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Search on : RIBEIRO, ANTONIO FERNANDO [Author]
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 Romaneli, Mariana Tresoldi das Neves et al. Hirschsprung's disease - Postsurgical intestinal dysmotility. Rev. paul. pediatr., Sept 2016, vol.34, no.3, p.388-392. ISSN 0103-0582


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 Pu, Mariana Zorrón Mei Hsia et al. Insulin therapy in patients with cystic fibrosis in the pre-diabetes stage: a systematic review. Rev. paul. pediatr., Sept 2016, vol.34, no.3, p.367-373. ISSN 0103-0582


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 Hortencio, Taís Daiene Russo et al. Factors impacting the growth and nutritional status of cystic fibrosis patients younger than 10 years of age who did not undergo neonatal screening. Rev. paul. pediatr., Mar 2015, vol.33, no.1, p.3-11. ISSN 0103-0582


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 Sundell, Michelle de Oliveira T. et al. Kwashiorkor e distúrbio de coagulação: apresentação atípica de fibrose cística. Rev. paul. pediatr., 2012, vol.30, no.1, p.139-143. ISSN 0103-0582


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 Carmo, Rafael L.M.L. et al. Colonic transit in children and adolescents with chronic constipation. J. Pediatr. (Rio J.), Aug 2015, vol.91, no.4, p.386-391. ISSN 0021-7557


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 Faria, Elisangela Jacinto de et al. Associação entre deficiência de alfa-1-antitripsina e a gravidade da fibrose cística. J. Pediatr. (Rio J.), Dez 2005, vol.81, no.6, p.485-490. ISSN 0021-7557


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 Ribeiro, Jose Dirceu, Ribeiro, Maria Ângela G. de O. and Ribeiro, Antonio Fernando Controvérsias na fibrose cística: do pediatra ao especialista. J. Pediatr. (Rio J.), Dez 2002, vol.78, suppl.2, p.171-186. ISSN 0021-7557


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 Cohen, Milena Antonelli et al. Avaliação da qualidade de vida de pacientes com fibrose cística por meio do Cystic Fibrosis Questionnaire. J. bras. pneumol., Abr 2011, vol.37, no.2, p.184-192. ISSN 1806-3713


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 Lima, Carmen Silvia Passos et al. Mutações do gene cystic fibrosis transmembrane conductance regulator e deleções dos genes glutationa S-transferase em pacientes com fibrose cística no Brasil. J. bras. pneumol., Fev 2012, vol.38, no.1, p.50-56. ISSN 1806-3713


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 Franco, Caroline Buarque et al. Effects of Pilates mat exercises on muscle strength and on pulmonary function in patients with cystic fibrosis. J. bras. pneumol., Oct 2014, vol.40, no.5, p.521-527. ISSN 1806-3713


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