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Universal spreading of water drops on complex surfaces

Soft matter, 2014-04, Vol.1 (15), p.2641-2648

2014

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Re: Azathioprine Monotherapy for Maintenance of Remission in Pediatric Patients With Autoimmune Hepatitis

Journal of pediatric gastroenterology and nutrition, 2007-10, Vol.45 (4), p.490-490

2007

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The Rise of Economic Societies in the Eighteenth Century: Patriotic Reform in Europe and North America

1, 2012

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P448 Long term effectiveness of first-line infliximab treatment compared to conventional treatment in paediatric moderate-to-severe Crohn’s disease – an update from the TISKids study

Journal of Crohn's and colitis, 2023-01, Vol.17 (Supplement_1), p.i579-i580

2023

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DOP67 First-line infliximab is cost-effective compared to conventional treatment in paediatric Crohn’s Disease – Results from the TISKids study

Journal of Crohn's and colitis, 2022-01, Vol.16 (Supplement_1), p.i111-i112

2022

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P398 Effect of Intravenous versus Oral Iron Therapy on Physical Fitness and Haemoglobin in Paediatric IBD Patients with Anaemia

Journal of Crohn's and colitis, 2021-05, Vol.15 (Supplement_1), p.S407-S408

2021

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OP38 Top-down infliximab superior to step-up in children with Moderate-to-Severe Crohn’s disease: A multicentre randomised controlled trial

Journal of Crohn's and colitis, 2020-01, Vol.14 (Supplement_1), p.S039-S039

2020

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Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis

Hepatology (Baltimore, Md.), 2006-01, Vol.43 (1), p.51-53

2006

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The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis

Journal of hepatology, 2004-11, Vol.41 (5), p.758-763

2004

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O0009 A LOCUS FOR ARTHROGRYPOSIS, RENAL DYSFUNCTION AND CHOLESTASIS SYNDROME MAPS TO CHROMOSOME 15Q

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (S1), p.S10-S10

2004

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O0009 A LOCUS FOR ARTHROGRYPOSIS, RENAL DYSFUNCTION AND CHOLESTASIS SYNDROME MAPS TO CHROMOSOME 15Q

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (Supplement 1), p.S10

2004

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From gene to disease; Wilson disease: copper storage due to mutations in ATP7B

Nederlands tijdschrift voor geneeskunde, 2003-03, Vol.147 (13), p.603

2003

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NASOBILIARY DRAINAGE INDUCES REMISSION IN BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS: H-03

Journal of pediatric gastroenterology and nutrition, 2005-05, Vol.40 (5), p.628

2005

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NASOBILIARY DRAINAGE INDUCES REMISSION IN BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS

Journal of pediatric gastroenterology and nutrition, 2005-05, Vol.40 (5), p.628-628

2005

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Farnesoid X receptor (FXR) activation and FXR genetic variation in inflammatory bowel disease

PloS one, 2011-08, Vol.6 (8), p.e23745-e23745

2011

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Reduced expression of ATP7B affected by Wilson disease–causing mutations is rescued by pharmacological folding chaperones 4‐phenylbutyrate and curcumin

Hepatology (Baltimore, Md.), 2009-12, Vol.50 (6), p.1783-1795

2009

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Familial cholestasis: Progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy

Baillière's best practice & research. Clinical gastroenterology, 2010-10, Vol.24 (5), p.541-553

2010

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Liver disease associated with canalicular transport defects: Current and future therapies

Journal of hepatology, 2010-02, Vol.52 (2), p.258-271

2010

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ATP8B1 is essential for maintaining normal hearing

Proceedings of the National Academy of Sciences - PNAS, 2009-06, Vol.106 (24), p.9709-9714

2009

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Mutations in VPS33B , encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome

Nature genetics, 2004-04, Vol.36 (4), p.400-404

2004

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Mutational analysis of ATP8B1 in patients with chronic pancreatitis

PloS one, 2013-11, Vol.8 (11), p.e80553-e80553

2013

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Paraneoplastic pemphigus associated with post‐transplant lymphoproliferative disorder after small bowel transplantation

Pediatric transplantation, 2021-09, Vol.25 (6), p.e14023-n/a

2021

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Loss of Syntaxin 3 Causes Variant Microvillus Inclusion Disease

Gastroenterology (New York, N.Y. 1943), 2014-07, Vol.147 (1), p.65-68.e10

2014

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Ferric Carboxymaltose Versus Ferrous Fumarate in Anemic Children with Inflammatory Bowel Disease: The POPEYE Randomized Controlled Clinical Trial

The Journal of pediatrics, 2023-05, Vol.256, p.113-119.e4

2023

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Universal spreading of water drops on complex surfaces

Re: Azathioprine Monotherapy for Maintenance of Remission in Pediatric Patients With Autoimmune Hepatitis

The Rise of Economic Societies in the Eighteenth Century: Patriotic Reform in Europe and North America

P448 Long term effectiveness of first-line infliximab treatment compared to conventional treatment in paediatric moderate-to-severe Crohn’s disease – an update from the TISKids study

DOP67 First-line infliximab is cost-effective compared to conventional treatment in paediatric Crohn’s Disease – Results from the TISKids study

P398 Effect of Intravenous versus Oral Iron Therapy on Physical Fitness and Haemoglobin in Paediatric IBD Patients with Anaemia

OP38 Top-down infliximab superior to step-up in children with Moderate-to-Severe Crohn’s disease: A multicentre randomised controlled trial

Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis

The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis

O0009 A LOCUS FOR ARTHROGRYPOSIS, RENAL DYSFUNCTION AND CHOLESTASIS SYNDROME MAPS TO CHROMOSOME 15Q

O0009 A LOCUS FOR ARTHROGRYPOSIS, RENAL DYSFUNCTION AND CHOLESTASIS SYNDROME MAPS TO CHROMOSOME 15Q

From gene to disease; Wilson disease: copper storage due to mutations in ATP7B

NASOBILIARY DRAINAGE INDUCES REMISSION IN BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS: H-03

NASOBILIARY DRAINAGE INDUCES REMISSION IN BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS

Farnesoid X receptor (FXR) activation and FXR genetic variation in inflammatory bowel disease

Reduced expression of ATP7B affected by Wilson disease–causing mutations is rescued by pharmacological folding chaperones 4‐phenylbutyrate and curcumin

Familial cholestasis: Progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy

Liver disease associated with canalicular transport defects: Current and future therapies

ATP8B1 is essential for maintaining normal hearing

Mutations in VPS33B , encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome

Mutational analysis of ATP8B1 in patients with chronic pancreatitis

First-line treatment with infliximab versus conventional treatment in children with newly diagnosed moderate-to-severe Crohn’s disease: an open-label multicentre randomised controlled trial

Paraneoplastic pemphigus associated with post‐transplant lymphoproliferative disorder after small bowel transplantation

Loss of Syntaxin 3 Causes Variant Microvillus Inclusion Disease

Ferric Carboxymaltose Versus Ferrous Fumarate in Anemic Children with Inflammatory Bowel Disease: The POPEYE Randomized Controlled Clinical Trial

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