Outcome of partial internal biliary diversion for intractable pruritus in children with cholestatic liver disease

Author:

Ramachandran P.,Shanmugam N. P.,Sinani S. Al,Shanmugam V.,Srinivas S.,Sathiyasekaran M.,Tamilvanan V.,Rela M.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Surgery,Pediatrics, Perinatology, and Child Health

Reference19 articles.

1. Jacquemin E (2012) Progressive familial intrahepatic cholestasis. Clin Res Hepatol Gastroenterol 36:S26–S35

2. Bull LN, Carlton VE, Stricker NL, Bhaharloo S, De Young JA, Freimer NB et al (1997) Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity. Hepatology 26(1):155–164

3. Lee CN, Tiao MM, Chen HJ et al (2013) Characteristics and outcome of liver transplantation in children with alagille syndrome. A single-center experience. Pediatr Neonatol 55(2):135–138

4. Kronsten V, Fitzpatrick E, Baker A (2013) Management of cholestatic pruritus in pediatric patients with Alagille syndrome: the King’s College Hospital experience. J Pediatr Gastroenterol Nutr 57(2):149–154

5. Wanty C, Joomye R, Van Hoorebeek N et al (2004) Fifteen years single center experience in the management of progressive familial intrahepatic cholestasis of infancy. Acta Gastroenterol Belg 67(4):313–319

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