About: 3 Developmental and Inherited Liver Disease

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Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	3 Developmental and Inherited Liver Disease
Creator	Quaglia, Alberto Torbenson, Michael Roberts, Eve
Source	Elsevier
abstract	Abstract A new section on the approach to diagnostic histological interpretation, is the overture to this chapter on inherited and developmental disorders. This initial section is split chronologically into the early neonatal and infantile period and later childhood and adulthood; with the intention of reflecting clinical practice as closely and succinctly as possible. Disorders of the biliary tree, bile formation and secretion, and hepatocyte metabolism are the core of this chapter, a merger of chapters 3 and 4 of the previous edition. Considerations on the pathogenetic and/or clinical overlap between developmental, genetic and metabolic disorders were the rationale behind this change. The complexity of hepatocyte metabolism is reflected into the miriad of related pathological conditions. Recent technological advances, particularly in genomics in the last five years, have resulted in a plethora of new entities and changes in terminology, challenging the authors to balance detail and application to clinical practice. Tables and figures from previous editions have been largely kept due to their quality and contemporary relevance, whilst new ones have been added to accommodate new advances (e.g. classification of mitochondrial disorders), a compromise to bridge between the two editions for the accustomed reader. Liver involvement in immunodeficiency and miscellaneous disorders precede the final section on anatomical anomalies. Vascular anomalies are now included in the chapters on vascular disorders.
has issue date	2018-12-31(xsd:dateTime)
bibo:doi	10.1016/b978-0-7020-6697-9.00003-0
has license	els-covid
sha1sum (hex)	b6ae4d88a03ac0b1142577db37678d6d59080bf3
schema:url	https://doi.org/10.1016/b978-0-7020-6697-9.00003-0
resource representing a document's title	3 Developmental and Inherited Liver Disease
resource representing a document's body	covid:b6ae4d88a03ac0b1142577db37678d6d59080bf3#body_text
is schema:about of	named entity 'bile salt' named entity 'galactose' named entity 'hepatobiliary' named entity 'varicella' named entity 'Immunohistochemical staining' named entity 'urine' named entity 'oxidative burst' named entity 'Cytogenetic studies' named entity 'liver' named entity 'cirrhosis' named entity 'mutation analysis' named entity 'biliary tract obstruction' named entity 'intestine' named entity 'long-term' named entity 'choledochal cyst' named entity 'cardiac disease' named entity 'False-positive' named entity 'Wilsonian' named entity 'liver biopsy' named entity 'quadriplegia' named entity 'Crigler-Najjar syndrome' named entity 'cholestyramine' named entity 'bile' named entity 'collagen' named entity 'histological' named entity 'cirrhosis' named entity 'infection' named entity 'Hepatocytes' named entity 'enlargement of the liver and spleen' named entity 'alcohol' named entity 'Sly syndrome' named entity 'cholestasis' named entity 'kidney stones' named entity 'cirrhosis' named entity 'cholesterol' named entity 'µmol/L' named entity 'intrahepatic bile ducts' named entity 'endocrine cells' named entity 'Niemann-Pick disease' named entity 'perinatal' named entity 'hyperbilirubinaemia' named entity 'Light microscopic' named entity 'crystal accumulation' named entity 'liver biopsy' named entity 'aspiration pneumonia' named entity 'percutaneous' named entity 'LFT' named entity 'cholestatic liver disease' named entity 'long-term' named entity 'macrophages' named entity 'uric acid' named entity 'cirrhosis' named entity 'cholestasis' named entity 'GSD' named entity 'biopsy' named entity 'peroxisomal' named entity 'common hepatic duct' named entity 'mutation' named entity 'bile' named entity 'HCC' named entity 'Kawasaki disease' named entity 'AST and ALT' named entity 'CGD' named entity 'sucrose' named entity 'liver transplantation' named entity 'perinatal' named entity 'Notch 2' named entity 'screening test' named entity 'factor VIII' named entity 'steatosis' named entity 'infection' named entity 'cytochrome-c oxidase' named entity 'hepatocytes' named entity 'chromosome 11q13' named entity 'cirrhosis' named entity 'bile duct' named entity 'systemic hypertension' named entity 'haemophagocytic syndrome' named entity 'haem synthesis' named entity 'inherited disorders' named entity 'mutation' named entity 'bile' named entity 'ecchymoses'

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