학술논문


EBSCO Discovery Service
발행년
-
(예 : 2010-2015)
전자자료 공정이용 안내

우리 대학 도서관에서 구독·제공하는 모든 전자자료(데이터베이스, 전자저널, 전자책 등)는 국내외 저작권법과 출판사와의 라이선스 계약에 따라 엄격하게 보호를 받고 있습니다.
전자자료의 비정상적 이용은 출판사로부터의 경고, 서비스 차단, 손해배상 청구 등 학교 전체에 심각한 불이익을 초래할 수 있으므로, 아래의 공정이용 지침을 반드시 준수해 주시기 바랍니다.

공정이용 지침
  • 전자자료는 개인의 학습·교육·연구 목적의 비영리적 사용에 한하여 이용할 수 있습니다.
  • 합리적인 수준의 다운로드 및 출력만 허용됩니다. (일반적으로 동일 PC에서 동일 출판사의 논문을 1일 30건 이하 다운로드할 것을 권장하며, 출판사별 기준에 따라 다를 수 있습니다.)
  • 출판사에서 제공한 논문의 URL을 수업 관련 웹사이트에 게재할 수 있으나, 출판사 원문 파일 자체를 복제·배포해서는 안 됩니다.
  • 본인의 ID/PW를 타인에게 제공하지 말고, 도용되지 않도록 철저히 관리해 주시기 바랍니다.
불공정 이용 사례
  • 전자적·기계적 수단(다운로딩 프로그램, 웹 크롤러, 로봇, 매크로, RPA 등)을 이용한 대량 다운로드
  • 동일 컴퓨터 또는 동일 IP에서 단시간 내 다수의 원문을 집중적으로 다운로드하거나, 전권(whole issue) 다운로드
  • 저장·출력한 자료를 타인에게 배포하거나 개인 블로그·웹하드 등에 업로드
  • 상업적·영리적 목적으로 자료를 전송·복제·활용
  • ID/PW를 타인에게 양도하거나 타인 계정을 도용하여 이용
  • EndNote, Mendeley 등 서지관리 프로그램의 Find Full Text 기능을 이용한 대량 다운로드
  • 출판사 콘텐츠를 생성형 AI 시스템에서 활용하는 행위(업로드, 개발, 학습, 프로그래밍, 개선 또는 강화 등)
위반 시 제재
  • 출판사에 의한 해당 IP 또는 기관 전체 접속 차단
  • 출판사 배상 요구 시 위반자 개인이 배상 책임 부담
'학술논문' 에서 검색결과 2건 | 목록 1~20
Academic Journal
Guerrini R; Neuroscience Department, Children's Hospital Meyer, University of Florence, Florence, Italy.; Mei D; Neuroscience Department, Children's Hospital Meyer, University of Florence, Florence, Italy.; Kerti-Szigeti K; Institute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.; Pepe S; Department of Experimental Medicine, University of Genoa, Italy.; Center for Synaptic Neuroscience and Technology, Istituto Italiano di Tecnologia, Genova, Italy.; Koenig MK; Department of Pediatrics, Division of Child and Adolescent Neurology, The University of Texas McGovern Medical School, Houston, TX, USA.; Von Allmen G; Department of Pediatrics, Division of Child and Adolescent Neurology, The University of Texas McGovern Medical School, Houston, TX, USA.; Cho MT; GeneDx, Gaithersburg, MD 20877, USA.; McDonald K; Pediatric Neurology, University of Mississippi Medical Center, Jackson, MS, USA.; Baker J; Genetics and Genomics, Children's Minnesota, Minneapolis, MN, USA.; Bhambhani V; Genetics and Genomics, Children's Minnesota, Minneapolis, MN, USA.; Powis Z; Ambry Genetics, Aliso Viejo, CA, USA.; Rodan L; Division of Genetics and Genomics and Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.; Nabbout R; Reference Centre for Rare Epilepsies, Department of Genetics, Necker Enfants Malades Hospital, APHP, member of ERN EpiCARE, Université de Paris, Paris, France.; Barcia G; Reference Centre for Rare Epilepsies, Department of Genetics, Necker Enfants Malades Hospital, APHP, member of ERN EpiCARE, Université de Paris, Paris, France.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Bacino CA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Mignot C; APHP, Sorbonne Université, Départément de Génétique, Centre de Référence Déficiences Intellectuelles de Causes Rares, Paris, France.; Institut du Cerveau (ICM), UMR S 1127, Inserm U1127, CNRS UMR 7225, Sorbonne Université, 75013 Paris, France.; Power LH; Pediatric Neurology, Stead Family Department of Pediatrics, University of Iowa Stead Family Children's Hospital, Iowa City, IA, USA.; Harris CJ; Department of Pediatric Genetics, University of Missouri Medical Center, Columbia, MO 65212, USA.; Marjanovic D; Danish Epilepsy Centre Filadelfia, Adult Neurology, Dianalund, Denmark.; Møller RS; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center Filadelfia, Dianalund, Denmark.; Department of Regional Health Services, University of Southern Denmark, Odense, Denmark.; Hammer TB; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center Filadelfia, Dianalund, Denmark.; Keski Filppula R; Department of Clinical Genetics, Oulu University Hospital, Medical Research Center Oulu and PEDEGO Research Unit, University of Oulu, Oulu, Finland.; Vieira P; Clinic for Children and Adolescents, Oulu University Hospital, Medical Research Center Oulu and PEDEGO Research Unit, University of Oulu, Oulu, Finland.; Hildebrandt C; Division of Genetics and Genomics, Metabolism Program, Boston Children's Hospital, Boston, MA, USA.; Sacharow S; Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.; Maragliano L; Center for Synaptic Neuroscience and Technology, Istituto Italiano di Tecnologia, Genova, Italy.; Department of Life and Environmental Sciences, Polytechnic University of Marche, Ancona, Italy.; Benfenati F; Center for Synaptic Neuroscience and Technology, Istituto Italiano di Tecnologia, Genova, Italy.; IRCCS Ospedale Policlinico San Martino, Genova, Italy.; Lachlan K; Wessex Clinical Genetics Service, University Hospital Southampton NHS Foundation Trust, Southampton, UK.; Human Development and Health, Faculty of Medicine University of Southampton, Southampton, UK.; Benneche A; Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway.; Petit F; CHU Lille, Clinique de Génétique, F-59000 Lille, France.; de Sainte Agathe JM; Laboratoire de Biologie Médicale Multi Sites SeqOIA, Laboratoire de Médecine Génomique, APHP. Sorbonne Université, Paris, France.; Hallinan B; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.; Division of Child Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.; Si Y; GeneDx, Gaithersburg, MD 20877, USA.; Wentzensen IM; GeneDx, Gaithersburg, MD 20877, USA.; Zou F; GeneDx, Gaithersburg, MD 20877, USA.; Narayanan V; Neurogenomics Division, Center for Rare Childhood Disorders, Translational Genomics Research Institute (TGen), Phoenix, AZ 85012, USA.; Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.; Boncristiano A; Neuroscience Department, Children's Hospital Meyer, University of Florence, Florence, Italy.; la Marca G; Newborn Screening, Clinical Chemistry and Pharmacology Laboratory, Meyer Children's University Hospital, Florence, Italy.; Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy.; Kato M; Department of Pediatrics, Showa University School of Medicine and Epilepsy Medical Center, Showa University Hospital, Tokyo, Japan.; Anderson K; Founder and Research Liaison, 'ATP6V1A Families' Facebook group.; Barba C; Neuroscience Department, Children's Hospital Meyer, University of Florence, Florence, Italy.; Sturiale L; CNR, Institute for Polymers, Composites and Biomaterials, IPCB, 95126 Catania, Italy.; Garozzo D; CNR, Institute for Polymers, Composites and Biomaterials, IPCB, 95126 Catania, Italy.; Bei R; Department of Clinical Sciences and Translational Medicine, University of Rome 'Tor Vergata', Rome, Italy.; Masuelli L; Department of Experimental Medicine, University of Rome 'Sapienza', Rome, Italy.; Conti V; Neuroscience Department, Children's Hospital Meyer, University of Florence, Florence, Italy.; Novarino G; Institute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.; Fassio A; Department of Experimental Medicine, University of Genoa, Italy.; IRCCS Ospedale Policlinico San Martino, Genova, Italy.
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
검색 결과 제한하기
제한된 항목
[AR] de Sainte Agathe, Jean Madeleine
발행연도 제한
-
학술DB(Database Provider)
저널명(출판물, Title)
출판사(Publisher)
자료유형(Source Type)
주제어
언어