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For: Wilschanski M, Durie PR. Patterns of GI disease in adulthood associated with mutations in the CFTR gene. Gut 2007;56:1153-63. [PMID: 17446304 DOI: 10.1136/gut.2004.062786] [Cited by in Crossref: 116] [Cited by in F6Publishing: 103] [Article Influence: 7.7] [Reference Citation Analysis]
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21 Wilschanski M, Yaakov Y, Omari I, Zaman M, Martin CR, Cohen-Cymberknoh M, Shoseyov D, Kerem E, Dasilva D, Sheth S, Uluer A, OʼSullivan BP, Freedman S. Comparison of Nasal Potential Difference and Intestinal Current Measurements as Surrogate Markers for CFTR Function. J Pediatr Gastroenterol Nutr 2016;63:e92-7. [PMID: 27496797 DOI: 10.1097/MPG.0000000000001366] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 1.4] [Reference Citation Analysis]
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25 Cohen-cymberknoh M, Yaakov Y, Shoseyov D, Shteyer E, Schachar E, Rivlin J, Bentur L, Picard E, Aviram M, Israeli E, Kerem E, Wilschanski M. Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis. Pediatr Pulmonol 2013;48:229-35. [DOI: 10.1002/ppul.22586] [Cited by in Crossref: 22] [Cited by in F6Publishing: 18] [Article Influence: 2.2] [Reference Citation Analysis]
26 Calvo-Lerma J, Martinez-Jimenez CP, Lázaro-Ramos JP, Andrés A, Crespo-Escobar P, Stav E, Schauber C, Pannese L, Hulst JM, Suárez L, Colombo C, Barreto C, de Boeck K, Ribes-Koninckx C; MyCyFAPP. Innovative approach for self-management and social welfare of children with cystic fibrosis in Europe: development, validation and implementation of an mHealth tool (MyCyFAPP). BMJ Open 2017;7:e014931. [PMID: 28302638 DOI: 10.1136/bmjopen-2016-014931] [Cited by in Crossref: 20] [Cited by in F6Publishing: 19] [Article Influence: 4.0] [Reference Citation Analysis]
27 Capurso G, Sbrozzi-Vanni A, Piane M, Begini P, Panzuto F, Libi F, Margagnoni G, Capotondi C, Marignani M, Chessa L, Delle Fave G. Phenotype expression in a case of adult cystic fibrosis caused by an extremely rare compound heterozygous genotype (2183AA>G/2789+5G>A). Pancreas 2009;38:599-601. [PMID: 19550280 DOI: 10.1097/MPA.0b013e3181967657] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
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31 Gridelli B. Benefit of liver transplantation in patients with cystic fibrosis. Nat Rev Gastroenterol Hepatol 2011;8:187-8. [DOI: 10.1038/nrgastro.2011.39] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
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33 Jakab RL, Collaco AM, Ameen NA. Physiological relevance of cell-specific distribution patterns of CFTR, NKCC1, NBCe1, and NHE3 along the crypt-villus axis in the intestine. Am J Physiol Gastrointest Liver Physiol. 2011;300:G82-G98. [PMID: 21030607 DOI: 10.1152/ajpgi.00245.2010] [Cited by in Crossref: 91] [Cited by in F6Publishing: 82] [Article Influence: 7.6] [Reference Citation Analysis]
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43 Kunovský L, Dítě P, Jabandžiev P, Eid M, Poredská K, Vaculová J, Sochorová D, Janeček P, Tesaříková P, Blaho M, Trna J, Hlavsa J, Kala Z. Causes of Exocrine Pancreatic Insufficiency Other Than Chronic Pancreatitis. J Clin Med 2021;10:5779. [PMID: 34945075 DOI: 10.3390/jcm10245779] [Reference Citation Analysis]
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45 Coderre L, Debieche L, Plourde J, Rabasa-Lhoret R, Lesage S. The Potential Causes of Cystic Fibrosis-Related Diabetes. Front Endocrinol (Lausanne) 2021;12:702823. [PMID: 34394004 DOI: 10.3389/fendo.2021.702823] [Reference Citation Analysis]
46 Mousa MS, Feldman JC, Mahajan P. Microgallbladder: Self-Remitting Acute Cholecystitis-Like Condition Unique to Patients with Cystic Fibrosis. Case Rep Radiol 2019;2019:6737428. [PMID: 31321111 DOI: 10.1155/2019/6737428] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
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48 Mezencev R, Auerbach SS. Inferred inactivation of the Cftr gene in the duodena of mice exposed to hexavalent chromium (Cr(VI)) in drinking water supports its tumor-suppressor status and implies its potential role in Cr(VI)-induced carcinogenesis of the small intestines. Toxicol Appl Pharmacol 2021;433:115773. [PMID: 34688701 DOI: 10.1016/j.taap.2021.115773] [Reference Citation Analysis]
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55 Sojo Aguirre A, Martínez Ezquerra N, Bousoño García C, García Novo MD, Heredia González S, Manzanares López-Manzanares J, Baranda García F, Vázquez Cordero C. [Pancreatitis in cystic fibrosis: association with genotype and pancreatic status]. An Pediatr (Barc) 2011;75:401-8. [PMID: 21820373 DOI: 10.1016/j.anpedi.2011.06.005] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
56 Dhooghe B, Noël S, Bouzin C, Behets-Wydemans G, Leal T. Correction of chloride transport and mislocalization of CFTR protein by vardenafil in the gastrointestinal tract of cystic fibrosis mice. PLoS One 2013;8:e77314. [PMID: 24204804 DOI: 10.1371/journal.pone.0077314] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 1.8] [Reference Citation Analysis]
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