Bile composition in Alagille Syndrome and PFIC patients having Partial External Biliary Diversion (Q33378260)

26 July 2017

Bile composition in Alagille Syndrome and PFIC patients having Partial External Biliary Diversion (English)

1 reference

26 July 2017

1 reference

Richard J Thompson

5

0 references

Peter F. Whitington

8

object named as

Peter F Whitington

1 reference

26 July 2017

Karan M Emerick

1

1 reference

26 July 2017

Marc S Elias

2

1 reference

26 July 2017

Hector Melin-Aldana

3

1 reference

26 July 2017

Sandra Strautnieks

4

1 reference

26 July 2017

Laura N Bull

6

1 reference

26 July 2017

A s Knisely

7

1 reference

26 July 2017

Richard M Green

9

1 reference

26 July 2017

20 October 2008

1 reference

26 July 2017

1 reference

26 July 2017

8

1 reference

26 July 2017

47

1 reference

Creative Commons Attribution 2.0 Generic

26 July 2017

start time

20 October 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1186/1471-230x-8-47

0 references

cites work

Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Molecular basis of intrahepatic cholestasis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Fifteen years single center experience in the management of progressive familial intrahepatic cholestasis of infancy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Partial external biliary diversion for intractable pruritus and xanthomas in Alagille syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Outcome of liver disease in children with Alagille syndrome: a study of 163 patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Clinical aspects of familial cholestasis (with molecular explanations).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Clinical and molecular genetics of Alagille syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Histologic pathology of the liver in progressive familial intrahepatic cholestasis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Clinical and biochemical findings in progressive familial intrahepatic cholestasis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Correctable plasma lipoprotein abnormalities in infants with choledochal cysts

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Quantitative estimation of the hydrophilic-hydrophobic balance of mixed bile salt solutions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Effects of plasma cholesterol lowering agents on hepatobiliary lipid metabolism and cholesterol turnover in the rhesus monkey

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Platelet adhesion in hypertension: application of a novel assay of platelet adhesion

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-8-47

Biliary diversion for progressive familial intrahepatic cholestasis: improved liver morphology and bile acid profile

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-8-47

Peripheral bile duct paucity and cholestasis in the liver of a patient with Alagille syndrome: further evidence supporting a lack of postnatal bile duct branching and elongation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-8-47

Evaluation of risk for atherosclerosis in Alagille syndrome and progressive familial intrahepatic cholestasis: two congenital cholestatic diseases with different lipoprotein metabolisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-230X-8-47

Phenotypic characterization of Lith genes that determine susceptibility to cholesterol cholelithiasis in inbred mice: physical-chemistry of gallbladder bile.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2585081

Bile acid profiles in siblings with progressive intrahepatic cholestasis: absence of biliary chenodeoxycholate

31 October 2018

1 reference

12 December 2020

Parameters of lipoprotein metabolism and cholestasis in healthy and cholestatic infants and children

1 reference

12 December 2020

Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease)

1 reference

12 December 2020

Lipoprotein pattern and plasma lecithin cholesterol acyl transferase activity in children with Alagille syndrome

1 reference

12 December 2020

Abnormal lipoprotein pattern in patients with Alagille syndrome depends on Icterus severity

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Biliary lipid composition in healthy and diseased infants, children, and young adults

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-230X-8-47

1 reference

Dimensions Publication ID

26 July 2017

0 references

1 reference

26 July 2017

1 reference