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Anticoagulation Monitoring Under ECMO Support: A Comparative Study Between the Activated Coagulation Time and the Anti-Xa Activity Assay

Journal of intensive care medicine, 2020-07, Vol.35 (7), p.679-686

2020

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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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Divergent Roles for Macrophage C-type Lectin Receptors, Dectin-1 and Mannose Receptors, in the Intestinal Inflammatory Response

Cell reports (Cambridge), 2020-03, Vol.30 (13), p.4386-4398.e5

2020

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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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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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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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Serum club cell protein 16 is associated with asymptomatic airway responsiveness in adults: Findings from the French epidemiological study on the genetics and environment of asthma

Respirology (Carlton, Vic.), 2015-11, Vol.20 (8), p.1198-1205

2015

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Liver glycogen storage diseases due to phosphorylase system deficiencies: Diagnosis thanks to non invasive blood enzymatic and molecular studies

Molecular genetics and metabolism, 2011-09, Vol.104 (1-2), p.137-143

2011

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Hepatorenal Syndrome: Diagnosis and Effect of Terlipressin Therapy in 4 Pediatric Patients

Journal of pediatric gastroenterology and nutrition, 2010-07, Vol.51 (1), p.100-102

2010

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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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Prophylactic endoscopic sclerotherapy of large esophagogastric varices in infants with biliary atresia

Gastrointestinal endoscopy, 2008-04, Vol.67 (4), p.732-737

2008

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Transient neonatal cholestasis: Origin and outcome

The Journal of pediatrics, 1998-10, Vol.133 (4), p.563-567

1998

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Defect of multidrug‐resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasis

Hepatology (Baltimore, Md.), 1996-04, Vol.23 (4), p.904-908

1996

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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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Prehospital Abciximab in ST-Segment Elevation Myocardial Infarction: Results of the Randomized, Double-Blind MISTRAL Study

Circulation. Cardiovascular interventions, 2012-02, Vol.5 (1), p.69-76

2012

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Delayed Postnatal Presentation of Biliary Atresia in 2 Premature Neonates

Journal of pediatric gastroenterology and nutrition, 2011-04, Vol.52 (4), p.489-491

2011

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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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Alagille syndrome and nephroblastoma: Unusual coincidence of two rare disorders

Pediatric blood & cancer, 2008-04, Vol.50 (4), p.908-911

2008

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Peliosis hepatis with initial presentation as acute hepatic failure and intraperitoneal hemorrhage in children

Journal of hepatology, 1999-06, Vol.30 (6), p.1146-1150

1999

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A novel therapy for atopic dermatitis with allergen-antibody complexes: A double-blind, placebo-controlled study

Journal of the American Academy of Dermatology, 1993-02, Vol.28 (2), p.232-239

1993

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Anticoagulation Monitoring Under ECMO Support: A Comparative Study Between the Activated Coagulation Time and the Anti-Xa Activity Assay

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

Divergent Roles for Macrophage C-type Lectin Receptors, Dectin-1 and Mannose Receptors, in the Intestinal Inflammatory Response

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

Corrosive substances ingestion: a review

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

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

Serum club cell protein 16 is associated with asymptomatic airway responsiveness in adults: Findings from the French epidemiological study on the genetics and environment of asthma

Liver glycogen storage diseases due to phosphorylase system deficiencies: Diagnosis thanks to non invasive blood enzymatic and molecular studies

Hepatorenal Syndrome: Diagnosis and Effect of Terlipressin Therapy in 4 Pediatric Patients

Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis

Prophylactic endoscopic sclerotherapy of large esophagogastric varices in infants with biliary atresia

Transient neonatal cholestasis: Origin and outcome

Defect of multidrug‐resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasis

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

Prehospital Abciximab in ST-Segment Elevation Myocardial Infarction: Results of the Randomized, Double-Blind MISTRAL Study

Delayed Postnatal Presentation of Biliary Atresia in 2 Premature Neonates

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

Alagille syndrome and nephroblastoma: Unusual coincidence of two rare disorders

Peliosis hepatis with initial presentation as acute hepatic failure and intraperitoneal hemorrhage in children

A novel therapy for atopic dermatitis with allergen-antibody complexes: A double-blind, placebo-controlled study

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