(Q34479253)

2 August 2017

title

Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis (English)

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benign recurrent intrahepatic cholestasis

2 August 2017

main subject

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2

Karel J van Erpecum

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2 August 2017

author name string

Janneke M Stapelbroek

1

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2 August 2017

Leo W J Klomp

3

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2 August 2017

Niels G Venneman

4

1 reference

2 August 2017

Thijs P Schwartz

5

1 reference

2 August 2017

Gerard P van Berge Henegouwen

6

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2 August 2017

John Devlin

7

1 reference

2 August 2017

Carin M J van Nieuwkerk

8

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2 August 2017

A S Knisely

9

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2 August 2017

Roderick H J Houwen

10

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2 August 2017

language of work or name

English

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publication date

1 January 2006

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2 August 2017

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2 August 2017

volume

43

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2 August 2017

issue

1

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2 August 2017

page(s)

51-53

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

2 August 2017

cites work

1 reference

7 January 2021

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

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

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Progressive familial intrahepatic cholestasis: partial biliary diversion normalizes serum lipids and improves growth in noncirrhotic patients

1 reference

7 January 2021

Surgical treatment of progressive familial intrahepatic cholestasis: comparison of partial external biliary diversion and ileal bypass

1 reference

7 January 2021

Benign recurrent intrahepatic cholestasis progressing to progressive familial intrahepatic cholestasis: low GGT cholestasis is a clinical continuum

1 reference

7 January 2021

Small gallstones, preserved gallbladder motility, and fast crystallization are associated with pancreatitis

1 reference

7 January 2021

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

1 reference

7 January 2021

A mouse genetic model for familial cholestasis caused by ATP8B1 mutations reveals perturbed bile salt homeostasis but no impairment in bile secretion

1 reference

7 January 2021

Familial intrahepatic cholestasis 1: studies of localization and function

1 reference

7 January 2021

Identifiers

DOI

10.1002/HEP.20998

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2 August 2017

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