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Immunosuppressive therapy for indeterminate acute hepatitis or pediatric acute liver failure

The Journal of pediatrics, 2019-11, Vol.214, p.243-244

2019

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Complications of Congenital Portosystemic Shunts in Children: Therapeutic Options and Outcomes

Journal of pediatric gastroenterology and nutrition, 2010-09, Vol.51 (3), p.322-330

2010

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ATP8B1 and ABCB11 analysis in 62 children with normal gamma‐glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): Phenotypic differences between PFIC1 and PFIC2 and natural history

Hepatology (Baltimore, Md.), 2010-05, Vol.51 (5), p.1645-1655

2010

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Long‐term outcome of pediatric liver transplantation for biliary atresia: A 10‐year follow‐up in a single center

Liver transplantation, 2005-02, Vol.11 (2), p.152-160

2005

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Corrosive substances ingestion: a review

Critical reviews in toxicology, 2019-09, Vol.49 (8), p.637-669

2019

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A Model for Early Endoscopic Detection of High‐Risk Gastroesophageal Varices in Children With Biliary Atresia

Journal of pediatric gastroenterology and nutrition, 2022-05, Vol.74 (5), p.643-650

2022

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The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood

Gastroenterology (New York, N.Y. 1943), 2001-05, Vol.120 (6), p.1448-1458

2001

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Obliterative Portal Venopathy: A Study of 48 Children

The Journal of pediatrics, 2014-07, Vol.165 (1), p.190-193.e2

2014

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Oral Cholic Acid for Hereditary Defects of Primary Bile Acid Synthesis: A Safe and Effective Long-term Therapy

Gastroenterology (New York, N.Y. 1943), 2009-10, Vol.137 (4), p.1310-1320.e3

2009

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Mutations in the novel gene FOPV are associated with familial autosomal dominant and non‐familial obliterative portal venopathy

Liver international, 2018-02, Vol.38 (2), p.358-364

2018

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Mutations in the MDR3 Gene Cause Progressive Familial Intrahepatic Cholestasis

Proceedings of the National Academy of Sciences - PNAS, 1998-01, Vol.95 (1), p.282-287

1998

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Progression to High‐Risk Gastroesophageal Varices in Children With Biliary Atresia With Low‐Risk Signs at First Endoscopy

Journal of pediatric gastroenterology and nutrition, 2015-05, Vol.60 (5), p.664-668

2015

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Experience With Endoscopic Management of High-Risk Gastroesophageal Varices, With and Without Bleeding, in Children With Biliary Atresia

Gastroenterology (New York, N.Y. 1943), 2013-10, Vol.145 (4), p.801-807

2013

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Acute Leukemia Presenting as Acute Hepatitis Without Liver Failure

Journal of pediatric gastroenterology and nutrition, 2014-11, Vol.59 (5), p.640-641

2014

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Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis

Hepatology (Baltimore, Md.), 1997-03, Vol.25 (3), p.519-523

1997

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Mutation spectrum in the French cohort of galactosemic patients and structural simulation of 27 novel missense variations

Molecular genetics and metabolism, 2012-11, Vol.107 (3), p.438-447

2012

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Budd‐Chiari Syndrome and Essential Thrombocythemia in a Child: Favorable Outcome After Transjugular Intrahepatic Portosystemic Shunt

Journal of pediatric gastroenterology and nutrition, 2008-03, Vol.46 (3), p.334-337

2008

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A new cause of progressive intrahepatic cholestasis : 3β-hydroxy-C27-steroid dehydrogenase/isomerase deficiency

The Journal of pediatrics, 1994-09, Vol.125 (3), p.379-384

1994

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Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease)

European journal of pediatrics, 1994-06, Vol.153 (6), p.424-428

1994

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Genetic cholestatic liver diseases: the example of progressive familial intrahepatic cholestasis and related disorders

Acta gastro-enterologica belgica, 2004-04, Vol.67 (2), p.179-183

2004

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Liver disease associated with ZZ alpha1-antitrypsin deficiency and ursodeoxycholic acid therapy in children

Journal of pediatric gastroenterology and nutrition, 2008-11, Vol.47 (5), p.623-629

2008

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Immunosuppressive therapy for indeterminate acute hepatitis or pediatric acute liver failure

Complications of Congenital Portosystemic Shunts in Children: Therapeutic Options and Outcomes

ATP8B1 and ABCB11 analysis in 62 children with normal gamma‐glutamyl transferase progressive familial intrahepatic cholestasis (PFIC): Phenotypic differences between PFIC1 and PFIC2 and natural history

Long‐term outcome of pediatric liver transplantation for biliary atresia: A 10‐year follow‐up in a single center

Corrosive substances ingestion: a review

A Model for Early Endoscopic Detection of High‐Risk Gastroesophageal Varices in Children With Biliary Atresia

The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood

Obliterative Portal Venopathy: A Study of 48 Children

Oral Cholic Acid for Hereditary Defects of Primary Bile Acid Synthesis: A Safe and Effective Long-term Therapy

Mutations in the novel gene FOPV are associated with familial autosomal dominant and non‐familial obliterative portal venopathy

Mutations in the MDR3 Gene Cause Progressive Familial Intrahepatic Cholestasis

Progression to High‐Risk Gastroesophageal Varices in Children With Biliary Atresia With Low‐Risk Signs at First Endoscopy

Experience With Endoscopic Management of High-Risk Gastroesophageal Varices, With and Without Bleeding, in Children With Biliary Atresia

Acute Leukemia Presenting as Acute Hepatitis Without Liver Failure

Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis

Mutation spectrum in the French cohort of galactosemic patients and structural simulation of 27 novel missense variations

Budd‐Chiari Syndrome and Essential Thrombocythemia in a Child: Favorable Outcome After Transjugular Intrahepatic Portosystemic Shunt

A new cause of progressive intrahepatic cholestasis : 3β-hydroxy-C27-steroid dehydrogenase/isomerase deficiency

Evidence for defective primary bile acid secretion in children with progressive familial intrahepatic cholestasis (Byler disease)

Genetic cholestatic liver diseases: the example of progressive familial intrahepatic cholestasis and related disorders

Liver disease associated with ZZ alpha1-antitrypsin deficiency and ursodeoxycholic acid therapy in children

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