Biliary Atresia: Aetiology, Diagnosis and Treatment

Despite extensive clinical and basic research, we know very little about the aetiology and pathomechanism of biliary atresia (BA). Today, it is a matter of common sense that early diagnosis (screening programs), sequential surgical treatment (the Kasai procedure and optional liver transplantation),...

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Detalles Bibliográficos
Formato:	Online
Idioma:	inglés
Publicado:	MDPI - Multidisciplinary Digital Publishing Institute 2024
Subjects:	biomarker cholangiocyte ductular reaction liver fibrosis pediatric liver disease pregnancy biliary atresia chorine esterase MELD score liver transplantation Kasai operation liver transplant etiology adjuvant therapy budesonide cholangitis Kasai hepatoportoenterostomy cytomegalovirus survival native liver antiviral treatment newborn screening public health epidemiology liver nodules hepatocellular carcinoma regenerative nodules focal nodular hyperplasia Kasai portoenterostomy transplant waiting list pediatric liver transplantation referral practice outcome kasai portoenterostomy primary liver transplantation outcomes perinatal liver inflammation innate immune system monocytes cholangiopathy liver histology transplant-free survival corticosteroids ursodeoxycholic acid cytotoxic T cells perinatal liver injury hematopoietic stem and progenitor cells myeloid progenitor cells liver transition adolescence adherence readiness professionals parents pediatric liver surgery hepatoblastoma pediatric surgery workforce subspecialization thema EDItEUR::M Medicine and Nursing thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJH Gastroenterology
Acceso en liña:	ONIX_20240704_9783725812172_96
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Biliary Atresia: Aetiology, Diagnosis and Treatment

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