(Q34024783)

30 July 2017

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title

Advances in familial and congenital cholestatic diseases. Clinical and diagnostic implications (English)

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30 July 2017

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C Colombo

1

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30 July 2017

L Okolicsanyi

series ordinal

2

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30 July 2017

M Strazzabosco

series ordinal

3

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30 July 2017

publication date

1 March 2000

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Digestive and Liver Disease

30 July 2017

published in

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30 July 2017

volume

32

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30 July 2017

issue

2

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30 July 2017

page(s)

152-159

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New insights into cholangiocyte physiology

30 July 2017

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

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Normal serum gamma-glutamyl-transpeptidase activity identifies groups of infants with idiopathic cholestasis with poor prognosis

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A new cause of progressive intrahepatic cholestasis: 3 beta-hydroxy-C27-steroid dehydrogenase/isomerase deficiency

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Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region

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

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Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis

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Heterozygous non-sense mutation of the MDR3 gene in familial intrahepatic cholestasis of pregnancy

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Identifiers

DOI

1 reference

30 July 2017

1 reference