(Q41191189)

28 September 2017

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title

Genetic diseases of bilirubin metabolism: the inherited unconjugated hyperbilirubinemias (English)

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bilirubin metabolic disorder

28 September 2017

main subject

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Jansen PL

1

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28 September 2017

publication date

1 September 1996

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28 September 2017

published in

Journal of Hepatology

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28 September 2017

volume

25

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28 September 2017

issue

3

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28 September 2017

page(s)

398-404

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Crigler-Najjar syndrome types I and II. Clinical experience--King's College Hospital 1972-1978. Phenobarbitone, phototherapy and liver transplantation

28 September 2017

cites work

1 reference

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7 January 2021

Crigler-Najjar type II disease inheritance: a family study

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https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Crigler-Najjar syndrome: an unusual course with development of neurologic damage at age eighteen

1 reference

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7 January 2021

The differential diagnosis of Crigler-Najjar disease, types 1 and 2, by bile pigment analysis

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7 January 2021

Unconjugated Bilirubin and an Increased Proportion of Bilirubin Monoconjugates in the Bile of Patients with Gilbert's Syndrome and Crigler-Najjar Disease

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7 January 2021

Unconjugated hyperbilirubinemia. Physiologic evaluation and experimental approaches to therapy

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7 January 2021

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

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7 January 2021

Function and regulation of UDP-glucuronosyltransferase genes in health and liver disease: report of the Seventh International Workshop on Glucuronidation, September 1993, Pitlochry, Scotland.

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7 January 2021

Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

A new type of defect in the gene for bilirubin uridine 5'-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I.

1 reference

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7 January 2021

Identification of an A-to-G missense mutation in exon 2 of the UGT1 gene complex that causes Crigler-Najjar syndrome type 2

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Effective Phototherapy in Congenital Nonobstructive, Nonhemolytic Jaundice

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https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Congenital nonobstructive, nonhemolytic jaundice. Effect of phototherapy

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https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Crigler-Najjar syndrome: treatment at home with phototherapy

1 reference

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7 January 2021

Crigler-Najjar Type 1 syndrome: absence of hepatic bilirubin UDP-glucuronyl transferase activity and therapeutic responses to light.

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7 January 2021

Crigler-Najjar syndrome type I: management with phototherapy crib mattress

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7 January 2021

Orthotopic auxiliary liver transplantation for Crigler-Najjar syndrome type 1

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7 January 2021

Liver transplantation in Crigler-Najjar syndrome. A case report

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7 January 2021

Orthotopic liver transplantation for type I Crigler-Najjar syndrome

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7 January 2021

Crigler-Najjar syndrome type I: treatment by home phototherapy followed by orthotopic hepatic transplantation

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Reduced caloric intake and nicontinic acid provocation tests in the diagnosis of Gilbert's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Chromosomal assignment of human phenol and bilirubin UDP-glucuronosyltransferase genes (UGT1A-subfamily)

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Assignment of the human UDP glucuronosyltransferase gene (UGT1A1) to chromosome region 2q37

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Cloning and stable expression of a new member of the human liver phenol/bilirubin: UDP-glucuronosyltransferase cDNA family

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Cloning and substrate specificity of a human phenol UDP-glucuronosyltransferase expressed in COS-7 cells

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Chronic unconjugated hyperbilirubinemia without overt signs of hemolysis in adolescents and adults

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Inheritance of type 2 Crigler-Najjar hyperbilirubinaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Immunochemical analysis of uridine diphosphate-glucuronosyltransferase in four patients with the Crigler-Najjar syndrome type I.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Genetic defect of bilirubin UDP-glucuronosyltransferase in the hyperbilirubinemic Gunn rat

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

A mutation in bilirubin uridine 5'-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type II

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2896%2980129-2

7 January 2021

10.1016/S0168-8278(96)80129-2

Identifiers

DOI

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28 September 2017

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