Výsledky vyhledávání - "Martine Ropert Bouchet"

[Inorganic element determinations: Arguments for their reimbursement by French National system of health insurance]

Autor: Josiane Arnaud, Souleiman El Balkhi, Jean Pierre Goullé, Nouredine Sadeg, Robert Garnier, Ma’atem Béatrice Fofou-Caillierez, Bénédicte Lelièvre, Nicolas Beauval, Martine Ropert Bouchet, Muriel Bost, Sarah Romain

Publikováno v: Annales de Biologie Clinique
Annales de Biologie Clinique, John Libbey Eurotext, 2021, ⟨10.1684/abc.2021.1654⟩

International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35c77a762f60b673a62e5c5099f60382
https://hal.univ-angers.fr/hal-03283799

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Intérêts d’inclure la détermination d’éléments inorganiques à la nomenclature des actes de biologie médicale

Autor: Jean Pierre Goullé, Ma’atem Béatrice Fofou-Callierez, Nicolas Beauval, Robert Garnier, Martine Ropert Bouchet, Sarah Romain, Muriel Bost, Souleiman El Balkhi, Bénédicte Lelièvre, Josiane Arnaud, Nourédine Sadeg

Publikováno v: Toxicologie Analytique et Clinique
Toxicologie Analytique et Clinique, Elsevier, 2020, 32, pp.33-61. ⟨10.1016/j.toxac.2019.07.005⟩

Resume Objectif L’objectif de cette revue est de demontrer que la determination d’elements inorganiques ne figurant pas actuellement a la nomenclature des actes de biologie medicale (NABM), peut etre essentielle au diagnostic et a la prise en cha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3d51a580e5aaa0afba56c82bec9d382
https://hal.archives-ouvertes.fr/hal-03490085

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Iron metabolism imbalance at the time of listing increases overall and infectious mortality after liver transplantation

Autor: Karim Boudjema, Caroline Jezequel, Amandine Landrieux, Christophe Camus, Thomas Uguen, Dominique Guyader, Michel Rayar, Edouard Bardou-Jacquet, Pauline Houssel-Debry, Elodie Fallet, Martine Ropert-Bouchet, L. Legros

Publikováno v: World Journal of Gastroenterology
World Journal of Gastroenterology, Baishideng Publishing Group Co. Limited, 2020, 26 (16), pp.1938-1949. ⟨10.3748/wjg.v26.i16.1938⟩

International audience; BACKGROUND Liver transplantation (LT) is the best treatment for patients with liver cancer or end stage cirrhosis, but it is still associated with a significant mortality. Therefore identifying factors associated with mortalit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30fbf71456168dde06c9247ff3b5f94d
https://hal.archives-ouvertes.fr/hal-02885884

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External quality assessment schemes for inorganic elements in the clinical laboratory: Lessons from the OELM scheme

Autor: Martine Ropert-Bouchet, Josiane Arnaud, Montserrat Ventura Alemany, Carla Siebelder, Valeria Patriarca, Liesbeth Schröer-Janssen, Montserrat González-Estecha, Marieke Te Winkel, Cas Weykamp, Béatrice Ma'atem Fofou-Caillierez, Marina Patriarca, MªCarmen González Gómez, Irene De Graaf

Publikováno v: Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS). 59

Measurements of inorganic elements in clinical laboratories produce results used for the diagnosis, the treatment and the monitoring of deficiencies or overloads. The main objective of External Quality Assessment Schemes is to verify, on a regular fr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24a7b69ad86f0c4a33048fde912f7ecc
https://pubmed.ncbi.nlm.nih.gov/31810809

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Hepcidin: immunoanalytic characteristics

Autor: Séverine Cunat, Benoit Rucheton, Thibaud Lefebvre, Jérôme Vialaret, Constance Delaby, Hubert de Verneuil, Patricia Aguilar-Martinez, Fleur Wolff, Sylvain Lehmann, Martine Ropert-Bouchet

Publikováno v: Annales de Biologie Clinique
Annales de Biologie Clinique, John Libbey Eurotext, 2018, 76 (6), pp.705-715. ⟨10.1684/abc.2018.1382⟩

International audience; Hepcidin has progressively become essential in clinical practice for the diagnosis and follow-up of a large spectrum of diseases. Anyway, its own biochemical and structural characteristics have complicated and delayed the acqu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5f6393f704ce36e2ca6716876107468
https://pubmed.ncbi.nlm.nih.gov/30257815

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Hereditary hemochromatosis HFE: regulatory and economic aspects of diagnosis and medical management

Autor: Henri Michel, Martine Ropert-Bouchet, Isabelle Fajardy

Publikováno v: Annales de biologie clinique. 70:405-411

L’hemochromatose genetique HFE est une affection de longue duree (ALD n o 17 – Maladies metaboliques et hereditaires) qui reste la premiere maladie genetique en France (60 % de l’ensemble des maladies genetiques). Elle est parfaitement codifiee

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b3c42115c25246f83a7cec100f26cba
https://doi.org/10.1684/abc.2012.0731

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Over-expression of wild-type and mutant HFE in a human melanocytic cell line reveals an intracellular bridge between MHC class I pathway and transferrin iron uptake

Autor: Magali Orhant, Jean Mosser, Pascal Loyer, Jean-Yves Le Gall, Agnès Thénié, Martine Ropert-Bouchet, Stéphanie Lohyer, Patricia Fergelot

Publikováno v: Biology of the Cell. 95:243-255

Hereditary hemochromatosis (HH) is a frequent recessive disorder of iron metabolism characterised by systemic iron overload. In Northern Europe, more than 90% of HH patients are homozygous for a mis-sense mutation (C282Y) in the HFE1 gene product. Th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7174fb335d7abe2e797c4fd5f7b957fc
https://doi.org/10.1016/s0248-4900(03)00057-1

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Iron Overload in Mice Expressing HFE Exclusively in the Intestinal Villi Provides Evidence That HFE Regulates a Functional Cross-Talk between Crypt and Villi Enterocytes

Autor: Seiamak Bahram, Hélène Jouan, Emmanuelle Abgueguen, Susan Gilfillan, Jean-Yves Le Gall, Magali Orhant, Martine Ropert-Bouchet, Patricia Fergelot, Gisèle Grimber, Mirjana Radosavljevic, Jean Mosser

Publikováno v: Blood Cells, Molecules, and Diseases. 28:348-360

Hereditary hemochromatosis (HH), a common autosomal recessive disorder due to a mutation in HFE, which encodes an atypical MHC class I glycoprotein, is characterized by excessive absorption of dietary iron. Little is known however of the apparently c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11c376cf83982dd6ee60dc37f6493878
https://doi.org/10.1006/bcmd.2002.0512

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