Results 211 to 220 of about 9,336,073 (253)
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Variant Hirschsprung's disease
Journal of Pediatric Surgery, 1997There are many clinical conditions that resemble Hirschsprung's disease despite the presence of ganglia cells on rectal biopsy. This group has focused its research interest into delineating variant Hirschsprung's disease based on specific histochemical, immunohistochemical, silver staining and electron microscopic studies.
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“Acquired” Hirschsprung's disease
Journal of Pediatric Surgery, 1981A case of Hirschsprung's disease is presented in which the presence of a group of ganglion cells noted on a rectal biopsy done at age 3 wk resulted in a 10-yr delay in definitive treatment.
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Hirschsprung's disease. Management
Alimentary Pharmacology & TherapeuticsSummaryBackgroundHirschsprung's disease (HD) is a rare congenital disease that is characterised by the absence of ganglion cells in the myenteric plexus starting in the distal bowel. This results in distal functional obstruction and may lead to complications like enterocolitis.
Claudio Morera, Samuel Nurko
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Surgery (Oxford), 2016
Abstract Hirschsprung's disease (HSCR) is characterized by a lack of enteric nervous system ganglion cells (aganglionosis) in a variable extent of distal bowel. It is the most common congenital bowel motility disorder and affected neonates usually present with distal intestinal obstruction in the first few days of life.
Sumita Chhabra, Simon E. Kenny
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Abstract Hirschsprung's disease (HSCR) is characterized by a lack of enteric nervous system ganglion cells (aganglionosis) in a variable extent of distal bowel. It is the most common congenital bowel motility disorder and affected neonates usually present with distal intestinal obstruction in the first few days of life.
Sumita Chhabra, Simon E. Kenny
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A missense mutation of the endothelin-B receptor gene in multigenic hirschsprung's disease
Cell, 1994E. Puffenberger +6 more
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Mutations of the RET proto-oncogene in Hirschsprung's disease
Nature, 1994P. Edery +9 more
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