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Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis.
Sousa M, Servidoni MF, Vinagre AM, Ramalho AS, Bonadia LC, Felício V, Ribeiro MA, Uliyakina I, Marson FA, Kmit A, Cardoso SR, Ribeiro JD, Bertuzzo CS, Sousa L, Kunzelmann K, Ribeiro AF, Amaral MD. Sousa M, et al. Among authors: bertuzzo cs. PLoS One. 2012;7(10):e47708. doi: 10.1371/journal.pone.0047708. Epub 2012 Oct 17. PLoS One. 2012. PMID: 23082198 Free PMC article.
Classification of CFTR mutation classes.
Marson FAL, Bertuzzo CS, Ribeiro JD. Marson FAL, et al. Among authors: bertuzzo cs. Lancet Respir Med. 2016 Aug;4(8):e37-e38. doi: 10.1016/S2213-2600(16)30188-6. Epub 2016 Jul 1. Lancet Respir Med. 2016. PMID: 27377414 No abstract available.
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?
Faria AG, Marson FA, Gomez CC, Ribeiro MÂ, Morais LB, Servidoni MF, Bertuzzo CS, Sakano E, Goto M, Paschoal IA, Pereira MC, Hessel G, Levy CE, Toro AA, Peixoto AO, Simões MC, Lomazi EA, Nogueira RJ, Ribeiro AF, Ribeiro JD. Faria AG, et al. Among authors: bertuzzo cs. Diagn Pathol. 2016 Oct 26;11(1):103. doi: 10.1186/s13000-016-0555-6. Diagn Pathol. 2016. PMID: 27784314 Free PMC article.
72 results