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Pulmonary hypertension is a mild comorbidity in end-stage cystic fibrosis patients.
Belle-van Meerkerk G, Cramer MJ, Kwakkel-van Erp JM, Nugroho MA, Tahri S, de Valk HW, van de Graaf EA. Belle-van Meerkerk G, et al. Among authors: van de graaf ea, de valk hw. J Heart Lung Transplant. 2013 Jun;32(6):609-14. doi: 10.1016/j.healun.2013.03.006. Epub 2013 Apr 9. J Heart Lung Transplant. 2013. PMID: 23582476
Resting energy expenditure in cystic fibrosis patients decreases after lung transplantation, which improves applicability of prediction equations for energy requirement.
Hollander-Kraaijeveld FM, van Lanen AS, de Roos NM, van de Graaf EA, Heijerman HGM. Hollander-Kraaijeveld FM, et al. Among authors: van de graaf ea. J Cyst Fibros. 2020 Nov;19(6):975-980. doi: 10.1016/j.jcf.2020.03.013. Epub 2020 Apr 11. J Cyst Fibros. 2020. PMID: 32291160 Free article. No abstract available.
Cystic Fibrosis-Related Diabetes with strict glycaemic control is not associated with frequent intravenous antibiotics use for pulmonary infections.
Belle-van Meerkerk G, de Valk HW, Stam-Slob MC, Teding van Berkhout F, Zanen P, van de Graaf EA. Belle-van Meerkerk G, et al. Among authors: van de graaf ea, de valk hw. Diabetes Res Clin Pract. 2016 Jun;116:230-6. doi: 10.1016/j.diabres.2016.04.014. Epub 2016 Apr 27. Diabetes Res Clin Pract. 2016. PMID: 27321340
79 results