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

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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Constipation and cystic fibrosis. Slow movement

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

2022

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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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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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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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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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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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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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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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The relationship between energy intake and body-growth in children with cystic fibrosis

Clinical nutrition (Edinburgh, Scotland), 2019-04, Vol.38 (2), p.920-925

2019

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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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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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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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Genetics of familial intrahepatic cholestasis syndromes

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

2005

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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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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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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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Defective Plasma Membrane Targeting of P.I661T-ATP8B1, Associated with Familial Intrahepatic Cholestasis, Can be Rescued in Vitro by CFTR Correctors

Journal of hepatology, 2016, Vol.64 (2), p.S304-S304

2016

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O084 : Novel treatment options to improve aberrant pre-messenger RNA splicing and protein folding in ATP8B1 deficiency

Journal of hepatology, 2015-04, Vol.62, p.S232-S232

2015

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Retrospective Study to Assess Long-Term Outcomes of Chelator-Based Treatment with Trientine in Wilson Disease Patients Withdrawn from Therapy with D-Penicillamine

Journal of hepatology, 2016, Vol.64 (2), p.S293-S293

2016

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Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

Nature genetics, 1994-12, Vol.8 (4), p.380-386

1994

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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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Systematic Review: the Epidemiology, Natural History and Burden of Alagille Syndrome

Journal of pediatric gastroenterology and nutrition, 2018-08, Vol.67 (2), p.148-156

2018

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Immunoglobulin G antibodies against deamidated-gliadin-peptides outperform anti-endomysium and tissue transglutaminase antibodies in children <2 years age

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2011-12, Vol.119 (12), p.894-900

2011

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Mutation-specific reporter for optimization and enrichment of prime editing

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

Constipation and cystic fibrosis. Slow movement

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

Dietary intake in children and adolescents with cystic fibrosis

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

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

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

Impact of laparoscopic antireflux surgery on belching in pediatric GERD patients

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

The relationship between energy intake and body-growth in children with cystic fibrosis

A Child With Refractory Coeliac Disease

Nutritional intervention in patients with Cystic Fibrosis: A systematic review

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

Genetics of familial intrahepatic cholestasis syndromes

Constipation in pediatric Cystic Fibrosis patients: An underestimated medical condition

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

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

Defective Plasma Membrane Targeting of P.I661T-ATP8B1, Associated with Familial Intrahepatic Cholestasis, Can be Rescued in Vitro by CFTR Correctors

O084 : Novel treatment options to improve aberrant pre-messenger RNA splicing and protein folding in ATP8B1 deficiency

Retrospective Study to Assess Long-Term Outcomes of Chelator-Based Treatment with Trientine in Wilson Disease Patients Withdrawn from Therapy with D-Penicillamine

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

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

Systematic Review: the Epidemiology, Natural History and Burden of Alagille Syndrome

Immunoglobulin G antibodies against deamidated-gliadin-peptides outperform anti-endomysium and tissue transglutaminase antibodies in children <2 years age

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