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Infantile polycystic disease of the kidneys and liver: clinical, pathological and radiological correlations and comparison with congenital hepatic fibrosis.

作者信息

Lieberman E, Salinas-Madrigal L, Gwinn J L, Brennan L P, Fine R N, Landing B H

出版信息

Medicine (Baltimore). 1971 Jul;50(4):277-318. doi: 10.1097/00005792-197107000-00003.

DOI:10.1097/00005792-197107000-00003
PMID:5143572
Abstract
摘要

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Infantile polycystic disease of the kidneys and liver: clinical, pathological and radiological correlations and comparison with congenital hepatic fibrosis.婴儿型肝肾多囊病:临床、病理及影像学相关性分析以及与先天性肝纤维化的比较
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Congenital Hepatic Fibrosis as an Early Sign of Presentation of ADPKD.先天性肝纤维化作为常染色体显性多囊肾病的早期表现迹象
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Infant presenting with pyloric stenosis and autosomal recessive polycystic kidney disease at 36 weeks' postmenstrual age (PMA).婴儿在 36 周龄时出现幽门狭窄和常染色体隐性多囊肾病。
BMJ Case Rep. 2021 May 19;14(5):e242679. doi: 10.1136/bcr-2021-242679.
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Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects.
常染色体隐性遗传性多囊肾病:一种肝-肾纤维囊性疾病,具有多种表现型效应。
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Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease.73 例常染色体隐性多囊肾病患者的肾功能、体积和影像学表现与 PKHD1 突变的相关性。
Clin J Am Soc Nephrol. 2010 Jun;5(6):972-84. doi: 10.2215/CJN.07141009. Epub 2010 Apr 22.
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The Ivemark syndrome: prenatal diagnosis of an uncommon cystic renal lesion with heterogeneous associations.
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Association of congenital hepatic fibrosis with autosomal dominant polycystic kidney disease. Report of a family with review of literature.先天性肝纤维化与常染色体显性遗传性多囊肾病的关联。附文献复习的一家系报告。
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Renal and biliary abnormalities in a new murine model of autosomal recessive polycystic kidney disease.常染色体隐性多囊肾病新小鼠模型中的肾脏和胆道异常
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