Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Edouard Bardou–Jacquet"'
Autor:
Astrid Imbert, Pierre-Jean Gavlovsky, Jean-Paul Judor, Edouard Bardou-Jacquet, Laure Elkrief, Adrien Lannes, Christine Silvain, Mathieu Schnee, Florence Tanne, Caroline Chevalier, Fabienne Vavasseur, Marion Khaldi, Sophie Brouard, Jean-François Mosnier, Jérôme Gournay, Sophie Conchon, Amédée Renand
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Relapse after immunosuppression (IS) treatment withdrawal is frequent in patients with Autoimmune Hepatitis (AIH), and non-invasive biomarkers predictive of this risk are lacking. We assessed the frequency of circulating T cell subsets as po
Externí odkaz:
https://doaj.org/article/f249c91e0f4045b49ea2ccb0dae5c652
Autor:
Pierre Allaume, Noémie Rabilloud, Bruno Turlin, Edouard Bardou-Jacquet, Olivier Loréal, Julien Calderaro, Zine-Eddine Khene, Oscar Acosta, Renaud De Crevoisier, Nathalie Rioux-Leclercq, Thierry Pecot, Solène-Florence Kammerer-Jacquet
Publikováno v:
Diagnostics, Vol 13, Iss 10, p 1799 (2023)
Background: Artificial Intelligence (AI)-based Deep Neural Networks (DNNs) can handle a wide range of applications in image analysis, ranging from automated segmentation to diagnostic and prediction. As such, they have revolutionized healthcare, incl
Externí odkaz:
https://doaj.org/article/67621dd34d684f06bf1ca92a03c31e58
Autor:
Hervé Lobbes, Quitterie Reynaud, Sabine Mainbourg, Claire Savy-Stortz, Martine Ropert, Edouard Bardou-Jacquet, Stéphane Durupt
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Aceruloplasminemia is a rare autosomal recessive inherited disorder. Mutations in the ceruloplasmin gene cause depressed ferroxidase activity leading to iron accumulation. The clinical phenotype is highly variable: anemia, retinopathy, diabetes melli
Externí odkaz:
https://doaj.org/article/a9bf0aa8908248cd9ce2285c83a381fc
Autor:
Maëna Le Corvec, Caroline Jezequel, Valérie Monbet, Nadia Fatih, Frédéric Charpentier, Hugues Tariel, Catherine Boussard-Plédel, Bruno Bureau, Olivier Loréal, Olivier Sire, Edouard Bardou-Jacquet
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0185997 (2017)
Prognostic tests are critical in the management of patients with cirrhosis and ascites. Biological tests or scores perform poorly in that situation. Mid-infrared fibre evanescent wave spectroscopy (MIR-FEWS) which allows for global serum metabolic pr
Externí odkaz:
https://doaj.org/article/6b6f40a5d18944cc8ba9ebd0814ce698
Autor:
L. Tom Vlasveld, Roel Janssen, Edouard Bardou-Jacquet, Hanka Venselaar, Houda Hamdi-Roze, Hal Drakesmith, Dorine W. Swinkels
Publikováno v:
Pharmaceuticals, Vol 12, Iss 3, p 132 (2019)
Iron overloading disorders linked to mutations in ferroportin have diverse phenotypes in vivo, and the effects of mutations on ferroportin in vitro range from loss of function (LOF) to gain of function (GOF) with hepcidin resistance. We reviewed 359
Externí odkaz:
https://doaj.org/article/272b1b18cc874fa695a4194c670e34d3
Autor:
Caroline Jézéquel, Fabrice Lainé, Bruno Laviolle, Anita Kiani, Edouard Bardou-Jacquet, Yves Deugnier
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128530 (2015)
Hepatic iron is increased in dysmetabolic iron overload syndrome (DIOS). Whether this reflects elevated body iron stores is still debated. The study was aimed at assessing body iron stores in DIOS patients by calculating the amount of mobilized iron
Externí odkaz:
https://doaj.org/article/d34b187b586b4b59b15622d57828331a
Autor:
Caroline Kannengiesser, Anne-Marie Jouanolle, Gilles Hetet, Annick Mosser, Françoise Muzeau, Dominique Henry, Edouard Bardou-Jacquet, Martine Mornet, Pierre Brissot, Yves Deugnier, Bernard Grandchamp, Carole Beaumont
Publikováno v:
Haematologica, Vol 94, Iss 3 (2009)
Background Elevated serum ferritin levels are frequently encountered in clinical situations and once iron overload or inflammation has been ruled out, many cases remain unexplained. Genetic causes of hyperferritinemia associated to early cataract inc
Externí odkaz:
https://doaj.org/article/06c64fc91f304069becefeb258335c2d
Autor:
Baptiste Giguet, Arnaud Bruneel, Sandrine Vuillaumier Barrot, Romain Moirand, Edouard Bardou Jacquet
Publikováno v:
JHEP Reports, Vol 4, Iss 7, Pp 100494- (2022)
Externí odkaz:
https://doaj.org/article/2b0dd645a27442eabf1f5260ac484964
Autor:
Oumnia Masrour, Edouard Bardou-Jacquet
Publikováno v:
Nutrition Clinique et Métabolisme. 37:72-76
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::119b5cd0cb97b1b392bf27bbf20f214a
https://doi.org/10.1016/j.nupar.2022.12.003
https://doi.org/10.1016/j.nupar.2022.12.003
Autor:
Christelle Nilles, Mickael Alexandre Obadia, Rodolphe Sobesky, Jérôme Dumortier, Olivier Guillaud, Chloé Laurencin, Caroline Moreau, Claire Vanlemmens, Fabienne Ory‐Magne, Victor de Ledinghen, Edouard Bardou‐Jacquet, Frederique Fluchère, Corinne Collet, Nouzha Oussedik‐Djebrani, France Woimant, Aurélia Poujois
Publikováno v:
Movement Disorders. 38:321-332
Wilson's disease (WD) is usually diagnosed in children and young adults; limited data exist on late-onset forms.The aim was to characterize the clinical and paraclinical presentations, therapeutic management, and outcomes in patients with late-onset
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aab5a738f2123e609d3ee2e8a3a24425
https://doi.org/10.1002/mds.29292
https://doi.org/10.1002/mds.29292