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For: van der Doef HP, Kokke FT, van der Ent CK, Houwen RH. Intestinal obstruction syndromes in cystic fibrosis: meconium ileus, distal intestinal obstruction syndrome, and constipation. Curr Gastroenterol Rep. 2011;13:265-270. [PMID: 21384135 DOI: 10.1007/s11894-011-0185-9] [Cited by in Crossref: 78] [Cited by in F6Publishing: 57] [Article Influence: 7.1] [Reference Citation Analysis]
Number Citing Articles
1 Shah N, Tan HL, Sebire N, Suri R, Leuven K. The role of endoscopy and biopsy in the management of severe gastrointestinal disease in cystic fibrosis patients. Pediatr Pulmonol. 2013;Epub ahead of print. [PMID: 23825099 DOI: 10.1002/ppul.22697] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 0.7] [Reference Citation Analysis]
2 Chin M, Aaron SD, Bell SC. The treatment of the pulmonary and extrapulmonary manifestations of cystic fibrosis. Presse Med 2017;46:e139-64. [PMID: 28576636 DOI: 10.1016/j.lpm.2016.11.030] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
3 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]
4 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]
5 Reznikov LR. Cystic Fibrosis and the Nervous System. Chest 2017;151:1147-55. [PMID: 27876591 DOI: 10.1016/j.chest.2016.11.009] [Cited by in Crossref: 19] [Cited by in F6Publishing: 16] [Article Influence: 3.2] [Reference Citation Analysis]
6 Hortencio TD, Nogueira RJ, Marson FA, Hessel G, Ribeiro JD, Ribeiro AF. [Factors impacting the growth and nutritional status of cystic fibrosis patients younger than 10 years of age who did not undergo neonatal screening]. Rev Paul Pediatr 2015;33:3-11. [PMID: 25681074 DOI: 10.1016/j.rpped.2014.11.004] [Cited by in Crossref: 3] [Article Influence: 0.4] [Reference Citation Analysis]
7 Semaniakou A, Croll RP, Chappe V. Animal Models in the Pathophysiology of Cystic Fibrosis. Front Pharmacol 2018;9:1475. [PMID: 30662403 DOI: 10.3389/fphar.2018.01475] [Cited by in Crossref: 34] [Cited by in F6Publishing: 30] [Article Influence: 11.3] [Reference Citation Analysis]
8 Bazett M, Honeyman L, Stefanov AN, Pope CE, Hoffman LR, Haston CK. Cystic fibrosis mouse model-dependent intestinal structure and gut microbiome. Mamm Genome 2015;26:222-34. [PMID: 25721416 DOI: 10.1007/s00335-015-9560-4] [Cited by in Crossref: 21] [Cited by in F6Publishing: 19] [Article Influence: 3.0] [Reference Citation Analysis]
9 Haggie PM, Cil O, Lee S, Tan JA, Rivera AA, Phuan PW, Verkman AS. SLC26A3 inhibitor identified in small molecule screen blocks colonic fluid absorption and reduces constipation. JCI Insight 2018;3:121370. [PMID: 30046015 DOI: 10.1172/jci.insight.121370] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 4.5] [Reference Citation Analysis]
10 Vitko M, Valerio DM, Rye PD, Onsøyen E, Myrset AH, Dessen A, Drumm ML, Hodges CA. A novel guluronate oligomer improves intestinal transit and survival in cystic fibrosis mice. Journal of Cystic Fibrosis 2016;15:745-51. [DOI: 10.1016/j.jcf.2016.06.005] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 2.0] [Reference Citation Analysis]
11 Grant JJ, McDade EJ, Zobell JT, Young DC. The indispensable role of pharmacy services and medication therapy management in cystic fibrosis. Pediatr Pulmonol 2021. [PMID: 34347382 DOI: 10.1002/ppul.25613] [Reference Citation Analysis]
12 Tuggle KL, Birket SE, Cui X, Hong J, Warren J, Reid L, Chambers A, Ji D, Gamber K, Chu KK, Tearney G, Tang LP, Fortenberry JA, Du M, Cadillac JM, Bedwell DM, Rowe SM, Sorscher EJ, Fanucchi MV. Characterization of defects in ion transport and tissue development in cystic fibrosis transmembrane conductance regulator (CFTR)-knockout rats. PLoS One 2014;9:e91253. [PMID: 24608905 DOI: 10.1371/journal.pone.0091253] [Cited by in Crossref: 97] [Cited by in F6Publishing: 92] [Article Influence: 12.1] [Reference Citation Analysis]
13 Demeyer S, De Boeck K, Witters P, Cosaert K. Beyond pancreatic insufficiency and liver disease in cystic fibrosis. Eur J Pediatr 2016;175:881-94. [DOI: 10.1007/s00431-016-2719-5] [Cited by in Crossref: 18] [Cited by in F6Publishing: 13] [Article Influence: 3.0] [Reference Citation Analysis]
14 Bazett M, Bergeron ME, Haston CK. Streptomycin treatment alters the intestinal microbiome, pulmonary T cell profile and airway hyperresponsiveness in a cystic fibrosis mouse model. Sci Rep 2016;6:19189. [PMID: 26754178 DOI: 10.1038/srep19189] [Cited by in Crossref: 33] [Cited by in F6Publishing: 29] [Article Influence: 5.5] [Reference Citation Analysis]
15 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]
16 Kopke MA, Ruaux CG, Gal A. Myenteric ganglionitis and intestinal leiomyositis in a Jack Russell terrier. J Small Anim Pract 2020;61:772-5. [PMID: 30387492 DOI: 10.1111/jsap.12962] [Reference Citation Analysis]
17 Hort A, Hameed A, Middleton PG, Pleass HC. Distal intestinal obstruction syndrome: an important differential diagnosis for abdominal pain in patients with cystic fibrosis. ANZ J Surg 2020;90:681-6. [PMID: 31364217 DOI: 10.1111/ans.15357] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Munck A, Languepin J, Debray D, Lamireau T, Abely M, Huet F, Maudinas R, Michaud L, Mas E. Management of pancreatic, gastrointestinal and liver complications in adult cystic fibrosis. Revue des Maladies Respiratoires 2015;32:566-85. [DOI: 10.1016/j.rmr.2014.12.008] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 0.9] [Reference Citation Analysis]
19 Busslinger GA, Weusten BLA, Bogte A, Begthel H, Brosens LAA, Clevers H. Human gastrointestinal epithelia of the esophagus, stomach, and duodenum resolved at single-cell resolution. Cell Rep 2021;34:108819. [PMID: 33691112 DOI: 10.1016/j.celrep.2021.108819] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
20 Green J, Gilchrist FJ, Carroll W. Interventions for preventing distal intestinal obstruction syndrome (DIOS) in cystic fibrosis. Cochrane Database Syst Rev 2018;6:CD012619. [PMID: 29894558 DOI: 10.1002/14651858.CD012619.pub2] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
21 Alattar Z, Thornley C, Behbahaninia M, Sisley A. Proximal small bowel obstruction in a patient with cystic fibrosis: a case report. Surg Case Rep 2019;5:143. [PMID: 31520190 DOI: 10.1186/s40792-019-0701-y] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
22 van der Mark VA, de Jonge HR, Chang JC, Ho-Mok KS, Duijst S, Vidović D, Carlon MS, Oude Elferink RP, Paulusma CC. The phospholipid flippase ATP8B1 mediates apical localization of the cystic fibrosis transmembrane regulator. Biochim Biophys Acta 2016;1863:2280-8. [PMID: 27301931 DOI: 10.1016/j.bbamcr.2016.06.005] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
23 Nash EF, Ohri CM, Stephenson AL, Durie PR. Abdominal pain in adults with cystic fibrosis. Eur J Gastroenterol Hepatol 2014;26:129-36. [PMID: 24366450 DOI: 10.1097/MEG.0000000000000011] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
24 Puzik A, Morris-Rosendahl DJ, Rückauer KD, Otto C, Gessler P, Saueressig U, Hentschel R. Lethal course of meconium ileus in preterm twins revealing a novel cystic fibrosis mutation (p.Cys524Tyr). BMC Pediatr 2014;14:13. [PMID: 24433235 DOI: 10.1186/1471-2431-14-13] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
25 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]
26 Mentessidou A, Loukou I, Kampouroglou G, Livani A, Georgopoulos I, Mirilas P. Long-term intestinal obstruction sequelae and growth in children with cystic fibrosis operated for meconium ileus: expectancies and surprises. Journal of Pediatric Surgery 2018;53:1504-8. [DOI: 10.1016/j.jpedsurg.2017.11.040] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 2.8] [Reference Citation Analysis]
27 Ermund A, Recktenwald CV, Skjåk-Braek G, Meiss LN, Onsøyen E, Rye PD, Dessen A, Myrset AH, Hansson GC. OligoG CF-5/20 normalizes cystic fibrosis mucus by chelating calcium. Clin Exp Pharmacol Physiol 2017;44:639-47. [PMID: 28261854 DOI: 10.1111/1440-1681.12744] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 4.3] [Reference Citation Analysis]
28 Li YW, Yu YJ, Fei F, Zheng MY, Zhang SW. High-resolution colonic manometry and its clinical application in patients with colonic dysmotility: A review. World J Clin Cases 2019; 7(18): 2675-2686 [PMID: 31616684 DOI: 10.12998/wjcc.v7.i18.2675] [Cited by in CrossRef: 2] [Article Influence: 0.7] [Reference Citation Analysis]
29 Gibson-Corley KN, Meyerholz DK, Engelhardt JF. Pancreatic pathophysiology in cystic fibrosis. J Pathol 2016;238:311-20. [PMID: 26365583 DOI: 10.1002/path.4634] [Cited by in Crossref: 56] [Cited by in F6Publishing: 47] [Article Influence: 8.0] [Reference Citation Analysis]
30 Sommerburg O, Schenk JP. [Abdominal manifestations in cystic fibrosis : Clinical review]. Radiologe 2020;60:781-90. [PMID: 32776239 DOI: 10.1007/s00117-020-00729-8] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
31 Hedsund C, Gregersen T, Joensson IM, Olesen HV, Krogh K. Gastrointestinal transit times and motility in patients with cystic fibrosis. Scandinavian Journal of Gastroenterology 2012;47:920-6. [DOI: 10.3109/00365521.2012.699548] [Cited by in Crossref: 25] [Cited by in F6Publishing: 26] [Article Influence: 2.5] [Reference Citation Analysis]
32 Stonebraker JR, Ooi CY, Pace RG, Corvol H, Knowles MR, Durie PR, Ling SC. Features of Severe Liver Disease With Portal Hypertension in Patients With Cystic Fibrosis. Clin Gastroenterol Hepatol 2016;14:1207-1215.e3. [PMID: 27062904 DOI: 10.1016/j.cgh.2016.03.041] [Cited by in Crossref: 56] [Cited by in F6Publishing: 44] [Article Influence: 9.3] [Reference Citation Analysis]
33 Sharma A, Morton A, Peckham D, Jayne D. Gastrointestinal surgery in adult patients with cystic fibrosis. Frontline Gastroenterol 2012;3:242-7. [PMID: 28839675 DOI: 10.1136/flgastro-2012-100184] [Cited by in Crossref: 3] [Article Influence: 0.3] [Reference Citation Analysis]
34 Giguere-Rich C, Mathew A, Reid E, Autore K, Guill MF. Use of an In-line Digestive Cartridge With Enteral Nutrition Improves the Weight Trajectory of 2 Children With Cystic Fibrosis Complicated by Another Medical Diagnosis. Nutr Clin Pract 2018;33:286-94. [PMID: 29658186 DOI: 10.1002/ncp.10080] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
35 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]
36 Mchugh DR, Cotton CU, Moss FJ, Vitko M, Valerio DM, Kelley TJ, Hao S, Jafri A, Drumm ML, Boron WF, Stern RC, Mcbennett K, Hodges CA. Linaclotide improves gastrointestinal transit in cystic fibrosis mice by inhibiting sodium/hydrogen exchanger 3. American Journal of Physiology-Gastrointestinal and Liver Physiology 2018;315:G868-78. [DOI: 10.1152/ajpgi.00261.2017] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
37 de Sillos MD, Chiba SM, Soares ACF, Gomes CET, de Morais MB. Colonic Transit Time and Fecal Impaction in Children and Adolescents With Cystic Fibrosis-associated Constipation. J Pediatr Gastroenterol Nutr 2021;73:319-24. [PMID: 34128499 DOI: 10.1097/MPG.0000000000003202] [Reference Citation Analysis]
38 Quade BN, Parker MD, Occhipinti R. The therapeutic importance of acid-base balance. Biochem Pharmacol 2021;183:114278. [PMID: 33039418 DOI: 10.1016/j.bcp.2020.114278] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
39 Mariani A, Gambazza S, Carta F, Ambrogi F, Brivio A, Bulfamante AM, Daccò V, Bassotti G, Colombo C. Prevalence and factors associated with urinary incontinence in females with cystic fibrosis: An Italian single-center cross-sectional analysis. Pediatr Pulmonol 2022;57:132-41. [PMID: 34636479 DOI: 10.1002/ppul.25723] [Reference Citation Analysis]
40 Jawad M, Klafkowski G, Lenney W, Gilchrist FJ. Intestinal obstruction secondary to adhesions in an infant with cystic fibrosis. BMJ Case Rep 2013;2013:bcr2013010444. [PMID: 23897385 DOI: 10.1136/bcr-2013-010444] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
41 Morales Morales CA, Gonzalez-Urquijo M, Morales Flores LF, Quevedo-Fernandez E, Guzmán Huerta EA, Virgilio Hernández-Torre MM. Proximal intestinal obstruction syndrome (PIOS) in a patient with cystic fibrosis: A case report. Ann Med Surg (Lond) 2020;60:669-72. [PMID: 33312560 DOI: 10.1016/j.amsu.2020.11.063] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
42 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]
43 Stefano MA, Poderoso RE, Mainz JG, Ribeiro JD, Ribeiro AF, Lomazi EA. Prevalence of constipation in cystic fibrosis patients: a systematic review of observational studies. Jornal de Pediatria 2020;96:686-92. [DOI: 10.1016/j.jped.2020.03.004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
44 Banne E, Meiner V, Shaag A, Katz-Brull R, Gamliel A, Korman S, Cederboim SH, Duvdevani MP, Frumkin A, Zilkha A, Kapuller V, Arbell D, Cohen E, Eventov-Friedman S. Transaldolase Deficiency: A New Case Expands the Phenotypic Spectrum. JIMD Rep 2016;26:31-6. [PMID: 26238251 DOI: 10.1007/8904_2015_474] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
45 Haller W, Ledder O, Lewindon PJ, Couper R, Gaskin KJ, Oliver M. Cystic fibrosis: An update for clinicians. Part 1: Nutrition and gastrointestinal complications: Gastrointestinal disease in cystic fibrosis. J Gastroenterol Hepatol 2014;29:1344-55. [DOI: 10.1111/jgh.12546] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 2.0] [Reference Citation Analysis]
46 Ooi CY, Jeyaruban C, Lau J, Katz T, Matson A, Bell SC, Adams SE, Krishnan U. High ambient temperature and risk of intestinal obstruction in cystic fibrosis. J Paediatr Child Health 2016;52:430-5. [PMID: 27145507 DOI: 10.1111/jpc.13096] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 2.4] [Reference Citation Analysis]
47 Arys B, Mandelstam S, Rao P, Kernick S, Kumbla S. Sonography of the pediatric gastrointestinal system. Ultrasound Q. 2014;30:101-117. [PMID: 24850026 DOI: 10.1097/ruq.0b013e3182a38dcc] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
48 Banjar H, Qeretli R, Ramadan A, Al-ibraheem A, Bnatig F. The first report on CFTR mutations of meconium ileus in cystic fibrosis population in Saudi Arabia: A single center review. International Journal of Pediatrics and Adolescent Medicine 2021. [DOI: 10.1016/j.ijpam.2021.03.008] [Reference Citation Analysis]
49 Gilchrist FJ, Green J, Carroll W. Interventions for treating distal intestinal obstruction syndrome (DIOS) in cystic fibrosis. Cochrane Database Syst Rev 2021;12:CD012798. [PMID: 34936086 DOI: 10.1002/14651858.CD012798.pub3] [Reference Citation Analysis]
50 Green J, Carroll W, Gilchrist F. Comparing the management of constipation and distal intestinal obstruction syndrome between paediatricians and adult physicians. Journal of Cystic Fibrosis 2018;17:e6-7. [DOI: 10.1016/j.jcf.2017.09.007] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
51 Lord R, Fairbourn N, Mylavarapu C, Dbeis A, Bowman T, Chandrashekar A, Banayat T, Hodges CA, Al-Nakkash L. Consuming Genistein Improves Survival Rates in the Absence of Laxative in ΔF508-CF Female Mice. Nutrients 2018;10:E1418. [PMID: 30282922 DOI: 10.3390/nu10101418] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
52 van de Peppel IP, Bodewes FAJA, Verkade HJ, Jonker JW. Bile acid homeostasis in gastrointestinal and metabolic complications of cystic fibrosis. J Cyst Fibros 2019;18:313-20. [PMID: 30201330 DOI: 10.1016/j.jcf.2018.08.009] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 2.5] [Reference Citation Analysis]
53 Fraquelli M, Baccarin A, Corti F, Conti CB, Russo MC, Valle SD, Pozzi R, Cressoni M, Conte D, Colombo C. Bowel ultrasound imaging in patients with cystic fibrosis: Relationship with clinical symptoms and CFTR genotype. Digestive and Liver Disease 2016;48:271-6. [DOI: 10.1016/j.dld.2015.09.010] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
54 Liang X, Bouhamdan M, Hou X, Zhang K, Song J, Hao K, Jin JP, Zhang Z, Xu J. Intestinal Dysbiosis in Young Cystic Fibrosis Rabbits. J Pers Med 2021;11:132. [PMID: 33669429 DOI: 10.3390/jpm11020132] [Reference Citation Analysis]
55 Ogden HL, Kim H, Wikenheiser-Brokamp KA, Naren AP, Mun KS. Cystic Fibrosis Human Organs-on-a-Chip. Micromachines (Basel) 2021;12:747. [PMID: 34202364 DOI: 10.3390/mi12070747] [Reference Citation Analysis]
56 Farrelly PJ, Charlesworth C, Lee S, Southern KW, Baillie CT. Gastrointestinal surgery in cystic fibrosis: a 20-year review. J Pediatr Surg 2014;49:280-3. [PMID: 24528967 DOI: 10.1016/j.jpedsurg.2013.11.038] [Cited by in Crossref: 24] [Cited by in F6Publishing: 17] [Article Influence: 2.7] [Reference Citation Analysis]
57 Stoltz DA, Rokhlina T, Ernst SE, Pezzulo AA, Ostedgaard LS, Karp PH, Samuel MS, Reznikov LR, Rector MV, Gansemer ND, Bouzek DC, Abou Alaiwa MH, Hoegger MJ, Ludwig PS, Taft PJ, Wallen TJ, Wohlford-Lenane C, McMenimen JD, Chen JH, Bogan KL, Adam RJ, Hornick EE, Nelson GA 4th, Hoffman EA, Chang EH, Zabner J, McCray PB Jr, Prather RS, Meyerholz DK, Welsh MJ. Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs. J Clin Invest 2013;123:2685-93. [PMID: 23676501 DOI: 10.1172/JCI68867] [Cited by in Crossref: 96] [Cited by in F6Publishing: 62] [Article Influence: 10.7] [Reference Citation Analysis]
58 Stefano MA, Poderoso RE, Mainz JG, Ribeiro JD, Ribeiro AF, Lomazi EA. Prevalence of constipation in cystic fibrosis patients: a systematic review of observational studies. Jornal de Pediatria (Versão em Português) 2020;96:686-92. [DOI: 10.1016/j.jpedp.2020.03.002] [Reference Citation Analysis]
59 Green J, Carroll W, Gilchrist FJ. Interventions for treating distal intestinal obstruction syndrome (DIOS) in cystic fibrosis. Cochrane Database Syst Rev 2018;8:CD012798. [PMID: 30075058 DOI: 10.1002/14651858.CD012798.pub2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
60 Schauble AL, Bisaccia EK, Lee G, Nasr SZ. N-acetylcysteine for Management of Distal Intestinal Obstruction Syndrome. J Pediatr Pharmacol Ther 2019;24:390-7. [PMID: 31598102 DOI: 10.5863/1551-6776-24.5.390] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
61 Carroll W, Green J, Gilchrist FJ. Interventions for preventing distal intestinal obstruction syndrome (DIOS) in cystic fibrosis. Cochrane Database Syst Rev 2021;12:CD012619. [PMID: 34936085 DOI: 10.1002/14651858.CD012619.pub3] [Reference Citation Analysis]
62 Abraham JM, Taylor CJ. Cystic Fibrosis & disorders of the large intestine: DIOS, constipation, and colorectal cancer. Journal of Cystic Fibrosis 2017;16:S40-9. [DOI: 10.1016/j.jcf.2017.06.013] [Cited by in Crossref: 29] [Cited by in F6Publishing: 24] [Article Influence: 5.8] [Reference Citation Analysis]
63 Korzeniewska-eksterowicz A, Stelmach I, Stelmach W. Urinary incontinence in adolescent females with cystic fibrosis in Poland. Open Medicine 2014;9:778-83. [DOI: 10.2478/s11536-013-0331-x] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
64 Burkardt DD, Graham JM, Short SS, Frykman PK. Advances in Hirschsprung disease genetics and treatment strategies: an update for the primary care pediatrician. Clin Pediatr (Phila). 2014;53:71-81. [PMID: 24002048 DOI: 10.1177/0009922813500846] [Cited by in Crossref: 30] [Cited by in F6Publishing: 20] [Article Influence: 3.3] [Reference Citation Analysis]
65 Olivier AK, Gibson-Corley KN, Meyerholz DK. Animal models of gastrointestinal and liver diseases. Animal models of cystic fibrosis: gastrointestinal, pancreatic, and hepatobiliary disease and pathophysiology. Am J Physiol Gastrointest Liver Physiol 2015;308:G459-71. [PMID: 25591863 DOI: 10.1152/ajpgi.00146.2014] [Cited by in Crossref: 31] [Cited by in F6Publishing: 28] [Article Influence: 4.4] [Reference Citation Analysis]
66 Guillon A, Chevaleyre C, Barc C, Berri M, Adriaensen H, Lecompte F, Villemagne T, Pezant J, Delaunay R, Moënne-Loccoz J, Berthon P, Bähr A, Wolf E, Klymiuk N, Attucci S, Ramphal R, Sarradin P, Buzoni-Gatel D, Si-Tahar M, Caballero I. Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets. PLoS One 2015;10:e0143459. [PMID: 26600426 DOI: 10.1371/journal.pone.0143459] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
67 Xu J, Livraghi-Butrico A, Hou X, Rajagopalan C, Zhang J, Song J, Jiang H, Wei HG, Wang H, Bouhamdan M, Ruan J, Yang D, Qiu Y, Xie Y, Barrett R, McClellan S, Mou H, Wu Q, Chen X, Rogers TD, Wilkinson KJ, Gilmore RC, Esther CR Jr, Zaman K, Liang X, Sobolic M, Hazlett L, Zhang K, Frizzell RA, Gentzsch M, O'Neal WK, Grubb BR, Chen YE, Boucher RC, Sun F. Phenotypes of CF rabbits generated by CRISPR/Cas9-mediated disruption of the CFTR gene. JCI Insight 2021;6:139813. [PMID: 33232302 DOI: 10.1172/jci.insight.139813] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]