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For: Kelly T, Buxbaum J. Gastrointestinal Manifestations of Cystic Fibrosis. Dig Dis Sci 2015;60:1903-13. [DOI: 10.1007/s10620-015-3546-7] [Cited by in Crossref: 50] [Cited by in F6Publishing: 40] [Article Influence: 7.1] [Reference Citation Analysis]
Number Citing Articles
1 Timothy Adewale A, Rowe SM, Solomon GM. Colocolonic intussusception in an adult cystic fibrosis patient. J Cyst Fibros 2019;18:e11-3. [PMID: 30503033 DOI: 10.1016/j.jcf.2018.11.013] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
2 Trandafir LM, Leon MM, Frasinariu O, Baciu G, Dodi G, Cojocaru E. Current Practices and Potential Nanotechnology Perspectives for Pain Related to Cystic Fibrosis. J Clin Med 2019;8:E1023. [PMID: 31336857 DOI: 10.3390/jcm8071023] [Reference Citation Analysis]
3 Filbrun AG, Lahiri T, Ren CL. Clinical Features and Complications of Cystic Fibrosis. Handbook of Cystic Fibrosis. Cham: Springer International Publishing; 2016. pp. 9-41. [DOI: 10.1007/978-3-319-32504-0_3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
4 Lamothe S, Zhang S. Chapter Five - Ubiquitination of Ion Channels and Transporters. Ubiquitination and Transmembrane Signaling. Elsevier; 2016. pp. 161-223. [DOI: 10.1016/bs.pmbts.2016.02.005] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
5 Ngo AV, Stanescu AL, Phillips GS. Neonatal Bowel Disorders: Practical Imaging Algorithm for Trainees and General Radiologists. AJR Am J Roentgenol 2018;210:976-88. [PMID: 29528714 DOI: 10.2214/AJR.17.19378] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 1.3] [Reference Citation Analysis]
6 Gini A, Zauber AG, Cenin DR, Omidvari A, Hempstead SE, Fink AK, Lowenfels AB, Lansdorp-vogelaar I. Cost-Effectiveness of Screening Individuals With Cystic Fibrosis for Colorectal Cancer. Gastroenterology 2017. [DOI: 10.1053/j.gastro.2017.12.011] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.6] [Reference Citation Analysis]
7 Wilbert F, Grünert SC, Heinzmann A, Bode SFN. Cystic fibrosis in disguise - the wolf in sheep's clothing, a case report. BMC Pediatr 2021;21:174. [PMID: 33853553 DOI: 10.1186/s12887-021-02636-w] [Reference Citation Analysis]
8 Tabori H, Jaudszus A, Arnold C, Mentzel HJ, Lorenz M, Michl RK, Lehmann T, Renz DM, Mainz JG. Relation of Ultrasound Findings and Abdominal Symptoms obtained with the CFAbd-Score in Cystic Fibrosis Patients. Sci Rep 2017;7:17465. [PMID: 29234058 DOI: 10.1038/s41598-017-17302-4] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
9 Dos Santos ALM, de Melo Santos H, Nogueira MB, Távora HTO, de Lourdes Jaborandy Paim da Cunha M, de Melo Seixas RBP, de Freitas Velloso Monte L, de Carvalho E. Cystic Fibrosis: Clinical Phenotypes in Children and Adolescents. Pediatr Gastroenterol Hepatol Nutr 2018;21:306-14. [PMID: 30345244 DOI: 10.5223/pghn.2018.21.4.306] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
10 Desseyn J, Gouyer V, Gottrand F. Biological modeling of mucus to modulate mucus barriers. American Journal of Physiology-Gastrointestinal and Liver Physiology 2016;310:G225-7. [DOI: 10.1152/ajpgi.00274.2015] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
11 do Carmo TIT, Soares VEM, Wruck J, Dos Anjos F, de Resende E Silva DT, de Oliveira Maciel SFV, Bagatini MD. Hyperinflammation and airway surface liquid dehydration in cystic fibrosis: purinergic system as therapeutic target. Inflamm Res 2021;70:633-49. [PMID: 33904934 DOI: 10.1007/s00011-021-01464-z] [Reference Citation Analysis]
12 Pfahler MHC, Kratzer W, Leichsenring M, Graeter T, Schmidt SA, Wendlik I, Lormes E, Schmidberger J, Fabricius D. Point shear wave elastography of the pancreas in patients with cystic fibrosis: a comparison with healthy controls. Abdom Radiol 2018;43:2384-90. [DOI: 10.1007/s00261-018-1479-2] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.8] [Reference Citation Analysis]
13 Goetz D, Ren CL. Review of Cystic Fibrosis. Pediatr Ann 2019;48:e154-61. [PMID: 30986316 DOI: 10.3928/19382359-20190327-01] [Cited by in Crossref: 24] [Cited by in F6Publishing: 23] [Article Influence: 8.0] [Reference Citation Analysis]
14 Cil O, Haggie PM, Tan JT, Rivera AA, Verkman AS. SLC26A6-selective inhibitor identified in a small-molecule screen blocks fluid absorption in small intestine. JCI Insight 2021;6:147699. [PMID: 34100381 DOI: 10.1172/jci.insight.147699] [Reference Citation Analysis]
15 Lee TH, Daly D, Su M, Lehane C. Colocolic intussusception mimicking distal intestinal obstruction syndrome in a young adult with cystic fibrosis. ANZ J Surg 2021. [PMID: 34570398 DOI: 10.1111/ans.17238] [Reference Citation Analysis]
16 Ridley A, Chaussy Y, Mottet N, Auber F. Dual intestinal anomalies in dizygotic twins. BMJ Case Rep 2018;2018:bcr-2018-225176. [PMID: 30077982 DOI: 10.1136/bcr-2018-225176] [Reference Citation Analysis]
17 Bono-Neri F, Romano C, Isedeh A. Cystic Fibrosis: Advancing Along the Continuum. J Pediatr Health Care 2019;33:242-54. [PMID: 30529125 DOI: 10.1016/j.pedhc.2018.08.008] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
18 Prieur MG, Christon LM, Mueller A, Smith BA, Georgiopoulos AM, Boat TF, Filigno SS. Promoting emotional wellness in children with cystic fibrosis, Part I: Child and family resilience. Pediatr Pulmonol 2021;56 Suppl 1:S97-S106. [PMID: 32658376 DOI: 10.1002/ppul.24958] [Reference Citation Analysis]
19 Sandy NS, Lomazi EA. Incomplete Distal Intestinal Obstruction Syndrome Complicated by Oligosymptomatic Intussusception. ACG Case Rep J 2018;5:e53. [PMID: 30038925 DOI: 10.14309/crj.2018.53] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
20 Mentzel HJ, Renz DM. [Abdominal imaging in cystic fibrosis]. Radiologe 2020;60:831-8. [PMID: 32495009 DOI: 10.1007/s00117-020-00703-4] [Reference Citation Analysis]
21 Hauser B, De Schepper J, Malfroot A, De Wachter E, De Schutter I, Keymolen K, Vandenplas Y. Gastric emptying and gastro-oesophageal reflux in children with cystic fibrosis. J Cyst Fibros. 2016;15:540-547. [PMID: 26778614 DOI: 10.1016/j.jcf.2015.12.015] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 2.2] [Reference Citation Analysis]
22 Beyder A, Farrugia G. Ion channelopathies in functional GI disorders. Am J Physiol Gastrointest Liver Physiol 2016;311:G581-6. [PMID: 27514480 DOI: 10.1152/ajpgi.00237.2016] [Cited by in Crossref: 27] [Cited by in F6Publishing: 22] [Article Influence: 4.5] [Reference Citation Analysis]
23 Castellani C, Duff AJA, Bell SC, Heijerman HGM, Munck A, Ratjen F, Sermet-Gaudelus I, Southern KW, Barben J, Flume PA, Hodková P, Kashirskaya N, Kirszenbaum MN, Madge S, Oxley H, Plant B, Schwarzenberg SJ, Smyth AR, Taccetti G, Wagner TOF, Wolfe SP, Drevinek P. ECFS best practice guidelines: the 2018 revision. J Cyst Fibros 2018;17:153-78. [PMID: 29506920 DOI: 10.1016/j.jcf.2018.02.006] [Cited by in Crossref: 229] [Cited by in F6Publishing: 175] [Article Influence: 57.3] [Reference Citation Analysis]
24 Seidler U, Nikolovska K. Slc26 Family of Anion Transporters in the Gastrointestinal Tract: Expression, Function, Regulation, and Role in Disease. In: Terjung R, editor. Comprehensive Physiology. Wiley; 2011. pp. 839-72. [DOI: 10.1002/cphy.c180027] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 6.3] [Reference Citation Analysis]
25 Reis FPD, Campos SV, Aiello VD, Duarte MIS, Samano MN, Pego-fernandes PM. Gastrointestinal mucormycosis post lung transplantation. The Brazilian Journal of Infectious Diseases 2019;23:368-70. [DOI: 10.1016/j.bjid.2019.07.003] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
26 Gini A, Zauber AG, Cenin DR, Omidvari AH, Hempstead SE, Fink AK, Lowenfels AB, Lansdorp-Vogelaar I. Cost Effectiveness of Screening Individuals With Cystic Fibrosis for Colorectal Cancer. Gastroenterology 2018;154:556-567.e18. [PMID: 29102616 DOI: 10.1053/j.gastro.2017.10.036] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 2.4] [Reference Citation Analysis]
27 Jaudszus A, Zeman E, Jans T, Pfeifer E, Tabori H, Arnold C, Michl RK, Lorenz M, Beiersdorf N, Mainz JG. Validity and Reliability of a Novel Multimodal Questionnaire for the Assessment of Abdominal Symptoms in People with Cystic Fibrosis (CFAbd-Score). Patient 2019;12:419-28. [PMID: 30887269 DOI: 10.1007/s40271-019-00361-2] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
28 Shan W, Hu Y, Ding J, Yang X, Lou J, Du Q, Liao Q, Luo L, Xu J, Xie R. Advances in Ca2+ modulation of gastrointestinal anion secretion and its dysregulation in digestive disorders (Review). Exp Ther Med 2020;20:8. [PMID: 32934673 DOI: 10.3892/etm.2020.9136] [Reference Citation Analysis]
29 Woods JD, Payton KSE, Sanchez-Lara PA, Au M, Simmons CF, Graham JM Jr. Non-Cystic Fibrosis-Related Meconium Ileus: GUCY2C-Associated Disease Discovered through Rapid Neonatal Whole-Exome Sequencing. J Pediatr 2019;211:207-10. [PMID: 31079856 DOI: 10.1016/j.jpeds.2019.04.022] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
30 Soares VEM, do Carmo TIT, Dos Anjos F, Wruck J, de Oliveira Maciel SFV, Bagatini MD, de Resende E Silva DT. Role of inflammation and oxidative stress in tissue damage associated with cystic fibrosis: CAPE as a future therapeutic strategy. Mol Cell Biochem 2021. [PMID: 34529223 DOI: 10.1007/s11010-021-04263-6] [Reference Citation Analysis]
31 Klymiuk N, Seeliger F, Bohlooly-Y M, Blutke A, Rudmann DG, Wolf E. Tailored Pig Models for Preclinical Efficacy and Safety Testing of Targeted Therapies. Toxicol Pathol. 2016;44:346-357. [PMID: 26511847 DOI: 10.1177/0192623315609688] [Cited by in Crossref: 29] [Cited by in F6Publishing: 24] [Article Influence: 4.1] [Reference Citation Analysis]
32 Al Sinani S, Al-Mulaabed S, Al Naamani K, Sultan R. Cystic Fibrosis Liver Disease: Know More. Oman Med J 2019;34:482-9. [PMID: 31745411 DOI: 10.5001/omj.2019.90] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Schnúr A, Hegyi P, Rousseau S, Lukacs GL, Veit G. Epithelial Anion Transport as Modulator of Chemokine Signaling. Mediators Inflamm 2016;2016:7596531. [PMID: 27382190 DOI: 10.1155/2016/7596531] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
34 Waldhausen JHT, Richards M. Meconium Ileus. Clin Colon Rectal Surg 2018;31:121-6. [PMID: 29487495 DOI: 10.1055/s-0037-1609027] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
35 Tabori H, Arnold C, Jaudszus A, Mentzel HJ, Renz DM, Reinsch S, Lorenz M, Michl R, Gerber A, Lehmann T, Mainz JG. Abdominal symptoms in cystic fibrosis and their relation to genotype, history, clinical and laboratory findings. PLoS One 2017;12:e0174463. [PMID: 28472055 DOI: 10.1371/journal.pone.0174463] [Cited by in Crossref: 32] [Cited by in F6Publishing: 20] [Article Influence: 6.4] [Reference Citation Analysis]
36 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]
37 Mandaliya R, Hadjiliadis D, Cohen S. Gastroparesis Concurrent with Adult Cystic Fibrosis; Are They Related? Am J Med 2016;129:e21-2. [PMID: 26836386 DOI: 10.1016/j.amjmed.2016.01.017] [Reference Citation Analysis]
38 Lavelle GM, White MM, Browne N, McElvaney NG, Reeves EP. Animal Models of Cystic Fibrosis Pathology: Phenotypic Parallels and Divergences. Biomed Res Int 2016;2016:5258727. [PMID: 27340661 DOI: 10.1155/2016/5258727] [Cited by in Crossref: 67] [Cited by in F6Publishing: 62] [Article Influence: 11.2] [Reference Citation Analysis]
39 Sathe MN, Freeman AJ. Gastrointestinal, Pancreatic, and Hepatobiliary Manifestations of Cystic Fibrosis. Pediatr Clin North Am 2016;63:679-98. [PMID: 27469182 DOI: 10.1016/j.pcl.2016.04.008] [Cited by in Crossref: 18] [Cited by in F6Publishing: 12] [Article Influence: 3.6] [Reference Citation Analysis]
40 Trouvé P, Génin E, Férec C. In silico search for modifier genes associated with pancreatic and liver disease in Cystic Fibrosis. PLoS One 2017;12:e0173822. [PMID: 28339466 DOI: 10.1371/journal.pone.0173822] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.8] [Reference Citation Analysis]
41 Buddington RK, Wong T, Howard SC. Paracellular Filtration Secretion Driven by Mechanical Force Contributes to Small Intestinal Fluid Dynamics. Med Sci (Basel) 2021;9:9. [PMID: 33572202 DOI: 10.3390/medsci9010009] [Reference Citation Analysis]
42 Arigliani M, Rech Morassutti F, Fabris M, Melli P, Tonutti E, Cogo P. Coeliac disease in infants: antibodies to deamidated gliadin peptide come first! Ital J Pediatr 2017;43:70. [PMID: 28797308 DOI: 10.1186/s13052-017-0392-6] [Cited by in Crossref: 3] [Article Influence: 0.6] [Reference Citation Analysis]
43 Olszowiec-Chlebna M, Koniarek-Maniecka A, Stelmach W, Smejda K, Jerzyńska J, Majak P, Białas M, Stelmach I. Predictors of deterioration of lung function in Polish children with cystic fibrosis. Arch Med Sci 2016;12:402-7. [PMID: 27186187 DOI: 10.5114/aoms.2016.59268] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]