Search Results - "Pecchini, Rogério"

Parainfluenza virus as a cause of acute respiratory infection in hospitalized children by Pecchini, Rogério, Berezin, Eitan Naaman, Souza, Maria Cândida, de Andrade Vaz-de-Lima, Lourdes, Sato, Neuza, Salgado, Maristela, Ueda, Mirthes, Passos, Saulo Duarte, Rangel, Raphael, Catebelota, Ana

“…Human parainfluenza viruses account for a significant proportion of lower respiratory tract infections in children. To assess the prevalence of Human…”
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Incidence and clinical characteristics of the infection by the respiratory syncytial virus in children admitted in Santa Casa de São Paulo Hospital by Pecchini, Rogério, Berezin, Eitan N, Felício, Maria C Calahani, Passos, Saulo D, Souza, Maria Cândido O de, Lima, Lourdes Rehder de Andrade Vaz de, Ueda, Mirthes, Matsumoto, Tokiko Kyomen, Durigon, Edison L

“…The purpose of this study was to identify the rate of infections due to RSV and other viruses in children. In addition we have analyzed demographic data and…”
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Parainfluenza virus as a cause of acute respiratory infection in hospitalized childrens by Pecchini, Rogério, Berezin, Eitan Naaman, Souza, Maria Cândida, Vaz-de-Lima, Lourdes de Andrade, Sato, Neuza, Salgado, Maristela, Ueda, Mirthes, Passos, Saulo Duarte, Rangel, Raphael, Catebelota, Ana

“…Background: Human parainfluenza viruses account for a significant proportion of lower respiratory tract infections in children.Objective: To assess the…”
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Phylodynamics and dispersal of HRSV entails its permanence in the general population in between yearly outbreaks in children by Katzov-Eckert, Hagit, Botosso, Viviane F, Neto, Eurico Arruda, Zanotto, Paolo Marinho de Andrade

“…Human respiratory syncytial virus (HRSV) is one of the major etiologic agents of respiratory tract infections among children worldwide. Here through a…”
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Pompe disease in a Brazilian series: clinical and molecular analyses with identification of nine new mutations by Oba-Shinjo, Sueli M., da Silva, Roseli, Andrade, Fernanda G., Palmer, Rachel E., Pomponio, Robert J., Ciociola, Kristina M., S. Carvalho, Mary, Gutierrez, Paulo S., Porta, Gilda, Marrone, Carlo D., Munoz, Verônica, Grzesiuk, Anderson K., Llerena, Juan C., Berditchevsky, Célia R., Sobreira, Claudia, Horovitz, Dafne, Hatem, Thamine P., Frota, Elizabeth R. C., Pecchini, Rogerio, Kouyoumdjian, João Aris, Werneck, Lineu, Amado, Veronica M., Camelo, José S., Mattaliano, Robert J., Marie, Suely K. N.

“…Pompe disease (glycogen storage disease type II or acid maltase deficiency) is an inherited autosomal recessive deficiency of acid α-glucosidase (GAA), with…”
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