Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Eurico Camargo Neto"'
Autor:
Heydy Bravo, Eurico Camargo Neto, Jaqueline Schulte, Jamile Pereira, Claudio Sampaio Filho, Fernanda Bittencourt, Fernanda Sebastião, Fernanda Bender, Ana Paula Scholz de Magalhães, Régis Guidobono, Franciele Barbosa Trapp, Kristiane Michelin-Tirelli, Carolina F.M. Souza, Diana Rojas Málaga, Gabriela Pasqualim, Ana Carolina Brusius-Facchin, Roberto Giugliani
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 12, Iss C, Pp 92-97 (2017)
Lysosomal storage diseases (LSDs) are genetic disorders, clinically heterogeneous, mainly caused by defects in genes encoding lysosomal enzymes that degrade macromolecules. Several LSDs already have specific therapies that may improve clinical outcom
Externí odkaz:
https://doaj.org/article/a2fe1b980788428984281a4eabc80911
Autor:
Eurico Camargo Neto, Jaqueline Schulte, Jamile Pereira, Heydy Bravo, Claudio Sampaio-Filho, Roberto Giugliani
Publikováno v:
Genetics and Molecular Biology, Iss 0 (2018)
Abstract We describe the initial results of a neonatal screening program for four lysosomal storage diseases (MPS I, Pompe, Gaucher and Fabry) using the digital microfluidics methodology. The method successfully identified patients previously diagnos
Externí odkaz:
https://doaj.org/article/0beabbf544b647ca91b1aa99311dbb22
Autor:
Clarissa Gutiérrez Carvalho, Renato Soibelmann Procianoy, Eurico Camargo Neto, Rita C. Silveira
Publikováno v:
Journal of Immunology Research, Vol 2018 (2018)
Ventilator-induced lung injury is well recognized, and appropriate arterial saturation target is unknown, so gentle modes of ventilation and minimizing oxidative stress have been well studied. Our objective was to analyze any association between the
Externí odkaz:
https://doaj.org/article/52c1d8fd2e2d4c7a8afcba7847ad20e1
Autor:
Clarissa Gutierrez Carvalho, Rita de Cassia Silveira, Eurico Camargo Neto, Renato Soibelmann Procianoy
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120486 (2015)
Early nCPAP seems to prevent ventilator-induced lung injury in humans, although the pathophysiological mechanisms underlying this beneficial effect have not been clarified yet.To evaluate plasma levels IL-1β, IL-6, IL-8, IL-10, and TNF-α immediatel
Externí odkaz:
https://doaj.org/article/2db90ce059774f1cbbf7541a2262c113
Publikováno v:
Emerging Infectious Diseases, Vol 10, Iss 6, Pp 1069-1073 (2004)
To estimate the prevalence of congenital toxoplasmosis, Chagas disease, cytomegalovirus, and rubella, blood samples on dried blood spot (DBS) from neonates (day 3–20 of life) were screened for immunoglobulin (Ig) M against Toxoplasma gondii, cytome
Externí odkaz:
https://doaj.org/article/d26418efb8b64316996ed9629f28c480
Autor:
Liane Esteves Daudt, Débora Zechmaister, Liliana Portal, Eurico Camargo Neto, Lúcia Mariano da Rocha Silla, Roberto Giugliani
Publikováno v:
Cadernos de Saúde Pública, Vol 18, Iss 3, Pp 833-841 (2002)
Este estudo, tem como o objetivo determinar a freqüência das hemoglobinopatias em neonatos, que realizaram a coleta para o Teste de Triagem Neonatal para Distúrbios Metabólicos no Hospital de Clínicas de Porto Alegre. O método utilizado para a
Externí odkaz:
https://doaj.org/article/bc9066a5162140e299a81dfa8dd41eb3
Triagem neonatal para hemoglobinopatias: um estudo piloto em Porto Alegre, Rio Grande do Sul, Brasil
Autor:
Liane Esteves Daudt, Débora Zechmaister, Liliana Portal, Eurico Camargo Neto, Lúcia Mariano da Rocha Silla, Roberto Giugliani
Publikováno v:
Cadernos de Saúde Pública, Vol 18, Iss 3, Pp 833-841
Este estudo, tem como o objetivo determinar a freqüência das hemoglobinopatias em neonatos, que realizaram a coleta para o Teste de Triagem Neonatal para Distúrbios Metabólicos no Hospital de Clínicas de Porto Alegre. O método utilizado para a
Externí odkaz:
https://doaj.org/article/41541be2973a4a2d8354f7407c3f6a13
Triagem neonatal para hemoglobinopatias: um estudo piloto em Porto Alegre, Rio Grande do Sul, Brasil
Autor:
Liane Esteves Daudt, Débora Zechmaister, Liliana Portal, Eurico Camargo Neto, Lúcia Mariano da Rocha Silla, Roberto Giugliani
Publikováno v:
Cadernos de Saúde Pública, Vol 18, Iss 3, Pp 833-841
Este estudo, tem como o objetivo determinar a freqüência das hemoglobinopatias em neonatos, que realizaram a coleta para o Teste de Triagem Neonatal para Distúrbios Metabólicos no Hospital de Clínicas de Porto Alegre. O método utilizado para a
Externí odkaz:
https://doaj.org/article/99ae8ad287754aa784a6bc543f561d5a
Autor:
Fernanda Machado Bittencourt, Jaqueline Schulte, Kristiane Michelin-Tirelli, Carolina Fischinger Moura de Souza, Eurico Camargo Neto, Franciele Barbosa Trapp, Jamile Pereira, Roberto Giugliani, Gabriela Pasqualim, Ana Paula Pereira Scholz de Magalhães, Ana Carolina Brusius-Facchin, Diana Rojas Málaga, Heydy Bravo, Fernanda Bender, Claudio Sampaio Filho, Regis Rolim Guidobono, Fernanda Medeiros Sebastião
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 12, Iss C, Pp 92-97 (2017)
Molecular Genetics and Metabolism Reports, Vol 12, Iss C, Pp 92-97 (2017)
Lysosomal storage diseases (LSDs) are genetic disorders, clinically heterogeneous, mainly caused by defects in genes encoding lysosomal enzymes that degrade macromolecules. Several LSDs already have specific therapies that may improve clinical outcom
Autor:
Jamile Pereira, Heydy Bravo, Claudio Sampaio-Filho, Roberto Giugliani, Jaqueline Schulte, Eurico Camargo Neto
Publikováno v:
Genetics and Molecular Biology v.41 n.2 2018
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Iss 0 (2018)
Genetics and Molecular Biology, Volume: 41, Issue: 2, Pages: 414-416, Published: 04 JUN 2018
Genetics and Molecular Biology, Issue: ahead, Published: 04 JUN 2018
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Iss 0 (2018)
Genetics and Molecular Biology, Volume: 41, Issue: 2, Pages: 414-416, Published: 04 JUN 2018
Genetics and Molecular Biology, Issue: ahead, Published: 04 JUN 2018
We describe the initial results of a neonatal screening program for four lysosomal storage diseases (MPS I, Pompe, Gaucher and Fabry) using the digital microfluidics methodology. The method successfully identified patients previously diagnosed with t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88d0da7ac814f2355d546f170746d90c
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572018000300414
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572018000300414