부산대학교 도서관

Bigotte M; FORGETTING Team-Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR 5292, Claude Bernard Lyon 1 University, 69675 Bron, France.; Gimenez M; FORGETTING Team-Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR 5292, Claude Bernard Lyon 1 University, 69675 Bron, France.; Gavoille A; Service de neurologie, sclérose en plaques, pathologies de la myéline et neuroinflammation, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, 69500 Bron, France.; Service de Biostatistique-Bioinformatique, Hospices Civils de Lyon, 69495 Pierre-Bénitem, France.; Deligiannopoulou A; FORGETTING Team-Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR 5292, Claude Bernard Lyon 1 University, 69675 Bron, France.; El Hajj A; FORGETTING Team-Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR 5292, Claude Bernard Lyon 1 University, 69675 Bron, France.; Croze S; Profilexpert, Genomic and Microgenomic Service, Claude Bernard Lyon 1 University, SFR santé LYON-EST, UCBL-INSERM US 7-CNRS UMS 3453, 69008 Lyon, France.; Goumaidi A; Viroscan3D SAS, 69008 Lyon, France.; Malleret G; FORGETTING Team-Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR 5292, Claude Bernard Lyon 1 University, 69675 Bron, France.; Salin P; FORGETTING Team-Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR 5292, Claude Bernard Lyon 1 University, 69675 Bron, France.; Giraudon P; FORGETTING Team-Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR 5292, Claude Bernard Lyon 1 University, 69675 Bron, France.; Ruiz A; FORGETTING Team-Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR 5292, Claude Bernard Lyon 1 University, 69675 Bron, France.; Marignier R; FORGETTING Team-Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR 5292, Claude Bernard Lyon 1 University, 69675 Bron, France.; Service de neurologie, sclérose en plaques, pathologies de la myéline et neuroinflammation, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, 69500 Bron, France.; Centre de référence des maladies inflammatoires rares du cerveau et de la moelle (MIRCEM), 69500 Bron, France.

Publisher: Oxford University Press Country of Publication: England NLM ID: 101755125 Publication Model: eCollection Cited Medium: Internet ISSN: 2632-1297 (Electronic) Linking ISSN: 26321297 NLM ISO Abbreviation: Brain Commun Subsets: PubMed not MEDLINE

Poggio E; Department of Biology, University of Padua, Padua, Italy.; Barazzuol L; Department of Biomedical Sciences, University of Padua, Padua, Italy.; Salmaso A; Department of Biology, University of Padua, Padua, Italy.; Milani C; Department of Biology, University of Padua, Padua, Italy.; Deligiannopoulou A; Department of Biomedical Sciences, University of Padua, Padua, Italy.; Cazorla ÁG; European Reference Network for Hereditary Metabolic Diseases (MetabERN), Madrid, Spain; Neurometabolic Unit and Synaptic Metabolism Laboratory, Neurology Department Sant Joan de Déu Hospital, IPR, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Jang SS; Seoul National University (SNU) College of Medicine, Seoul, South Korea.; Juliá-Palacios N; Neurology Department, Neurometabolic Unit, Institut de Recerca, CIBERER and MetabERN, Hospital Sant Joan de Déu, Barcelona, Spain.; Keren B; APHP.Sorbonne Université, Department of Medical Genetics, Pitié-Salpêtrière University Hospital, and Centre de Référence Maladies Rares Déficiences Intellectuelles de Causes Rares, Paris, France.; Kopajtich R; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.; Lynch SA; Department of Clinical Genetics, Temple Street Children's University Hospital, Dublin, Ireland.; Mignot C; APHP.Sorbonne Université, Department of Medical Genetics, Pitié-Salpêtrière University Hospital, and Centre de Référence Maladies Rares Déficiences Intellectuelles de Causes Rares, Paris, France.; Moorwood C; Exeter Genomics Laboratory, Royal Devon University Healthcare NHS Foundation Trust, Exeter, United Kingdom.; Neuhofer C; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.; Nigro V; Department of Precision Medicine, University of Campania, Luigi Vanvitelli, Napoli, Italy.; Oostra A; Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Ghent University Hospital, Ghent, Belgium.; Prokisch H; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.; Saillour V; Laboratoire de biologie médicale multisites Seqoia - FMG2025, Paris, France.; Schuermans N; Center for Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium; Department of Biomolecular Medicine, Ghent University Hospital, Ghent, Belgium.; Torella A; Department of Precision Medicine, University of Campania, Luigi Vanvitelli, Napoli, Italy.; Verloo P; Department of Pediatric Neurology, Center for Inherited Metabolic Disorders and metabERN, University Hospital Ghent, Ghent, Belgium.; Yazbeck E; Pediatric Neurology Department, Assistance Publique-Hôpitaux de Paris, Hôpitaux Universitaires Paris Saclay, Bicêtre Hospital, Le Kremlin Bicêtre, France.; Zollino M; Unit of Medical Genetics, Section of Genomic Medicine, Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.; Jech R; Department of Neurology, Charles University in Prague, 1st Faculty of Medicine and General University Hospital in Prague, Prague, Czech Republic.; Winkelmann J; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany; Munich Cluster for Systems Neurology, SyNergy, Munich, Germany.; Necpal J; 2nd Department of Neurology, Faculty of Medicine, Comenius University, Bratislava, Slovakia; Department of Neurology, Zvolen Hospital, Zvolen, Slovakia.; Calì T; Department of Biomedical Sciences, University of Padua, Padua, Italy; Centro Studi per la Neurodegenerazione (CESNE), University of Padua, Padua, Italy; Neuroscience Center (PNC), University of Padua, Padua, Italy.; Brini M; Department of Biology, University of Padua, Padua, Italy; Centro Studi per la Neurodegenerazione (CESNE), University of Padua, Padua, Italy.; Zech M; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany; Institute for Advanced Study, Technical University of Munich, Garching, Germany. Electronic address: michael.zech@mri.tum.de.

Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Tidière, Morgane; Thevenot, Xavier; Deligiannopoulou, Adamantia; Douay, Guillaume; Whipple, Mylisa; Siberchicot, Aurélie; Gaillard, Jean-Michel; Lemaître, Jean-François

Proceedings: Biological Sciences, 2018 Sep 01. 285(1886), 1-6.

Deligiannopoulou, A.; Karalis, V.

Physica Medica. 104:S59-S59

Morgane Tidière; Xavier Thevenot; Adamantia Deligiannopoulou; Guillaume Douay; Mylisa Whipple; Aurélie Siberchicot; Jean-Michel Gaillard; Jean-François Lemaître

Proceedings of the Royal Society B: Biological Sciences. 285:20181479

Tidière, Morgane; Thevenot, Xavier; Deligiannopoulou, Adamantia; Douay, Guillaume; Mylisa Whipple; Siberchicot, Aurélie; Jean-Michel Gaillard; Jean-François Lemaître