학술논문


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'학술논문' 에서 검색결과 1,629건 | 목록 1~20
Academic Journal
Coudert A; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Le Tanno P; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Dufour W; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Edery P; Hospices Civils de Lyon, Lyon, France.; Jacquette A; Service de génétique, CHICAM Site Alençon, Alençon, France.; Delplancq G; Unité de génétique constitutionnelle, service de biologie médicale, CH Versailles, Le Chesnay, France.; Chambon P; Laboratoire de Cytogénétique, CHU Rouen, Rouen, France.; Missirian C; Département de Génétique médicale, Hôpital de la Timone-Enfant, Assistance Publique Hôpitaux de Marseille, Hopital de la Timone, Marseille, France.; Caumes R; Service de génétique clinique, CHU Lille, Lille, France.; Faivre L; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, CHU Dijon, Dijon, France.; Callier P; Laboratoire de génétique chromosomique et moléculaire, CHU Dijon, Dijon, France.; Mosca AL; Laboratoire de génétique chromosomique et moléculaire, CHU Dijon, Dijon, France.; Marle N; Laboratoire de génétique chromosomique et moléculaire, CHU Dijon, Dijon, France.; Geneviève D; Université Montpellier, U1183, Service de Génétique Médicale, CHU Montpellier, Montpellier, France.; Lacombe D; Service de Génétique Médicale et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, CHU Bordeaux; INSERM U1211, Bordeaux, France.; Pebrel-Richard C; Service de Cytogénétique - Secteur constitutionnel, CHU Clermont-Ferrand, Clermont-Ferrand, France.; Redon S; Service de Génétique Médicale et Biologie de la Reproduction, CHU de Brest, Brest, France and Univ Brest, Inserm, EFS, UMR 1078, GGB, F-29200, Brest, France.; Touraine R; Service de génétique clinique chromosomique et moléculaire, CHU Saint-Etienne, Saint Etienne, France.; Fradin M; Service de génétique clinique, centre de référence maladies rares anomalies du développement CLAD-Ouest, CHU, Rennes, France.; Odent S; Service de génétique clinique, centre de référence maladies rares anomalies du développement CLAD-Ouest, CHU, Rennes, France.; Pasquier L; Service de génétique clinique, centre de référence maladies rares anomalies du développement CLAD-Ouest, CHU, Rennes, France.; Guichet A; Department of Genetics, University Hospital of Angers, Angers, France.; Mercier S; Université de Rennes 1, UEB, IFR 140, Faculté de Médecine, CNRS, UMR 6061, Institut Génétique et Développement de Rennes, Rennes, France.; Medical Genetics, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Nizon M; Medical Genetics, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Isidor B; Medical Genetics, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Vincent M; Medical Genetics, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Le Guillou Horn XM; LabCom I3M-Dactim mis/LMA CNRS 7348, Université de Poitiers, Poitiers, France.; Egloff M; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Schaefer E; Hôpitaux Universitaires de Strasbourg, Service de Génétique Médicale, Strasbourg, France.; Guerrot AM; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Ruaud L; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Chemaly N; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Nadeau G; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Coutton C; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Dieterich K; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France KDieterich@chu-grenoble.fr.
Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Academic Journal
Barcia G; Service de Médecine Génomique, Necker Enfants-Malades Hospital, APHP, Université de Paris, Paris, France.; INSERM U1163, Imagine Institute for Rare Diseases, Université de Paris, Paris, France.; Necker Enfants-Malades Hospital, Membre of EPICARE, Reference Center for Rare Epilepsies, Paris, France.; Chemaly N; Necker Enfants-Malades Hospital, Membre of EPICARE, Reference Center for Rare Epilepsies, Paris, France.; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.; Gobin-Limballe S; Service de Médecine Génomique, Necker Enfants-Malades Hospital, APHP, Université de Paris, Paris, France.; Losito E; Necker Enfants-Malades Hospital, Membre of EPICARE, Reference Center for Rare Epilepsies, Paris, France.; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.; Department of Clinical Neurophysiology, Necker Enfants-Malades Hospital, APHP, Paris, France.; Aubart M; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.; Sarda E; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.; Assouline Z; Service de Médecine Génomique, Necker Enfants-Malades Hospital, APHP, Université de Paris, Paris, France.; INSERM U1163, Imagine Institute for Rare Diseases, Université de Paris, Paris, France.; Plante-Bordeneuve P; Service de Médecine Génomique, Necker Enfants-Malades Hospital, APHP, Université de Paris, Paris, France.; INSERM U1163, Imagine Institute for Rare Diseases, Université de Paris, Paris, France.; Hully M; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.; Barrois R; Necker Enfants-Malades Hospital, Membre of EPICARE, Reference Center for Rare Epilepsies, Paris, France.; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.; Department of Clinical Neurophysiology, Necker Enfants-Malades Hospital, APHP, Paris, France.; Barnerias C; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.; Sareidaki D; Necker Enfants-Malades Hospital, Membre of EPICARE, Reference Center for Rare Epilepsies, Paris, France.; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.; Zeitoun DC; Necker Enfants-Malades Hospital, Membre of EPICARE, Reference Center for Rare Epilepsies, Paris, France.; Department of Clinical Neurophysiology, Necker Enfants-Malades Hospital, APHP, Paris, France.; Eisermann M; Necker Enfants-Malades Hospital, Membre of EPICARE, Reference Center for Rare Epilepsies, Paris, France.; Department of Clinical Neurophysiology, Necker Enfants-Malades Hospital, APHP, Paris, France.; Fourrage C; Service de Médecine Génomique, Necker Enfants-Malades Hospital, APHP, Université de Paris, Paris, France.; Hanein S; INSERM U1163, Imagine Institute for Rare Diseases, Université de Paris, Paris, France.; Rio M; Service de Médecine Génomique, Necker Enfants-Malades Hospital, APHP, Université de Paris, Paris, France.; Boddaert N; Department of Pediatric Radiology, Necker Enfants-Malades Hospital, APHP, Paris, France.; Desguerre I; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.; Kaminska A; Necker Enfants-Malades Hospital, Membre of EPICARE, Reference Center for Rare Epilepsies, Paris, France.; Department of Clinical Neurophysiology, Necker Enfants-Malades Hospital, APHP, Paris, France.; Steffann J; Service de Médecine Génomique, Necker Enfants-Malades Hospital, APHP, Université de Paris, Paris, France.; INSERM U1163, Imagine Institute for Rare Diseases, Université de Paris, Paris, France.; Nabbout R; INSERM U1163, Imagine Institute for Rare Diseases, Université de Paris, Paris, France.; Necker Enfants-Malades Hospital, Membre of EPICARE, Reference Center for Rare Epilepsies, Paris, France.; Department of Pediatric Neurology, Necker Enfants-Malades Hospital Université de Paris Cité, Paris, France.
Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101692036 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2470-9239 (Electronic) Linking ISSN: 24709239 NLM ISO Abbreviation: Epilepsia Open Subsets: MEDLINE
Academic Journal
Bakouh N; Translational Research in Neuroscience Lab, Institut Imagine, Université Paris Cité, INSERM U1163, 75015 Paris, France.; Castaño-Martín R; Translational Research in Neuroscience Lab, Institut Imagine, Université Paris Cité, INSERM U1163, 75015 Paris, France.; Metais A; Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, INSERM U1266, 75014 Paris, France.; Service de Neuropathologie, GHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, F-75014 Paris, France.; Dan EL; STAR-UBB Institute, Babeş-Bolyai University, 400084 Cluj-Napoca, Romania.; Balducci E; Department of Pediatric Neurosurgery Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Department of Pediatric Neurology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Chhuon C; INSERM US24, Proteomic platform, SFR Necker, 75015 Paris, France.; Lepicka J; INSERM US24, Proteomic platform, SFR Necker, 75015 Paris, France.; Barcia G; Translational Research in Neuroscience Lab, Institut Imagine, Université Paris Cité, INSERM U1163, 75015 Paris, France.; Department of Pediatric Neurosurgery Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Department of Pediatric Neurology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Losito E; Department of Pediatric Neurosurgery Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Department of Pediatric Neurology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Lourdel S; Cordeliers Research Center, INSERM, Sorbonne University, Paris Cité University, 75006 Paris, France.; CNRS EMR 8228-Laboratory of Renal Physiology and Tubulopathies, Université de Paris Cité, Centre de Recherche des Cordeliers, 75006 Paris, France.; Planelles G; Cordeliers Research Center, INSERM, Sorbonne University, Paris Cité University, 75006 Paris, France.; CNRS EMR 8228-Laboratory of Renal Physiology and Tubulopathies, Université de Paris Cité, Centre de Recherche des Cordeliers, 75006 Paris, France.; Muresan RC; STAR-UBB Institute, Babeş-Bolyai University, 400084 Cluj-Napoca, Romania.; Moca VV; STAR-UBB Institute, Babeş-Bolyai University, 400084 Cluj-Napoca, Romania.; Kaminska A; Department of Pediatric Neurosurgery Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Department of Pediatric Neurology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Bourgeois M; Department of Pediatric Neurosurgery Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Department of Pediatric Neurology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Chemaly N; Department of Pediatric Neurosurgery Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Department of Pediatric Neurology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Rguez Y; Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, INSERM U1266, 75014 Paris, France.; Auvin S; Hôpital Robert Debré, Assistance Publique Hôpitaux de Paris, 75019 Paris, France.; Huberfeld G; Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, INSERM U1266, 75014 Paris, France.; Varlet P; Institute of Psychiatry and Neuroscience of Paris (IPNP), Université Paris Cité, INSERM U1266, 75014 Paris, France.; Service de Neuropathologie, GHU-Paris Psychiatrie et Neurosciences, Hôpital Sainte Anne, F-75014 Paris, France.; Asnafi V; Department of Pediatric Neurosurgery Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Department of Pediatric Neurology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Guerrera IC; INSERM US24, Proteomic platform, SFR Necker, 75015 Paris, France.; Kabashi E; Translational Research in Neuroscience Lab, Institut Imagine, Université Paris Cité, INSERM U1163, 75015 Paris, France.; Nabbout R; Translational Research in Neuroscience Lab, Institut Imagine, Université Paris Cité, INSERM U1163, 75015 Paris, France.; Department of Pediatric Neurosurgery Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Department of Pediatric Neurology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Ciura S; Translational Research in Neuroscience Lab, Institut Imagine, Université Paris Cité, INSERM U1163, 75015 Paris, France.; Blauwblomme T; Translational Research in Neuroscience Lab, Institut Imagine, Université Paris Cité, INSERM U1163, 75015 Paris, France.; Department of Pediatric Neurosurgery Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.; Department of Pediatric Neurology, Hôpital Necker, Assistance Publique Hôpitaux de Paris, 75015 Paris, France.
Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE
Academic Journal
Chemaly N; Department of Pediatric Neurology, Reference Center for Rare Epilepsies, Hôpital Necker-Enfants Malades, Member of ERN EpiCARE, Paris, France.; Kuchenbuch M; Department of Pediatric Neurology, Reference Center for Rare Epilepsies, Hôpital Necker-Enfants Malades, Member of ERN EpiCARE, Paris, France.; Université de Lorraine, CNRS, IMoPA, F-54000 Nancy, France.; Service de Pédiatrie, Reference Center for Rare Epilepsies, Member of ERN EpiCARE, Université de Lorraine, CHRU-Nancy, F-54000 Nancy, France.; Losito E; Department of Pediatric Neurology, Reference Center for Rare Epilepsies, Hôpital Necker-Enfants Malades, Member of ERN EpiCARE, Paris, France.; Kaminska A; Unit of Pediatric Neurophysiology, Necker Enfants Malades Hospital, AP-HP, Paris, France.; Coste-Zeitoun D; Unit of Pediatric Neurophysiology, Necker Enfants Malades Hospital, AP-HP, Paris, France.; Barcia G; Université de Paris Cité, Paris, France.; Desguerre I; Department of Pediatric Neurology, Reference Center for Rare Epilepsies, Hôpital Necker-Enfants Malades, Member of ERN EpiCARE, Paris, France.; Hully M; Department of Pediatric Neurology, Reference Center for Rare Epilepsies, Hôpital Necker-Enfants Malades, Member of ERN EpiCARE, Paris, France.; Nabbout R; Department of Pediatric Neurology, Reference Center for Rare Epilepsies, Hôpital Necker-Enfants Malades, Member of ERN EpiCARE, Paris, France.; Université de Paris Cité, Paris, France.; Laboratory of Translational Research for Neurological Disorders, INSERM MR1163, Imagine Institute, Paris, France.
Publisher: Wiley Country of Publication: England NLM ID: 9506311 Publication Model: Print Cited Medium: Internet ISSN: 1468-1331 (Electronic) Linking ISSN: 13515101 NLM ISO Abbreviation: Eur J Neurol Subsets: MEDLINE
Academic Journal
Scorrano G; Department of Pediatric Neurology, Reference Centre for Rare Epilepsies, Necker Enfants Malades University Hospital, AP-HP, Université Paris Cité, Paris, France.; Barcia G; Department of Genetics, Necker Enfants Malades University Hospital, AP-HP, Université Paris Cité, Paris, France.; Laboratory of Translational Research for Neurological Disorders, INSERM UMR 1163, Imagine Institute, Paris, France.; Champ J; Laboratoire de Biologie Médicale Multi-Sites SeqOIA Assistance-Publique, Paris, France.; Courtin T; Department of Genetics, Necker Enfants Malades University Hospital, AP-HP, Université Paris Cité, Paris, France.; Boddaert N; Department of Pediatric Radiology, Necker Enfants Malades Hospital, AP-HP, Université Paris Cité, Paris, France.; Kaminska A; Clinical Neurophysiology Department, Necker Enfants Malades University Hospital, AP-HP, Université Paris Cité, Paris, France.; Chemaly N; Department of Pediatric Neurology, Reference Centre for Rare Epilepsies, Necker Enfants Malades University Hospital, AP-HP, Université Paris Cité, Paris, France.; Nabbout R; Department of Pediatric Neurology, Reference Centre for Rare Epilepsies, Necker Enfants Malades University Hospital, AP-HP, Université Paris Cité, Paris, France.; Department of Genetics, Necker Enfants Malades University Hospital, AP-HP, Université Paris Cité, Paris, France.; Laboratory of Translational Research for Neurological Disorders, INSERM UMR 1163, Imagine Institute, Paris, France.
Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101692036 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2470-9239 (Electronic) Linking ISSN: 24709239 NLM ISO Abbreviation: Epilepsia Open Subsets: MEDLINE
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[검색어] Chemaly, N.
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