4.3 Article

Trafficking and Transporter Disorders in Pediatric Cholestasis

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CLINICS IN LIVER DISEASE
卷 14, 期 4, 页码 619-+

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W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.cld.2010.08.001

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Pediatric cholestasis; Bile salt export pump; Multidrug resistance protein; Genetic diagnosis; Cell polarity

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This article describes the uses of immunostaining in the diagnosis of cholestasis To immunostain for bile salt export pump (BSEP) and multidrug resistance protein 3 in severe hepatobiliary disease manifest early in life can rapidly identify whether sequencing of ABCB11 or ABCB4 is likely to yield a genetic diagnosis To immunostain for canalicular ectoenzymes as well as transporters with transmission electron microscopy can suggest whether sequencing of ATP8B1 is likely to yield a genetic diagnosis Demonstrating BSEP expression can direct attention to bile acid synthesis disorders Immunostaining for multidrug resistance-associated protein 2 serves principally as a control for adequacy of processing

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CLINICS IN LIVER DISEASE (2024)

Article Gastroenterology & Hepatology

Treatment of Primary Biliary Cholangitis including Transplantation

Yasameen Muzahim, Ali Wakil, Mehak Bassi, Nikolaos Pyrsopoulos

CLINICS IN LIVER DISEASE (2024)

Article Gastroenterology & Hepatology

Phenotypes of Primary Sclerosing Cholangitis and Differential Diagnosis

Brian H. Horwich, Douglas T. Dieterich

CLINICS IN LIVER DISEASE (2024)

Article Gastroenterology & Hepatology

Treatment of Autoimmune Hepatitis

Aparna Goel, Paul Kwo

Summary: The goal of autoimmune hepatitis treatment is achieving clinical and biochemical remission. Standard care involves induction treatment with corticosteroids and gradual tapering of steroids. Alternatives to standard therapy can be considered for patients with intolerance or inadequate response. Treatment withdrawal is achievable in less than 20% of patients after 2 years of sustained remission, and liver transplantation should be considered for patients with progressive disease or complications.

CLINICS IN LIVER DISEASE (2024)

Article Gastroenterology & Hepatology

Systemic Complications of Primary Biliary Cholangitis

Mariana Zapata, Hendrick Pagan-Torres, Marlyn J. Mayo

CLINICS IN LIVER DISEASE (2024)

Article Gastroenterology & Hepatology

Primary Sclerosing Cholangitis Epidemiology, Diagnosis, and Presentation

Aalam Sohal, Sanya Kayani, Kris Kowdley

Summary: Primary sclerosing cholangitis (PSC) is an immune-mediated liver disease characterized by inflammation and fibrosis of bile ducts. It is commonly associated with inflammatory bowel disease, especially ulcerative colitis. The natural history of the disease varies among patients, but most will develop cirrhosis.

CLINICS IN LIVER DISEASE (2024)