Hirschprung's disease (Q34733361)

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Language	Label	Description	Also known as
English	Hirschprung's disease	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

Hirschprung's disease (English)

1 reference

Europe PubMed Central

4 August 2017

author name string

Sullivan PB

1

1 reference

Europe PubMed Central

4 August 2017

language of work or name

0 references

publication date

1 January 1996

1 reference

Europe PubMed Central

4 August 2017

Archives of Disease in Childhood

1 reference

Europe PubMed Central

4 August 2017

74

1 reference

Europe PubMed Central

4 August 2017

5-7

1 reference

Europe PubMed Central

4 August 2017

1

1 reference

Europe PubMed Central

4 August 2017

Contemporary approaches toward understanding the pathogenesis of Hirschsprung disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

From neural crest to bowel: development of the enteric nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Mutations of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Isosorbide dinitrate and nifedipine treatment of achalasia: a clinical, manometric and radionuclide evaluation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Inability of neural crest cells to colonize the presumptive aganglionic bowel of ls/ls mutant mice: requirement for a permissive microenvironment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Development profile of neuron-specific enolase in human gut and its implications in Hirschsprung's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Accumulation of components of basal laminae: association with the failure of neural crest cells to colonize the presumptive aganglionic bowel of ls/ls mutant mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Immunohistochemical investigations of gut hormones in the colon of patients with Hirschsprung's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Familial Hirschsprung's disease: report of autosomal dominant and probable recessive X-linked kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

New insights into peptidergic abnormalities in Hirschsprung's disease by wholemount immunohistochemistry.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

A novel neuropeptide, pituitary adenylate cyclase-activating polypeptide (PACAP), in human intestine: evidence for reduced content in Hirschsprung's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Quantitative and qualitative analysis of the extracellular matrix protein, laminin, in Hirschsprung's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

7 July 2018

Effect of nitric oxide on the colonic smooth muscle of patients with Hirschsprung's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511606

26 October 2018

Immunocytochemistry for neuronal markers shows deficiencies in conventional histology in the treatment of Hirschsprung's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hirschsprung's disease: a comparison of the nervous control of ganglionic and aganglionic smooth muscle in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Hirschsprung's disease: 20 cases in 12 kindreds.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities of nitric-oxide-producing neurons in Hirschsprung's disease: morphology and implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial occurrence of Hirschsprung's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of neuronal nitric oxide synthase in nerve fibers of aganglionic intestine: a clue to Hirschsprung's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study of the extracellular matrix protein as the migration pathway of neural crest cells in the gut: analysis in human embryos with special reference to the pathogenesis of Hirschsprung's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine structure of neurons synthesizing vasoactive intestinal peptide in the human colon from patients with Hirschsprung's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is the reduction of VIP the clue to the pathophysiology of Hirschsprung's disease?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Involvement of nitric oxide in nerve-mediated inhibition and action of vasoactive intestinal peptide in colonic smooth muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aggregation chimeras demonstrate that the primary defect responsible for aganglionic megacolon in lethal spotted mice is not neuroblast autonomous.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nitric oxide synthase distribution in the enteric nervous system of Hirschsprung's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8660047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/ADC.74.1.5

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

ResearchGate publication ID

0 references

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