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Combined cystic disease of the liver and kidney.

作者信息

D'Agata I D, Jonas M M, Perez-Atayde A R, Guay-Woodford L M

机构信息

Center for Childhood Liver Disease, Children's Hospital, Boston, Massachusetts.

出版信息

Semin Liver Dis. 1994 Aug;14(3):215-28. doi: 10.1055/s-2007-1007313.

DOI:10.1055/s-2007-1007313
PMID:7939783
Abstract
摘要

相似文献

1
Combined cystic disease of the liver and kidney.肝肾联合性囊肿病
Semin Liver Dis. 1994 Aug;14(3):215-28. doi: 10.1055/s-2007-1007313.
2
[Investigation of the gene locus in autosomal polycystic kidney disease in a 21 year old female patient with congenital hepatic fibrosis and polycystic liver].[对一名患有先天性肝纤维化和多囊肝的21岁女性常染色体显性多囊肾病患者的基因位点研究]
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Bile duct dysplasia and congenital hepatic fibrosis associated with polycystic kidney (Caroli syndrome) in a rat.大鼠中与多囊肾相关的胆管发育异常和先天性肝纤维化(卡罗里综合征)
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4
Congenital hepatic fibrosis in a child with autosomal dominant polycystic kidney disease.一名患有常染色体显性多囊肾病儿童的先天性肝纤维化。
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Kidney and liver cysts in autosomal dominant polycystic kidney disease.常染色体显性多囊肾病中的肾囊肿和肝囊肿
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The hepatic fibrocystic diseases.肝脏纤维囊性疾病
Clin Liver Dis. 2006 Feb;10(1):55-71, v-vi. doi: 10.1016/j.cld.2005.10.003.
7
[Fibropolycystic disease of the liver].[肝脏纤维多囊病]
Ryoikibetsu Shokogun Shirizu. 1995(8):90-3.
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Pathology teach and tell: perinatal recessive polycystic kidney disease with congenital hepatic fibrosis.病理学教学案例:围产期隐性多囊肾病合并先天性肝纤维化
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[Congenital hepatic fibrosis and autosomal recessive polycystic kidney disease].
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[Polycystic kidney diseases: molecular genetics and counselling].[多囊肾病:分子遗传学与遗传咨询]
Nephrol Ther. 2006 Jul;2(3):120-6. doi: 10.1016/j.nephro.2006.03.001. Epub 2006 Jun 27.

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Pathology of Fibropolycystic Liver Diseases.纤维多囊性肝病的病理学
Clin Liver Dis (Hoboken). 2021 May 1;17(4):238-243. doi: 10.1002/cld.1044. eCollection 2021 Apr.
3
Persistent pruritus as a rare and potentially serious manifestation of liver involvement in autosomal dominant polycystic kidney disease.
持续性瘙痒是常染色体显性遗传性多囊肾病肝脏受累的一种罕见且可能严重的表现。
Clin Kidney J. 2018 Jul 6;12(3):380-381. doi: 10.1093/ckj/sfy057. eCollection 2019 Jun.
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Congenital hepatic fibrosis in a 9-year-old female patient - a case report.一名9岁女性患者的先天性肝纤维化——病例报告
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Inhibiting heat shock protein 90 (HSP90) limits the formation of liver cysts induced by conditional deletion of Pkd1 in mice.抑制热休克蛋白90(HSP90)可限制小鼠中Pkd1条件性缺失诱导的肝囊肿形成。
PLoS One. 2014 Dec 4;9(12):e114403. doi: 10.1371/journal.pone.0114403. eCollection 2014.
6
Polycystic liver disease presenting as pruritus.以瘙痒为表现的多囊肝病。
Ann Gastroenterol. 2014;27(1):76-78.
7
Pathophysiology, epidemiology, classification and treatment options for polycystic liver diseases.多囊肝疾病的病理生理学、流行病学、分类和治疗选择。
World J Gastroenterol. 2013 Sep 21;19(35):5775-86. doi: 10.3748/wjg.v19.i35.5775.
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Treatment of polycystic liver disease with resection-fenestration and a new classification.采用切除-开窗术治疗多囊肝疾病及一种新分类法
World J Gastroenterol. 2008 Aug 28;14(32):5066-72. doi: 10.3748/wjg.14.5066.
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Developments in the management of autosomal dominant polycystic kidney disease.常染色体显性遗传性多囊肾病的治疗进展。
Ther Clin Risk Manag. 2008 Apr;4(2):393-407. doi: 10.2147/tcrm.s1617.
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Surgical management of polycystic liver disease.多囊肝疾病的外科治疗
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