Results 341 to 350 of about 184,117 (387)
Some of the next articles are maybe not open access.
Lancet, The, 2009
Biliary atresia is a rare disease of infancy, which has changed within 30 years from being fatal to being a disorder for which effective palliative surgery or curative liver transplantation, or both, are available. Good outcomes for infants depend on early referral and timely Kasai portoenterostomy, and thus a high index of suspicion is needed for ...
Mark Davenport
exaly +3 more sources
Biliary atresia is a rare disease of infancy, which has changed within 30 years from being fatal to being a disorder for which effective palliative surgery or curative liver transplantation, or both, are available. Good outcomes for infants depend on early referral and timely Kasai portoenterostomy, and thus a high index of suspicion is needed for ...
Mark Davenport
exaly +3 more sources
Current Opinion in Gastroenterology, 2019
Purpose of review Biliary atresia is a poorly understood deadly disease. Genetic predisposition factors are suspected albeit not firmly established. This review summarizes recent evidence of genetic alterations in biliary atresia.
M. Girard, G. Panasyuk
semanticscholar +1 more source
Purpose of review Biliary atresia is a poorly understood deadly disease. Genetic predisposition factors are suspected albeit not firmly established. This review summarizes recent evidence of genetic alterations in biliary atresia.
M. Girard, G. Panasyuk
semanticscholar +1 more source
The Indian Journal of Pediatrics, 1970
A case of duodenal atresia is presented in a child of 1 1/2 years. Duodeno-jejunostomy was done and the patient recovered.
V. B. Bhatnagar, H. S. Asopa
openaire +3 more sources
A case of duodenal atresia is presented in a child of 1 1/2 years. Duodeno-jejunostomy was done and the patient recovered.
V. B. Bhatnagar, H. S. Asopa
openaire +3 more sources
The Indian Journal of Pediatrics, 2000
Intestinal atresia accounts for about one third of all cases of neonatal intestinal obstruction. The survival rate has improved to 90% in most of the series with the operative mortality being < 1%. The survival rate improves with distal atresias. An increased mortality is observed in multiple atresias (57%), apple peel atresia (71%), and when atresia ...
Minu Bajpai, T. R. Sai Prasad
openaire +3 more sources
Intestinal atresia accounts for about one third of all cases of neonatal intestinal obstruction. The survival rate has improved to 90% in most of the series with the operative mortality being < 1%. The survival rate improves with distal atresias. An increased mortality is observed in multiple atresias (57%), apple peel atresia (71%), and when atresia ...
Minu Bajpai, T. R. Sai Prasad
openaire +3 more sources
Journal of Pediatric Surgery, 2010
We present a case of a female newborn with a single air bubble on abdominal x-ray by pyloric atresia and a short review of the literature.
Andriessen, M.J.G. +2 more
openaire +4 more sources
We present a case of a female newborn with a single air bubble on abdominal x-ray by pyloric atresia and a short review of the literature.
Andriessen, M.J.G. +2 more
openaire +4 more sources
The Indian Journal of Pediatrics, 1983
During a period from 1970 to 1981, a total of 38 neonates of intestinal atresia have been treated at the Kobe Children’s Hospital. Three of nine patients occurring prior to 1973 died due to inadequare preoperative management and delay in closure of enterostomy which had been created for perforation of the bowel.
openaire +3 more sources
During a period from 1970 to 1981, a total of 38 neonates of intestinal atresia have been treated at the Kobe Children’s Hospital. Three of nine patients occurring prior to 1973 died due to inadequare preoperative management and delay in closure of enterostomy which had been created for perforation of the bowel.
openaire +3 more sources
Pediatrics In Review, 1995
Choanal atresia is an abnormality of canalization during development of the nasal passages. It involves bone and/or soft tissue and may result in either partial (choanal stenosis) or complete obstruction of the posterior nasal airway. The most widely accepted mechanism for the development of choanal atresia is the persistence of the oronasal membrane ...
L, Menasse-Palmer +2 more
openaire +2 more sources
Choanal atresia is an abnormality of canalization during development of the nasal passages. It involves bone and/or soft tissue and may result in either partial (choanal stenosis) or complete obstruction of the posterior nasal airway. The most widely accepted mechanism for the development of choanal atresia is the persistence of the oronasal membrane ...
L, Menasse-Palmer +2 more
openaire +2 more sources
The Annals of Thoracic Surgery, 1978
Bronchial atresia is a rare congenital anomaly usually producing an extrahilar mass and associated distal hyperinflation on chest roentogenogram. Bronchography reveals nonfilling of the atretic bronchus and displacement of neighboring normal bronchi. Characteristically, the patient is young and asymptomatic but has an abnormal chest roentgenogram.
R L, Meng +4 more
openaire +2 more sources
Bronchial atresia is a rare congenital anomaly usually producing an extrahilar mass and associated distal hyperinflation on chest roentogenogram. Bronchography reveals nonfilling of the atretic bronchus and displacement of neighboring normal bronchi. Characteristically, the patient is young and asymptomatic but has an abnormal chest roentgenogram.
R L, Meng +4 more
openaire +2 more sources
Archives of Pediatrics & Adolescent Medicine, 1978
A case of pyloric atresia was treated successfully with side-to-side gastroduodenostomy. The mortality in treated cases is high, due to delay in diagnosis and inadequate relief of the obstruction. Side-to-side gastroduodenostomy or excision of the atresia with pyloroplasty offer the greatest opportunity for a successful outcome, as indicated by a ...
C W, Konvolinka, R E, Steward
openaire +2 more sources
A case of pyloric atresia was treated successfully with side-to-side gastroduodenostomy. The mortality in treated cases is high, due to delay in diagnosis and inadequate relief of the obstruction. Side-to-side gastroduodenostomy or excision of the atresia with pyloroplasty offer the greatest opportunity for a successful outcome, as indicated by a ...
C W, Konvolinka, R E, Steward
openaire +2 more sources
Neonatal diagnosis of biliary atresia: a practical review and update
Pediatric Radiology, 2021D. Brahee, B. Lampl
semanticscholar +1 more source