Page last updated: 2024-10-25

dapi and Hirschsprung Disease

dapi has been researched along with Hirschsprung Disease in 1 studies

DAPI: RN given refers to parent cpd.

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 (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Garavelli, L1
Zollino, M1
Mainardi, PC1
Gurrieri, F1
Rivieri, F1
Soli, F1
Verri, R1
Albertini, E1
Favaron, E1
Zignani, M1
Orteschi, D1
Bianchi, P1
Faravelli, F1
Forzano, F1
Seri, M1
Wischmeijer, A1
Turchetti, D1
Pompilii, E1
Gnoli, M1
Cocchi, G1
Mazzanti, L1
Bergamaschi, R1
De Brasi, D1
Sperandeo, MP1
Mari, F1
Uliana, V1
Mostardini, R1
Cecconi, M1
Grasso, M1
Sassi, S1
Sebastio, G1
Renieri, A1
Silengo, M1
Bernasconi, S1
Wakamatsu, N1
Neri, G1

Reviews

1 review available for dapi and Hirschsprung Disease

ArticleYear
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.
    American journal of medical genetics. Part A, 2009, Volume: 149A, Issue:3

    Topics: Abnormalities, Multiple; Adolescent; Aging; Child; Child, Preschool; Chromosomes, Artificial, Bacter

2009