Pathologic lower extremity fractures in children with Alagille syndrome (Q33945515)

30 July 2017

title

Pathologic lower extremity fractures in children with Alagille syndrome (English)

1 reference

30 July 2017

1 reference

Christina B Bales

1

1 reference

30 July 2017

Binita M Kamath

2

1 reference

30 July 2017

Pedro S Munoz

3

1 reference

30 July 2017

Alexander Nguyen

4

1 reference

30 July 2017

David A Piccoli

5

1 reference

30 July 2017

Nancy B Spinner

6

1 reference

30 July 2017

David Horn

7

1 reference

30 July 2017

Justine Shults

8

1 reference

30 July 2017

Mary B Leonard

9

1 reference

30 July 2017

Adda Grimberg

10

1 reference

30 July 2017

Kathleen M Loomes

11

1 reference

30 July 2017

language of work or name

English

0 references

publication date

1 July 2010

1 reference

Journal of Pediatric Gastroenterology and Nutrition

30 July 2017

published in

1 reference

30 July 2017

volume

51

1 reference

30 July 2017

issue

1

1 reference

30 July 2017

page(s)

66-70

1 reference

Dimorphic effects of Notch signaling in bone homeostasis.

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Notch signaling maintains bone marrow mesenchymal progenitors by suppressing osteoblast differentiation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Bone fragility contributes to the risk of fracture in children, even after moderate and severe trauma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Deficits in size-adjusted bone mass in children with Alagille syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Consequences of JAG1 mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Alagille syndrome: case report with bilateral radio-ulnar synostosis and a literature review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Features of Alagille syndrome in 92 patients: frequency and relation to prognosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Bone mineral content in infants and children with chronic cholestatic liver disease.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Growth hormone insensitivity associated with elevated circulating growth hormone-binding protein in children with Alagille syndrome and short stature.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Studies of the aetiology of neonatal hepatitis and biliary atresia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Histiocytic osteolysis secondary to hyperbilirubinaemia: a case report

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2893241

Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients

29 October 2018

1 reference

12 December 2020

Centers for Disease Control and Prevention 2000 Growth Charts for the United States: Improvements to the 1977 National Center for Health Statistics Version

1 reference

12 December 2020

Arteriohepatic dysplasia: radiologic features of a new syndrome

1 reference

12 December 2020

Consequences of childhood-onset growth hormone deficiency for adult bone mass

1 reference

12 December 2020

Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy

1 reference

12 December 2020

Bone fractures in children undergoing orthotopic liver transplantation

1 reference

12 December 2020

[Evolution of post-fracture bone deformities in an infant with hepatic osteodystrophy on Alagille syndrome]

1 reference

12 December 2020

Epidemiology of Childhood Fractures in Britain: A Study Using the General Practice Research Database

1 reference

12 December 2020

Impairment of bone mass development in children with chronic cholestatic liver disease

1 reference

12 December 2020

10.1097/MPG.0B013E3181CB9629

Identifiers

DOI

1 reference

release_vxlpw3dgnjcqfkgdrhkiofuknu

30 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/vxlpw3dgnjcqfkgdrhkiofuknu

24 November 2022

mapped directly with Wikidata item

PMC publication ID

2893241

1 reference

30 July 2017

1 reference