Zobrazeno 21 - 30
of 318
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:
Emma Wischlen, Noémie Laverdure, Domitille Erard, Barbara Rohmer, Olivier Boillot, Rémi Dubois, Alain Lachaux, Sophie Collardeau-Frachon, Valérie Hervieu, Jérôme Dumortier
Publikováno v:
Clinics and Research in Hepatology and Gastroenterology. 47:102139
Autor:
Laura Tourvieilhe, Elise Jandot, Thierry Quessada, Christine Barreto, Stéphanie Marotte, Sophie Heissat, Pierre Poinsot, Anais Sierra-Torre, Rémi Duclaux-Loras, Alain Lachaux, Irène Loras-Duclaux, Muriel Rabilloud, Noël Peretti
Publikováno v:
Clinical Nutrition
Clinical Nutrition, 2022, 41 (9), pp.1961-1968. ⟨10.1016/j.clnu.2022.07.030⟩
Clinical Nutrition, 2022, 41 (9), pp.1961-1968. ⟨10.1016/j.clnu.2022.07.030⟩
International audience; BACKGROUND AND AIMS: Central line-associated bloodstream infections (CLABSIs) are the main complication in children with home parenteral nutrition (HPN) and some patients develop recurrent CLABSIs (REC-CLABSIs), defined as two
Autor:
Patrick McKiernan, Ekkehard Sturm, Binita M Kamath, Richard J Thompson, Emmanuel Gonzalès, Alain Lachaux, Ulrich Baumann, Eyal Shteyer, Piotr Czubkowski, Reha Artan, Buket Dalgic, Hasan Özen, Girish Gupte, Tassos Grammatikopoulos, Saul J Karpen, Quanhong Ni, Lise Kjems, Patrick Horn
Publikováno v:
Tuesday 25th April 2022.
Autor:
Girish Gupte, Richard J. Thompson, Lorenzo D’Antiga, Tassos Grammatikopoulos, Emmanuel Gonzalès, Florence Lacaille, Alain Lachaux, Bertrand Roquelaure, Ulrich Baumann, Elke Lainka, Ekkehard Sturm, Eyal Shteyer, Piotr Czubkowski, Reha Artan, Buket Dalgic, Hasan Ozen, Kathleen M. Loomes, Jennifer M. Vittorio, Saul J. Karpen, Patrick McKiernan, Cara L. Mack, Angelo Di Giorgio, Qifeng Yu, Lise Kjems, Patrick Horn
Poster-Abstract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be7881e6f1466690a7a399a43814166b
Autor:
Aurélia Poujois, Rodolphe Sobesky, Wassilios G. Meissner, Anne-Sophie Brunet, Emmanuel Broussolle, Chloé Laurencin, Laurence Lion-François, Olivier Guillaud, Alain Lachaux, François Maillot, Jérémie Belin, Ephrem Salamé, Claire Vanlemmens, Bruno Heyd, Céline Bellesme, Dalila Habes, Christophe Bureau, Fabienne Ory-Magne, Pascal Chaine, Jean-Marc Trocello, Daniel Cherqui, Didier Samuel, Victor de Ledinghen, Jean-Charles Duclos-Vallée, France Woimant
Publikováno v:
Neurology
Neurology, American Academy of Neurology, 2020, 94 (21), pp.e2189--e2202. ⟨10.1212/wnl.0000000000009474⟩
Neurology, 2020, 94 (21), pp.e2189--e2202. ⟨10.1212/wnl.0000000000009474⟩
Neurology, American Academy of Neurology, 2020, 94 (21), pp.e2189--e2202. ⟨10.1212/wnl.0000000000009474⟩
Neurology, 2020, 94 (21), pp.e2189--e2202. ⟨10.1212/wnl.0000000000009474⟩
ObjectiveTo evaluate the effect of liver transplantation (LT) in patients with Wilson disease (WD) with severe neurologic worsening resistant to active chelation.MethodsFrench patients with WD who underwent LT for pure neurologic indication were retr
Autor:
Eduardo Couchonnal, Sophie Bouchard, Thomas Damgaard Sandahl, Cecile Pagan, Laurence Lion-François, Olivier Guillaud, Dalila Habes, Dominique Debray, Thierry Lamireau, Pierre Broué, Alexandre Fabre, Claire Vanlemmens, Rodolphe Sobesky, Frederic Gottrand, Laure Bridoux-Henno, Abdelouahed Belmalih, Aurelia Poujois, Corinne Collet, Micheline Misrahi, Bruno Francou, Anne Sophie Brunet, Alain Lachaux, Muriel Bost
Publikováno v:
Couchonnal, E, Bouchard, S, Sandahl, T D, Pagan, C, Lion-François, L, Guillaud, O, Habes, D, Debray, D, Lamireau, T, Broué, P, Fabre, A, Vanlemmens, C, Sobesky, R, Gottrand, F, Bridoux-Henno, L, Belmalih, A, Poujois, A, Brunet, A S, Lachaux, A & Bost, M 2021, ' Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64(10) (2021) 104305] ', European Journal of Medical Genetics, vol. 64, no. 11, pp. 104341 . https://doi.org/10.1016/j.ejmg.2021.104341
European Journal of Medical Genetics
European Journal of Medical Genetics, Elsevier, 2021, 64 (11), pp.104341. ⟨10.1016/j.ejmg.2021.104341⟩
European Journal of Medical Genetics
European Journal of Medical Genetics, Elsevier, 2021, 64 (11), pp.104341. ⟨10.1016/j.ejmg.2021.104341⟩
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34a648abc67dca1b7458242e2fc0865d
http://hdl.handle.net/20.500.12278/123774
http://hdl.handle.net/20.500.12278/123774
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:
Jean-William Dupuy, Céline Léon, Frédéric Saltel, Sophie Collardeau-Frachon, Mathias Ruiz, Esra Karatas, Nathalie Senant, Marion Bouchecareilh, Sylvaine Di-Tommaso, Alain Lachaux, Anne-Aurélie Raymond
Publikováno v:
JHEP Reports
JHEP Reports Innovation in Hepatology
JHEP Reports Innovation in Hepatology, Elsevier, 2021, 3 (4), pp.100297. ⟨10.1016/j.jhepr.2021.100297⟩
JHEP Reports Innovation in Hepatology, 2021, 3 (4), pp.100297. ⟨10.1016/j.jhepr.2021.100297⟩
JHEP Reports, Vol 3, Iss 4, Pp 100297-(2021)
JHEP Reports Innovation in Hepatology
JHEP Reports Innovation in Hepatology, Elsevier, 2021, 3 (4), pp.100297. ⟨10.1016/j.jhepr.2021.100297⟩
JHEP Reports Innovation in Hepatology, 2021, 3 (4), pp.100297. ⟨10.1016/j.jhepr.2021.100297⟩
JHEP Reports, Vol 3, Iss 4, Pp 100297-(2021)
Background & Aims A single point mutation in the Z-variant of alpha 1-antitrypsin (Z-AAT) alone can lead to both a protein folding and trafficking defect, preventing its exit from the endoplasmic reticulum (ER), and the formation of aggregates that a
Autor:
Ritva Koskela, Jennifer Hollis, Frank M. Ruemmele, Giuseppe Castaldo, Lorenzo Norsa, Giusi Grimaldi, Emeline Bequet, Peter Heinz-Erian, Holm H. Uhlig, Saara Leskinen, Remi Duclaux-Loras, Simon Travis, Alain Lachaux, Roberto Berni Canani, Kaija-Leena Kolho, Astor Rodrigues, Lukasz Dembinski, Jaques Deflandre, Neil Shah, Richard K. Russell, Andreas R. Janecke, Satu Wedenoja, Jutta Köglmeier, Sibylle Koletzko
Publikováno v:
Journal of Crohn'scolitis. 15(10)
Background Congenital chloride diarrhoea [CLD] is a rare autosomal recessive disease caused by mutations in the solute family carrier 26 member 3 [SLC26A3] gene. Patients suffer from life-long watery diarrhoea and chloride loss. Inflammatory bowel di