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A False-Negative Newborn Screen for Tyrosinemia Type 1-Need for Re-Evaluation of Newborn Screening with Succinylacetone

International journal of neonatal screening, 2023-12, Vol.9 (4), p.66

2023

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Cholic acid induces a Cftr dependent biliary secretion and liver growth response in mice

PloS one, 2015-02, Vol.10 (2), p.e0117599-e0117599

2015

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Rationale and design of TransplantLines: a prospective cohort study and biobank of solid organ transplant recipients

BMJ open, 2018-12, Vol.8 (12), p.e024502-e024502

2018

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Reversal of secondary protein‐losing enteropathy after surgical revision of a jejunal Roux‐en‐Y loop in a patient after liver transplantation

American journal of transplantation, 2019-07, Vol.19 (7), p.2116-2121

2019

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First report of successful transplantation of a pediatric donor liver graft after hypothermic machine perfusion

Pediatric transplantation, 2019-05, Vol.23 (3), p.e13362-n/a

2019

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Treatment of Infants and Toddlers With Cystic Fibrosis–related Pancreatic Insufficiency and Fat Malabsorption With Pancrelipase MT

Journal of pediatric gastroenterology and nutrition, 2011-07, Vol.53 (1), p.61-64

2011

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Cirrhosis and Portal Hypertension in Compound Heterozygous People With Cystic Fibrosis Harboring One F508del CFTR Gene Mutation

Gastroenterology (New York, N.Y. 1943), 2022-10, Vol.163 (4), p.1098-1100

2022

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Towards a Standardized Classification of the Hepatobiliary Manifestations in Cystic Fibrosis (CFHBI): A Joint ESPGHAN/NASPGHAN Position Paper

Journal of pediatric gastroenterology and nutrition, 2024-01, Vol.78 (1), p.153-165

2024

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Cystic Fibrosis Related Liver Disease: Research Challenges and Future Perspectives

Journal of pediatric gastroenterology and nutrition, 2017-10, Vol.65 (4), p.443-448

2017

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Human extrahepatic and intrahepatic cholangiocyte organoids show region-specific differentiation potential and model cystic fibrosis-related bile duct disease

Scientific reports, 2020-12, Vol.10 (1), p.21900-21900, Article 21900

2020

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Time‐to‐reach Target Calprotectin Level in Newly Diagnosed Patients With Inflammatory Bowel Disease

Journal of pediatric gastroenterology and nutrition, 2019-10, Vol.69 (4), p.466-473

2019

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Bile acid homeostasis in gastrointestinal and metabolic complications of cystic fibrosis

Journal of cystic fibrosis, 2019-05, Vol.18 (3), p.313-320

2019

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IVACAFTOR restores FGF19 regulated bile acid homeostasis in cystic fibrosis patients with an S1251N or a G551D gating mutation

Journal of cystic fibrosis, 2019-03, Vol.18 (2), p.286-293

2019

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Defective FXR-FGF15 signaling and bile acid homeostasis in cystic fibrosis mice can be restored by the laxative polyethylene glycol

American journal of physiology: Gastrointestinal and liver physiology, 2019-03, Vol.316 (3), p.G404-G411

2019

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Diagnosis, follow-up and treatment of cystic fibrosis-related liver disease

Current opinion in pulmonary medicine, 2017-11, Vol.23 (6), p.562-569

2017

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Increase of Serum γ‐Glutamyltransferase Associated With Development of Cirrhotic Cystic Fibrosis Liver Disease

Journal of pediatric gastroenterology and nutrition, 2015-07, Vol.61 (1), p.113-118

2015

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Cystic fibrosis and the role of gastrointestinal outcome measures in the new era of therapeutic CFTR modulation

Journal of cystic fibrosis, 2015-03, Vol.14 (2), p.169-177

2015

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Routine Postoperative Antithrombotic Therapy in Pediatric Liver Transplantation: Impact on Bleeding and Thrombotic Complications

Thrombosis and haemostasis, 2020-04, Vol.120 (4), p.627-637

2020

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Gastroenterological endpoints in drug trials for cystic fibrosis

Pediatric pulmonology, 2016-10, Vol.51 (S44), p.S18-S22

2016

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Altered intestinal bile salt biotransformation in a cystic fibrosis ( Cftr−/− ) mouse model with hepato-biliary pathology

Journal of cystic fibrosis, 2015-07, Vol.14 (4), p.440-446

2015

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Solitary Rectal Ulcer Syndrome as a Sign of Unrecognized Hirschsprung Disease

The Journal of pediatrics, 2016-10, Vol.177, p.321-321.e1

2016

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Abnormal Liver Function Tests in Patients With COVID‐19: Relevance and Potential Pathogenesis

Hepatology (Baltimore, Md.), 2020-11, Vol.72 (5), p.1864-1872

2020

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A novel phenotype of a hepatocyte nuclear factor homeobox A ( HNF1A ) gene mutation, presenting with neonatal cholestasis

Journal of hepatology, 2015-11, Vol.63 (5), p.1295-1297

2015

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Calciprotein particle counts associate with vascular remodelling in chronic kidney disease

Cardiovascular research, 2024-08

2024

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Sleep quality, fatigue, societal participation and health-related quality of life in kidney transplant recipients: a cross-sectional and longitudinal cohort study

Nephrology, dialysis, transplantation, 2023-12, Vol.39 (1), p.74-83

2023

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A False-Negative Newborn Screen for Tyrosinemia Type 1-Need for Re-Evaluation of Newborn Screening with Succinylacetone

Cholic acid induces a Cftr dependent biliary secretion and liver growth response in mice

Rationale and design of TransplantLines: a prospective cohort study and biobank of solid organ transplant recipients

Reversal of secondary protein‐losing enteropathy after surgical revision of a jejunal Roux‐en‐Y loop in a patient after liver transplantation

First report of successful transplantation of a pediatric donor liver graft after hypothermic machine perfusion

Treatment of Infants and Toddlers With Cystic Fibrosis–related Pancreatic Insufficiency and Fat Malabsorption With Pancrelipase MT

Cirrhosis and Portal Hypertension in Compound Heterozygous People With Cystic Fibrosis Harboring One F508del CFTR Gene Mutation

Towards a Standardized Classification of the Hepatobiliary Manifestations in Cystic Fibrosis (CFHBI): A Joint ESPGHAN/NASPGHAN Position Paper

Cystic Fibrosis Related Liver Disease: Research Challenges and Future Perspectives

Human extrahepatic and intrahepatic cholangiocyte organoids show region-specific differentiation potential and model cystic fibrosis-related bile duct disease

Time‐to‐reach Target Calprotectin Level in Newly Diagnosed Patients With Inflammatory Bowel Disease

Bile acid homeostasis in gastrointestinal and metabolic complications of cystic fibrosis

IVACAFTOR restores FGF19 regulated bile acid homeostasis in cystic fibrosis patients with an S1251N or a G551D gating mutation

Defective FXR-FGF15 signaling and bile acid homeostasis in cystic fibrosis mice can be restored by the laxative polyethylene glycol

Diagnosis, follow-up and treatment of cystic fibrosis-related liver disease

Increase of Serum γ‐Glutamyltransferase Associated With Development of Cirrhotic Cystic Fibrosis Liver Disease

Cystic fibrosis and the role of gastrointestinal outcome measures in the new era of therapeutic CFTR modulation

Routine Postoperative Antithrombotic Therapy in Pediatric Liver Transplantation: Impact on Bleeding and Thrombotic Complications

Gastroenterological endpoints in drug trials for cystic fibrosis

Altered intestinal bile salt biotransformation in a cystic fibrosis ( Cftr−/− ) mouse model with hepato-biliary pathology

Solitary Rectal Ulcer Syndrome as a Sign of Unrecognized Hirschsprung Disease

Abnormal Liver Function Tests in Patients With COVID‐19: Relevance and Potential Pathogenesis

A novel phenotype of a hepatocyte nuclear factor homeobox A ( HNF1A ) gene mutation, presenting with neonatal cholestasis

Calciprotein particle counts associate with vascular remodelling in chronic kidney disease

Sleep quality, fatigue, societal participation and health-related quality of life in kidney transplant recipients: a cross-sectional and longitudinal cohort study

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