Editorial: Infants with cholestasis.
作者信息
Uchida Hiroo, Tiao Gregory M, Shivakumar Pranavkumar, Wong Kenneth K Y, Asai Akihiro, Amano Hizuru
机构信息
Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Division of Pediatric General and Thoracic Surgery, Cincinnati Children's, Hospital Medical Center, Cincinnati, OH, United States.
出版信息
Front Pediatr. 2023 Mar 28;11:1175231. doi: 10.3389/fped.2023.1175231. eCollection 2023.
Abstract
摘要
相似文献
1
Editorial: Infants with cholestasis.社论：胆汁淤积症患儿
Front Pediatr. 2023 Mar 28;11:1175231. doi: 10.3389/fped.2023.1175231. eCollection 2023.
2
Phenobarbital-enhanced hepatobiliary scintigraphy in the diagnosis of biliary atresia: two decades of experience at a tertiary center.苯巴比妥增强肝胆闪烁显像在胆道闭锁诊断中的应用：一家三级中心二十年的经验。
Pediatr Radiol. 2013 Oct;43(10):1365-75. doi: 10.1007/s00247-013-2704-3. Epub 2013 May 11.
3
Quantification of Serum Matrix Metallopeptide 7 Levels May Assist in the Diagnosis and Predict the Outcome for Patients with Biliary Atresia.血清基质金属蛋白酶 7 水平的定量检测可能有助于胆道闭锁患者的诊断和预后预测。
J Pediatr. 2019 May;208:30-37.e1. doi: 10.1016/j.jpeds.2018.12.006. Epub 2019 Mar 8.
4
Cholestasis in the newborn and infant.新生儿及婴儿胆汁淤积症
Clin Res Hepatol Gastroenterol. 2014 Jun;38(3):263-7. doi: 10.1016/j.clinre.2014.03.010. Epub 2014 Apr 18.
5
Diffusion-Weighted Imaging for Differentiation of Biliary Atresia and Grading of Hepatic Fibrosis in Infants with Cholestasis.扩散加权成像在胆汁淤积症婴儿胆道闭锁和肝纤维化分级中的鉴别诊断。
Korean J Radiol. 2021 Feb;22(2):253-262. doi: 10.3348/kjr.2020.0055. Epub 2020 Aug 28.
6
Atypical causes of cholestasis.胆汁淤积的非典型病因。
World J Gastroenterol. 2014 Jul 28;20(28):9418-26. doi: 10.3748/wjg.v20.i28.9418.
7
Body composition of children aged 1 to 12 years with biliary atresia or Alagille syndrome.1至12岁患有胆道闭锁或阿拉吉列综合征儿童的身体组成。
J Pediatr Gastroenterol Nutr. 2005 Feb;40(2):146-50. doi: 10.1097/00005176-200502000-00012.
8
Neonatal intrahepatic cholestasis caused by citrin deficiency with no hepatic steatosis: a case report.无肝脂肪变性的瓜氨酸血症所致新生儿肝内胆汁淤积症：一例报告
BMC Pediatr. 2021 May 18;21(1):237. doi: 10.1186/s12887-021-02717-w.
9
Diversity of disorders causing neonatal cholestasis - the experience of a tertiary pediatric center in Germany.导致新生儿胆汁淤积症的疾病多样性 - 德国一家三级儿科中心的经验。
Front Pediatr. 2014 Jun 23;2:65. doi: 10.3389/fped.2014.00065. eCollection 2014.
10
Biochemical characteristics of neonatal cholestasis induced by citrin deficiency.由 citrin 缺乏引起的新生儿胆汁淤积的生化特征。
World J Gastroenterol. 2012 Oct 21;18(39):5601-7. doi: 10.3748/wjg.v18.i39.5601.
引用本文的文献
1
Determination of Optimal Vitamin D Dosage in Children with Cholestasis.确定胆汁淤积症患儿的最佳维生素 D 剂量。
BMC Pediatr. 2023 Jun 21;23(1):313. doi: 10.1186/s12887-023-04113-y.
本文引用的文献
1
Intraoperative indocyanine green fluorescence cholangiography can rule out biliary atresia: A preliminary report.术中吲哚菁绿荧光胆管造影可排除胆道闭锁：初步报告。
Front Pediatr. 2022 Nov 4;10:1005879. doi: 10.3389/fped.2022.1005879. eCollection 2022.
2
Re-evaluation of Laparoscopic Hepatic Subcapsular Spider-Like Telangiectasis Sign: A Highly Accurate Method to Diagnose Biliary Atresia in Infants.腹腔镜肝包膜下蜘蛛样毛细血管扩张征的重新评估：一种诊断婴儿胆道闭锁的高度准确方法。
Front Pediatr. 2022 Apr 25;10:850449. doi: 10.3389/fped.2022.850449. eCollection 2022.
3
Serum MMP-7 in the Diagnosis of Biliary Atresia.血清 MMP-7 在胆道闭锁诊断中的应用。
Pediatrics. 2019 Nov;144(5). doi: 10.1542/peds.2019-0902. Epub 2019 Oct 11.
4
Diagnostic Accuracy of Serum Matrix Metalloproteinase-7 for Biliary Atresia.血清基质金属蛋白酶-7对胆道闭锁的诊断准确性。
Hepatology. 2018 Dec;68(6):2069-2077. doi: 10.1002/hep.30234. Epub 2018 Nov 15.
5
Biliary tract: MMP7 - a diagnostic biomarker for biliary atresia.胆道：基质金属蛋白酶7——一种用于胆道闭锁的诊断生物标志物。
Nat Rev Gastroenterol Hepatol. 2018 Feb;15(2):68. doi: 10.1038/nrgastro.2017.175. Epub 2017 Dec 13.
Zotero 插件