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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.)
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불공정 이용 사례
  • 전자적·기계적 수단(다운로딩 프로그램, 웹 크롤러, 로봇, 매크로, RPA 등)을 이용한 대량 다운로드
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위반 시 제재
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'e-Article' searched 102results | List 1~20
Conference
2025 17th International Conference on Bioinformatics and Biomedical Technology (ICBBT) Bioinformatics and Biomedical Technology (ICBBT), 2025 17th International Conference on. :1-5 May, 2025
Academic Journal
In The American Journal of Human Genetics 6 July 2023 110(7):1098-1109
Binoy S; Center for Accessible Neuropsychology and Sagol School of Neuroscience, Tel Aviv University, Tel Aviv-Yafo, Israel.; Department of Occupational Therapy, Faculty of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.; Loyola Stritch School of Medicine, Chicago, IL, United States.; Montaser-Kouhsari L; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, United States.; Ponger P; Movement Disorders Division, Department of Neurology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.; Saban W; Center for Accessible Neuropsychology and Sagol School of Neuroscience, Tel Aviv University, Tel Aviv-Yafo, Israel.; Department of Occupational Therapy, Faculty of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.
Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101477954 Publication Model: eCollection Cited Medium: Print ISSN: 1662-5161 (Print) Linking ISSN: 16625161 NLM ISO Abbreviation: Front Hum Neurosci Subsets: PubMed not MEDLINE
Academic Journal
Tolonen JP; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Kavli Institute of Nanoscience Discovery, University of Oxford, Oxford, UK.; Parolin Schnekenberg R; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Oxford Center for Genomic Medicine, Oxford University Hospitals National Health Service Foundation Trust, University of Oxford, Oxford, UK.; McGowan S; Centre for Computational Biology, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.; Sims D; Centre for Computational Biology, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.; McEntagart M; South West Regional Genetics Service, St. George's University Hospitals, London, UK.; Elmslie F; South West Regional Genetics Service, St. George's University Hospitals, London, UK.; Shears D; Oxford Center for Genomic Medicine, Oxford University Hospitals National Health Service Foundation Trust, University of Oxford, Oxford, UK.; Stewart H; Oxford Center for Genomic Medicine, Oxford University Hospitals National Health Service Foundation Trust, University of Oxford, Oxford, UK.; Tofaris GK; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Kavli Institute of Nanoscience Discovery, University of Oxford, Oxford, UK.; Dabir T; Northern Ireland Regional Genetics Service, Belfast City Hospital, Belfast, UK.; Morrison PJ; Patrick G. Johnston Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, UK.; Johnson D; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.; Hadjivassiliou M; Department of Neurology, Royal Hallamshire Hospital, Sheffield Teaching Hospital NHS Foundation Trust, Sheffield, UK.; Ellard S; Exeter Genomics Laboratory, Royal Devon University Healthcare NHS Foundation Trust, UK.; Shaw-Smith C; Peninsula Clinical Genetics Service, Royal Devon University Hospital, Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.; Znaczko A; Peninsula Clinical Genetics Service, Royal Devon University Hospital, Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.; Dixit A; Department of Clinical Genetics, Nottingham University Hospitals NHS Trust, Nottingham, UK.; Suri M; Department of Clinical Genetics, Nottingham University Hospitals NHS Trust, Nottingham, UK.; Sarkar A; Department of Clinical Genetics, Nottingham University Hospitals NHS Trust, Nottingham, UK.; Harrison RE; Department of Clinical Genetics, Nottingham University Hospitals NHS Trust, Nottingham, UK.; Jones G; Department of Clinical Genetics, Nottingham University Hospitals NHS Trust, Nottingham, UK.; Houlden H; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, University College London, London, UK.; Ceravolo G; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, University College London, London, UK.; Unit of Pediatric Emergency, Department of Adult and Childhood Human Pathology, University Hospital of Messina, Messina, Italy.; Jarvis J; Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.; Williams J; Oxford Regional Genetics Laboratory, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.; Shanks ME; Oxford Regional Genetics Laboratory, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.; Clouston P; Oxford Regional Genetics Laboratory, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.; Rankin J; Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.; Blumkin L; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.; Pediatric Movement Disorders Service, Pediatric Neurology Unit, Edith Wolfson Medical Center, Holon, Israel.; Lerman-Sagie T; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.; Magen Center for Rare Diseases-Metabolic, Neurogenetic, Wolfson Medical Center, Holon, Israel.; Ponger P; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.; Movement Disorders Unit, Department of Neurology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.; Raskin S; Genetika Centro de Aconselhamento e Laboratório, Curitiba, Brazil.; Granath K; Research Unit of Clinical Medicine, Medical Research Center, Oulu University Hospital and University of Oulu, Oulu, Finland.; Uusimaa J; Research Unit of Clinical Medicine, Medical Research Center, Oulu University Hospital and University of Oulu, Oulu, Finland.; Conti H; All Wales Medical Genomics Service, Wrexham Maelor Hospital, Wrexham, UK.; McCann E; Liverpool Women's Hospital Foundation Trust, Liverpool, UK.; Joss S; West of Scotland Centre for Genomic Medicine, Queen Elizabeth University Hospital, Glasgow, UK.; Blakes AJM; Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Manchester Centre for Genomic Medicine, University of Manchester, St. Mary's Hospital, Manchester Academic Health Science Centre, Manchester, UK.; Metcalfe K; Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Manchester Centre for Genomic Medicine, University of Manchester, St. Mary's Hospital, Manchester Academic Health Science Centre, Manchester, UK.; Kingston H; Manchester Centre for Genomic Medicine, University of Manchester, St. Mary's Hospital, Manchester Academic Health Science Centre, Manchester, UK.; Bertoli M; Northern Genetics Service, International Centre for Life, Newcastle upon Tyne, UK.; Kneen R; Department of Neurology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.; Lynch SA; Department of Clinical Genetics, Children's Health Ireland (CHI) at Crumlin, Dublin, Ireland.; Martínez Albaladejo I; Neurology in Pediatrics, Hospital Santa Lucía, Murcia, Spain.; Moore AP; The Walton Centre NHS Foundation Trust, Liverpool, UK.; Jones WD; North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children, Great Ormond Street NHS Foundation Trust, London, UK.; Becker EBE; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Kavli Institute of Nanoscience Discovery, University of Oxford, Oxford, UK.; Németh AH; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Oxford Center for Genomic Medicine, Oxford University Hospitals National Health Service Foundation Trust, University of Oxford, Oxford, UK.
Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE
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