Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Alain Lachaux"'
Autor:
Dany Hermann Ngwanou, Eduardo Couchonnal, François Parant, Abdelouahed Belmalih, Olivier Guillaud, Jérôme Dumortier, Muriel Bost, Alain Lachaux
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 75(4)
Determining 24-hour urinary copper excretion (UCE) levels is useful for diagnosing Wilson's disease (WD) and for treatment monitoring. Exchangeable copper (ExC) is a novel potential marker, but its long-term changes have never been described in patie
Autor:
Thierry Lamireau, Muriel Girard, Martina Fanna, Florent Guérin, Carmen Capito, Guillaume Masson, Alain Lachaux, Frédéric Gottrand, Christophe Chardot, Alain Dabadie, Bertrand Roquelaure, Bogdan Hermeziu, Pierre Broué, Emmanuel Jacquemin
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2019, 69 (4), pp.416-424. ⟨10.1097/MPG.0000000000002446⟩
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2019, 69 (4), pp.416-424. ⟨10.1097/MPG.0000000000002446⟩
Objectives: This study analyses the prognosis of biliary atresia (BA) in France since 1986, when both Kasai operation (KOp) and liver transplantation (LT) became widely available. Methods: The charts of all patients diagnosed with BA born between 198
Autor:
C. Maurage, D. Dobbelaere, Alain Lachaux, A. Morali, M Larchet, Jean-Philippe Girardet, Pascale Benlian, Daniel Rieu, M. Meyer, Olivier Mouterde, F. Lacaille, Jacques Sarles, C Lenearts, J.L. Ginies, S. Viola, O. Goulet
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 33:122-126
Background Familial defective apolipoprotein B-100, a dominantly inherited form of hypercholesterolemia caused by a single Arg3500Gln mutation, is silent in childhood but may confer a high risk of cardiovascular disease in adulthood. The objective wa
Autor:
Véronique Chirouze, Alexandre Lapillonne, Alain Lachaux, Michelle Chambon, Valérie Mamoux, Vincent Fournier, Christine Hakme
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 30:528-532
BACKGROUND The long-chain polyunsaturated fatty acid (LC-PUFA) status of infants with untreated biliary atresia (BA) is known to be poor and is correlated to the severity of the liver disease. Liver transplantation (LT) markedly increases survival of
Autor:
Stéphanie Coopman, Nicolas Kalach, Laurent Michaud, Julie Rebeuh, Guy Molitor, Laurent Rebouissoux, Amandine Georges, Alain Lachaux, Alain Dabadie
Publikováno v:
ResearcherID
Objectives An inlet patch (IP) is defined as heterotopic gastric mucosa located in the proximal esophagus. Little information is available in children. The aim of this retrospective study was to assess clinical significance, endoscopic and histologic
Autor:
Raymonde Bouvier, Alain Lachaux, Carlos Robles-Medranda, Catherine Le Gall, Jérôme Dumortier, F Villard, Hannah P. Lukashok, Christine Rivet
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 50(5)
Background Esophageal stricture is one of the most severe complications in eosinophilic esophagitis (EoE). Clinical practice is based on limited data and some treatments are still considered controversial. We report on our experience in the treatment
Autor:
Alain Lachaux, Irène Loras-Duclaux, Jean-Paul Ortonne, Jean-paul Chappuis, Raymonde Bouvier, G. Meneguzzi
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 29(4)
Background: An infant born with pyloric atresia had development of intractable diarrhea and was found to have total epithelial detachment of gastric and small and large bowel mucosa. She had no skin abnormalities. Parental consanguinity and pyloric a
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 27(4)
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 27(2)
Autor:
L. Michel-Calemard, A. Sassolas, M. Bovier-Lapierre, Alain Lachaux, L. Pugnet-Chardon, P. Moulin
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 39:S272-S273