Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Edna Lucia Souza"'
Autor:
Edna Lucia Souza, Renata Silva Girão, Juçara Magalhães Simões, Carolina Ferraz Reis, Naiara Araújo Galvão, Sandra Cristina S. Andrade, Denise Mattedi F. Werneck, César A. Araújo-Neto, Leda Solano F. Souza
Publikováno v:
Jornal de Pediatria, Vol 88, Iss 5, Pp 423-429 (2012)
OBJETIVOS: Determinar a prevalência de infecção do trato respiratório inferior (ITRI) por Chlamydia trachomatis em lactentes internados e descrever as características clínicas, laboratoriais e radiológicas da doença. MÉTODOS: Este foi um est
Externí odkaz:
https://doaj.org/article/0280891b12254a3da2de23e249a34124
Publikováno v:
Cadernos de Saúde Pública, Vol 40, Iss 7 (2024)
Abstract: The Brazilian Unified National Health System (SUS) has incorporated newborn screening for cystic fibrosis since 2001. The protocol involves two samples of immunoreactive trypsinogen (IRT1/IRT2). This study aims to analyze fixed and floating
Externí odkaz:
https://doaj.org/article/2083f15edf81403798a9b659eaf502c6
Autor:
Adson Santos Martins, Samara Alves Santos, Cláudia Alves da Silva Lisboa, Tânia Fraga Barros, Tereza Cristina Medrado Ribeiro, Hugo da Costa-Ribeiro, Ângela Peixoto de Mattos, Patrícia Silva de Almeida Mendes, Carlos Maurício Cardeal Mendes, Edna Lúcia Souza, Ana Lúcia Moreno Amor, Neci Matos Soares, Márcia Cristina Aquino Teixeira
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 44, Iss 1, Pp 80-91 (2024)
Introduction. The multifactorial etiology of gastroenteritis emphasizes the need for different laboratory methods to identify or exclude infectious agents and evaluate the severity of diarrheal disease. Objective. To diagnose the infectious etiology
Externí odkaz:
https://doaj.org/article/b369d92cf90a4f7e8cec233b141b6e35
Autor:
Carolina Godoy, Igor Radel, Laís Ribeiro Mota, Marília Augusta Santos, Regina Terse, Edna Lúcia Souza
Publikováno v:
Revista Brasileira de Saúde Materno Infantil, Vol 24 (2024)
Abstract Introduction: cystic fibrosis newborn screening must enable its earlier diagnosis, which may enhance outcomes. This study was a series case of delayed-diagnosis children submitted to cystic fibrosis newborn screening. Description: fourteen c
Externí odkaz:
https://doaj.org/article/012aa7f975fe45b5a41251dee512d6d1
Five-year performance analysis of a cystic fibrosis newborn screening program in northeastern Brazil
Autor:
Carolina Godoy, Danielle C. Paixão, Ney C.A. Boa-Sorte, Tatiana Amorim, Luiz Vicente R.F. da Silva Filho, Edna Lúcia Souza
Publikováno v:
Jornal de Pediatria, Vol 99, Iss 1, Pp 23-30 (2023)
Objective: To analyze the performance of the cystic fibrosis (CF) newborn screening (NBS) program over its first five years in a Brazilian northeastern state. Method: A population-based study using a screening algorithm based on immunoreactive trypsi
Externí odkaz:
https://doaj.org/article/df89df86ac6846edb3dcb42b64c80f40
Autor:
Rodrigo Abensur Athanazio, Suzana Erico Tanni, Juliana Ferreira, Paulo de Tarso Roth Dalcin, Marcelo B de Fuccio, Concetta Esposito, Mariane Gonçalves Martynychen Canan, Liana Sousa Coelho, Mônica de Cássia Firmida, Marina Buarque de Almeida, Paulo José Cauduro Marostica, Luciana de Freitas Velloso Monte, Edna Lúcia Souza, Leonardo Araujo Pinto, Samia Zahi Rached, Verônica Stasiak Bednarczuk de Oliveira, Carlos Antonio Riedi, Luiz Vicente Ribeiro Ferreira da Silva Filho
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 49, Iss 2 (2023)
ABSTRACT Cystic fibrosis (CF) is a genetic disease that results in dysfunction of the CF transmembrane conductance regulator (CFTR) protein, which is a chloride and bicarbonate channel expressed in the apical portion of epithelial cells of various or
Externí odkaz:
https://doaj.org/article/2ee12dd8b3bd413899822534cd8fd4b1
Autor:
Fernanda Matos Fontenelle, Lucas da Silva Vieira, Adriana Virgínia Barros Faiçal, Marcia Cristina Aquino Teixeira, Juliana Cana Brazil, Edna Lúcia Souza
Publikováno v:
Jornal de Assistência Farmacêutica e Farmacoeconomia, Vol 1, Iss s.2 (2023)
Introdução: A fibrose cística (FC) é uma doença hereditária, autossômica recessiva, causada por mutações no gene Cystic Fibrosis Transmembrane Regulator. Este gene codifica a proteína de mesmo nome, responsável pelo transporte de íons atr
Externí odkaz:
https://doaj.org/article/eed24c1908504222848af716dfaa2a39
Autor:
Fernanda de S. Nascimento, Nelson A. Sena, Tatiane da A. Ferreira, Cibele D.F. Marques, Luciana R. Silva, Edna Lúcia Souza
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 94, Iss 5, Pp 504-510 (2018)
Objectives: The aims of the study were to determine the frequency of hepatobiliary disease in patients with cystic fibrosis and to describe the sociodemographic, clinical, and laboratory profile of these patients. Methods: This was a retrospective, d
Externí odkaz:
https://doaj.org/article/12412ee899724f8bb8898b390a9374ab
Autor:
Fernanda de S. Nascimento, Nelson A. Sena, Tatiane da A. Ferreira, Cibele D.F. Marques, Luciana R. Silva, Edna Lúcia Souza
Publikováno v:
Jornal de Pediatria, Vol 94, Iss 5, Pp 504-510 (2018)
Objectives: The aims of the study were to determine the frequency of hepatobiliary disease in patients with cystic fibrosis and to describe the sociodemographic, clinical, and laboratory profile of these patients. Methods: This was a retrospective, d
Externí odkaz:
https://doaj.org/article/fa9db40d02234ee0b7c42755e93c60e0
Autor:
Paloma Horejs Bittencourt, Carlos Sidney Silva Pimentel, Bianca Sampaio Bonfim, Paulo José Marostica, Edna Lúcia Souza
Publikováno v:
Brazilian Journal of Infectious Diseases, Vol 21, Iss 1, Pp 107-111 (2017)
In Brazil the knowledge about methicillin-resistant Staphylococcus aureus infection in cystic fibrosis patients is scarce. This study aimed to determine the incidence of respiratory tract colonization and the identification rates after a standardized
Externí odkaz:
https://doaj.org/article/a46a36d8591e4ee4b2256a35b6cdd894