(Q34975714)

5 August 2017

title

Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia (English)

1 reference

5 August 2017

Carol L Clericuzio

1

1 reference

5 August 2017

Rick A Martin

series ordinal

2

1 reference

5 August 2017

language of work or name

English

0 references

publication date

1 March 2009

1 reference

5 August 2017

1 reference

5 August 2017

volume

11

1 reference

5 August 2017

issue

3

1 reference

5 August 2017

page(s)

220-222

1 reference

Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: a critical review of the evidence and suggested guidelines for local practice

5 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Risk of tumorigenesis in overgrowth syndromes: A comprehensive review

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Serum alpha-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Recognition and management of childhood cancer syndromes: a systems approach

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Isolated hemihyperplasia (hemihypertrophy): report of a prospective multicenter study of the incidence of neoplasia and review

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Childhood cancer predisposition: applications of molecular testing and future implications

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Alpha-fetoprotein (AFP) levels in normal children

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Evaluation of alpha-fetoprotein in early infancy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111026

Paternal uniparental disomy in monozygotic twins discordant for hemihypertrophy

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1097%2FGIM.0B013E31819436CF

Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1097%2FGIM.0B013E31819436CF

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1097%2FGIM.0B013E31819436CF

Late relapse of adrenocortical carcinoma in Beckwith-Wiedemann syndrome. Clinical, endocrinological and genetic aspects

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19367194

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Chromosome 11 uniparental isodisomy predisposing to embryonal neoplasms

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19367194

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

LIT1 and H19 methylation defects in isolated hemihyperplasia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19367194

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1097/GIM.0B013E31819436CF

1 reference

Dimensions Publication ID

5 August 2017

0 references

1 reference

5 August 2017

1 reference