(Q69267890)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2515370%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

title

Crigler-Najjar type II disease inheritance: a family study (English)

1 reference

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30 September 2019

author name string

P Labrune

1

1 reference

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30 September 2019

A Myara

2

1 reference

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30 September 2019

C Hennion

3

1 reference

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30 September 2019

J P Gout

4

1 reference

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30 September 2019

F Trivin

5

1 reference

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30 September 2019

M Odievre

6

1 reference

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30 September 2019

publication date

1 January 1989

1 reference

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Journal of Inherited Metabolic Disease

30 September 2019

published in

1 reference

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30 September 2019

volume

12

1 reference

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30 September 2019

issue

3

1 reference

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30 September 2019

page(s)

302-306

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf01799221

30 September 2019

exact match

0 references

cites work

Congenital familial nonhemolytic jaundice with kernicterus

1 reference

12 December 2020

Inheritance of type 2 Crigler-Najjar hyperbilirubinaemia

1 reference

12 December 2020

Measurement of the activity of bilirubin UDP-glucuronyl transferase: application to needle biopsy specimens

1 reference

12 December 2020

Hepatic Bilirubin UDP-Glucuronyl Transferase Activity in Liver Disease and Gilbert's Syndrome

1 reference

12 December 2020

Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity

1 reference

12 December 2020

Nonhemolytic unconjugated hyperbilirubinemia with hepatic glucuronyl transferase deficiency: a genetic study in four generations

1 reference

12 December 2020

Prolonged survival in three brothers with severe type 2 Crigler-Najjar syndrome. Ultrastructural and metabolic studies

1 reference

12 December 2020

Inheritable and congenital hyperbilirubinemia. Models for the study of drug metabolism

1 reference

12 December 2020

Hepatic bilirubin glucuronidation in Gilbert's syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01799221

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2515370%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

30 September 2019

0 references

1 reference