Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Fernando Antonio de Abreu e Silva"'
Autor:
Clarissa Pitrez Abarno, Maria do Carmo Rocha Laurent, Nair Regina Ritter Ribeiro, Fernando Antonio de Abreu e Silva
Publikováno v:
Clinical and Biomedical Research, Vol 31, Iss 2 (2011)
Trata-se de um estudo documental retrospectivo quantitativo, com o objetivo de caracterizar as crianças e adolescentes com Fibrose Cística atendidos no Hospital de Clínicas de Porto Alegre no período de 2007 e 2008. A população deste estudo car
Externí odkaz:
https://doaj.org/article/70b8e00b063548889719f3855328074d
Publikováno v:
Clinical and Biomedical Research, Vol 31, Iss 2 (2011)
A fibrose cística (FC) completa 73 anos de história desde a sua descrição inicial. Foi a Dra. Dorothy Andersen – uma patologista no Babies’ and Children Hospital at Columbia Presbyterian Medical Center em Nova Iorque que publicou estudo em 19
Externí odkaz:
https://doaj.org/article/1c238a5ab12742378f3f42ec1683070c
Autor:
Paul M. Quinton, Fernando Antonio de Abreu e Silva, Paulo José Cauduro Marostica, Elenara da Fonseca Andrade Procianoy
Publikováno v:
Lung, vol 198, iss 1
PurposeCystic fibrosis (CF) is a multisystem genetic disease caused by dysfunction of the epithelial anionic channel Cystic Fibrosis Transmembrane conductance Regulator (CFTR). Decreased mucociliary clearance because of thickened mucus is part of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a931ab233b315081c03f9c1778adeef4
https://escholarship.org/uc/item/6f05j54m
https://escholarship.org/uc/item/6f05j54m
Autor:
Rodrigo Abensur Athanazio, Luiz Vicente Ribeiro Ferreira da Silva Filho, Alberto Andrade Vergara, Antônio Fernando Ribeiro, Carlos Antônio Riedi, Elenara da Fonseca Andrade Procianoy, Fabíola Villac Adde, Francisco José Caldeira Reis, José Dirceu Ribeiro, Lídia Alice Torres, Marcelo Bicalho de Fuccio, Matias Epifanio, Mônica de Cássia Firmida, Neiva Damaceno, Norberto Ludwig-Neto, Paulo José Cauduro Maróstica, Samia Zahi Rached, Suzana Fonseca de Oliveira Melo, Leonardo Araújo Pinto, Luciana Freitas Velloso Monte, Laurinda Yoko Shinzato Higa, Tania Wrobel Folescu, Fernando Augusto de Lima Marson, Isabela Sad, Maria de Fátima Correa Pimenta Servidoni, Paulo Kussek, Salmo Raskin, Adriana Della Zuana, Albin Augustin, Anneliese Hoffmann, Beatriz Barbisan, Bruno Hochhegger, Carlos Emilio Levy, Claudine Sarmento da Veiga, Claudio Ricachinevsky, Concetta Esposito, Dante Escuissato, Diego Brandemburgo, Elisabeth Marques, Evanirso de Aquino, Gilberto Bueno Fischer, Joaquim Carlos Rodrigues, Leticia Machado, Lucia Muramato, Lusmaia Damasceno Camargo Costa, Marcio Donadio, Marcos César Santos de Castro, Maria Angela Ribeiro, Maria Angélica Santana, Mariane Canan, Marina Buarque de Almeida, Murilo Britto, Paulo Roth Tarso Dalcin, Regina Terse Trindade Ramos, Sonia Chiba, Valéria de Carvalho Martins, Claudine Lacerda, Eliana Barbosa, Elizabet Vilar Guimarães, Gabriel Hessel, Jocemara Gurmini, Lenycia Neri, Marcelo Coelho Nogueira, Mônica Chang Wayhs, Miriam Isabel Santos Simon, Arlene Gonçalves dos Santos Fernandes, Claudia de Castro de Silva, Cristiano Túlio Maciel Albuquerque, Edna Lúcia Souza, Fernando Antonio de Abreu e Silva, Paulo de Tarso Dalcin, Renata Maria de Noronha, Ricardo Teixeira, Sandra Helena Machado, Spencer Marcantonio Camargo, Tatiana Rozov, Ticiana da Costa Rodrigues
Publikováno v:
Jornal Brasileiro de Pneumologia v.43 n.3 2017
Jornal Brasileiro de Pneumologia
Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)
instacron:SBPT
Jornal Brasileiro de Pneumologia, Vol 43, Iss 3, Pp 219-245
Jornal Brasileiro de Pneumologia, Volume: 43, Issue: 3, Pages: 219-245, Published: JUN 2017
Jornal Brasileiro de Pneumologia
Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)
instacron:SBPT
Jornal Brasileiro de Pneumologia, Vol 43, Iss 3, Pp 219-245
Jornal Brasileiro de Pneumologia, Volume: 43, Issue: 3, Pages: 219-245, Published: JUN 2017
Cystic fibrosis (CF) is an autosomal recessive genetic disorder characterized by dysfunction of the CFTR gene. It is a multisystem disease that most often affects White individuals. In recent decades, various advances in the diagnosis and treatment o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::907f2733abedf1cb23fbf66bc14b0cc1
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132017000300219
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132017000300219
Autor:
Themis Reverbel da Silveira, Larisse Longo, Giovana Regina Weber Hoss, Sandra Maria Gonçalves Vieira, Jéssica Tonin Ferrari, Maria Teresa Vieira Sanseverino, Fernando Antonio de Abreu e Silva, Jorge Luiz dos Santos, Leila Xavier Sinigaglia Fratta
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Clinical & Biomedical Research; Vol. 37 No. 2 (2017)
Clinical and Biomedical Research; v. 37 n. 2 (2017)
Clinical and Biomedical Research
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Clinical and Biomedical Research, Vol 37, Iss 2 (2017)
Repositório Institucional da UFRGS
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Clinical & Biomedical Research; Vol. 37 No. 2 (2017)
Clinical and Biomedical Research; v. 37 n. 2 (2017)
Clinical and Biomedical Research
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Clinical and Biomedical Research, Vol 37, Iss 2 (2017)
Repositório Institucional da UFRGS
Biliary atresia (BA) seems to be a multifactorial disorder in which environmental factors interact with the patient’s genetic constitution. This study aimed to analyze information concerning environmental risk factors associated with BA in southern
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bfa5b4a979fae3a23ee7f3061d87d1f
Autor:
Fernando Antonio de Abreu e Silva, Danilo C. Berton, Luiz Felipe Fröhlich, Paulo José Zimermann Teixeira, Paulo J.C. Vieira, Jorge Pinto Ribeiro
Publikováno v:
Pediatric Pulmonology. 49:911-918
Background: Post-infectious bronchiolitis obliterans (PBO) is a chronic lung disease characterized by the persistence of continuous obstructive respiratory symptoms following an acute and severe respiratory infection in children under 3 years old. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cea3ef6d347df8124b5eb616a95ad26a
https://doi.org/10.1002/ppul.22929
https://doi.org/10.1002/ppul.22929
Publikováno v:
Jornal Brasileiro de Pneumologia v.34 n.5 2008
Jornal Brasileiro de Pneumologia
Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)
instacron:SBPT
Jornal Brasileiro de Pneumologia, Volume: 34, Issue: 5, Pages: 280-287, Published: MAY 2008
Jornal Brasileiro de Pneumologia
Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)
instacron:SBPT
Jornal Brasileiro de Pneumologia, Volume: 34, Issue: 5, Pages: 280-287, Published: MAY 2008
OBJETIVO: Estudar as relações entre função pulmonar, radiologia de tórax e estado clínico em fibrose cística. MÉTODOS: Em estudo transversal e retrospectivo, analisaram-se prontuários e radiografias de pacientes do Hospital de Clínicas de P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a92edbe8b28409129a8069ca9963880e
https://doi.org/10.1590/s1806-37132008000500006
https://doi.org/10.1590/s1806-37132008000500006
Autor:
Rodolpho Mattos Albano, Elizabeth de Andrade Marques, Alexandre P. Zavascki, Afonso Luis Barth, Anneliese Hoffmann, Fernando Antonio de Abreu e Silva, Alex Guerra Ferreira, Luiz Gonzaga da Cunha, Maria Izolete Vieira
Publikováno v:
Journal of Clinical Microbiology. 45:4077-4080
Burkholderia pseudomallei is rarely isolated from cystic fibrosis patients outside known areas of endemicity. We report the recovery of B. pseudomallei from the sputum of a cystic fibrosis patient who lives in Brazil. We highlight the importance of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc63d04bc82978f4e33a53289329237d
https://doi.org/10.1128/jcm.01386-07
https://doi.org/10.1128/jcm.01386-07
Publikováno v:
Revista Brasileira de Otorrinolaringologia v.73 n.4 2007
Revista Brasileira de Otorrinolaringologia
Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial (ABORL-CCF)
instacron:ABORL-F
Revista Brasileira de Otorrinolaringologia
Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial (ABORL-CCF)
instacron:ABORL-F
The combination of factors, such as abnormal viscosity of the paranasal sinus secretions, decreased sinus drainage, and impaired mucociliary clearance may account for the establishment of a suitable and opportune environment for the colonization of b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00a868bfa21f5b4930d581766b6707f6
https://doi.org/10.1590/s0034-72992007000400007
https://doi.org/10.1590/s0034-72992007000400007
Autor:
Fernando Antonio de Abreu e Silva, Afonso Luis Barth, Elizabeth Andrade Marques, Mônica de Cássia Firmida, Vilma Almeida Paixão, Tania Wrobel Folescu, Alex Guerra Ferreira, Maria Angélica Santana, Robson Souza Leão, Érica Aparecida Dos Santos Ribeiro da Silva, Ana Paula D'Alincourt Carvalho-Assef
Publikováno v:
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica. 123(12)
A prospective study was conducted in Brazil to evaluate antimicrobial resistance patterns and molecular epidemiology of Pseudomonas aeruginosa isolates from cystic fibrosis (CF) patients with chronic lung infection. All isolates were obtained between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c766ed85fb5c1769a7d39880b0bb33cb
https://pubmed.ncbi.nlm.nih.gov/26522829
https://pubmed.ncbi.nlm.nih.gov/26522829