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The loss of calretinin expression indicates aganglionosis in Hirschsprung’s disease
Background: Hirschsprung’s disease (HD) is a congenital disorder characterised by the absence of ganglion cells in the large bowel, leading to functional obstruction and colonic dilatation proximal to the affected segment. A subclass of nerve cell bodies in both submucosa and myenteric ganglia of th...
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Main Authors: | , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Copyright 2004 Journal of Clinical Pathology
2004
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1770342/ https://ncbi.nlm.nih.gov/pubmed/15220363 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jcp.2004.016030 |
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