Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Alain Lachaux"'
Autor:
Mounzer Koudsi, Christine Martinez-Vinson, Bénédicte Pigneur, Stéphanie Willot, Djeddi Djamal, Raphael Enaud, Julie Rebeuh, Claire Dupont, Alain Dabadie, Valérie Bertrand, Jean-Pierre Hugot, Alain Lachaux, Franck Ruemmele, Jérôme Viala, Rémi Duclaux-Loras, GETAID Pédiatrique
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 76:763-770
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:
Pierre Broué, Anne Sophie Brunet, Dominique Debray, Alain Lachaux, Muriel Bost, Abdelouahed Belmalih, Thierry Lamireau, Eduardo Couchonnal, Olivier Guillaud, Claire Vanlemmens, Dalila Habes, Frédéric Gottrand, Laurence Lion-François, Aurélia Poujois, Jérôme Dumortier, Emmanuel Jacquemin, Alexandre Fabre, Rodolphe Sobesky, Laure Bridoux-Henno
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2021, ⟨10.1097/mpg.0000000000003196⟩
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2021, ⟨10.1097/mpg.0000000000003196⟩
OBJECTIVES To describe a cohort of Wilson disease (WD) pediatric cases, and to point out the diagnostic particularities of this age group and the long-term outcome. METHODS Clinical data of 182 pediatric patients included in the French WD national re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aab9f3bd34236e7e2308481f18d82264
http://hdl.handle.net/20.500.12278/109258
http://hdl.handle.net/20.500.12278/109258
Autor:
Esra Karatas, Lioara Restier, Christine Lombard, Magali Dechomet, Mathias Ruiz, Abdelouahed Belmalih, Roman Garin, Alain Lachaux, Céline Renoux, Philippe Joly, Marion Bouchecareilh
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2021, 73 (3), pp.e68-e72. ⟨10.1097/MPG.0000000000003125⟩
Journal of Pediatric Gastroenterology and Nutrition, 2021, 73 (3), pp.e68-e72. ⟨10.1097/MPG.0000000000003125⟩
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2021, 73 (3), pp.e68-e72. ⟨10.1097/MPG.0000000000003125⟩
Journal of Pediatric Gastroenterology and Nutrition, 2021, 73 (3), pp.e68-e72. ⟨10.1097/MPG.0000000000003125⟩
International audience; The presence of modifier genes is now well recognized in severe liver disease outcome associated with alpha-1-antitrypsin deficiency (A1ATD) but their identification remains to be fully elucidated. To address this goal, we per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b13466906b7b7b6162a16747e7223e2
https://hal.archives-ouvertes.fr/hal-03436289
https://hal.archives-ouvertes.fr/hal-03436289
Autor:
S. Sissaoui, Claire Bordat, Florence Lacaille, Sophie Collardeau-Frachon, Noël Peretti, Manon Cochet, Alain Lachaux, Pierre Poinsot
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2021, 73 (1), pp.4-8. ⟨10.1097/mpg.0000000000003145⟩
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2021, 73 (1), pp.4-8. ⟨10.1097/mpg.0000000000003145⟩
International audience; Familial intestinal hypocholesterolemias, such as abetalipoproteinemia, hypobetalipoproteinemia, and chylomicron retention disease, are rare genetic diseases that result in a defect in the synthesis or secretion of lipoprotein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f92115543d35ddf03a14e991c1af9577
https://www.hal.inserm.fr/inserm-03452104
https://www.hal.inserm.fr/inserm-03452104
Autor:
Laurent Michaud, Jérôme Viala, Alain Lachaux, Frédéric Gottrand, Pierre Fayoux, Delphine Ley, Marie Bridenne, Bruno Hauser, Laurent Rebouissoux, Julie Lemale
OBJECTIVES: Research on long-term use of mitomycin C (MC) for recurrent esophageal stenoses is limited. We assessed the long-term efficacy and safety of local application of MC for recurrent esophageal stenoses in children. METHODS: This was a retros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69079689c0d05d1b8af551fe7ce54844
https://biblio.vub.ac.be/vubir/efficacy-and-safety-of-the-local-application-of-mitomycin-c-to-recurrent-esophageal-strictures-in-children(c3467766-c850-44b7-9b8d-663cd43a9c36).html
https://biblio.vub.ac.be/vubir/efficacy-and-safety-of-the-local-application-of-mitomycin-c-to-recurrent-esophageal-strictures-in-children(c3467766-c850-44b7-9b8d-663cd43a9c36).html
Autor:
G. de Saint Basile, Yves Bertrand, N. Peretti, J. Fayard, Alain Lachaux, C. Malcus, T. Louazon, Marie-Pierre Cordier, Pierre-Yves Mure, B. Rohmer, S. Collardeau, Rémi Dubois, R. Duclaux
Publikováno v:
Archives de Pédiatrie. 25:334-339
TTC7A mutations cause multiple neonatal intestinal atresias with early inflammatory bowel disease and severe combined immunodeficiency. There are no treatment protocols for this rare disease. Two new cases are described for which radical early treatm
Autor:
Bernard Benoit, Corinne Boyer, Bérengère Francois, Frédéric Gottrand, Alain Lachaux, Stéphanie De Smet
Publikováno v:
European Journal of Pediatrics. 176:1613-1618
We analyzed the characteristics of the population with congenital portosystemic shunt diagnosed during the antenatal period and the organization of their perinatal care. This multicentric retrospective study included all the patients with a prenatal
Autor:
Frédérique Dijoud, Damien Dupont, Corentin Tanné, Sophie Collardeau-Frachon, Meja Rabodonirina, Frédéric Hameury, Yves Gillet, Rémi Dubois, Alain Lachaux, Christine Rivet, Jérôme Dumortier
Publikováno v:
Pediatric Infectious Disease Journal. 36:805-808
This first observation of donor-transmitted coccidioidomycosis in a pediatric liver-transplant recipient underlines a rare condition in transplanted patients in a nonendemic area. This transmission was observed after a liver split, the patient being
Publikováno v:
Archives de Pédiatrie. 24:391-398
Small-bowel capsule endoscopy (CE) has recently been used in children. During the past few years, an intense research activity has defined the advantages and limitations of CE. Its uses have been established in several small-bowel pathologies such as