胆道闭锁(biliary atresia)和婴儿肝炎综合症(NH)是新生儿阻塞性黄疸中最常见的疾病，两者鉴别困难，目前尚无特异性的诊断方法。
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先天性胆道闭锁(congenital biliary atresia)是新生儿期一种少见的急急黄疸性疾病，是招致新生儿障碍性黄疸并需动刀子治疗的疾病。听说null。
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...IDA肝胆断层显像对婴儿持续性黄疸常见病因的鉴别诊断价值 【中文摘要】：目的：先天性胆道闭锁(extrahepatic biliary atresia, EHBA)与婴儿肝炎综合征(infant hepatitis syndrome, IHS)是引起婴儿期持续性黄...
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先天性胆道闭锁 congenital biliary atresia ; biliary atresia ; Diagnostic value ; congenital atresia of biliary duct
胆道闭锁症 biliary atresia
后天性胆道闭锁 congenital biliary atresia
肝外胆道闭锁 extrahepatic biliary atresia ; EHBA
和胆道闭锁 biliary atresia
为胆道闭锁 biliary atresia
在胆道闭锁 biliary atresia
目的胆道闭锁 biliary atresia
检测胆道闭锁 biliary atresia
·2,447,543篇论文数据，部分数据来源于NoteExpress
在儿童肝脏移植最常见的原因是胆道闭锁。
In children, the most common reason for liver transplantation is biliary atresia.
目的：探讨活体肝移植治疗儿童先天性胆道闭锁的临床体会。
Objective: To summarize the clinical experience of living related liver transplantation for biliary atresia.
对14例胆道闭锁患儿进行葛西手术后肝脏病理变化的研究。
The pathology of liver was studied in 14 patients with congenial biliary atresia after Kasai's operation.
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