Characteristics of Congenital Hepatic Fibrosis in a Large Cohort of Patients With Autosomal Recessive Polycystic Kidney Disease-Reference-Cited by-同舟云学术

Characteristics of Congenital Hepatic Fibrosis in a Large Cohort of Patients With Autosomal Recessive Polycystic Kidney Disease

Published:2013-01 Issue:1 Volume:144 Page:112-121.e2
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Gunay–Aygun Meral,Font–Montgomery Esperanza,Lukose Linda,Tuchman Gerstein Maya,Piwnica–Worms Katie,Choyke Peter,Daryanani Kailash T.,Turkbey Baris,Fischer Roxanne,Bernardini Isa,Sincan Murat,Zhao Xiongce,Sandler Netanya G.,Roque Annelys,Douek Daniel C.,Graf Jennifer,Huizing Marjan,Bryant Joy C.,Mohan Parvathi,Gahl William A.,Heller Theo

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

National Human Genome Research Institute

National Cancer Institute

NIH Clinical Center

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference41 articles.

1. Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender;Zerres;Acta Paediatr,1996

2. Autosomal recessive polycystic kidney disease: outcomes from a single-center experience;Capisonda;Pediatr Nephrol,2003