검색어 : 통합검색[Devos Emmanuelle]
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- Distribution of <i>Clostridioides difficile</i> ribotypes and sequence types across humans, animals and food in 13 European countries
- Rupnik, Maja; Viprey, Virginie; Janezic, Sandra; Tkalec, Valerija; Davis, Georgina; Sente, Bé atrice; Devos, Nathalie; Muller, Bruno H.; Santiago-Allexant, Emmanuelle; Cleuziat, Philippe; Wilcox, Mark; Davies, Kerrie; National Laboratory for Health, Environment and Food, Maribor, Slovenia; Leeds Institute of Medical Research, University of Leeds, Leeds, UK; National Laboratory for Health, Environment and Food, Maribor, Slovenia; National Laboratory for Health, Environment and Food, Maribor, Slovenia; Leeds Institute of Medical Research, University of Leeds, Leeds, UK; GSK Vaccines, Rixensart, Belgium; GSK Vaccines, Rixensart, Belgium; bioMé rieux, Marcy-l'Etoile, France; bioMé rieux, Marcy-l'Etoile, France; bioMé rieux, Marcy-l'Etoile, France; European Study Group Clostridioidies difficile, ESCMID; European Study Group Clostridioidies difficile, ESCMID; (Emerging microbes & infections, v.13, 2024, pp.2427804)
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- Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex
- Brun, Jennifer; Chiaverini, Christine; Devos, Caroline; Leclerc-Mercier, Sté phanie; Mazereeuw, Juliette; Bourrat, Emmanuelle; Maruani, Annabel; Mallet, Sté phanie; Abasq, Claire; Phan, Alice; Vabres, Pierre; Martin, Ludovic; Bodemer, Christine; Lagrange, Sylvie; Lacour, Jean-Philippe; Reference Centre for Inherited Epidermolysis Bullosa, Archet 2 Hospital, University of Nice Sophia Antipolis, Nice, France; Reference Centre for Inherited Epidermolysis Bullosa, Archet 2 Hospital, University of Nice Sophia Antipolis, Nice, France; Department of Algology, Archet 2 Hospital, University of Nice Sophia Antipolis, Nice, France; Reference Centre for Cutaneous Rare Diseases (MAGEC), Necker Enfants Malades Hospital, University Paris Descartes, Institut Imagine, APHP, Paris, France; Reference Centre of Rare Diseases of the Skin, Larrey Hospital, Toulouse, France; Reference Centre for Cutaneous Rare Diseases (MAGEC), Saint-Louis Hospital, Paris, France; Department of Dermatology, CHRU de Tours, Tours, France; Department of Dermatology, |La Timone Hospital, Marseille, France; Department of Dermatology, CHRU de Brest, Brest, France; Department of Dermatology, Claude Bernard-Lyon 1 University and Hospices Civils de Lyon, Lyon, France; Department of Dermatology, Dijon Univ; (Orphanet journal of rare diseases, v.12, 2017, pp.119)
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- MUC1 Expression in Papillary Thyroid Carcinoma Is Associated with <i>BRAF</i> Mutation and Lymph Node Metastasis; the Latter is the Most Important Risk Factor of Relapse
- Renaud, Florence; Gnemmi, Viviane; Devos, Patrick; Aubert, Sé bastien; Cré pin, Michel; Coppin, Lucie; Ramdane, Nassima; Bouchindhomme, Brigitte; d'Herbomez, Michelle; Van Seuningen, Isabelle; Do Cao, Christine; Pattou, Franç ois; Carnaille, Bruno; Pigny, Pascal; Wé meau, Jean-Louis; Leteurtre, Emmanuelle; Institute of Pathology, Lille University Hospital, Lille, France.; Institute of Pathology, Lille University Hospital, Lille, France.; Faculty of Medicine, North of France University, Lille, France.; Institute of Pathology, Lille University Hospital, Lille, France.; Molecular Oncology and Genetics, Lille University Hospital, Lille, France.; Inserm, UMR837, team 5 “Mucins, epithelial differentiation and carcinogenesis,” Jean-Pierre Aubert Research Center, Lille, France.; Department of Research, EA2694, Lille University Hospital, Lille, France.; Institute of Pathology, Lille University Hospital, Lille, France.; Faculty of Medicine, North of France University, Lille, France.; Inserm, UMR837, team 5 “Mucins, epithelial differentiation and carcinogenesis,” Jean-Pierre Aubert Research Center, Lille, France.; Endocrinology and Metabolic Diseases, Lille University Hospital, Lille, France.; Faculty of Medicine, North of France University, Lille, France.; Faculty of Medicine,; (Thyroid : official journal of the American Thyroid Association, v.24, 2014, pp.1375-1384)
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- Spectrum of movement disorders associated with glutaric aciduria type 1: A study of 16 patients
- Gitiaux, Cyril; Roze, Emmanuel; Kinugawa, Kiyoka; Flamand-Rouviè re, Constance; Boddaert, Nathalie; Apartis, Emmanuelle; Valayannopoulos, Vassili; Touati, Guy; Motte, Jacques; Devos, David; Mention, Karine; Dobbelaere, Dries; Rodriguez, Diana; Roubertie, Agathe; Chabrol, Brigitte; Feillet, Franç ois; Vidailhet, Marie; Bahi-Buisson, Nadia; Université Paris-Descartes, Service de Neurologie Pé diatrique et Maladies mé taboliques, Hô pital Necker Enfants Malades, AP-HP, Paris, France; Pô le des Maladies du Systè me Nerveux, Fé dé ration de Neurologie, groupe hospitalier Pitié -Salpê triè re, AP-HP, Paris, France; Pô le des Maladies du Systè me Nerveux, Fé dé ration de Neurologie, groupe hospitalier Pitié -Salpê triè re, AP-HP, Paris, France; Service de Neurologie, Bicê tre, AP-HP, Paris, France; Université Paris-Descartes, Service de Radiologie Pé diatrique, Hô pital Necker Enfants Malades, AP-HP, Paris, France; Service de Neurophysiologie Hô pital Saint-Antoine, AP-HP, Paris, France; Université Paris-Descartes, Service de Neurologie Pé diatrique et Maladies mé taboliques, Hô pital Necker Enfants Malades, AP-HP, Paris, France; Université Paris-Descartes, Se; (Movement disorders : official journal of the Movement Disorder Society, v.23, 2008, pp.2392-2397)
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- The ubiquitin-like modifier FAT10 is induced in MASLD and impairs the lipid-regulatory activity of PPARα
- Clavreul, Ludivine; Bernard, Lucie; Cotte, Alexia K.; Hennuyer, Nathalie; Bourouh, Cyril; Devos, Claire; Helleboid, Audrey; Haas, Joel T.; Verrijken, An; Gheeraert, Cé line; Derudas, Bruno; Guille, Loï c; Chevalier, Julie; Eeckhoute, Jé rô me; Vallez, Emmanuelle; Dorchies, Emilie; Van Gaal, Luc; Lassailly, Guillaume; Francque, Sven; Staels, Bart; Paumelle, Ré jane; ; (Metabolism : clinical and experimental, v.151, 2024, pp.155720)
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- Early clindamycin for bacterial vaginosis in pregnancy (PREMEVA): a multicentre, double-blind, randomised controlled trial
- Subtil, Damien; Brabant, Gilles; Tilloy, Emma; Devos, Patrick; Canis, Fré dé rique; Fruchart, Annie; Bissinger, Marie-Christine; Dugimont, Jean-Charles; Nolf, Catherine; Hacot, Christophe; Gautier, Sophie; Chantrel, Jé rô me; Jousse, Marielle; Desseauve, David; Plennevaux, Jean Louis; Delaeter, Christine; Deghilage, Sylvie; Personne, Anne; Joyez, Emmanuelle; Guinard, Elisabeth; Kipnis, Eric; Faure, Karine; Grandbastien, Bruno; Ancel, Pierre-Yves; Goffinet, Franç ois; Dessein, Rodrigue; Pô le Femme Mè re Nouveau-né , Centre Hospitalier Universitaire de Lille; Service de Gyné cologie-Obsté trique, Groupement des Hô pitaux de l'Institut Catholique de Lille, Hô pital Saint Vincent; Pô le Femme Mè re Nouveau-né , Centre Hospitalier Universitaire de Lille; Epidé miologie et Qualité des soins (EA 2694), Université de Lille; Laboratoire de Biologie Mé dicale, Centre Hospitalier de Valenciennes; Institut de Microbiologie, Centre Hospitalier Universitaire de Lille; Institut de Microbiologie, Centre Hospitalier Universitaire de Lille; Association des Biologistes des Ré gions Nord Picardie; Association des Biologistes des Ré gions Nord Picardie; As; (The Lancet, v.392, 2018, pp.2171-2179)
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- Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression
- Mignot, Cyril; Apartis, Emmanuelle; Durr, Alexandra; Marques Lourenç o, Charles; Charles, Perrine; Devos, David; Moreau, Caroline; de Lonlay, Pascale; Drouot, Nathalie; Burglen, Lydie; Kempf, Nadine; Nourisson, Elsa; Chantot-Bastaraud, Sandra; Lebre, Anne-Sophie; Rio, Marlè ne; Chaix, Yves; Bieth, Eric; Roze, Emmanuel; Bonnet, Isabelle; Canaple, Sandrine; Rastel, Coralie; Brice, Alexis; Rö tig, Agnè s; Desguerre, Isabelle; Tranchant, Christine; Koenig, Michel; Anheim, Mathieu; Department of Genetics and Cytogenetics, AP-HP, Hô pital de la Salpê triè re, Paris, F-75013, France; Department of Physiology, APHP, Saint-Antoine Hospital, Paris, France; Department of Genetics and Cytogenetics, AP-HP, Hô pital de la Salpê triè re, Paris, F-75013, France; Department of Neuroscience and Behaviour Sciences, School of Medicine of Ribeirã o Preto, University of Sao Polo, Sao Polo, Brazil; Department of Genetics and Cytogenetics, AP-HP, Hô pital de la Salpê triè re, Paris, F-75013, France; Department of Medical Pharmacology & Department of Movement Disorders and Neurology, EA 4559/1046, Lille Nord de France University, CHU Lille, Lille, France; Department of Movement Disorders and Neurology, EA 4559/1046, Lille Nord de France University, CHU Lille, Lille, France; Inserm U781, Imagine Institut des Maladies Gé né tiques, Université Paris Descartes et Centre de Ré fé rence des Maladie; (Orphanet journal of rare diseases, v.8, 2013, pp.173-173)
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