Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Proteinose Alveolar Pulmonar"'
Autor:
Dorneles, Alice Alves Resende, Leão, Amanda Santos, Nascimento, Brenno Barreto, Oliveira, Davison Rodrigues Lima, de Miranda, Eduardo Alves, da Silva, Isadora Arantes Pereira, Leal, Letícia Araujo, Cariello, Louise Habka, Castro, Luana Cristina Farias, Lacerda, Ludymilla Oliveira Portilho, Naves, Maria Eduarda Costa, Pelegrini, Maria Paula Roncaglia, Lopes, Mariana Guimarães, Assunção, Mariana Silva, Oliveira, Mayza Maressa, de Sousa, Melina Bequer, de Oliveira, Renato Domingues Melo, Fernandes, Rogério Wilson Brandão, de Resende, Vitor Coelho Capel, Souza, Vitória de Castro, Legname, Vivian Zulzke Barboza, Anesi, Wellington Airton, Braga, Yan Costa
Publikováno v:
Brazilian Journal of Health Review; Vol. 5 No. 5 (2022); 18268-18277
Brazilian Journal of Health Review; v. 5 n. 5 (2022); 18268-18277
Brazilian Journal of Health Review
Federação das Indústrias do Estado do Paraná (FIEP)
instacron:BJRH
Brazilian Journal of Health Review; v. 5 n. 5 (2022); 18268-18277
Brazilian Journal of Health Review
Federação das Indústrias do Estado do Paraná (FIEP)
instacron:BJRH
INTRODUÇÃO: A Proteinose Alveolar Pulmonar (PAP) é uma síndrome rara causada pelo acúmulo de surfactante no espaço alveolar, mais comumente encontrada em homens com idade média de 20 a 50 anos. É uma patologia com apresentação clínica vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3d59e793f3fbdabf007332c735027b0
https://doi.org/10.34119/bjhrv5n5-039
https://doi.org/10.34119/bjhrv5n5-039
Autor:
João Carlos Thompson, Marina Kishima, Mariana Ulbricht Gomes, Mariano de Almeida Menezes, José Perandré Neto, Paula Tapia Gomes Pereira
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 32, Iss 3, Pp 261-266 (2006)
OBJETIVO: Apresentar a evolução de quatro casos de proteinose alveolar pulmonar atendidos na Faculdade de Medicina da Universidade Estadual de Londrina, enfocando a importância da lavagem pulmonar total como tratamento de escolha. MÉTODOS: Trata-
Externí odkaz:
https://doaj.org/article/eb47cb13abe34121bbb2cd755dd046db
Autor:
Athayde, Rodolfo Augusto Bacelar de, Arimura, Fábio Eiji, Kairalla, Ronaldo Adib, Carvalho, Carlos Roberto Ribeiro, Baldi, Bruno Guedes
Publikováno v:
Jornal Brasileiro de Pneumologia v.44 n.3 2018
Jornal Brasileiro de Pneumologia
Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)
instacron:SBPT
Jornal Brasileiro de Pneumologia, Volume: 44, Issue: 3, Pages: 231-236, Published: MAY 2018
Jornal Brasileiro de Pneumologia
Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)
instacron:SBPT
Jornal Brasileiro de Pneumologia, Volume: 44, Issue: 3, Pages: 231-236, Published: MAY 2018
Objective: Pulmonary alveolar proteinosis (PAP) is a rare disease, characterized by the alveolar accumulation of surfactant, which is composed of proteins and lipids. PAP is caused by a deficit of macrophage activity, for which the main treatment is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::48fa5000b962eb28c4e6d79b65182e29
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132018000300231
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132018000300231
Autor:
Ronaldo Adib Kairalla, F. E. Arimura, Bruno Guedes Baldi, Rodolfo Augusto Bacelar de Athayde, Carlos Roberto Ribeiro de Carvalho
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Jornal Brasileiro de Pneumologia
Jornal Brasileiro de Pneumologia, Vol 44, Iss 3, Pp 231-236
Universidade de São Paulo (USP)
instacron:USP
Jornal Brasileiro de Pneumologia
Jornal Brasileiro de Pneumologia, Vol 44, Iss 3, Pp 231-236
Objective: Pulmonary alveolar proteinosis (PAP) is a rare disease, characterized by the alveolar accumulation of surfactant, which is composed of proteins and lipids. PAP is caused by a deficit of macrophage activity, for which the main treatment is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c838f5ccb786d15a7c96ca6549af1c0
Publikováno v:
Revista Brasileira de Anestesiologia v.62 n.6 2012
Revista Brasileira de Anestesiologia
Sociedade Brasileira de Anestesiologia (SBA)
instacron:SBA
Revista Brasileira de Anestesiologia, Volume: 62, Issue: 6, Pages: 873-877, Published: DEC 2012
Revista Brasileira de Anestesiologia, Vol 62, Iss 6, Pp 873-877 (2012)
Revista Brasileira de Anestesiologia
Sociedade Brasileira de Anestesiologia (SBA)
instacron:SBA
Revista Brasileira de Anestesiologia, Volume: 62, Issue: 6, Pages: 873-877, Published: DEC 2012
Revista Brasileira de Anestesiologia, Vol 62, Iss 6, Pp 873-877 (2012)
JUSTIFICATIVA E OBJETIVOS: O primeiro caso de proteinose alveolar pulmonar (PAP) foi descrito por Rose em 1958, mas ainda é um distúrbio raro. PAP é caracterizada pela deposição de material lipoproteico secundário ao processamento anormal de su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49f8eff75df77ef3f82e860c4e28b7cc
https://doi.org/10.1590/s0034-70942012000600012
https://doi.org/10.1590/s0034-70942012000600012
Publikováno v:
Brazilian Journal of Anesthesiology. 62:869-877
Summary Background and objectives The first case of Pulmonary Alveolar Proteinosis (PAP) was described by Rose in 1958, but it is still a rare disorder. PAP is characterized by deposition of lipoproteinaceous material secondary to abnormal processing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29de5fe5592423c593ec0cab07efdeee
https://doi.org/10.1016/s0034-7094(12)70187-3
https://doi.org/10.1016/s0034-7094(12)70187-3
Publikováno v:
Revista Portuguesa de Pneumologia, Vol 17, Iss 3, Pp 139-142 (2011)
Resumo: A proteinose alveolar pulmonar (PAP) é uma doença rara caracterizada pela acumulação anormal de material lipoproteináceo nos alvéolos, que pode levar a insuficiência respiratória, estando associada a um risco elevado de infecções. O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2a9dc31a370ce418839820b60850993
http://www.sciencedirect.com/science/article/pii/S0873215911000110
http://www.sciencedirect.com/science/article/pii/S0873215911000110
Publikováno v:
Revista Portuguesa de Pneumologia (English Edition), Vol 20, Iss 5, Pp 254-259 (2014)
Revista Portuguesa de Pneumologia, Vol 20, Iss 5, Pp 254-259 (2014)
Revista Portuguesa de Pneumologia, Vol 20, Iss 5, Pp 254-259 (2014)
Whole lung lavage (WLL) is the gold standard technique for the treatment of Pulmonary Alveolar Proteinosis (PAP). In this paper we evaluated and discuss bilateral WLL, namely the procedure work-up and the therapeutic efficacy.Six bilateral WLL perfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9849b200e78d6582d9574a19276b38ca
https://pubmed.ncbi.nlm.nih.gov/25042291
https://pubmed.ncbi.nlm.nih.gov/25042291
Autor:
Rodolfo Augusto Bacelar de Athayde, Fábio Eiji Arimura, Ronaldo Adib Kairalla, Carlos Roberto Ribeiro Carvalho, Bruno Guedes Baldi
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 44, Iss 3, Pp 231-236
ABSTRACT Objective: Pulmonary alveolar proteinosis (PAP) is a rare disease, characterized by the alveolar accumulation of surfactant, which is composed of proteins and lipids. PAP is caused by a deficit of macrophage activity, for which the main trea
Externí odkaz:
https://doaj.org/article/acb6ca9f757b4a6ca86497a097da4364
Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by abnormal accumulation of a lipoproteinaceous material in the alveoli, which may lead to respiratory failure and has an associated high risk for infections. The mainstay treatmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2346::c97bc8835641631520ef1651d7eaa3f1
https://hdl.handle.net/10400.16/869
https://hdl.handle.net/10400.16/869