Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Lioara Restier"'
Autor:
Ahmad Fneich, Pierre Poinsot, Christelle Elias, Lioara Restier, Philippe Vanhems, Florent Wallet, Cyrielle Caussy, Antoine Duclos, Noël Peretti
Publikováno v:
Clinical Nutrition Open Science, Vol 44, Iss , Pp 9-14 (2022)
Background: Undernutrition has been previously identified as a deleterious factor in acute infections. In covid-19 infection, obesity is a risk-factor of severe evolution, but initial undernutrition has not been evaluated yet. Methods: We retrospecti
Externí odkaz:
https://doaj.org/article/a195870f81ff401fa0bf98a809adad28
Autor:
Typhaine Louazon, Pierre Poinsot, Lioara Restier, Abdelouahed Belmalih, Irène Loras-Duclaux, Stéphanie Marotte, Sophie Heissat, Didier Barnoud, Cécile Chambrier, Cyrille B. Confavreux, Alain Lachaux, Justine Bacchetta, Noel Peretti
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Long-term parenteral nutrition (PN) may induce bone complications. Tridimensional bone imaging techniques such as high-resolution peripheral quantitative computed tomography (HR-pQCT) allow the assessment of both compartmental volumetric den
Externí odkaz:
https://doaj.org/article/299298a6867f4b5ebf86aa6ccc64f6a7
Autor:
Charlotte Cuerq, Emilie Henin, Lioara Restier, Emilie Blond, Jocelyne Drai, Christophe Marçais, Mathilde Di Filippo, Christian Laveille, Marie-Caroline Michalski, Pierre Poinsot, Cyrielle Caussy, Agnès Sassolas, Philippe Moulin, Emmanuelle Reboul, Sybil Charriere, Emile Levy, Alain Lachaux, Noël Peretti
Publikováno v:
Journal of Lipid Research, Vol 59, Iss 9, Pp 1640-1648 (2018)
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 often supplemented in the
Externí odkaz:
https://doaj.org/article/d3ae3482ce1842fd8028966debda54e5
Autor:
Caroline Demily, François Parant, David Cheillan, Emmanuel Broussolle, Alice Pavec, Olivier Guillaud, Lioara Restier, MOPSY Consortium, Alain Lachaux, Muriel Bost
Publikováno v:
Annals of General Psychiatry, Vol 16, Iss 1, Pp 1-8 (2017)
Abstract Background Wilson’s disease (WD) is a rare autosomal-recessive, inherited disorder caused by a mutation in the copper-transporting gene ATP7B affecting the liver and nervous system. About 30% of patients with WD may initially present with
Externí odkaz:
https://doaj.org/article/1d67d3ca25fa4f90bbd934bee2643c75
Autor:
Philippe Joly, Hélène Vignaud, Julie Di Martino, Mathias Ruiz, Roman Garin, Lioara Restier, Abdelouahed Belmalih, Christelle Marchal, Christophe Cullin, Benoit Arveiler, Patricia Fergelot, Aaron D Gitler, Alain Lachaux, Julien Couthouis, Marion Bouchecareilh
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0179369 (2017)
The most common and severe disease causing allele of Alpha 1-Antitrypsin Deficiency (1ATD) is Z-1AT. This protein aggregates in the endoplasmic reticulum, which is the main cause of liver disease in childhood. Based on recent evidences and on the fre
Externí odkaz:
https://doaj.org/article/7cf097c7bb7d421ca4fb799dbd93f347
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:
Alain Lachaux, Julie Traclet, Lioara Restier, Olivier Guillaud, Jérôme Dumortier, Colette Chapuis-Cellier, Philippe Joly, Jean François Mornex
Publikováno v:
Clinics and Research in Hepatology and Gastroenterology
Clinics and Research in Hepatology and Gastroenterology, Elsevier, 2019, 43 (1), pp.77-81. ⟨10.1016/j.clinre.2018.08.016⟩
Clinics and Research in Hepatology and Gastroenterology, Elsevier, 2019, 43 (1), pp.77-81. ⟨10.1016/j.clinre.2018.08.016⟩
BACKGROUND: Alpha-1-antitrypsin deficiency (A1ATD) is a common genetic condition which predisposes to emphysema and liver disorders. It is estimated that 10-15% of homozygous individuals for the Z allele (PiZZ) may develop liver fibrosis. The optimal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e330bdb14ec510e030b845054ef1595a
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02191902/document
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02191902/document
Autor:
Lioara Restier, Mathias Ruiz, Groupe Francophone d’Hépatologie Gastroentérologie et Nutrition Pédiatriques, Madeleine Aumar, Laure Bridoux-Henno, Thierry Lamireau, Philippe Joly, Abdelouahed Belmalih, Emmanuel Jacquemin, Colette Chapuis-Cellier, Julien Berthiller, Pierre Broué, Christine Rivet, Marion Bouchecareilh, Florence Lacaille, Jérôme Dumortier, Alain Lachaux
Publikováno v:
Liver International
Liver International, Wiley-Blackwell, 2019, 39 (6), pp.1136--1146. ⟨10.1111/liv.14035⟩
Liver Int
Liver Int, 2019, 39 (6), pp.1136--1146. ⟨10.1111/liv.14035⟩
Liver International, Wiley-Blackwell, 2019, 39 (6), pp.1136--1146. ⟨10.1111/liv.14035⟩
Liver Int
Liver Int, 2019, 39 (6), pp.1136--1146. ⟨10.1111/liv.14035⟩
International audience; BACKGROUND & AIMS: To identify prognostic factors for liver disease in children with alpha-1 antitrypsin deficiency, irrespective of phenotype, using the DEFI-ALPHA cohort. METHODS: Retrospective, then prospective from 2010, m