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Query Trace: Osteoporosis and CFTR[original query]

Disease burden in people with cystic fibrosis heterozygous for F508del and a minimal function mutation. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2021 7 21 (1): 96-103. Sawicki Gregory S, Van Brunt Kate, Booth Jason, Bailey Evan, Millar Stefanie J, Konstan Michael W, Flume Patrick Similar articles in PubMed
Evaluation of bone disease in patients with cystic fibrosis and end-stage lung disease. Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia 2019 Feb 45 (1): e20170280. Robinson Cécile A, Hofer Markus, Benden Christian, Schmid Christo Similar articles in PubMed
Association of clinical severity of cystic fibrosis with variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1 and SLC9A3). Gene 2017 7 629 117-126. Pereira Stéphanie Villa-Nova, Ribeiro José Dirceu, Bertuzzo Carmen Sílvia, Marson Fernando Augusto Li Similar articles in PubMed
Polymorphisms in the glutathione pathway modulate cystic fibrosis severity: a cross-sectional study. BMC medical genetics 2014 15 (1): 27. Marson Fernando Augusto de Lima, Bertuzzo Carmen Silvia, Ribeiro Antonio Fernando, Ribeiro Jose Dirc Similar articles in PubMed
TNF gene polymorphisms in cystic fibrosis patients: contribution to the disease progression. Journal of translational medicine 2013 Jan 11 (1): 1. Shmarina G, Pukhalsky A, Petrova N, Zakharova E, Avakian L, Kapranov N, Alioshkin V Similar articles in PubMed