Titlebook: Diseases of the Liver in Children; Evaluation and Manag Karen F. Murray,Simon Horslen Book 2014 Springer Science+Business Media New York 20

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Biliary Atresiartoenterostomy can survive more than 10 years with their native liver and achieve good quality of life. However, a large proportion of children with BA will require liver transplantation at some stage, especially if the Kasai portoenterostomy is unsuccessful. In the largest follow-up study of BA chi

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Combinatorial Evolution of DNA with RECODE era in the understanding of this topic. In the late 1880s, after the introduction of anaesthesia and antisepsis, the first liver resections were attempted. Further advances in hepatic anatomy were made at the turn of the nineteenth century, but it was not until the late 1950s that the segmental str

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https://doi.org/10.1007/978-3-658-10988-2ver relies on a multidisciplinary approach involving clinical chemistry, hematology, immunology, imaging studies, endoscopy, histopathology, and microbiology. Mutational analyses for many genetic liver diseases are now available. This chapter will outline the basic laboratory assessment of the liver

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Munehito Arai,Yuuki Hayashi,Hisashi Kudo native or transplanted liver. The primary imaging modalities that are routinely called upon to evaluate the pediatric liver include ultrasound (US), computed tomography (CT), magnetic resonance imaging (MRI), and nuclear scintigraphy. The detailed anatomical capabilities offered by US, CT, and MRI

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https://doi.org/10.1007/978-981-13-0854-3they read about during their training but may never have encountered. The aim of this chapter is to describe hepatic disease phenotypes based on age and primary manifestation of liver disease such as cholestasis, hepatomegaly, or acute liver failure and to provide a reasonably comprehensive list of

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