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Features of Severe Liver Disease With Portal Hypertension in Patients With Cystic Fibrosis.
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SERPINA1 Z allele is associated with cystic fibrosis liver disease.
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A single centre experience of liver disease in adults with cystic fibrosis 1995-2006.
J Cyst Fibros. 2008 May;7(3):252-7. doi: 10.1016/j.jcf.2007.10.004. Epub 2007 Nov 26.
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Long-term follow-up and liver outcomes in children with cystic fibrosis and nodular liver on ultrasound in a multi-center study.
J Cyst Fibros. 2023 Mar;22(2):248-255. doi: 10.1016/j.jcf.2022.07.017. Epub 2022 Aug 16.
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Genetic modifiers of liver disease in cystic fibrosis.
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Correlation of Transient Elastography With Severity of Cystic Fibrosis-related Liver Disease.
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Obliterative Portal Venopathy Without Cirrhosis Is Prevalent in Pediatric Cystic Fibrosis Liver Disease With Portal Hypertension.
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Cystic fibrosis-associated liver disease in children.
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Rare Mutation in Cystic Fibrosis as a Cause of Early-Onset Liver Disease and Esophageal Varices.
Cureus. 2025 Feb 3;17(2):e78408. doi: 10.7759/cureus.78408. eCollection 2025 Feb.
2
Genetic modifiers of body mass index in individuals with cystic fibrosis.
Am J Hum Genet. 2024 Oct 3;111(10):2203-2218. doi: 10.1016/j.ajhg.2024.08.004. Epub 2024 Sep 10.
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Genetic variation in severe cystic fibrosis liver disease is associated with novel mechanisms for disease pathogenesis.
Hepatology. 2024 Nov 1;80(5):1012-1025. doi: 10.1097/HEP.0000000000000863. Epub 2024 Mar 27.
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Cystic fibrosis screening, evaluation, and management of hepatobiliary disease consensus recommendations.
Hepatology. 2024 May 1;79(5):1220-1238. doi: 10.1097/HEP.0000000000000646. Epub 2023 Oct 26.
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Heterogeneous liver on research ultrasound identifies children with cystic fibrosis at high risk of advanced liver disease.
J Cyst Fibros. 2023 Jul;22(4):745-755. doi: 10.1016/j.jcf.2023.03.019. Epub 2023 Apr 7.
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Ameliorating liver disease in an autosomal recessive polycystic kidney disease mouse model.
Am J Physiol Gastrointest Liver Physiol. 2023 May 1;324(5):G404-G414. doi: 10.1152/ajpgi.00255.2022. Epub 2023 Mar 7.
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Modifier Factors of Cystic Fibrosis Phenotypes: A Focus on Modifier Genes.
Int J Mol Sci. 2022 Nov 17;23(22):14205. doi: 10.3390/ijms232214205.
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Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis.
Am J Hum Genet. 2022 Oct 6;109(10):1894-1908. doi: 10.1016/j.ajhg.2022.09.004.
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Role of transient elastography and APRI in the assessment of pediatric cystic fibrosis liver disease.
Can Liver J. 2021 Feb 24;4(1):23-32. doi: 10.3138/canlivj-2020-0008. eCollection 2021 Winter.
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Cystic fibrosis liver disease: A condition in need of structured transition and continuity of care.
Can Liver J. 2019 Aug 27;2(3):71-83. doi: 10.3138/canlivj-2018-0019. eCollection 2019 Summer.

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2
Circulating microRNAs as noninvasive diagnostic biomarkers of liver disease in children with cystic fibrosis.
J Pediatr Gastroenterol Nutr. 2015 Feb;60(2):247-54. doi: 10.1097/MPG.0000000000000600.
3
Ursodeoxycholic acid for cystic fibrosis-related liver disease.
Cochrane Database Syst Rev. 2014 Dec 15(12):CD000222. doi: 10.1002/14651858.CD000222.pub3.
4
Outcome in patients with cystic fibrosis liver disease.
J Cyst Fibros. 2015 Jan;14(1):120-6. doi: 10.1016/j.jcf.2014.05.013. Epub 2014 Jun 7.
5
Serum proteome profiling identifies novel and powerful markers of cystic fibrosis liver disease.
PLoS One. 2013;8(3):e58955. doi: 10.1371/journal.pone.0058955. Epub 2013 Mar 14.
6
Utility of transient elastography in the non-invasive evaluation of cystic fibrosis liver disease.
Liver Int. 2013 May;33(5):698-705. doi: 10.1111/liv.12113. Epub 2013 Feb 22.
7
Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in pancreatitis.
J Cyst Fibros. 2012 Sep;11(5):355-62. doi: 10.1016/j.jcf.2012.05.001. Epub 2012 Jun 2.
9
A clinical prediction rule and platelet count predict esophageal varices in children.
Gastroenterology. 2011 Dec;141(6):2009-16. doi: 10.1053/j.gastro.2011.08.049. Epub 2011 Sep 16.
10
Nongenetic influences on cystic fibrosis outcomes.
Curr Opin Pulm Med. 2011 Nov;17(6):448-54. doi: 10.1097/MCP.0b013e32834ba899.

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