首页 文献索引 SCI期刊 AI助手
期刊目录筛选

期刊名:Seminars in pediatric surgery

缩写:SEMIN PEDIATR SURG

ISSN:1055-8586

e-ISSN:1532-9453

IF/分区:2.5/Q1

文章目录 更多期刊信息

共收录本刊相关文章索引999
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Isabelle Lane Curran,Robert A Cowles Isabelle Lane Curran
Biliary atresia can be a challenging diagnosis to make as there is no single definitive diagnostic laboratory or imaging study available and no single agreed upon diagnostic algorithm. The purpose of this article is to review the complex pu...
Iiris Nyholm,Maria Hukkinen,Mikko P Pakarinen Iiris Nyholm
Regardless of the underlying etiology and success of PE, progressive liver fibrosis and eventually cirrhosis represent the dominant pathology and the end-stage of BA. Ascending bile duct injury-induced cholestasis, inflammation and ductular...
Renos M Jeropoulos,Jorge Arroyo,Mark Davenport Renos M Jeropoulos
Biliary atresia (BA) remains a disease of significant morbidity and mortality world-wide. Early and accurate diagnosis facilitates early intervention and improves outcomes. The gold standard in diagnosing BA is a liver biopsy followed by ch...
Alyssa Stetson,Alexander Bondoc,Greg Tiao Alyssa Stetson
The Kasai portoenterostomy (KPE) can provide a surgical cure for children with biliary atresia (BA), without the need for a liver transplant (OLTxp). Revision KPE can be attempted following a failed initial KPE where biliary clearance is no...
Ana M Calinescu,Barbara E Wildhaber Ana M Calinescu
Cholangitis, defined as the inflammation of the bile ducts, is the most frequent complication after Kasai hepatoportoenterostomy in patients with biliary atresia (BA). This review seeks to provide a comprehensive synthesis of current knowle...
Qiongfen Lin,Paul Kwong-Hang Tam,Clara Sze-Man Tang Qiongfen Lin
Biliary atresia (BA) is a severe neonatal cholestatic disorder marked by fibro-obliteration of the extrahepatic and intrahepatic bile ducts. It is the most common cause of pediatric end-stage liver disease and the leading indication for liv...
Phoebe N Miller,Suruthi Baskaran,Amar Nijagal Phoebe N Miller
Biliary atresia is a progressive neonatal cholangiopathy that leads to liver failure. Characterized by inflammation-mediated liver injury, the immune system plays a critical role in the pathogenesis of this disease. Though several types of ...
Carmen Mesas Burgos,Natalie Rintoul,Lars Mikael Broman Carmen Mesas Burgos
Despite ECMO being a well-accepted and established life-saving support for newborns, prematurity ( 2.0 kg) deserves to be challenge. The authors suggest that Prem-ECMO (GA 32-33) could be considered when restricted to experienced high-volum...