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Titlebook: Introduction to Biliary Atresia; Masaki Nio Book 2021 The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer

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Pathology of Biliary Atresia,ompare them with the liver histological features in other two major diseases, namely Alagille syndrome (AGS) [5–7] and progressive familial intrahepatic cholestasis type 2 (PFIC2) [8, 9] that we need to distinguish from BA. Next, we will review the association between pathological changes of BA and
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Biomarkers of Biliary Atresia,is urgently needed to simplify the diagnostic algorithm and ideally avoid an operative procedure. Recently, serum matrix metalloproteinase-7 (MMP-7) has shown promise in diagnosing BA, achieving a more favorable area under the receiver operating characteristic curves than other noninvasive biomarker
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Differential Diagnosis of Biliary Atresia, atresia include various diseases, such as congenital biliary dilatation, genetic diseases, metabolic disorders, infections, and idiopathic neonatal hepatitis. In cases with neonatal cholestasis, biliary atresia is considered first, and diagnosis and treatment are performed as quickly as possible. I
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Diagnostic Modalities for Biliary Atresia,lude invasive and noninvasive methods. The noninvasive methods include ultrasonography (US), duodenal tube test, hepatobiliary scintigraphy, magnetic resonance cholangiopancreatography, and endoscopic retrograde cholangiopancreatography; whereas the invasive methods include cholangiography, explorat
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Ryoji Ohik spielt, läßt den großen Umfang der Literatur über die analytischen Bestimmungsverfahren dieses Elementes verständlich erscheinen. Da der Orthophosphorsäure unter den Verbindungen des Phosphors die größte Bedeutung zukommt, weil sie in den Organismen in verschiedenen Verbindungen vorkommt, weil sie
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