Association between the IVS4G > T mutation in the TCF7L2 gene and susceptibility to diabetes in cystic fibrosis patients

Por Furgeri, Daniela Tenório, Marson, Fernando Augusto de Lima, Ribeiro, Antonio Fernando, Bertuzzo, Carmen Silvia
Publicado em 2012

Polymorphisms in the glutathione pathway modulate cystic fibrosis severity: a cross-sectional study

Por Marson, Fernando Augusto de Lima, Bertuzzo, Carmen Silvia, Ribeiro, Antonio Fernando, Ribeiro, Jose Dirceu
Publicado em 2014

Genetic interaction of GSH metabolic pathway genes in cystic fibrosis

Por Marson, Fernando Augusto de Lima, Bertuzzo, Carmen Sílvia, Secolin, Rodrigo, Ribeiro, Antônio Fernando, Ribeiro, José Dirceu
Publicado em 2013

Effects of Pilates mat exercises on muscle strength and on pulmonary function in patients with cystic fibrosis

Por Franco, Caroline Buarque, Ribeiro, Antonio Fernando, Morcillo, André Moreno, Zambon, Mariana Porto, Almeida, Marina Buarque, Rozov, Tatiana
Publicado no J Bras Pneumol (2014)

Hirschsprung's disease - Postsurgical intestinal dysmotility

Por Romaneli, Mariana Tresoldi das Neves, Ribeiro, Antonio Fernando, Bustorff-Silva, Joaquim Murray, de Carvalho, Rita Barbosa, Lomazi, Elizete Aparecida
Publicado no Rev Paul Pediatr (2016)

Cystic fibrosis transmembrane conductance regulator mutations at a referral center for cystic fibrosis

Por Coutinho, Cyntia Arivabeni de Araújo Correia, Marson, Fernando Augusto de Lima, Ribeiro, Antônio Fernando, Ribeiro, José Dirceu, Bertuzzo, Carmen Silvia
Publicado em 2013

Screening for F508del as a first step in the molecular diagnosis of cystic fibrosis,

Por Marson, Fernando Augusto de Lima, Bertuzzo, Carmen Silvia, Ribeiro, Maria Ângela Gonçalves de Oliveira, Ribeiro, Antônio Fernando, Ribeiro, José Dirceu
Publicado em 2013

Assessment of IgG antibodies to Pseudomonas aeruginosa in patients with cystic fibrosis by an enzyme-linked immunosorbent assay (ELISA)

Por Mauch, Renan Marrichi, Rossi, Cláudio Lúcio, Ribeiro, José Dirceu, Ribeiro, Antônio Fernando, Nolasco da Silva, Marcos Tadeu, Levy, Carlos Emílio
Publicado em 2014

Factors impacting the growth and nutritional status of cystic fibrosis patients younger than 10 years of age who did not undergo neonatal screening

Por Hortencio, Taís Daiene Russo, Nogueira, Roberto José Negrão, Marson, Fernando Augusto de Lima, Hessel, Gabriel, Ribeiro, José Dirceu, Ribeiro, Antônio Fernando
Publicado no Rev Paul Pediatr (2015)

Insulin therapy in patients with cystic fibrosis in the pre-diabetes stage: a systematic review

Por Pu, Mariana Zorrón Mei Hsia, Christensen-Adad, Flávia Corrêa, Gonçalves, Aline Cristina, Minicucci, Walter José, Ribeiro, José Dirceu, Ribeiro, Antonio Fernando
Publicado no Rev Paul Pediatr (2016)

Saliva as a potential tool for cystic fibrosis diagnosis

Por Gonçalves, Aline Cristina, Marson, Fernando Augusto de Lima, Mendonça, Regina Maria de Holanda, Ribeiro, José Dirceu, Ribeiro, Antonio Fernando, Paschoal, Ilma Aparecida, Levy, Carlos Emílio
Publicado em 2013

Nasal Potential Difference in Cystic Fibrosis considering Severe CFTR Mutations

Por Ng, Ronny Tah Yen, Marson, Fernando Augusto de Lima, Ribeiro, Jose Dirceu, Ribeiro, Antonio Fernando, Bertuzzo, Carmen Silvia, Ribeiro, Maria Angela Gonçalves de Oliveira, Severino, Silvana Dalge, Sakano, Eulalia
Publicado no Dis Markers (2015)

The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype: Transcriptome Comparative Analysis Searching for the Protective Factors

Por Calyjur, Priscila Clara, Almeida, Camila de Freitas, Ayub-Guerrieri, Danielle, Ribeiro, Antonio Fernando, Fernandes, Stephanie de Alcântara, Ishiba, Renata, dos Santos, Andre Luis Fernandes, Onofre-Oliveira, Paula, Vainzof, Mariz
Publicado no PLoS One (2016)

Pulsed direct and constant direct currents in the pilocarpine iontophoresis sweat chloride test

Por Gomez, Carla Cristina Souza, Servidoni, Maria de Fatima, Marson, Fernando Augusto de Lima, Canavezi, Paulo Jose Coelho, Vinagre, Adriana Mendes, Costa, Eduardo Tavares, Ribeiro, Antonio Fernando, Ribeiro, Maria Angela Gonçalves de Oliveira, Toro, Adyleia Aparecida Dalbo Contrera, Pavan, Celia Regina, Rondon, Michelle Vivine Sá dos Santos, Lorena, Sonia Leticia Silva, Vieria, Francisco Ubaldi, Ribeiro, Jose Dirceu
Publicado no BMC Pulm Med (2014)

Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?

Por Faria, Alethéa Guimarães, Marson, Fernando Augusto Lima, Gomez, Carla Cristina de Souza, Ribeiro, Maria Ângela Gonçalves de Oliveira, Morais, Lucas Brioschi, Servidoni, Maria de Fátima, Bertuzzo, Carmen Sílvia, Sakano, Eulália, Goto, Maura, Paschoal, Ilma Aparecida, Pereira, Mônica Corso, Hessel, Gabriel, Levy, Carlos Emílio, Toro, Adyléia Aparecida Dalbo Contrera, Peixoto, Andressa Oliveira, Simões, Maria Cristina Ribeiro, Lomazi, Elizete Aparecida, Nogueira, Roberto José Negrão, Ribeiro, Antônio Fernando, Ribeiro, José Dirceu
Publicado no Diagn Pathol (2016)

Erratum to: Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?

Por Faria, Alethéa Guimarães, Marson, Fernando Augusto Lima, de Souza Gomez, Carla Cristina, Ribeiro, Maria Ângela Gonçalves de Oliveira, Morais, Lucas Brioschi, de Fátima Servidoni, Maria, Bertuzzo, Carmen Sílvia, Sakano, Eulália, Goto, Maura, Paschoal, Ilma Aparecida, Pereira, Mônica Corso, Hessel, Gabriel, Levy, Carlos Emílio, Toro, Adyléia Aparecida Dalbo Contrera, Peixoto, Andressa Oliveira, Simões, Maria Cristina Ribeiro, Lomazi, Elizete Aparecida, Nogueira, Roberto José Negrão, Ribeiro, Antônio Fernando, Ribeiro, José Dirceu
Publicado no Diagn Pathol (2017)