W. de Vries

发表

Twenty-year transplant-free survival rate among patients with biliary atresia.

R. Houwen, J. Hoekstra-Weebers, H. Verkade, 2011, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Cholic Acid Induces a Cftr Dependent Biliary Secretion and Liver Growth Response in Mice

H. Verkade, H. D. de Jonge, J. Baller, 2015, PloS one.

Pulmonary medium vessel vasculitis in an 11 year old boy: Hughes Stovin syndrome as a variant of polyarteritis nodosa?

G. Koppelman, H. Bootsma, W. Armbrust, 2011, Pediatric rheumatology online journal.

Biliary atresia in the Netherlands: outcome of patients diagnosed between 1987 and 2008.

H. Verkade, H. Groen, J. Hulscher, 2012, The Journal of pediatrics.

Towards an individual screening strategy for first-degree relatives of celiac patients

M. Mearin, Margreet Wessels, L. Roovers, 2018, European Journal of Pediatrics.

Hydrolysed Formula Is a Risk Factor for Vitamin K Deficiency in Infants With Unrecognised Cholestasis

H. Verkade, K. Kok, R. Houwen, 2010, Journal of pediatric gastroenterology and nutrition.

Health Status and Quality of Life in Adult Biliary Atresia Patients Surviving with Their Native Livers

J. Hoekstra-Weebers, H. Verkade, J. Hulscher, 2014, European Journal of Pediatric Surgery.

Overall Quality of Life in Adult Biliary Atresia Survivors with or without Liver Transplantation: Results from a National Cohort

J. Hoekstra-Weebers, R. Porte, H. Verkade, 2015, European Journal of Pediatric Surgery.

Course of life into adulthood of patients with biliary atresia: the achievement of developmental milestones in a nationwide cohort.

R. Houwen, J. Hoekstra-Weebers, R. Porte, 2012, Journal of Adolescent Health.