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For: Lobo J, Rojas-Balcazar JM, Noone PG. Recent advances in cystic fibrosis. Clin Chest Med 2012;33:307-28. [PMID: 22640848 DOI: 10.1016/j.ccm.2012.02.006] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 1.4] [Reference Citation Analysis]
Number Citing Articles
1 AbdulWahab A, Zahraldin K, Sid Ahmed MA, Jarir SA, Muneer M, Mohamed SF, Hamid JM, Hassan AAI, Ibrahim EB. The emergence of multidrug-resistant Pseudomonas aeruginosa in cystic fibrosis patients on inhaled antibiotics. Lung India 2017;34:527-31. [PMID: 29098998 DOI: 10.4103/lungindia.lungindia_39_17] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.4] [Reference Citation Analysis]
2 Jadhav AB, Lurie AG, Tadinada A. Chronic osteitic rhinosinusitis as a manifestation of cystic fibrosis: A case report. Imaging Sci Dent 2014;44:243-7. [PMID: 25279346 DOI: 10.5624/isd.2014.44.3.243] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
3 Tynan A, Mawhinney L, Armstrong ME, O'Reilly C, Kennedy S, Caraher E, Jülicher K, O'Dwyer D, Maher L, Schaffer K, Fabre A, McKone EF, Leng L, Bucala R, Bernhagen J, Cooke G, Donnelly SC. Macrophage migration inhibitory factor enhances Pseudomonas aeruginosa biofilm formation, potentially contributing to cystic fibrosis pathogenesis. FASEB J 2017;31:5102-10. [PMID: 28768722 DOI: 10.1096/fj.201700463R] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
4 Deighan M, Ash S, McMorrow R. Anaesthesia for parturients with severe cystic fibrosis: a case series. Int J Obstet Anesth 2014;23:75-9. [PMID: 24361190 DOI: 10.1016/j.ijoa.2013.10.006] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
5 Naderi N, Peiman S, Alamdari A, Dormohammadi Toosi T, Taghdiri F. A salty cause of cough in a 24-year-old man. Oxf Med Case Reports 2014;2014:71-3. [PMID: 25988033 DOI: 10.1093/omcr/omu029] [Reference Citation Analysis]
6 Vazquez Guillamet R, Ursu O, Iwamoto G, Moseley PL, Oprea T. Chronic obstructive pulmonary disease phenotypes using cluster analysis of electronic medical records. Health Informatics J 2018;24:394-409. [PMID: 27856785 DOI: 10.1177/1460458216675661] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 2.5] [Reference Citation Analysis]
7 Cronly J, Duff A, Riekert K, Horgan A, Lehane E, Perry I, Fitzgerald A, Howe B, Chroinin MN, Savage E. Positive mental health and wellbeing in adults with cystic fibrosis: A cross sectional study. Journal of Psychosomatic Research 2019;116:125-30. [DOI: 10.1016/j.jpsychores.2018.11.016] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
8 Hentschel J, Jäger M, Beiersdorf N, Fischer N, Doht F, Michl RK, Lehmann T, Markert UR, Böer K, Keller PM, Pletz MW, Mainz JG. Dynamics of soluble and cellular inflammatory markers in nasal lavage obtained from cystic fibrosis patients during intravenous antibiotic treatment. BMC Pulm Med 2014;14:82. [PMID: 24885494 DOI: 10.1186/1471-2466-14-82] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.4] [Reference Citation Analysis]
9 Bayomy OF, Ramos KJ, Goss CH. Improving lung transplant outcomes in France: the high emergency lung transplantation programme. Eur Respir J 2022;59:2102209. [PMID: 35086845 DOI: 10.1183/13993003.02209-2021] [Reference Citation Analysis]
10 Jang M, Kim S, Jeong B, Park HY, Jeon K, Kim J, Ki C, Koh W. Association of CFTR gene variants with nontuberculous mycobacterial lung disease in a Korean population with a low prevalence of cystic fibrosis. J Hum Genet 2013;58:298-303. [DOI: 10.1038/jhg.2013.19] [Cited by in Crossref: 17] [Cited by in F6Publishing: 15] [Article Influence: 1.9] [Reference Citation Analysis]
11 Chalasani S, Bettadahalli SS, Bhupathi SV, Aswani VH. A novel case of diabetic muscle necrosis in a patient with cystic fibrosis-related diabetes. Clin Med Res 2013;11:113-6. [PMID: 23656801 DOI: 10.3121/cmr.2013.1124] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
12 Li J, Hao C, Ren L, Xiao Y, Wang J, Qin X. Data Mining of Lung Microbiota in Cystic Fibrosis Patients. PLoS One 2016;11:e0164510. [PMID: 27741283 DOI: 10.1371/journal.pone.0164510] [Cited by in Crossref: 17] [Cited by in F6Publishing: 15] [Article Influence: 2.8] [Reference Citation Analysis]
13 Abdulwahab A, Allangawi M, Thomas M, Bettahi I, Sivaraman SK, Jerobin J, Chandra P, Abou-samra A, Ramanjaneya M. Sputum and plasma adiponectin levels in clinically stable adult cystic fibrosis patients with CFTR I1234V mutation. transl med commun 2020;5. [DOI: 10.1186/s41231-020-00053-2] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
14 Putman MS, Baker JF, Uluer A, Herlyn K, Lapey A, Sicilian L, Tillotson AP, Gordon CM, Merkel PA, Finkelstein JS. Trends in bone mineral density in young adults with cystic fibrosis over a 15 year period. J Cyst Fibros 2015;14:526-32. [PMID: 25698451 DOI: 10.1016/j.jcf.2015.01.011] [Cited by in Crossref: 26] [Cited by in F6Publishing: 24] [Article Influence: 3.7] [Reference Citation Analysis]
15 Kay DM, Maloney B, Hamel R, Pearce M, Demartino L, Mcmahon R, Mcgrath E, Krein L, Vogel B, Saavedra-matiz CA, Caggana M, Tavakoli NP. Screening for cystic fibrosis in New York State: considerations for algorithm improvements. Eur J Pediatr 2016;175:181-93. [DOI: 10.1007/s00431-015-2616-3] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 1.9] [Reference Citation Analysis]
16 Leonardi S, Praticò AD, Rotolo N, Di Dio G, Lionetti E, La Rosa M. Early acute pancreatitis in a child with compound heterozygosis ∆F508/R1438W/Y1032C cystic fibrosis: a case report. J Med Case Rep 2013;7:188. [PMID: 23883480 DOI: 10.1186/1752-1947-7-188] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]