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Mutation-specific reporter for optimization and enrichment of prime editing

Nature communications, 2022-03, Vol.13 (1), p.1028-1028, Article 1028

2022

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Constipation and cystic fibrosis. Slow movement

Journal of cystic fibrosis, 2022-05, Vol.21 (3), p.385-386

2022

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Systematic review: clinical efficacy of chelator agents and zinc in the initial treatment of Wilson disease

Alimentary pharmacology & therapeutics, 2009-05, Vol.29 (9), p.947-958

2009

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Novel Orally Formulated Mixed Micelles Optimize Vitamin K Absorption Under Bile-Deficient Conditions

Gastroenterology (New York, N.Y. 1943), 2021-09, Vol.161 (3), p.1056-1059.e5

2021

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The long-term outcome of the Kasai operation in patients with biliary atresia: a systematic review

Netherlands journal of medicine, 2013-05, Vol.71 (4), p.170-173

2013

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Effects and efficacy of laparoscopic fundoplication in children with GERD: a prospective, multicenter study

Surgical endoscopy, 2017-03, Vol.31 (3), p.1101-1110

2017

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Progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP

Scientific reports, 2017-08, Vol.7 (1), p.8671-10, Article 8671

2017

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Dietary intake in children and adolescents with cystic fibrosis

Clinical nutrition (Edinburgh, Scotland), 2014-06, Vol.33 (3), p.528-532

2014

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Cirrhosis associated with decreased survival and a 10-year lower median age at death of cystic fibrosis patients in the Netherlands

Journal of cystic fibrosis, 2019-05, Vol.18 (3), p.385-389

2019

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Preterm Infants With Biliary Atresia: A Nationwide Cohort Analysis From The Netherlands

Journal of pediatric gastroenterology and nutrition, 2017-10, Vol.65 (4), p.370-374

2017

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Serum retinol levels and pulmonary function in children and adolescents with cystic fibrosis

Journal of cystic fibrosis, 2016-03, Vol.15 (2), p.e16-e16

2016

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Nutritional intervention in patients with Cystic Fibrosis: A systematic review

Journal of cystic fibrosis, 2013-03, Vol.12 (2), p.102-115

2013

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Impact of laparoscopic antireflux surgery on belching in pediatric GERD patients

Neurogastroenterology and motility, 2016-10, Vol.28 (10), p.1525-1532

2016

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Constipation in pediatric Cystic Fibrosis patients: An underestimated medical condition

Journal of cystic fibrosis, 2010-01, Vol.9 (1), p.59-63

2010

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A Child With Refractory Coeliac Disease

Journal of pediatric gastroenterology and nutrition, 2011-08, Vol.53 (2), p.216-218

2011

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Association of the CLCA1 p.S357N Variant With Meconium Ileus in European Patients With Cystic Fibrosis

Journal of pediatric gastroenterology and nutrition, 2010-03, Vol.50 (3), p.347-349

2010

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Serum retinol levels and pulmonary function in children and adolescents with cystic fibrosis

Journal of cystic fibrosis, 2015-05, Vol.14 (3), p.392-397

2015

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Genetics of familial intrahepatic cholestasis syndromes

Journal of Medical Genetics, 2005-06, Vol.42 (6), p.449-463

2005

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FIC1 Disease: A Spectrum of Intrahepatic Cholestatic Disorders

Seminars in liver disease, 2001-01, Vol.21 (4), p.535-544

2001

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

Journal of pediatric gastroenterology and nutrition, 2010-12, Vol.51 (6), p.773-776

2010

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Vitamin K deficiency bleeding in cholestatic infants with alpha-1-antitrypsin deficiency

Archives of disease in childhood. Fetal and neonatal edition, 2009-11, Vol.94 (6), p.F456-F460

2009

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Heterozygous alpha-i antitrypsin deficiency as a co-factor in the development of chronic liver disease: a review

Netherlands journal of medicine, 2007-05, Vol.65 (5), p.160-166

2007

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Copper: two sides of the same coin

Netherlands journal of medicine, 2008-09, Vol.66 (8), p.325

Houwen, R H J

2008

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Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients

Genes and immunity, 2004-05, Vol.5 (3), p.215-220

2004

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IFIC, a new cholestatic liver disease?

European journal of gastroenterology & hepatology, 1998-12, Vol.10 (12), p.A53

1998

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Mutation-specific reporter for optimization and enrichment of prime editing

Constipation and cystic fibrosis. Slow movement

Systematic review: clinical efficacy of chelator agents and zinc in the initial treatment of Wilson disease

Novel Orally Formulated Mixed Micelles Optimize Vitamin K Absorption Under Bile-Deficient Conditions

The long-term outcome of the Kasai operation in patients with biliary atresia: a systematic review

Effects and efficacy of laparoscopic fundoplication in children with GERD: a prospective, multicenter study

Progress towards non-invasive diagnosis and follow-up of celiac disease in children; a prospective multicentre study to the usefulness of plasma I-FABP

Dietary intake in children and adolescents with cystic fibrosis

Cirrhosis associated with decreased survival and a 10-year lower median age at death of cystic fibrosis patients in the Netherlands

Preterm Infants With Biliary Atresia: A Nationwide Cohort Analysis From The Netherlands

Serum retinol levels and pulmonary function in children and adolescents with cystic fibrosis

Nutritional intervention in patients with Cystic Fibrosis: A systematic review

Impact of laparoscopic antireflux surgery on belching in pediatric GERD patients

Constipation in pediatric Cystic Fibrosis patients: An underestimated medical condition

A Child With Refractory Coeliac Disease

Association of the CLCA1 p.S357N Variant With Meconium Ileus in European Patients With Cystic Fibrosis

Serum retinol levels and pulmonary function in children and adolescents with cystic fibrosis

Genetics of familial intrahepatic cholestasis syndromes

FIC1 Disease: A Spectrum of Intrahepatic Cholestatic Disorders

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

Vitamin K deficiency bleeding in cholestatic infants with alpha-1-antitrypsin deficiency

Heterozygous alpha-i antitrypsin deficiency as a co-factor in the development of chronic liver disease: a review

Copper: two sides of the same coin

Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients

IFIC, a new cholestatic liver disease?

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