Results 161 to 170 of about 4,891,717 (200)

Hirschsprung?s disease as a neurochristopathy

Pediatric Surgery International, 1996
Recent molecular-genetic and histochemical studies of intestinal aganglionosis have confirmed the initial classification established by Bolande, who considered Hirschsprung's disease (HD) a neurocristopathy. This paper is a critical review of the results of molecular-genetic studies carried out from 1992 to date.
openaire   +3 more sources

Hirschsprung's Disease in the Newborn

Clinics in Perinatology, 1978
Although the specific pathogenesis of Hirschsprung's disease is still unclear, there have been continuing advances in both an understanding of the disturbances? in bowel motility in this disorder and in the means for diagnosing it.
S J, Boley, G, Dinari, M I, Cohen
openaire   +2 more sources

Hirschsprung's disease in the newborn

Journal of Pediatric Surgery, 1984
Hirschsprung's disease has become a more common cause of newborn intestinal obstruction in the past 30 years. In a group of 137 newborns with intestinal obstruction the most common diagnosis was necrotizing enterocolitis. The second most common cause, however, was Hirschsprung's disease.
M D, Klein, A G, Coran, J R, Wesley, R A, Drongowski   +3 more
openaire   +2 more sources

Variant Hirschsprung's disease

Journal of Pediatric Surgery, 1997
There 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.
openaire   +2 more sources

Hirschsprung's disease. Management

Alimentary Pharmacology & Therapeutics
SummaryBackgroundHirschsprung'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
openaire   +2 more sources

Hirschsprung Disease

Pediatrics In Review, 2021
Mark, Mahon, Julie, Khlevner
openaire   +2 more sources

Hirschsprung’s Disease

Digestion, 1950
M, BODIAN, F D, STEPHENS, B C H, WARD
openaire   +3 more sources

The Surgery of Hirschsprung’s Disease

Surgical Clinics of North America, 1983
The author concisely describes what Hirschsprung’s disease is, how it can be diagnosed, and what advantages accrue to the various “definitive” treatments proposed by surgeons.
openaire   +2 more sources

HIRSCHSPRUNG'S DISEASE

The Lancet, 1951
M, BODIAN, C O, CARTER, B C H, WARD
openaire   +2 more sources

“Acquired” Hirschsprung's disease

Journal of Pediatric Surgery, 1981
A 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.
openaire   +2 more sources