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Hepatology (Baltimore, Md.)|December 31, 2013
MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion diseaseMuriel Girard, Florence Lacaille, Virginie Verkarre, et al.
Journal of Pediatric Surgery|July 25, 2022
Antithrombin supplementation for prevention of vascular thrombosis after pediatric liver transplantationMaria Hukkinen, Michela Wong, Zeynep Demir, et al.
Orphanet Journal of Rare Diseases|June 15, 2014
Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?Laurent Enaud, Alice Hadchouel, Aurore Coulomb, et al.
The American Journal of Gastroenterology|February 26, 2026
Histogenetic Classification Predicts Outcomes in 130 Adults with Chronic Intestinal Pseudo-ObstructionMinh-Chau Ta, Dominique Cazals-Hatem, Lore Billiauws, et al.
Journal of Inherited Metabolic Disease|September 1, 2017
Autism spectrum disorders in propionic acidemia patientsCaroline Dejean de la Bâtie, Valérie Barbier, Célina Roda, et al.
Journal of Autoimmunity|September 16, 2023
Hepatic safety and efficacy of immunomodulatory drugs used in patients with autoimmune hepatitisBenedetta Terziroli Beretta-Piccoli, Gustav Buescher, George Dalekos, et al.
Diagnostics (Basel, Switzerland)|May 28, 2022
Targeted-Capture Next-Generation Sequencing in Diagnosis Approach of Pediatric CholestasisMarion Almes, Anne Spraul, Mathias Ruiz, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 31, 2024
Noninvasive scores are poorly predictive of histological fibrosis in paediatric fatty liver diseaseLaura Kalveram, Ulrich Baumann, Ruth De Bruyne, et al.
Journal of Inherited Metabolic Disease|October 24, 2020
Long term outcome of MPI-CDG patients on D-mannose therapyMuriel Girard, Claire Douillard, Dominique Debray, et al.
Pediatric Nephrology (Berlin, Germany)|November 9, 2020
Long-term kidney and liver outcome in 50 children with autosomal recessive polycystic kidney diseaseGuillaume Dorval, Olivia Boyer, Anne Couderc, et al.
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