings in a series of 60 p
Externí odkaz:
https://doaj.org/article/1404f8816b534ad7ab3e8938299915ab
Autor:
Estela Azeka, Marcelo Biscegli Jatene, Ana Cristina Tanaka, Filomena Regina Galas, Ludhmilla Abrahao Hajjar, Nana Miura, Jose Otavio Costa Auler Junior
Publikováno v:
Clinics, Vol 69, Iss suppl 1, Pp 47-50 (2014)
Heart transplantation is an option for children with complex congenital heart disease and cardiomyopathies. A patient's quality of life and long-term survival depend on successful management of the surgical complications and adverse side effects of i
Externí odkaz:
https://doaj.org/article/9b68f5f2f57c40229802ce500561ecb7
Autor:
Marcelo Biscegli Jatene, Décio Cavalet Soares Abuchaim, Marcos G. Tiveron, Carla Tanamati, Nana Miura, Arlindo Riso, Edmar Atik, Antonio Augusto Lopes, Miguel Barbero Marcial
Publikováno v:
Brazilian Journal of Cardiovascular Surgery, Vol 26, Iss 1, Pp 93-97 (2011)
OBJETIVO: Analisar uma série de 34 pacientes adultos submetidos ao tratamento cirúrgico da persistência do canal arterial. MÉTODOS: Estudo retrospectivo, com coleta de dados dos prontuários de 34 pacientes consecutivos, com idade superior a 18 a
Externí odkaz:
https://doaj.org/article/3d6fe045c1bd4765b4e2e923f3200df1
Autor:
Marcelo Biscegli Jatene, Décio Cavalet Soares Abuchaim, José de Lima Oliveira Junior, Arlindo Riso, Carla Tanamati, Nana Miura, Antonio Augusto Lopes, Miguel L Barbero-Marcial
Publikováno v:
Brazilian Journal of Cardiovascular Surgery, Vol 24, Iss 3, Pp 346-353 (2009)
OBJETIVO: Reportar a experiência no tratamento cirúrgico da coarctação da aorta (CoAo) em pacientes adultos, avaliando os resultados imediatos e a médio prazo. MÉTODOS: Entre janeiro de 1987 e março de 2000, 50 pacientes consecutivos adultos f
Externí odkaz:
https://doaj.org/article/d9bb134d8b8e49d0ae3f77a0c5224098