(Q49138858)

18 February 2018

title

A father and son with cholestasis and peripheral pulmonic stenosis: a distinct form of intrahepatic cholestasis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A632979

17 July 2022

1 reference

1 reference

LaBrecque DR

2

1 reference

18 February 2018

C. A. Riely

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A632979

17 July 2022

D. R. LaBrecque

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A632979

17 July 2022

C. Ghent

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A632979

17 July 2022

A. Horwich

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A632979

17 July 2022

G. Klatskin

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A632979

17 July 2022

language of work or name

English

0 references

publication date

1 March 1978

1 reference

18 February 2018

The Journal of Pediatrics

published in

1 reference

18 February 2018

volume

92

1 reference

18 February 2018

issue

3

1 reference

18 February 2018

page(s)

406-411

1 reference

18 February 2018

Intrahepatic cholestasis in childhood

cites work

1 reference

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Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease

7 January 2021

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7 January 2021

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The metabolism of 3alpha, 7alpha, 12alpha-trihydorxy-5beta-cholestan-26-oic acid in two siblings with cholestasis due to intrahepatic bile duct anomalies. An apparent inborn error of cholic acid synthesis

7 January 2021

1 reference

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A syndrome of multiple developmental defects including polycystic kidneys and intrahepatic biliary dysgenesis in 2 siblings.

7 January 2021

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Hereditary recurrent intrahepatic cholestasis from birth

7 January 2021

1 reference

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Effect of phenobarbital on hyperbilirubinemia, bile acid metabolism, and microsomal enzyme activity in chronic intrahepatic cholestasis of childhood

7 January 2021

1 reference

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Biliary transport and hepatic storage of sulfobromophthalein sodium in the unanesthetized dog, in normal man, and in patients with hepatic disease

7 January 2021

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Quantitative estimation of bile salts in serum

7 January 2021

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An improved method for measuring human blood bile acids.

7 January 2021

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Bile salts and liver disease in childhood

7 January 2021

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Congenital absence of the intrahepatic bile ducts

7 January 2021

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Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur

7 January 2021

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Familial intrahepatic cholestatic jaundice in infancy

7 January 2021

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A case of familial intrahepatic cholestasis

7 January 2021

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Severe familial intrahepatic cholestasis

7 January 2021

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Neonatal Hepatitis and Biliary Atresia Associated with Trisomy 17–18 Syndrome

7 January 2021

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FAMILIAL EXTRAHEPATIC BILIARY ATRESIA.

7 January 2021

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Prolonged obstructive jaundice in infancy. V. The genetic components in neonatal hepatitis

7 January 2021

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FAMILIAL "GIANT-CELL HEPATITIS" IN INFANCY. CLINICAL, PATHOLOGIC, AND GENETIC STUDIES ON A LARGE FAMILY

7 January 2021

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Hereditary lymphedema and obstructive jaundice

7 January 2021

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Hereditary recurrent cholestasis with lymphoedema--two new families.

7 January 2021

1 reference

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Trihydroxycoprostanic acid in the duodenal fluid of two children with intrahepatic bile duct anomalies

7 January 2021

1 reference

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Hereditary cholestasis combined with peripheral pulmonary stenosis and other anomalies

7 January 2021

1 reference

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Byler's disease: fatal intrahepatic cholestasis

7 January 2021

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Progressive familial cholestatic cirrhosis and bile acid metabolism

7 January 2021

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10.1016/S0022-3476(78)80428-4

7 January 2021

Identifiers

DOI

1 reference

18 February 2018

1 reference

18 February 2018