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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1978 1
1986 11
1987 30
1988 38
1989 48
1990 35
1991 30
1992 35
1993 41
1994 39
1995 32
1996 43
1997 47
1998 40
1999 33
2000 52
2001 61
2002 25
2003 46
2004 47
2005 56
2006 50
2007 60
2008 72
2009 60
2010 55
2011 59
2012 75
2013 50
2014 58
2015 90
2016 66
2017 80
2018 88
2019 43
2020 1
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1,587 results
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Page 1
Incidence of Biliary Atresia and Timing of Hepatoportoenterostomy in the United States.
Hopkins PC, et al. J Pediatr 2017. PMID 28746031
OBJECTIVE: To evaluate the incidence, trends, seasonality, and age at the time of hepatoportoenterostomy (Kasai procedure) for biliary atresia in the US. ...Implementation of systematic screening measures for biliary atresia in the US are needed....
OBJECTIVE: To evaluate the incidence, trends, seasonality, and age at the time of hepatoportoenterostomy (Kasai procedure) for biliary
Prophylactic Antibiotics for Prevention of Cholangitis in Patients With Biliary Atresia Status Post-Kasai Portoenterostomy: A Systematic Review.
Decharun K, et al. Clin Pediatr (Phila) 2016 - Review. PMID 26183324
PURPOSE: To determine effectiveness of prophylactic antibiotics in preventing cholangitis, we conducted a systematic review comparing cholangitis occurrence in biliary atresia patients after Kasai portoenterostomy (KP) with and without antibiotics. METHODS: We searched online bibliographic databases from April 1, 2013, using search terms "biliary atresia" OR "cholangitis" AND "antibiotics," selecting studies with control group data. ...
PURPOSE: To determine effectiveness of prophylactic antibiotics in preventing cholangitis, we conducted a systematic review comparing cholan …
Biliary atresia.
Kobayashi H and Stringer MD. Semin Neonatol 2003 - Review. PMID 15001126
Biliary atresia (BA) is a congenital obliterative cholangiopathy of unknown aetiology, affecting both the intra- and extrahepatic bile ducts. Although relatively rare, BA must be excluded in any infant with conjugated hyperbilirubinaemia since the prognosis is improved by early diagnosis and prompt surgery. ...
Biliary atresia (BA) is a congenital obliterative cholangiopathy of unknown aetiology, affecting both the intra- and extrahepa
Biliary atresia.
Nio M and Ohi R. Semin Pediatr Surg 2000 - Review. PMID 11112835
Although the prognosis of biliary atresia has been dramatically improved in the era of liver transplantation, the Kasai operation is still the first line of surgical treatment. Successful hepatic portoenterostomy depends on early diagnosis and surgery, adequate surgical technique, prevention of cholangitis, and precise postoperative management....
Although the prognosis of biliary atresia has been dramatically improved in the era of liver transplantation, the Kasai operat …
Biliary atresia.
Chardot C. Orphanet J Rare Dis 2006 - Review. PMID 16872500 Free PMC article.
Biliary atresia (BA) is a rare disease characterised by a biliary obstruction of unknown origin that presents in the neonatal period. ...Liver transplantation may be needed later if the Kasai operation fails to restore the biliary flow or if cirrhotic complications occur. ...
Biliary atresia (BA) is a rare disease characterised by a biliary obstruction of unknown origin that presents in the ne
Biliary atresia.
Davenport M. Semin Pediatr Surg 2005 - Review. PMID 15770587
Biliary atresia (BA) remains a devastating disease of infants. It is still a disease of largely unknown etiology although many hypotheses such as an aberrant early bile duct development, perinatal viral infection, aberrant immune response, and abnormalities of bile acids have all been suggested as possibly etiologically important. ...
Biliary atresia (BA) remains a devastating disease of infants. It is still a disease of largely unknown etiology although many
Surgery for biliary atresia.
Ohi R. Liver 2001 - Review. PMID 11422780
Although the prognosis of biliary atresia has been improved in recent years, particularly in the era of liver transplantation, hepatic portoenterostomy, e.g., the Kasai operation, is still the first line of surgical treatment. ...
Although the prognosis of biliary atresia has been improved in recent years, particularly in the era of liver transplantation, …
Advances in paediatric gastroenterology
Tam PKH, et al. Lancet 2017 - Review. PMID 28901937
Although minimally invasive surgery has been extended to neonatal surgery, it is difficult to establish its role for neonatal disorders such as oesophageal atresia and biliary atresia through clinical trials because of the rarity of these disorders. Advances in treatments for biliary atresia and necrotising enterocolitis have been achieved through specialisation, multidisciplinary management, and multicentre collaboration in research; similarly robust clinical evidence for other rare gastrointestinal disorders is needed. ...
Although minimally invasive surgery has been extended to neonatal surgery, it is difficult to establish its role for neonatal …
[Biliary atresia: a severe illness].
Ramonet M, et al. Arch Argent Pediatr 2014. PMID 25362914 Spanish. Free article.
Neonatal cholestasis could be due to several different diseases, thus a diagnosis of biliary atresia and early derivation for surgical treatment are necessary to allow a restoration of the bile flow. ...Biliary atresia must be diagnosed before the first month of life and must be considered as a surgical emergency....
Neonatal cholestasis could be due to several different diseases, thus a diagnosis of biliary atresia and early derivation for …
[Biliary tract surgery in childhood].
Dübbers M. Chirurg 2020 - Review. PMID 31691142 German.
For children with biliary atresia Kasai portoenterostomy is a therapeutic option in the first weeks of life. Most affected children, however, require a liver transplantation before they enter adulthood. ...This requires early resection of the biliary tree and reconstruction with a bilioenteric anastomosis. While laparoscopic cholecystectomy has become the standard approach also for children, the value of minimally invasive procedures for more complex surgical procedures of the biliary tract has not yet been defined....
For children with biliary atresia Kasai portoenterostomy is a therapeutic option in the first weeks of life. Most affected chi …
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