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For: Michl RK, Tabori H, Hentschel J, Beck JF, Mainz JG. Clinical approach to the diagnosis and treatment of cystic fibrosis and CFTR-related disorders. Expert Review of Respiratory Medicine 2016;10:1177-86. [DOI: 10.1080/17476348.2016.1240032] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Cazzola M, Calzetta L, Page C, Rogliani P, Matera MG. Thiol-Based Drugs in Pulmonary Medicine: Much More than Mucolytics. Trends in Pharmacological Sciences 2019;40:452-63. [DOI: 10.1016/j.tips.2019.04.015] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 5.0] [Reference Citation Analysis]
2 Martinez-Millana A, Zettl A, Floch J, Calvo-Lerma J, Sevillano JL, Ribes-Koninckx C, Traver V. The Potential of Self-Management mHealth for Pediatric Cystic Fibrosis: Mixed-Methods Study for Health Care and App Assessment. JMIR Mhealth Uhealth 2019;7:e13362. [PMID: 30998222 DOI: 10.2196/13362] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
3 Iwanicki C, Logomarsino JV. Impaired glucose tolerance, body mass index and respiratory function in patients with cystic fibrosis: A systematic review. Clin Respir J 2019;13:341-54. [PMID: 30919537 DOI: 10.1111/crj.13019] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
4 Kilinc AA, Alishbayli G, Taner HE, Cokugras FC, Cokugras H. Clinical characteristics and genetic analysis of cystic fibrosis transmembrane conductance reseptor-related disease. Pediatr Int 2020;62:629-33. [PMID: 32003094 DOI: 10.1111/ped.14173] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
5 Westholm E, Wendt A, Eliasson L. Islet Function in the Pathogenesis of Cystic Fibrosis-Related Diabetes Mellitus. Clin Med Insights Endocrinol Diabetes 2021;14:11795514211031204. [PMID: 34345195 DOI: 10.1177/11795514211031204] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Freitas DA, Chaves GS, Santino TA, Ribeiro CT, Dias FA, Guerra RO, Mendonça KM. Standard (head-down tilt) versus modified (without head-down tilt) postural drainage in infants and young children with cystic fibrosis. Cochrane Database Syst Rev 2018;3:CD010297. [PMID: 29684249 DOI: 10.1002/14651858.CD010297.pub3] [Reference Citation Analysis]
7 Castaldo A, Cimbalo C, Castaldo RJ, D'Antonio M, Scorza M, Salvadori L, Sepe A, Raia V, Tosco A. Cystic Fibrosis-Screening Positive Inconclusive Diagnosis: Newborn Screening and Long-Term Follow-Up Permits to Early Identify Patients with CFTR-Related Disorders. Diagnostics (Basel) 2020;10:E570. [PMID: 32784480 DOI: 10.3390/diagnostics10080570] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]