Biliary atresia: the King's College Hospital experience (1974-1995) (Q53602822)

16 May 2018

title

Biliary atresia: the King's College Hospital experience (1974-1995) (English)

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1

M Davenport

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author name string

N Kerkar

2

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G Mieli-Vergani

3

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A P Mowat

4

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E R Howard

5

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language of work or name

English

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publication date

1 March 1997

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Journal of Pediatric Surgery

published in

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volume

32

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issue

3

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page(s)

479-485

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Results of surgical treatment for extrahepatic biliary atresia in United Kingdom 1980-2. Survey conducted on behalf of the British Paediatric Association Gastroenterology Group and the British Association of Paediatric Surgeons.

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Extrahepatic biliary atresia: preoperative assessment and surgical results in 47 consecutive cases

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Liver transplantation in 100 children: Cambridge and King's College Hospital series

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Hepatic portoenterostomy for biliary atresia. A comparative study of histology and prognosis after surgery

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Late referral for biliary atresia--missed opportunities for effective surgery

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Does the morphology of the extrahepatic biliary remnants in biliary atresia influence survival? A review of 205 cases

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Endoscopic sclerotherapy in the management of esophageal varices in 61 children with biliary atresia

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Hepatic histology and the development of esophageal varices in biliary atresia

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Hepatic lymphatic drainage to the jejunum for congenital biliary atresia

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Pulmonary arteriovenous shunting in children with liver disease

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Macroscopic appearance at portoenterostomy--a prognostic variable in biliary atresia

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Jaundice at 14 days of age: exclude biliary atresia

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Biliary atresia registry, 1976 to 1989

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Current concept of the treatment of biliary atresia

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The surgery of biliary atresia

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Prognosis of extrahepatic biliary atresia

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Surgical limitation for biliary atresia: indication for liver transplantation

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Long-term outcome after surgery for biliary atresia. Study of 40 patients surviving for more than 10 years

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The surgery of "correctable" biliary atresia

7 January 2021

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7 January 2021

Acquired biliary atresia

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A patient with biliary atresia who died 28 years after hepatic portojejunostomy

7 January 2021

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Outcome of 21 patients with biliary atresia living more than 10 years

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Optimal therapy for patients with biliary atresia: portoenterostomy ("Kasai" procedures) versus primary transplantation

7 January 2021

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Primary management of biliary atresia: don't change the rules

7 January 2021

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10 years of pediatric liver transplantation

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Liver transplantation in babies and children with extrahepatic biliary atresia

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3468(97)90611-4

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16 May 2018

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16 May 2018