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Liver and biliary problems in cystic fibrosis.囊性纤维化中的肝脏和胆道问题。
J R Soc Med. 1992;85 Suppl 19(Suppl 19):20-4.
2
Liver and biliary problems in cystic fibrosis.囊性纤维化中的肝脏和胆道问题。
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Long-term prospective study of the effect of ursodeoxycholic acid on cystic fibrosis-related liver disease.熊去氧胆酸对囊性纤维化相关肝病影响的长期前瞻性研究。
J Clin Gastroenterol. 2001 Apr;32(4):324-8. doi: 10.1097/00004836-200104000-00009.
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Ursodeoxycholic acid treatment in patients with cystic fibrosis at risk for liver disease.熊去氧胆酸治疗有发生肝病风险的囊性纤维化患者。
Dig Liver Dis. 2010 Jun;42(6):428-31. doi: 10.1016/j.dld.2009.07.022. Epub 2010 Jan 19.
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Bile acid therapy in pediatric hepatobiliary disease: the role of ursodeoxycholic acid.胆汁酸疗法在小儿肝胆疾病中的应用：熊去氧胆酸的作用
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Ursodeoxycholic acid for cystic fibrosis-related liver disease.熊去氧胆酸用于治疗囊性纤维化相关肝病。
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Hepatobiliary disease in cystic fibrosis: a survey of current issues and concepts.囊性纤维化中的肝胆疾病：当前问题与概念综述
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Hepatobiliary abnormalities and disease in cystic fibrosis: epidemiology and outcomes through adulthood.囊性纤维化肝胆异常和疾病：成人期的流行病学和转归。
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10
Delayed intestinal visualization at hepatobiliary scintigraphy is associated with response to long-term treatment with ursodeoxycholic acid in patients with cystic fibrosis-associated liver disease.在患有囊性纤维化相关肝病的患者中，肝胆闪烁显像时肠道显影延迟与对熊去氧胆酸长期治疗的反应相关。
J Hepatol. 1999 Oct;31(4):672-7. doi: 10.1016/s0168-8278(99)80347-x.

引用本文的文献

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Ursodeoxycholic acid for cystic fibrosis-related liver disease.熊去氧胆酸用于治疗囊性纤维化相关肝病。
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2
Ursodeoxycholic acid in cystic fibrosis-related liver disease: a systematic review.熊去氧胆酸在囊性纤维化相关肝病中的应用：一项系统评价
J R Soc Med. 1997;90 Suppl 31(Suppl 31):6-12. doi: 10.1177/014107689709031S03.
3
Liver transplantation for hepatic cirrhosis in cystic fibrosis.囊性纤维化患者肝硬化的肝移植
J R Soc Med. 1996;89 Suppl 27(Suppl 27):31-7.
4
Liver transplantation for hepatic cirrhosis in cystic fibrosis.囊性纤维化患者肝硬化的肝移植治疗
Arch Dis Child. 1994 Oct;71(4):349-52. doi: 10.1136/adc.71.4.349.
5
Liver disease in cystic fibrosis.囊性纤维化中的肝脏疾病
Arch Dis Child. 1995 Apr;72(4):281-4. doi: 10.1136/adc.72.4.281.

本文引用的文献

1
Intestinal bile acid malabsorption in cystic fibrosis: a primary mucosal cell defect.囊性纤维化中的肠道胆汁酸吸收不良：一种原发性黏膜细胞缺陷。
Pediatr Res. 1982 Jun;16(6):494-8. doi: 10.1203/00006450-198206000-00019.
2
Conjugated bile acids in serum and secretions in response to cholecystokinin/secretin stimulation in children with cystic fibrosis.囊性纤维化患儿血清中结合胆汁酸及胆囊收缩素/促胰液素刺激后的分泌物情况
Gut. 1985 Nov;26(11):1246-56. doi: 10.1136/gut.26.11.1246.
3
Serum bile acid composition in patients with cystic fibrosis.囊性纤维化患者的血清胆汁酸成分
Clin Chim Acta. 1985 Sep 30;151(2):101-10. doi: 10.1016/0009-8981(85)90313-4.
4
Lesser omental thickness in normal children: baseline for detection of portal hypertension.正常儿童小网膜厚度：检测门静脉高压的基线
AJR Am J Roentgenol. 1985 Oct;145(4):693-6. doi: 10.2214/ajr.145.4.693.
5
The relation of leukotrienes to liver injury.
Hepatology. 1985 Sep-Oct;5(5):883-91. doi: 10.1002/hep.1840050530.
6
Bile acid malabsorption in cystic fibrosis; membrane vesicles, a tool for revealing the role of the ileal brush border membrane.
Acta Paediatr Scand Suppl. 1985;317:28-30. doi: 10.1111/j.1651-2227.1985.tb14931.x.
7
Bile acid secretion in cystic fibrosis: evidence for a defect unrelated to fat malabsorption.囊性纤维化中的胆汁酸分泌：与脂肪吸收不良无关的缺陷证据。
Gut. 1986 Sep;27(9):1043-8. doi: 10.1136/gut.27.9.1043.
8
Ultrasound findings in children with cystic fibrosis.囊性纤维化患儿的超声检查结果
Br J Radiol. 1987 Feb;60(710):137-41. doi: 10.1259/0007-1285-60-710-137.
9
Current clinical management of hepatic problems in cystic fibrosis.囊性纤维化肝脏问题的当前临床管理
J R Soc Med. 1986;79 Suppl 12(Suppl 12):38-43.
10
In vivo bile acid uptake from terminal ileum in cystic fibrosis.
Pediatr Res. 1988 Mar;23(3):323-8. doi: 10.1203/00006450-198803000-00018.

Liver and biliary problems in cystic fibrosis.

作者信息

Tanner M S

机构信息

Department of Paediatrics, Sheffield Children's Hospital, Western Bank.

出版信息

J R Soc Med. 1992;85 Suppl 19(Suppl 19):20-4.

PMID:1597836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1295449/
Abstract
摘要