Zobrazeno 1 - 10 of 68 pro vyhledávání: '"H. Clouzeau"'
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Proton pump inhibitors are still overprescribed for hospitalized children
Autor: A, Arnoux, M, Bailhache, C, Tetard, L, Rebouissoux, H, Clouzeau, T, Lamireau, R, Enaud
Publikováno v: Archives de Pédiatrie. 29:258-262
The use of proton pump inhibitors has increased exponentially over the past 20 years. Several side effects have been reported and concerns exist about the consequences of long-term proton pump inhibitors on health, leading to limitation of their use.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c334047bb66d1ca8a53cb188e09b2bb
https://doi.org/10.1016/j.arcped.2022.02.004
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3
Increased Fecal Calprotectin is Associated with Worse Gastrointestinal Symptoms and Quality of Life Scores in Children with Cystic Fibrosis
Autor: Fabien Beaufils, Michael Fayon, Raphaël Enaud, Stéphanie Bui, Laurence Delhaes, Thierry Lamireau, Emmanuel Mas, H. Clouzeau, François Galode, M. Mittaine, Martin Addra
Publikováno v: Journal of Clinical Medicine, Vol 9, Iss 4080, p 4080 (2020)
Journal of Clinical Medicine
Journal of Clinical Medicine, MDPI, 2020, 9 (12), ⟨10.3390/jcm9124080⟩
Journal of Clinical Medicine, 2020, 9 (12), ⟨10.3390/jcm9124080⟩
Volume 9
Issue 12
In cystic fibrosis (CF), cystic fibrosis transmembrane regulator (CFTR) dysfunction leads to digestive disorders that promote intestinal inflammation and dysbiosis enhancing gastrointestinal symptoms. In pancreatic insufficiency CF patients, both int
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f4c50813dcd88f56a5d4d116731a948
https://www.mdpi.com/2077-0383/9/12/4080
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5
Intestinal Inflammation in Children with Cystic Fibrosis Is Associated with Crohn's-Like Microbiota Disturbances
Autor: Patrick Berger, Thomas Bazin, Thierry Lamireau, Christophe Hubert, Michael Fayon, Thomas Barnetche, Thierry Schaeverbeke, Laurence Delhaes, H. Clouzeau, Katarzyna B. Hooks, Aurélien Barré, Philippe Lehours, Cécile Bébéar, Stéphanie Bui, Macha Nikolski, Raphaël Enaud, Marie Massot
Publikováno v: Journal of Clinical Medicine, Vol 8, Iss 5, p 645 (2019)
Journal of Clinical Medicine
Volume 8
Issue 5
Journal of Clinical Medicine, MDPI, 2019, 8 (5), pp.645. ⟨10.3390/jcm8050645⟩
Journal of Clinical Medicine, 2019, 8 (5), pp.645. ⟨10.3390/jcm8050645⟩
Journal of Clinical Medicine 5 (8), 1-13. (2019)
Cystic fibrosis (CF) is a systemic genetic disease that leads to pulmonary and digestive disorders. In the majority of CF patients, the intestine is the site of chronic inflammation and microbiota disturbances. The link between gut inflammation and m
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54d8426d38a303e808932f3ffb769048
http://hdl.handle.net/20.500.12278/7805
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7
J Pediatr Gastroenterol Nutr
Autor: Anne-Laure Gominon, Michael Fayon, Julien Vergniol, H. Clouzeau, Stéphanie Bui, Thierry Lamireau, Raphaël Enaud, Eric Frison, Victor de Ledinghen, Jean-Baptiste Hiriart
Publikováno v: Journal of Pediatric Gastroenterology and Nutrition
Journal of Pediatric Gastroenterology and Nutrition, Lippincott, Williams & Wilkins, 2018, 66 (3), pp.455-460. ⟨10.1097/mpg.0000000000001822⟩
Objectives Cystic fibrosis-related liver disease (CFLD) can develop silently in early life and approximately 10% of children with cystic fibrosis (CF) become cirrhotic before adulthood. Clinical, biological, and ultrasound criteria used to define CFL
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e60a4b49213f26906511836dc17d2d6c
https://hal.archives-ouvertes.fr/hal-03194289
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8
[Liver disease, gastrointestinal complications, nutritional management and feeding disorders in pediatric cystic fibrosis]
Autor: D, Debray, E, Mas, A, Munck, M, Gérardin, H, Clouzeau
Publikováno v: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 23(12S)
In cystic fibrosis (CF), approximately 5-8% of the patients develop multilobular cirrhosis during the first decade of life. Annual screening (clinical examination, liver biochemistry, ultrasonography) is recommended in order to identify early signs o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4bc9e2c3e217106219071dab0eddbd0b
https://pubmed.ncbi.nlm.nih.gov/28231889
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9
Étude des scores de dénutrition chez l’enfant hospitalisé
Autor: O. Zaghet, R. Enaud, Thierry Lamireau, H. Clouzeau, Laurent Rebouissoux
Publikováno v: Nutrition Clinique et Métabolisme. 33:53
Discipline Clinique. Introduction et but de l’etude La denutrition en France, touche environ 10 % des enfants hospitalises avec pour consequence une augmentation du taux de morbi-mortalite, de la duree d’hospitalisation et donc son cout. Le but d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::463df7e83eee6bf162509e4959c18355
https://doi.org/10.1016/j.nupar.2019.01.316
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10
Évaluation de l’état nutritionnel chez l’enfant polyhandicapé (étude Polynut)
Autor: Thierry Lamireau, H. Clouzeau, R. Enaud, O. Zaghet, Laurent Rebouissoux
Publikováno v: Nutrition Clinique et Métabolisme. 33:53
Discipline Clinique. Introduction et but de l’etude On estime actuellement a 15 000 le nombre de patients polyhandicapes âges de moins de 20 ans en France. Les progres dans la prise en charge globale ont permis une augmentation de l’esperance de
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8f8762c963c9dd6390a7d80324a472cd
https://doi.org/10.1016/j.nupar.2019.01.317
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