Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Lioara Restier"'
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
Autor:
Colette Chapuis-Cellier, Alain Francina, Mathias Ruiz, Philippe Joly, Alain Lachaux, Abdelhouaed Belmalih, Céline Renoux, Lioara Restier, Marion Bouchecareilh
Publikováno v:
Liver International
Liver International, Wiley-Blackwell, 2017, 37 (11), pp.1608-1611. ⟨10.1111/liv.13586⟩
Liver International, Wiley-Blackwell, 2017, 37 (11), pp.1608-1611. ⟨10.1111/liv.13586⟩
Background and Aims Fifteen to twenty percent of alpha-1 anti-trypsin deficiency patients (A1ATD) have a severe liver outcome (portal hypertension - PHT) during childhood. Since they all share the same ZZ SERPINA1 genotype and that environmental fact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d72209b86d957abe1d46686f3a18e7bd
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02329718
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02329718
Autor:
Laura Jarri, Irène Loras-Duclaux, Noël Peretti, Angélique Denis, Behrouz Kassai-Koupai, Alain Lachaux, Pauline Occelli, Cyrille Colin, Sandrine Touzet, Lioara Restier, Antoine Duclos
Publikováno v:
Journal of Evaluation in Clinical Practice. 21:958-962
Rationale, aims and objectives Malnutrition screening is essential to detect and to treat patients with stunting or wasting. The aim was to evaluate the subjective perception of frequency and assessment of malnutrition by health care professionals. R
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)
Annals of General Psychiatry
Annals of General Psychiatry
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 psychiatr
Autor:
Pierre Poinsot, Philippe Moulin, André Sérusclat, Sophie Collardeau Frachon, Noël Peretti, Lioara Restier, Alain Lachaux, Sybil Charrière, Mathilde Di Filippo
Publikováno v:
Journal of clinical lipidology
Journal of clinical lipidology, Elsevier, 2017, 11 (1), pp.167-177. ⟨10.1016/j.jacl.2016.11.008⟩
Journal of clinical lipidology, Elsevier, 2017, 11 (1), pp.167-177. ⟨10.1016/j.jacl.2016.11.008⟩
International audience; BACKGROUND: The childhood/adult-onset lysosomal acid lipase deficiency (LALD; late-onset LALD) is a rare genetic disease. Children present severe fatty liver disease with early cirrhosis. Before enzyme replacement therapy, sta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55169af4252a75600c2c0785cd8fd6d0
https://hal.archives-ouvertes.fr/hal-01848035
https://hal.archives-ouvertes.fr/hal-01848035
Autor:
Michael N'Guyen, Stéphanie Marotte, Sophie Heissat, Noël Peretti, Irène Loras-Duclaux, Eléa Mirabel-Chambaud, Lioara Restier, Thierry Quessada, Joëlle Goudable, Marie-Laure Valdeyron, Alain Lachaux
Publikováno v:
Clinical Nutrition
Clinical Nutrition, Elsevier, 2016, 35 (2), pp.446-52. ⟨10.1016/j.clnu.2015.03.011⟩
Clinical Nutrition, Elsevier, 2016, 35 (2), pp.446-52. ⟨10.1016/j.clnu.2015.03.011⟩
International audience; BACKGROUND & AIMS: This retrospective study evaluated the impact of new organization during the moving to a new university pediatric hospital on the incidence of central catheter-related blood stream infections (CRBSIs) among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f76dfdf525dbaed870b410fea53bd85c
https://hal.archives-ouvertes.fr/hal-01850030
https://hal.archives-ouvertes.fr/hal-01850030