Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Alain Lachaux"'
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:
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:
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:
Anthony Conway, Audrey Beringer, Roselyne Boulieu, Antony Citterio-Quentin, Aishling Ryan, Amal El Mahmoudi, Alain Lachaux, Thibault Perret
Publikováno v:
Basic and Clinical Pharmacology and Toxicology
Basic and Clinical Pharmacology and Toxicology, Wiley, 2019, 124 (5), pp.600--606. ⟨10.1111/bcpt.13176⟩
Basic and Clinical Pharmacology and Toxicology, Wiley, 2019, 124 (5), pp.600--606. ⟨10.1111/bcpt.13176⟩
Inosine monophosphate dehydrogenase (IMPDH) is considered as the limiting enzyme of thiopurine metabolism for the formation of 6-thioguanine nucleotides (6-TGN). No data are available on the influence of RBC IMPDH activity on the metabolism of thiopu
Autor:
Cécile Talbotec, Marc Bellaiche, Jacques Cardey, Catherine Le Gall, Laure Bridoux-Henno, Thierry Lamireau, Jérôme Viala, Alain Dabadie, Emmanuel Mas, Alain Lachaux, Lioara Restier-Miron, Laurent Michaud
Publikováno v:
Endoscopy
Endoscopy, 2019, 51 (1), pp.10--17. ⟨10.1055/a-0647-1709⟩
Endoscopy, 2019, 51 (1), pp.10--17. ⟨10.1055/a-0647-1709⟩
Background Esophagogastroduodenoscopy (EGD) is the standard method for diagnosis of esophageal and gastric varices in children. In this prospective study we evaluated the use of PillCam esophageal capsule endoscopy (ECE) in pediatric patients. Method
Autor:
Philippe Moulin, Jocelyne Drai, Emmanuelle Reboul, Emile Levy, Charlotte Cuerq, Lioara Restier, Noël Peretti, Mathilde Di Filippo, Marie-Caroline Michalski, Alain Lachaux, Emilie Blond, Pierre Poinsot, Agnès Sassolas, Sybil Charrière, Cyrielle Caussy, Christian Laveille, Christophe Marçais, Emilie Henin
Publikováno v:
Journal of Lipid Research
Journal of Lipid Research, American Society for Biochemistry and Molecular Biology, 2018, 59 (9), pp.1640--1648
Journal of Lipid Research, 2018, 59 (9), pp.1640-1648. ⟨10.1194/jlr.M085043⟩
Journal of Lipid Research, American Society for Biochemistry and Molecular Biology, 2018, 59 (9), pp.1640-1648. ⟨10.1194/jlr.M085043⟩
Journal of Lipid Research, Vol 59, Iss 9, Pp 1640-1648 (2018)
Journal of Lipid Research, 2018, 59 (9), pp.1640--1648
Journal of Lipid Research 9 (59), 1640-1648. (2018)
Journal of Lipid Research, American Society for Biochemistry and Molecular Biology, 2018, 59 (9), pp.1640--1648
Journal of Lipid Research, 2018, 59 (9), pp.1640-1648. ⟨10.1194/jlr.M085043⟩
Journal of Lipid Research, American Society for Biochemistry and Molecular Biology, 2018, 59 (9), pp.1640-1648. ⟨10.1194/jlr.M085043⟩
Journal of Lipid Research, Vol 59, Iss 9, Pp 1640-1648 (2018)
Journal of Lipid Research, 2018, 59 (9), pp.1640--1648
Journal of Lipid Research 9 (59), 1640-1648. (2018)
International audience; Abetalipoproteinemia (ABL) and chylomicron retention disease (CMRD) are extremely rare recessive forms of hypobetalipoproteinemia characterized by intestinal lipid malabsorption and severe vitamin E deficiency. Vitamin E is of
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:
Noël Peretti, Pierre-Marie Lavrut, Raphael Maudinas, Pauline Bonniaud-Blot, Marie Bournez, Alexandre Fabre, Patrice Bourgeois, Fabienne Charbit-Henrion, Nadine Cerf-Bensussan, Mathias Faure, Alain Lachaux, Rémi Duclaux-Loras
Publikováno v:
Clinics and Research in Hepatology and Gastroenterology
Clinics and Research in Hepatology and Gastroenterology, Elsevier, 2021, 45 (6), pp.101640. ⟨10.1016/j.clinre.2021.101640⟩
Clinics and Research in Hepatology and Gastroenterology, 2021, 45 (6), pp.101640. ⟨10.1016/j.clinre.2021.101640⟩
Clinics and Research in Hepatology and Gastroenterology, Elsevier, 2021, 45 (6), pp.101640. ⟨10.1016/j.clinre.2021.101640⟩
Clinics and Research in Hepatology and Gastroenterology, 2021, 45 (6), pp.101640. ⟨10.1016/j.clinre.2021.101640⟩
International audience; Proprotein convertase 1 (PCSK1, PC1/3) deficiency is an uncommon cause of neonatal malabsorptive diarrhoea associated with endocrinopathies that are due to the disrupted processing of a large number of prohormones, including p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3d19118e9f0e0fe9a4709d8813481f2
https://www.hal.inserm.fr/inserm-03337429/document
https://www.hal.inserm.fr/inserm-03337429/document
Autor:
Jean-Louis Stephan, Sophie Heissat, Laurent Michaud, Valérie Triolo, Hugues Patural, Camille Donnet, Sylvie Destombe, Alain Lachaux
Publikováno v:
Endoscopy international open
Endoscopy international open, 2020, 8 (7), pp.E830--e833. ⟨10.1055/a-0914-2711⟩
Endoscopy International Open, Vol 08, Iss 07, Pp E830-E833 (2020)
Endoscopy International Open
Endoscopy international open, 2020, 8 (7), pp.E830--e833. ⟨10.1055/a-0914-2711⟩
Endoscopy International Open, Vol 08, Iss 07, Pp E830-E833 (2020)
Endoscopy International Open
Background and study aims Eosinophilic esophagitis (EoE) is a chronic immune disease with increasing incidence. It is clinically defined by symptoms of esophageal dysfunction and histologically by eosinophilic polynuclear cell infiltration of the eso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c3348ab028ba15872741dfe242ba652
https://hal.archives-ouvertes.fr/hal-02902551
https://hal.archives-ouvertes.fr/hal-02902551