학술논문
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'학술논문'
에서 검색결과 173건 | 목록
1~20
Academic Journal
Piet MM; Department of Child Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, European Reference Network EpiCARE, Heidelberglaan 100, Utrecht, CX 3584, The Netherlands; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, European Reference Network EpiCARE, Heidelberglaan 100, Utrecht, CX 3584, The Netherlands.; Braun KPJ; Department of Child Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, European Reference Network EpiCARE, Heidelberglaan 100, Utrecht, CX 3584, The Netherlands.; Koeleman BPC; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, European Reference Network EpiCARE, Heidelberglaan 100, Utrecht, CX 3584, The Netherlands.; Stevelink R; Department of Child Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, European Reference Network EpiCARE, Heidelberglaan 100, Utrecht, CX 3584, The Netherlands; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, European Reference Network EpiCARE, Heidelberglaan 100, Utrecht, CX 3584, The Netherlands. Electronic address: R.Stevelink-4@umcutrecht.nl.
Publisher: Elsevier Trends Journals Country of Publication: England NLM ID: 8507085 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 0168-9525 (Print) Linking ISSN: 01689525 NLM ISO Abbreviation: Trends Genet Subsets: MEDLINE
Academic Journal
Stevelink R; Department of Child Neurology, University Medical Center Utrecht, member of European Reference Network EpiCARE, Utrecht, the Netherlands.; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, member of European Reference Network EpiCARE, Utrecht, the Netherlands.; Piet MM; Department of Child Neurology, University Medical Center Utrecht, member of European Reference Network EpiCARE, Utrecht, the Netherlands.; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, member of European Reference Network EpiCARE, Utrecht, the Netherlands.; Bos Y; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, member of European Reference Network EpiCARE, Utrecht, the Netherlands.; van 't Slot R; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, member of European Reference Network EpiCARE, Utrecht, the Netherlands.; Braun KPJ; Department of Child Neurology, University Medical Center Utrecht, member of European Reference Network EpiCARE, Utrecht, the Netherlands.; Koeleman BPC; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, member of European Reference Network EpiCARE, Utrecht, the Netherlands.
Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE
Academic Journal
Sanders MWCB; Department of Child Neurology, University Medical Center Utrecht Brain Center, Utrecht, the Netherlands.; Koeleman BPC; Department of Genetics, Center for Molecular Medicine, University Medical Center, Utrecht, the Netherlands.; Brilstra EH; Department of Genetics, Center for Molecular Medicine, University Medical Center, Utrecht, the Netherlands.; Jansen FE; Department of Child Neurology, University Medical Center Utrecht Brain Center, Utrecht, the Netherlands.; Baldassari S; Hôpital de la Pitié Salpêtrière, Institut du Cerveau-Paris Brain Institute, Sorbonne Université, Paris, France.; Chipaux M; Department of Pediatric Neurosurgery, Rothschild Foundation Hospital, Paris, France.; Sim NS; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.; Ko A; Division of Pediatric Neurology, Department of Pediatrics, Pediatric Epilepsy Clinics, Severance Children's Hospital, Seoul, Republic of Korea.; Kang HC; Division of Pediatric Neurology, Department of Pediatrics, Pediatric Epilepsy Clinics, Severance Children's Hospital, Seoul, Republic of Korea.; Blümcke I; Department of Neuropathology, University Hospital Erlangen, Erlangen, Germany.; Lal D; Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, United States.; Cologne Center for Genomics, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.; Baulac S; Hôpital de la Pitié Salpêtrière, Institut du Cerveau-Paris Brain Institute, Sorbonne Université, Paris, France.; Lee JH; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.; Aronica E; Department of (Neuro)Pathology, Amsterdam Neuroscience, Amsterdam University Medical Center, Amsterdam, the Netherlands.; Stichting Epilepsie Instellingen Nederland, Heemstede, the Netherlands.; Braun KPJ; Department of Child Neurology, University Medical Center Utrecht Brain Center, Utrecht, the Netherlands.
Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE
Academic Journal
van Oirsouw ASE; Graduate School of Life Sciences, Utrecht University, Heidelberglaan 8, 3584 CS Utrecht, The Netherlands.; UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, Utrecht 3584 CX, The Netherlands.; Department of Genetics, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, Utrecht 3584 CX, The Netherlands.; Hadders MA; Oncode Institute and Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Universiteitsweg 100, Utrecht 3584 CG, The Netherlands.; Koetsier M; Department of Genetics, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, Utrecht 3584 CX, The Netherlands.; Peters EDJ; Department of Genetics, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, Utrecht 3584 CX, The Netherlands.; Assia Batzir N; Pediatric Genetics Unit, Schneider Children's Medical Centerl, 14 Kaplan St., Petah Tikva 4920235, Israel.; Barakat TS; Department of Clinical Genetics, Erasmus MC University Medical Center, Dr. Molewaterplein 50, Rotterdam 3000 CA, The Netherlands.; Baralle D; Human Development and Health, Faculty of Medicine, University of Southampton, Southampton General Hospital, Tremona Road, Southampton SO16 6YD, United Kingdom.; Beil A; Department of Pediatrics, Division of Pediatric Genetics, Metabolism, and Genomic Medicine, University of Michigan, 1500 E. Medical Center Drive, Ann Arbor, MI 48109, United States.; Bonnet-Dupeyron MN; Consultations de Génétique, Centre Hospitalier de Valence, 179 Bd Maréchal Juin, Valence 26000, France.; Boone PM; Division of Genetics and Genomics, Boston Children's Hospital, 300 Longwood Ave., Boston, MA 02115, United States.; Bouman A; Department of Clinical Genetics, Erasmus MC University Medical Center, Dr. Molewaterplein 50, Rotterdam 3000 CA, The Netherlands.; Carere DA; GeneDx, LLC, 207 Perry Parkway, Gaithersburg, MD 20877, United States.; Cogne B; Nantes Université, Centre Hospitalier Universitaire de Nantes, Service de Génétique médicale 1, place Alexis Ricordeau, 44093 Nantes, France.; Dunnington L; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, 6431 Fannin Street, MSB 3144B, Houston, TX 77030, United States.; Farach LS; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, 6431 Fannin Street, MSB 3144B, Houston, TX 77030, United States.; Genetti CA; Division of Genetics and Genomics, Boston Children's Hospital, 300 Longwood Ave., Boston, MA 02115, United States.; Manton Center for Orphan Disease Research, Boston Children's Hospital, 300 Longwood Ave., Boston, MA 02115, United States.; Isidor B; Nantes Université, Centre Hospitalier Universitaire de Nantes, Service de Génétique médicale 1, place Alexis Ricordeau, 44093 Nantes, France.; Januel L; Department of Genetics, Hospices Civils de Lyon, 3 Quai des Célestins, Lyon 69002, France.; Joshi A; St. George's University of London & St. George's University Hospitals NHS Foundation Trust, Blackshaw Road, Tooting, London SW17 0QT, United Kingdom.; Lahiri N; St. George's University of London & St. George's University Hospitals NHS Foundation Trust, Blackshaw Road, Tooting, London SW17 0QT, United Kingdom.; Lee KN; Department of Pediatrics, Division of Pediatric Genetics, Metabolism, and Genomic Medicine, University of Michigan, 1500 E. Medical Center Drive, Ann Arbor, MI 48109, United States.; Maya I; Recanati Genetics Institute, Beilinson Hospital, Rabin Medical Center, 39 Jabotinski St., Petah Tikva 49100, Israel.; Gray Faculty of Medical and Health Sciences, Tel Aviv University, 35 Klatzkin St, Tel Aviv 6997801, Israel.; McEntagart M; St. George's University of London & St. George's University Hospitals NHS Foundation Trust, Blackshaw Road, Tooting, London SW17 0QT, United Kingdom.; Northrup H; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, 6431 Fannin Street, MSB 3144B, Houston, TX 77030, United States.; Pujalte M; Department of Genetics, Hospices Civils de Lyon, 3 Quai des Célestins, Lyon 69002, France.; Richardson K; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, 6431 Fannin Street, MSB 3144B, Houston, TX 77030, United States.; Walker S; Genomics England, Translational Genomics, One Canada Square, London E14 5AB, United Kingdom.; Koeleman BPC; UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, Utrecht 3584 CX, The Netherlands.; Alders M; Department of Human Genetics, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam 1105 AZ, The Netherlands.; Reproduction and Development Research Institute, Meibergdreef 9, Amsterdam 1105 AZ, The Netherlands.; van Jaarsveld RH; Department of Genetics, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, Utrecht 3584 CX, The Netherlands.; Oegema R; Department of Genetics, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, Utrecht 3584 CX, The Netherlands.
Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Academic Journal
de Kovel, Carolien G F; Brilstra, Eva H; van Kempen, Marjan J A; Van't Slot, Ruben; Nijman, Isaac J; Afawi, Zaid; De Jonghe, Peter; Djémié, Tania; Guerrini, Renzo; Hardies, Katia; Helbig, Ingo; Hendrickx, Rik; Kanaan, Moine; Kramer, Uri; Lehesjoki, Anna-Elina E; Lemke, Johannes R; Marini, Carla; Mei, Davide; Møller, Rikke S; Pendziwiat, Manuela; Stamberger, Hannah; Suls, Arvid; Weckhuysen, S; Balling, R; Barisic, N; Baulac, S; Caglayan, HS; Craiu, DC; Depienne, C; Gormley, P; Hjalgrim, H; Hoffman-Zacharska, D; Jähn, J; Klein, KM; Komarek, V; LeGuern, E; Lerche, H; May, P; Muhle, H; Pal, D; Palotie, A; Rosenow, F; Selmer, K; Serratosa, JM; Sisodiya, SM; Stephani, U; Sterbova, K; Striano, P; Talvik, T; van Haelst, M; Verbeek, N; von Spiczak, S; Weber, YG; Koeleman, BPC.
Mol Genet Genomic Med
EuroEPINOMICS RES Consortium 2016, 'Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients', Molecular Genetics and Genomic Medicine, vol. 4, no. 5, pp. 568-580. https://doi.org/10.1002/mgg3.235
Molecular Genetics & Genomic Medicine
Molecular genetics & genomic medicine
de Kovel, C G F, Brilstra, E H, van Kempen, M J A, Van't Slot, R, Nijman, I J, Afawi, Z, De Jonghe, P, Djémié, T, Guerrini, R, Hardies, K, Helbig, I, Hendrickx, R, Kanaan, M, Kramer, U, Lehesjoki, A-E E, Lemke, J R, Marini, C, Mei, D, Møller, R S, Pendziwiat, M, Stamberger, H, Suls, A, Weckhuysen, S,Koeleman , B P C & EuroEPINOMICS RES Consortium 2016, ' Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients ', Molecular Genetics & Genomic Medicine, vol. 4, no. 5, pp. 568-580 . https://doi.org/10.1002/mgg3.235
EuroEPINOMICS RES Consortium 2016, 'Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients', Molecular Genetics and Genomic Medicine, vol. 4, no. 5, pp. 568-580. https://doi.org/10.1002/mgg3.235
Molecular Genetics & Genomic Medicine
Molecular genetics & genomic medicine
de Kovel, C G F, Brilstra, E H, van Kempen, M J A, Van't Slot, R, Nijman, I J, Afawi, Z, De Jonghe, P, Djémié, T, Guerrini, R, Hardies, K, Helbig, I, Hendrickx, R, Kanaan, M, Kramer, U, Lehesjoki, A-E E, Lemke, J R, Marini, C, Mei, D, Møller, R S, Pendziwiat, M, Stamberger, H, Suls, A, Weckhuysen, S,
Academic Journal
Perucca, P; Anderson, A; Jazayeri, D; Hitchcock, A; Graham, J; Todaro, M; Tomson, T; Battino, D; Perucca, E; Martinez Ferri, M; Rochtus, A; Lagae, L; Canevini, MP; Zambrelli, E; Campbell, E; Koeleman, BPC; Scheffer, IE; Berkovic, SF; Kwan, P; Sisodiya, SM; Goldstein, DB; Petrovski, S; Craig, J; Vajda, FJE; O'Brien, TJ; EpiPGX and EPIGEN Consortia, .
Academic Journal
Leu C; Department of Neurology, McGovern Medical School, UTHealth Houston, Houston, TX, USA; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH, USA. Electronic address: Costin.Leu@uth.tmc.edu.; Avbersek A; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK; Chalfont Centre for Epilepsy, Chalfont-St-Peter, Buckinghamshire, UK.; Stevelink R; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands; Department of Child Neurology, UMC Utrecht Brain Centers, University Medical Center Utrecht, Utrecht, the Netherlands.; Custodio HM; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK; Chalfont Centre for Epilepsy, Chalfont-St-Peter, Buckinghamshire, UK.; Chen S; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.; Speed D; Center for Quantitative Genetics and Genomics, Aarhus University, Aarhus, Denmark.; Bennett CA; Department of Medicine, Epilepsy Research Centre, Austin Health, University of Melbourne, Melbourne, Australia.; Jonsson L; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Unnsteinsdóttir U; deCODE Genetics/Amgen Inc., Reykjavik, Iceland.; Jorgensen AL; Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.; Cavalleri GL; Department of Molecular and Cellular Therapeutics, Royal College of Surgeons in Ireland, Dublin, Ireland; FutureNeuro Research Centre, Science Foundation Ireland, Dublin, Ireland.; Delanty N; FutureNeuro Research Centre, Science Foundation Ireland, Dublin, Ireland; Department of Neurology, Beaumont Hospital, Dublin, Ireland.; Craig JJ; Department of Neurology, Belfast Health and Social Care Trust, Belfast, UK.; Depondt C; Department of Neurology, CUB Erasmus Hospital, Free University of Brussels, University Hospital Brussels, Brussels, Belgium.; Johnson MR; Department of Brain Sciences, Faculty of Medicine, Imperial College London, London, UK.; Koeleman BPC; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; Hassanin E; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Luxembourg.; Omidvar ME; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.; Krause R; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Luxembourg.; Lerche H; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.; Marson AG; Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, UK; The Walton Centre NHS Foundation Trust, Liverpool, UK; Liverpool Health Partners, Liverpool, UK.; O'Brien TJ; Departments of Medicine and Neurology, Royal Melbourne Hospital, University of Melbourne, Parkville, Australia; Departments of Neuroscience and Neurology, The School of Translational Medicine, Monash University and the Alfred Hospital, Melbourne, Australia.; Sander JW; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK; Chalfont Centre for Epilepsy, Chalfont-St-Peter, Buckinghamshire, UK; Stichting Epilepsie Instellingen Nederland (SEIN), Heemstede, the Netherlands; Department of Neurology, West China Hospital, Sichuan University, Chengdu, China.; Sills GJ; School of Life Sciences, University of Glasgow, Glasgow, UK.; Striano P; Paediatric Neurology and Muscular Diseases Unit, IRCCS 'G. Gaslini' Institute, Genova, Italy; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genova, Italy.; Zara F; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genova, Italy; Laboratory of Neurogenetics and Neuroscience, IRCCS 'G. Gaslini' Institute, Genova, Italy.; Stefansson H; deCODE Genetics/Amgen Inc., Reykjavik, Iceland.; Stefansson K; deCODE Genetics/Amgen Inc., Reykjavik, Iceland; Faculty of Medicine, University of Iceland, Reykjavik, Iceland.; May P; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Luxembourg.; Neale BM; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.; Lal D; Department of Neurology, McGovern Medical School, UTHealth Houston, Houston, TX, USA; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH, USA; Center of Neurogenetics, UTHealth Houston, TX, USA; Stanley Center for Psychiatric Research, Broad Institute of Harvard and M.I.T, Cambridge, MA, USA.; Berkovic SF; Department of Medicine, Epilepsy Research Centre, Austin Health, University of Melbourne, Melbourne, Australia; Department of Neurology, Austin Health, Heidelberg, Australia.; Sisodiya SM; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK; Chalfont Centre for Epilepsy, Chalfont-St-Peter, Buckinghamshire, UK. Electronic address: s.sisodiya@ucl.ac.uk.
Publisher: Elsevier B.V Country of Publication: Netherlands NLM ID: 101647039 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2352-3964 (Electronic) Linking ISSN: 23523964 NLM ISO Abbreviation: EBioMedicine Subsets: MEDLINE
Academic Journal
Nijboer TCW; UMCU Brain Center and Center of Excellence for Rehabilitation Medicine, University Medical Center Utrecht and De Hoogstraat Rehabilitation, Utrecht, The Netherlands.; Department of Experimental Psychology and Helmholtz Institute, Utrecht University, Utrecht, The Netherlands.; Hessel EVS; UMCU Brain Center and Center of Excellence for Rehabilitation Medicine, University Medical Center Utrecht and De Hoogstraat Rehabilitation, Utrecht, The Netherlands.; Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; van Haaften GW; Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; van Zandvoort MJ; Department of Experimental Psychology and Helmholtz Institute, Utrecht University, Utrecht, The Netherlands.; van der Spek PJ; Department of Pathology, Erasmus Medical Center Rotterdam, Rotterdam, the Netherlands.; Troelstra C; Department of Pathology, Erasmus Medical Center Rotterdam, Rotterdam, the Netherlands.; de Kovel CGF; Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Koeleman BPC; Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; van der Zwaag B; Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Brilstra EH; Department of Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Burbach JPH; UMCU Brain Center, Department of Translational Neuroscience, University Medical Center Utrecht, Utrecht, the Netherlands.
Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
Academic Journal
Martins Custodio H; University College London Queen Square Institute of Neurology, Department of Clinical and Experimental Epilepsy, London, WC1N 3BG, UK.; Chalfont Centre for Epilepsy, Chalfont St Peter SL9 0RJ, UK.; Clayton LM; University College London Queen Square Institute of Neurology, Department of Clinical and Experimental Epilepsy, London, WC1N 3BG, UK.; Chalfont Centre for Epilepsy, Chalfont St Peter SL9 0RJ, UK.; Bellampalli R; University College London Queen Square Institute of Neurology, Department of Clinical and Experimental Epilepsy, London, WC1N 3BG, UK.; Chalfont Centre for Epilepsy, Chalfont St Peter SL9 0RJ, UK.; Pagni S; University College London Queen Square Institute of Neurology, Department of Clinical and Experimental Epilepsy, London, WC1N 3BG, UK.; Chalfont Centre for Epilepsy, Chalfont St Peter SL9 0RJ, UK.; Silvennoinen K; University College London Queen Square Institute of Neurology, Department of Clinical and Experimental Epilepsy, London, WC1N 3BG, UK.; Chalfont Centre for Epilepsy, Chalfont St Peter SL9 0RJ, UK.; Kuopio Epilepsy Center, Neurocenter, Kuopio University Hospital, Kuopio 70210, Finland.; Caswell R; Exeter Genomics Laboratory, Royal Devon University Healthcare NHS Foundation Trust, Exeter EX2 5DW, UK.; Brunklaus A; Paediatric Neuroscience Research Group, Royal Hospital for Children, Glasgow G51 4TF, UK.; Institute of Health and Wellbeing, University of Glasgow, Glasgow G12 8TB, UK.; Guerrini R; Neuroscience Department, Meyer Children's Hospital IRCSS, University of Florence, 50139 Florence, Italy.; Koeleman BPC; Department of Genetics, University Medical Centre Utrecht, 3584CX Utrecht, The Netherlands.; Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig 04103, Germany.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig 04103, Germany.; Møller RS; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, DK-4293 Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, DK-5230 Odense, Denmark.; Scheffer IE; Epilepsy Research Centre, Florey Institute, University of Melbourne, Austin Health and Royal Children's Hospital, Melbourne, VIC 3084, Australia.; Murdoch Children's Research Institute, Parkville, VIC 3052, Australia.; Weckhuysen S; Applied and Translational Neurogenomics Group, VIB Centre for Molecular Neurology, VIB, Antwerp 2610, Belgium.; Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, Antwerp 2650, Belgium.; Department of Neurology, University Hospital Antwerp, Antwerp 2650, Belgium.; µNEURO Research Centre of Excellence, University of Antwerp, Antwerp 2610, Belgium.; Zara F; Unit of Medical Genetics, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.; Department of Neurosciences Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, 16132 Genoa, Italy.; Zuberi S; Paediatric Neuroscience Research Group, Royal Hospital for Children, Glasgow G51 4TF, UK.; Institute of Health and Wellbeing, University of Glasgow, Glasgow G12 8TB, UK.; Kuchenbaecker K; University College London Division of Psychiatry, London W1T 7BN, UK.; Balestrini S; University College London Queen Square Institute of Neurology, Department of Clinical and Experimental Epilepsy, London, WC1N 3BG, UK.; Chalfont Centre for Epilepsy, Chalfont St Peter SL9 0RJ, UK.; Neuroscience Department, Meyer Children's Hospital IRCSS, University of Florence, 50139 Florence, Italy.; Mills JD; University College London Queen Square Institute of Neurology, Department of Clinical and Experimental Epilepsy, London, WC1N 3BG, UK.; Chalfont Centre for Epilepsy, Chalfont St Peter SL9 0RJ, UK.; Amsterdam UMC, University of Amsterdam, Department of (Neuro)Pathology, Amsterdam Neuroscience, 1105 AZ Amsterdam, The Netherlands.; Sisodiya SM; University College London Queen Square Institute of Neurology, Department of Clinical and Experimental Epilepsy, London, WC1N 3BG, UK.; Chalfont Centre for Epilepsy, Chalfont St Peter SL9 0RJ, UK.
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
Dirkx N; Applied & Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium. nina.dirkx@uantwerpen.vib.be.; Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium. nina.dirkx@uantwerpen.vib.be.; Weuring WJ; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584 CX, The Netherlands. woutweuring2@gmail.com.; De Vriendt E; Applied & Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Smal N; Applied & Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.; van de Vondervoort J; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584 CX, The Netherlands.; van 't Slot R; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584 CX, The Netherlands.; Koetsier M; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584 CX, The Netherlands.; Zonnekein N; Applied & Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.; De Pooter T; Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.; Neuromics Support Facility, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Weckhuysen S; Applied & Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; Department of Neurology, Antwerp University Hospital, Antwerp, Belgium.; Koeleman BPC; Department of Genetics, University Medical Center Utrecht, Utrecht, 3584 CX, The Netherlands.
Publisher: BioMed Central Country of Publication: England NLM ID: 101190720 Publication Model: Electronic Cited Medium: Internet ISSN: 1741-7007 (Electronic) Linking ISSN: 17417007 NLM ISO Abbreviation: BMC Biol Subsets: MEDLINE
Academic Journal
Stevelink R; Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.; Department of Child Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands.; Koeleman BPC; Department of Child Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands.; Sisodiya SM; Department of Clinical and Experimental Epilepsy, University College London Queen Square Institute of Neurology, London, UK.; Chalfont Centre for Epilepsy, Bucks, UK.; Chalfont Centre for Epilepsy, Chalfont St. Peter, UK.
Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE
Academic Journal
Martin JE; Carmona FD; Broen JCA; Simeon CP; Vonk MC; Carreira P; Rios-Fernandez R; Espinosa G; Vicente-Rabaneda E; Tolosa C; Garcia-Hernandez FJ; Castellvi I; Fonollosa V; Gonzalez-Gay MA; Saez-Comet L; Portales RG; de la Pena PG; Fernandez-Castro M; Diaz B; Martinez-Estupinan L; Coenen M; Voskuyl AE; Schuerwegh AJ; Vanthuyne M; Houssiau F; Smith V; de Keyser F; De Langhe E; Riemekasten G; Witte T; Hunzelmann N; Kreuter A; Palm O; Chee MM; van Laar JM; Denton C; Herrick A; Worthington J; Koeleman BPC; Radstake TRDJ; Fonseca C; Martin J; Spanish Scleroderma Grp
GENES AND IMMUNITY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Institut dInvestigació Biomèdica Sant Pau (IIB Sant Pau)
Martin, J E, Carmona, F D, Broen, J C A, Simeon, C P, Vonk, M C, Carreira, P, Rios-Fernandez, R, Espinosa, G, Vicente-Rabaneda, E, Tolosa, C, Garcia-Hernandez, F J, Castellvi, I, Fonollosa, V, Gonzalez-Gay, M A, Saez-Comet, L, Portales, R G, de la Pena, P G, Fernandez-Castro, M, Diaz, B, Martinez-Estupinan, L, Coenen, M, Voskuyl, A E, Schuerwegh, A J, Vanthuyne, M, Houssiau, F, Smith, V, de Keyser, F, De Langhe, E, Riemekasten, G, Witte, T, Hunzelmann, N, Kreuter, A, Palm, O, Chee, M M, van Laar, J M, Denton, C, Herrick, A, Worthington, J,Koeleman , B P C, Radstake, T R D J, Fonseca, C & Martin, J 2012, 'The autoimmune disease-associated IL2RA locus is involved in the clinical manifestations of systemic sclerosis', Genes and Immunity, vol. 13, no. 2, pp. 191-196. https://doi.org/10.1038/gene.2011.72
Genes and Immunity, 13, 2, pp. 191-6
Martin, J E, Carmona, F D, Broen, J C A, Simeón, C P, Vonk, M C, Carreira, P, Ríos-Fernández, R, Espinosa, G, Vicente-Rabaneda, E, Tolosa, C, García-Hernández, F J, Castellví, I, Fonollosa, V, González-Gay, M A, Sáez-Comet, L, Portales, R G, De La Pẽa, P G, Fernández-Castro, M, Díaz, B, Martínez-Estupĩán, L, Coenen, M, Voskuyl, A E, Schuerwegh, A J, Vanthuyne, M, Houssiau, F, Smith, V, De Keyser, F, De Langhe, E, Riemekasten, G, Witte, T, Hunzelmann, N, Kreuter, A, Palm, Ø, Chee, M M, Van Laar, J M, Denton, C, Herrick, A, Worthington, J,Koeleman , B P C, Radstake, T R D J, Fonseca, C & Martín, J 2012, 'The autoimmune disease-associated IL2RA locus is involved in the clinical manifestations of systemic sclerosis', Genes and Immunity, vol. 13, no. 2, pp. 191-196. https://doi.org/10.1038/gene.2011.72
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Institut dInvestigació Biomèdica Sant Pau (IIB Sant Pau)
Martin, J E, Carmona, F D, Broen, J C A, Simeon, C P, Vonk, M C, Carreira, P, Rios-Fernandez, R, Espinosa, G, Vicente-Rabaneda, E, Tolosa, C, Garcia-Hernandez, F J, Castellvi, I, Fonollosa, V, Gonzalez-Gay, M A, Saez-Comet, L, Portales, R G, de la Pena, P G, Fernandez-Castro, M, Diaz, B, Martinez-Estupinan, L, Coenen, M, Voskuyl, A E, Schuerwegh, A J, Vanthuyne, M, Houssiau, F, Smith, V, de Keyser, F, De Langhe, E, Riemekasten, G, Witte, T, Hunzelmann, N, Kreuter, A, Palm, O, Chee, M M, van Laar, J M, Denton, C, Herrick, A, Worthington, J,
Genes and Immunity, 13, 2, pp. 191-6
Martin, J E, Carmona, F D, Broen, J C A, Simeón, C P, Vonk, M C, Carreira, P, Ríos-Fernández, R, Espinosa, G, Vicente-Rabaneda, E, Tolosa, C, García-Hernández, F J, Castellví, I, Fonollosa, V, González-Gay, M A, Sáez-Comet, L, Portales, R G, De La Pẽa, P G, Fernández-Castro, M, Díaz, B, Martínez-Estupĩán, L, Coenen, M, Voskuyl, A E, Schuerwegh, A J, Vanthuyne, M, Houssiau, F, Smith, V, De Keyser, F, De Langhe, E, Riemekasten, G, Witte, T, Hunzelmann, N, Kreuter, A, Palm, Ø, Chee, M M, Van Laar, J M, Denton, C, Herrick, A, Worthington, J,
Academic Journal
Gorlova, O; Martin, J-E; Rueda, B; Koeleman, BPC; Ying, J; Teruel, M; Diaz-Gallo, L-M; Broen, JC; Vonk, MC; Simeon, CP
PLOS GENETICS. 7(7):e1002178-e1002178
Conference
Silvennoinen K; de Lange N; Zagaglia S; Balestrini S; Androsova G; Borghei M; Wassenaar M; Auce P; Avbersek; Becker F; Berghuis B; Campbell E; Coppola A; Francis B; Wolking S; Cavalleri GL; Craig J; Delanty N; Johnson MR; Koeleman BPC; Kunz WS; Lerche H; Marson AG; O'Brien TJ; Sander JW; Sills GJ; Striano P; Zara F; Krause R; Depondt C; Sisodiya SM
Academic Journal
Academic Journal
Academic Journal
Pinto D; Kasteleijn-Nolst Trenite DGA; Cordell HJ; Mattheisen M; Strauch K; Lindhout D; Koeleman BPC
Pinto, D, Kasteleijn-Nolst Trenité, D G A, Cordell, H J, Mattheisen, M, Strauch, K, Lindhout, D & Koeleman , B P C 2007, 'Explorative two-locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures-related photosensitivity loci', Genetic Epidemiology, vol. 31, no. 1, pp. 42-50. https://doi.org/10.1002/gepi.20190
Academic Journal
Abumadini MS; Department of Psychiatry, King Fahd Hospital of the University, Al-Khobar and College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.; Al Ghamdi KS; Department of Physiology, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.; Alqahtani AH; Department of Psychiatry, King Fahd Hospital of the University, Al-Khobar and College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.; Almedallah DK; Department of Psychiatry, King Fahd Hospital of the University, Al-Khobar and College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.; Callans L; Department of Surgery, University of Pennsylvania School of Medicine, Philadelphia, PA, United States.; Jarad JA; Department of Psychiatry, King Fahd Hospital of the University, Al-Khobar and College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.; Cyrus C; Department of Clinical Biochemistry, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.; Koeleman BPC; Department of Genetics, Division Lab, University Medical Center Utrecht, Utrecht, Netherlands.; Keating BJ; Department of Surgery, University of Pennsylvania School of Medicine, Philadelphia, PA, United States.; Pankratz N; Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, United States.; Al-Ali AK; Department of Clinical Biochemistry, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101477914 Publication Model: eCollection Cited Medium: Print ISSN: 1662-5099 (Print) Linking ISSN: 16625099 NLM ISO Abbreviation: Front Mol Neurosci Subsets: PubMed not MEDLINE
Academic Journal
Alizadeh BZ; Hanifi-Moghaddam P; Eerligh P; van der Slik AR; Kolb H; Kharagjitsingh AV; Arias AMP; Ronkainen M; Knip M; Bonfanti R; Bonifacio E; Devendra D; Wilkin T; Giphart MJ; Koeleman BPC; Nolsoe R; Poulsen TM; Schloot NC; Roep BO
Clinical and Experimental Immunology. 145:480-484
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