Page last updated: 2024-11-02

oxotremorine and Hirschsprung Disease

oxotremorine has been researched along with Hirschsprung Disease in 2 studies

Oxotremorine: A non-hydrolyzed muscarinic agonist used as a research tool.

Hirschsprung Disease: Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Okasora, T1
Okamoto, E2
Toyosaka, A2
Nakai, K1
Niwamoto, H1
Inoue, M1
Ueki, S1
Kuwata, K1
Nagai, K1

Other Studies

2 other studies available for oxotremorine and Hirschsprung Disease

ArticleYear
[Comparative physiopathologic study on congenital Hirschsprung's disease and acquired esophageal achalasia].
    Nihon Heikatsukin Gakkai zasshi, 1990, Volume: 26, Issue:5

    Topics: Animals; Dose-Response Relationship, Drug; Esophageal Achalasia; Esophagus; Hirschsprung Disease; Hu

1990
Qualitative and quantitative analysis of muscarinic acetylcholine receptors in the piebald lethal mouse model of Hirschsprung's disease.
    Gastroenterology, 1985, Volume: 88, Issue:6

    Topics: Acetylcholine; Acetylcholinesterase; Animals; Colon; Disease Models, Animal; Female; Hirschsprung Di

1985