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You are here: Respiratory Tract » Cystic Fibrosis

10. August 2022

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	Articles 1 - 20 / 17219

	Achromobacter spp. prevalence and adaptation in cystic fibrosis lung infection. Microbiol Res Veschetti L, Boaretti M, Saitta GM, Passarelli Mantovani R, Lleò MM, Sandri A, Malerba G. PMID: 35931003 [PubMed - as supplied by publisher]
	Dornase alfa in Cystic Fibrosis: indications, comparative studies and effects on lung clearance index. Ital J Pediatr Terlizzi V, Castellani C, Taccetti G, Ferrari B. PMID: 35927765 [PubMed - indexed for MEDLINE]
	A step forward for an intermediate cystic fibrosis population. Eur Respir J Birket SE. PMID: 35926867 [PubMed - indexed for MEDLINE]
	A systematic review of lung clearance index in non-cystic fibrosis, non-primary ciliary dyskinesia bronchiectasis. Respir Med Hine C, Desai M, Davies J, Sapey E, Nagakumar P. PMID: 35926429 [PubMed - as supplied by publisher]
	Surgical considerations in cystic fibrosis: what every general surgeon needs to know. ANZ J Surg Chetwood JD, Volovets A, Sivam S, Koh C. PMID: 35920692 [PubMed - as supplied by publisher]
	Global prevalence of non-tuberculous mycobacteria in adults with non-cystic fibrosis bronchiectasis 2006-2021: a systematic review and meta-analysis. BMJ Open Zhou Y, Mu W, Zhang J, Wen SW, Pakhale S. PMID: 35914904 [PubMed - indexed for MEDLINE]
	Inhaled antibiotics for pulmonary exacerbations in cystic fibrosis. Cochrane Database Syst Rev Smith S, Rowbotham NJ, Charbek E. PMID: 35914011 [PubMed - indexed for MEDLINE]
	Educational achievements of children aged 10-11 years with cystic fibrosis. A data linkage study in Wales. Int J Popul Data Sci Schlüter DK, Griffiths R, Akbari A, Taylor-Robinson D. PMID: 35909577 [PubMed - indexed for MEDLINE]
	Continuous glucose monitoring versus self-monitoring of blood glucose in the management of cystic fibrosis related diabetes: A systematic review and meta-analysis. J Cyst Fibros Kumar S, Soldatos G, Ranasinha S, Teede H, Pallin M. PMID: 35906171 [PubMed - as supplied by publisher]
	Therapeutic applications of curcumin nanomedicine formulations in cystic fibrosis. Prog Biomater Quispe C, Herrera-Bravo J, Khan K, Javed Z, Semwal P, Painuli S, Kamiloglu S, Martorell M, Calina D, Sharifi-Rad J. PMID: 35904711 [PubMed - as supplied by publisher]
	Epidemiology of Eosinophilic Esophagitis in Patients with Cystic Fibrosis: A Population-Based 5-Year Study. Pediatr Gastroenterol Hepatol Nutr Alaber O, Sabe R, Baez-Socorro V, Sankararaman S, Roesch E, Sferra TJ. PMID: 35903489 [PubMed]
	Trends in Growth and Maturation in Children with Cystic Fibrosis Throughout Nine Decades. Front Endocrinol (Lausanne) Mason KA, Rogol AD. PMID: 35903281 [PubMed - indexed for MEDLINE]
	Gut Bifidobacteria enrichment following oral Lactobacillus-supplementation is associated with clinical improvements in children with cystic fibrosis. BMC Pulm Med Ray KJ, Santee C, McCauley K, Panzer AR, Lynch SV. PMID: 35902830 [PubMed - indexed for MEDLINE]
	Is there a role of viral infection in cystic fibrosis exacerbation in children? Turk J Pediatr Hamed DH, Soliman MS, Emam OS, El-Attar MM. PMID: 35899568 [PubMed - indexed for MEDLINE]
	Cystic fibrosis associated with Wernicke's encephalopathy in an older adult. BMJ Case Rep Vijayavel N, Koh SW, Goodman EL. PMID: 35896303 [PubMed - indexed for MEDLINE]
	Biologic drugs in treating allergic bronchopulmonary aspergillosis in patients with cystic fibrosis: a systematic review. Eur Respir Rev Manti S, Giallongo A, Parisi GF, Papale M, Mulè E, Aloisio D, Rotolo N, Leonardi S. PMID: 35896271 [PubMed - indexed for MEDLINE]
	Newborn Screening for Cystic Fibrosis: A Qualitative Study of Successes and Challenges from Universal Screening in the United States. Int J Neonatal Screen Sontag MK, Miller JI, McKasson S, Gaviglio A, Martiniano SL, West R, Vazquez M, Ren CL, Farrell PM, McColley SA, Kellar-Guenther Y. PMID: 35892468 [PubMed]
	The Use of Artificial Sputum Media to Enhance Investigation and Subsequent Treatment of Cystic Fibrosis Bacterial Infections. Microorganisms Aiyer A, Manos J. PMID: 35888988 [PubMed]
	Auxological and Endocrinological Features in Children and Adolescents with Cystic Fibrosis. J Clin Med Ferrari V, Terlizzi V, Stagi S. PMID: 35887806 [PubMed]
	Emerging Concepts in Defective Macrophage Phagocytosis in Cystic Fibrosis. Int J Mol Sci Jaganathan D, Bruscia EM, Kopp BT. PMID: 35887098 [PubMed - indexed for MEDLINE]

Articles 1 - 20 / 17219

Page 1 of 861



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