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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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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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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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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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23 Stratifying young children with cystic fibrosis for disease severity using intestinal organoid swelling, intestinal current measurements or sweat chloride concentration as CFTR-dependent biomarker

Journal of cystic fibrosis, 2016-06, Vol.15, p.S57-S57

2016

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1 EFFICACY AND SAFETY OF D-PENICILLAMINE AND TRIENTINE FOR THE TREATMENT OF WILSON DISEASE

Journal of hepatology, 2011-03, Vol.54, p.S1-S1

2011

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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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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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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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P-035: Elevated faecal calprotectin does not differentiate between IBD and a juvenile polyp

Journal of Crohn's and colitis, 2014-09, Vol.8, p.S407-S407

2014

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Atypical findings in a rat model for parenteral nutrition–induced cholestasis

Nutrition research (New York, N.Y.), 2006-12, Vol.26 (12), p.664-669

2006

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477 Immunohistochemically recognised bile salt export protein is unremarkably expressed at the canaliculus in persons with ATP8B1 disease

Hepatology (Baltimore, Md.), 2003, Vol.38, p.390-390

2003

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The tissue transglutaminase gene is not a primary factor predisposing to celiac disease

The American journal of gastroenterology, 2001-12, Vol.96 (12), p.3337-3340

2001

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The tissue transglutaminase gene is not a primary factor predisposing to celiac disease

The American journal of gastroenterology, 2001-12, Vol.96 (12), p.3337-3340

2001

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Catch-Up Growth and Endocrine Changes in Childhood Celiac Disease

Hormone research in paediatrics, 2002, Vol.58 (Suppl. 1), p.57-65

2002

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Unexpected lethal pulmonary hypertension in a 5-year-old girl successfully treated for biliary atresia

Journal of pediatric surgery, 1995-04, Vol.30 (4), p.589-590

1995

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Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene

Human genetics, 1992-08, Vol.89 (6), p.607-611

1992

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CIPROFLOXACIN FOR CHOLANGITIS AFTER HEPATIC PORTOENTEROSTOMY

The Lancet (British edition), 1987-06, Vol.329 (8546), p.1367-1367

1987

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Twenty years of childhood coeliac disease in the Netherlands: clinical presentation

Netherlands journal of medicine, 1996-01, Vol.48 (1), p.A20

1996

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Mapping the BRIC gene to chromosome 18q21

Netherlands journal of medicine, 1995-08, Vol.47 (2), p.A12

1995

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Isolation and regional localization of 25 anonymous DNA probes on a chromosome 13 hybrid panel

Cytogenetic and genome research, 1991-01, Vol.57 (2-3), p.87-90

1991

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Dietary intake in children and adolescents with cystic fibrosis

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

Nutritional intervention in patients with Cystic Fibrosis: A systematic review

Constipation in pediatric Cystic Fibrosis patients: An underestimated medical condition

A Child With Refractory Coeliac Disease

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

23 Stratifying young children with cystic fibrosis for disease severity using intestinal organoid swelling, intestinal current measurements or sweat chloride concentration as CFTR-dependent biomarker

1 EFFICACY AND SAFETY OF D-PENICILLAMINE AND TRIENTINE FOR THE TREATMENT OF WILSON DISEASE

Constipation and cystic fibrosis. Slow movement

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

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

P-035: Elevated faecal calprotectin does not differentiate between IBD and a juvenile polyp

Atypical findings in a rat model for parenteral nutrition–induced cholestasis

477 Immunohistochemically recognised bile salt export protein is unremarkably expressed at the canaliculus in persons with ATP8B1 disease

The tissue transglutaminase gene is not a primary factor predisposing to celiac disease

The tissue transglutaminase gene is not a primary factor predisposing to celiac disease

Catch-Up Growth and Endocrine Changes in Childhood Celiac Disease

Unexpected lethal pulmonary hypertension in a 5-year-old girl successfully treated for biliary atresia

Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene

CIPROFLOXACIN FOR CHOLANGITIS AFTER HEPATIC PORTOENTEROSTOMY

Twenty years of childhood coeliac disease in the Netherlands: clinical presentation

Mapping the BRIC gene to chromosome 18q21

Isolation and regional localization of 25 anonymous DNA probes on a chromosome 13 hybrid panel

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