(Q28254452)

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Sandra S Strautnieks

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Yvonne Meier

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Bruno Stieger

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Jane A Byrne

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Bernard C Portmann

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Laura N Bull

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Banu Bilezikçi

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Figen Ozçay

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Aranka László

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László Tiszlavicz

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Lynette Moore

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Jeremy Raftos

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Henrik Arnell

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Björn Fischler

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Nikos Papadogiannakis

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Hector Melín-Aldana

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Karan M Emerick

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Giorgina Mieli-Vergani

Hepatoma complicating Byler disease

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language of work or name

English

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publication date

August 2006

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478-86

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cites work

1 reference

Bile acids as carcinogens in human gastrointestinal cancers

21 January 2018

1 reference

Partial external diversion of bile for the treatment of intractable pruritus associated with intrahepatic cholestasis

21 January 2018

1 reference

7 January 2021

Selective surgical management of progressive familial intrahepatic cholestasis (Byler's disease).

1 reference

7 January 2021

Ileal exclusion for Byler's disease: an alternative surgical approach with promising early results for pruritus

1 reference

7 January 2021

A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

1 reference

7 January 2021

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

1 reference

7 January 2021

Atp8b1 deficiency in mice reduces resistance of the canalicular membrane to hydrophobic bile salts and impairs bile salt transport

1 reference

7 January 2021

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

1 reference

7 January 2021

Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis

1 reference

7 January 2021

The human bile salt export pump: characterization of substrate specificity and identification of inhibitors

1 reference

7 January 2021

Functional expression of the canalicular bile salt export pump of human liver

1 reference

7 January 2021

Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity

1 reference

7 January 2021

Hepatocellular Carcinoma Following Neonatal Hepatitis

1 reference

7 January 2021

Hepatocyte transplantation for inherited factor VII deficiency

1 reference

7 January 2021

Studies on the Mechanism of the Increase in Serum Alkaline Phosphatase Activity in Cholestasis: Significance of the Hepatic Bile Acid Concentration for the Leakage of Alkaline Phosphatase from Rat Liver

1 reference

7 January 2021

Hepatoma in Siblings with Progressive Familial Cholestatic Cirrhosis of Childhood

1 reference

7 January 2021

Impaired expression and function of the bile salt export pump due to three novel ABCB11 mutations in intrahepatic cholestasis

1 reference

7 January 2021

In situ localization of the hepatocytic Na+/Taurocholate cotransporting polypeptide in rat liver

1 reference

7 January 2021

Natural variation in human membrane transporter genes reveals evolutionary and functional constraints

1 reference

7 January 2021

Primary carcinoma of the liver after giant-cell hepatitis of infancy; report of a case

1 reference

7 January 2021

Primary carcinoma of the liver and giant-cell hepatitis in infancy

1 reference

7 January 2021

Hepatocellular carcinoma and liver cell dysplasia in children with chronic liver disease

1 reference

7 January 2021

Histologic pathology of the liver in progressive familial intrahepatic cholestasis

1 reference

7 January 2021

Clinical and biochemical findings in progressive familial intrahepatic cholestasis

1 reference

7 January 2021

Clinical characteristics and prognosis of pediatric hepatocellular carcinoma.

1 reference

7 January 2021

A progressive familial intrahepatic cholestasis type 2 mutation causes an unstable, temperature-sensitive bile salt export pump.

1 reference

7 January 2021

Two common PFIC2 mutations are associated with the impaired membrane trafficking of BSEP/ABCB11.

1 reference

7 January 2021

Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11

1 reference

7 January 2021

Deficiency of BSEP in PFIC with hepatocellular malignancy

1 reference

7 January 2021

Deficient DNA-ligase activity in the metabolic disease tyrosinemia type I.

1 reference

7 January 2021

Tyrosinaemia type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione).

1 reference

7 January 2021

Liver transplant pathology in pediatric metabolic disorders

1 reference

7 January 2021

The occurrence of hepatoma in the chronic form of hereditary tyrosinemia

1 reference

7 January 2021

Liver transplantation in nine Spanish patients with tyrosinaemia type I

1 reference

7 January 2021

Safety of living-related liver transplantation for progressive familial intrahepatic cholestasis

1 reference

7 January 2021