부산대학교 도서관

Bryson, F.; Meister, M. R.; Dichek, D. J.; Mullen, A.D.; Hurwitz, B. C.; Lawrence, J. D.; Spears, A. M.; Washam, P.; Quartini, E. S.; Kassabian, L.; Lopez, S.; Schmidt, B. E.

Global Oceans 2020: Singapore – U.S. Gulf Coast. :1-7 Oct, 2020

Dichek, D. J.; Lawrence, J. D.; Meister, M. R.; Spears, A. M.; Hurwitz, B. C.; Bryson, F.; Washam, P. M.; Quartini, E. S.; Kassabian, L.; Schmidt, B. E.

Global Oceans 2020: Singapore – U.S. Gulf Coast. :1-9 Oct, 2020

Bruschi, G.; Pellegrino, L.; Bisogno, A.L.; Ferreri, F.; Kassabian, B.; Seppi, D.; Favaretto, S.; Corbetta, M.; Dainese, F.

Epilepsy & Behavior. 156

See, William A., M.D.

Urologic Oncology: Seminars and Original Investigations. 24(3):274-275

Kassabian B; Neurology Unit, Department of Neuroscience (DNS), Università degli Studi di Padova, Padua, Italy.; Facco M; Laboratory of Hematology and Immunology, Department of Medicine (DIMED), Università degli Studi di Padova, Padua, Italy.; Miscioscia A; Neurology Unit, Department of Neuroscience (DNS), Università degli Studi di Padova, Padua, Italy.; Multiple Sclerosis Centre, Neurology Unit, Azienda Ospedaliera di Padova, Padua, Italy.; Carraro S; Laboratory of Hematology and Immunology, Department of Medicine (DIMED), Università degli Studi di Padova, Padua, Italy.; Rinaldi F; Multiple Sclerosis Centre, Neurology Unit, Azienda Ospedaliera di Padova, Padua, Italy.; Gallo P; Neurology Unit, Department of Neuroscience (DNS), Università degli Studi di Padova, Padua, Italy.; Multiple Sclerosis Centre, Neurology Unit, Azienda Ospedaliera di Padova, Padua, Italy.; Puthenparampil M; Neurology Unit, Department of Neuroscience (DNS), Università degli Studi di Padova, Padua, Italy.; Multiple Sclerosis Centre, Neurology Unit, Azienda Ospedaliera di Padova, Padua, Italy.

Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101560960 Publication Model: eCollection Cited Medium: Internet ISSN: 1664-3224 (Electronic) Linking ISSN: 16643224 NLM ISO Abbreviation: Front Immunol Subsets: MEDLINE

Coles, W. A.; Murphy Jr., T. W.; Melser, J. F.; Tu, J. K.; White, G. A.; Kassabian, K. H.; Bales, K.; Baumgartner, B. B.

PASP 124, 42-50, (2012)

Porcaro C; Department of Neuroscience and Padova Neuroscience Center (PNC), University of Padova, Padova, Italy.; Institute of Cognitive Sciences and Technologies (ISTC) - National Research Council (CNR), Rome, Italy.; Centre for Human Brain Health, School of Psychology, University of Birmingham, Birmingham, United Kingdom.; Seppi D; Neurology Clinics, Azienda Ospedale Università, Padua, Italy.; Unit of Clinical Neurophysiology, Azienda Ospedale Università, Padua, Italy.; Pellegrino G; Epilepsy Program, Schulich School of Medicine and Dentistry, Western University, London, ON, Canada.; Dainese F; Neurology Clinics, Azienda Ospedale Università, Padua, Italy.; Unit of Clinical Neurophysiology, Azienda Ospedale Università, Padua, Italy.; Kassabian B; Neurology Clinics, Azienda Ospedale Università, Padua, Italy.; Unit of Clinical Neurophysiology, Azienda Ospedale Università, Padua, Italy.; Pellegrino L; Neurology Clinics, Azienda Ospedale Università, Padua, Italy.; Unit of Clinical Neurophysiology, Azienda Ospedale Università, Padua, Italy.; De Nardi G; Neurology Clinics, Azienda Ospedale Università, Padua, Italy.; Unit of Clinical Neurophysiology, Azienda Ospedale Università, Padua, Italy.; Grego A; Neurology Clinics, Azienda Ospedale Università, Padua, Italy.; Unit of Clinical Neurophysiology, Azienda Ospedale Università, Padua, Italy.; Corbetta M; Department of Neuroscience and Padova Neuroscience Center (PNC), University of Padova, Padova, Italy.; Neurology Clinics, Azienda Ospedale Università, Padua, Italy.; Veneto Institute of Molecular Medicine (VIMM), Fondazione Biomedica, Padua, Italy.; Ferreri F; Department of Neuroscience and Padova Neuroscience Center (PNC), University of Padova, Padova, Italy.; Neurology Clinics, Azienda Ospedale Università, Padua, Italy.; Unit of Clinical Neurophysiology, Azienda Ospedale Università, Padua, Italy.

Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101478481 Publication Model: eCollection Cited Medium: Print ISSN: 1662-4548 (Print) Linking ISSN: 1662453X NLM ISO Abbreviation: Front Neurosci Subsets: PubMed not MEDLINE

Kassabian, Benedetta; Fenger, Christina Dühring; Willems, Marjolaine; Aledo-Serrano, Angel; Linnankivi, Tarja; McDonnell, Pamela Pojomovsky; Lusk, Laina; Jepsen, Birgit Susanne; Bayat, Michael; Kattentidt, Anja; Vidal, Anna Abulí; Valero-Lopez, Gabriel; Alarcon-Martinez, Helena; Goodspeed, Kimberly; van Slegtenhorst, Marjon; Barakat, Tahsin Stefan; Møller, Rikke S.; Johannesen, Katrine M.; Rubboli, Guido

Kassabian , B , Fenger , C D , Willems , M , Aledo-Serrano , A , Linnankivi , T , McDonnell , P P , Lusk , L , Jepsen , B S , Bayat , M , Kattentidt , A , Vidal , A A , Valero-Lopez , G , Alarcon-Martinez , H , Goodspeed , K , van Slegtenhorst , M , Barakat , T S , Møller , R S , Johannesen , K M & Rubboli , G 2023 , ' Intrafamilial variability in SLC6A1 -related neurodevelopmental disorders : [Inkl. Correction] ' , Frontiers in Neuroscience , vol. 17 , 1219262 .

Kassabian B; Department of Epilepsy Genetics and Precision Medicine, Danish Epilepsy Center Filadelfia, member of the European Reference Network EpiCARE, Dianalund, Denmark.; Neurology Unit, Department of Neurosciences, University of Padua, Padua, Italy.; Levy AM; Department of Clinical Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.; Gardella E; Department of Epilepsy Genetics and Precision Medicine, Danish Epilepsy Center Filadelfia, member of the European Reference Network EpiCARE, Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.; Aledo-Serrano A; Epilepsy and Neurogenetics Unit, Vithas la Milagrosa University Hospital, Vithas Hospital Group, Madrid, Spain.; Ananth AL; Division of Pediatric Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.; Brea-Fernández AJ; Grupo de Genómica y Bioinformática, Centro Singular de Investigación en Medicina Molecular y Enfermedades Crónicas (CiMUS), Centro de Investigación Biomédica en Red de Enfermedades Raras del Instituto de Salud Carlos III (CIBERER-ISCIII), Universidade de Santiago de Compostela, Santiago de Compostela, Spain.; Grupo de Genética, Fundación Pública Galega de Medicina Xenómica, Instituto de Investigación Biomédica de Santiago (IDIS), Santiago de Compostela, Spain.; Caumes R; CHU de Lille, Clinique de Génétique, Lille, France.; Chatron N; Service de Genetique, Hospices Civils de Lyon, Bron, France.; Institute NeuroMyoGène, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, Centre National de la recherche scientifique (CNRS) Unité mixte de recherche (UMR) 5261- L'Institut national de la santé et de la recherche médicale (INSERM) U1315, Université de Lyon-Université Claude Bernard Lyon 1, Lyon, France.; Dainelli A; Neuroscience Department, Meyer Children's Hospital IRCCS (Istituto di Ricovero e Cura a Carattere Scientifico), member of the European Reference Network EpiCARE, Florence, Italy.; De Wachter M; Department of Pediatric Neurology, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Denommé-Pichon AS; Functional Unit for Diagnostic Innovation in Rare Diseases, Fédération Hospitalo-Universitaire Médecine TRANSLationnelle et Anomalies du Développement (FHU-TRANSLAD), Dijon Bourgogne University Hospital, Dijon, France.; L'Institut national de la santé et de la recherche médicale (INSERM) Unité mixte de recherche (UMR) 1231, Génétique des Anomalies du Développement (GAD), Fédération Hospitalo-Universitaire Médecine TRANSLationnelle et Anomalies du Développement (FHU-TRANSLAD), University of Burgundy, Dijon, France.; Dye TJ; Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.; Fazzi E; Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.; Unit of Child Neurology and Psychiatry, Azienda Socio Sanitaria Territoriale (ASST) Spedali Civili of Brescia, Brescia, Italy.; Felt R; Department of Neurology, Kaiser Permanente Bellevue Medical Center, Bellevue, Washington, USA.; Fernández-Jaén A; Department of Pediatric Neurology, Neurogenetics Section, Hospital Universitario Quirónsalud, Madrid, Spain.; Facultad de Medicina, Universidad Europea, Madrid, Spain.; Fernández-Prieto M; Grupo de Genómica y Bioinformática, Centro Singular de Investigación en Medicina Molecular y Enfermedades Crónicas (CiMUS), Centro de Investigación Biomédica en Red de Enfermedades Raras del Instituto de Salud Carlos III (CIBERER-ISCIII), Universidade de Santiago de Compostela, Santiago de Compostela, Spain.; Grupo de Genética, Fundación Pública Galega de Medicina Xenómica, Instituto de Investigación Biomédica de Santiago (IDIS), Santiago de Compostela, Spain.; Gantz E; Division of Pediatric Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.; Gasperowicz P; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.; Gil-Nagel A; Neurology Department, Epilepsy Program, Ruber Internacional Hospital, Madrid, Spain.; Gómez-Andrés D; Child Neurology Unit, Hospital Universitari Vall d'Hebron, Vall d'Hebron Research Institute, Barcelona, Spain.; Greiner HM; Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.; Guerrini R; Neuroscience Department, Meyer Children's Hospital IRCCS (Istituto di Ricovero e Cura a Carattere Scientifico), member of the European Reference Network EpiCARE, Florence, Italy.; Haanpää MK; Department of Genomics, Turku University Hospital, Turku, Finland.; Helin M; Department of Pediatric Neurology, Turku University Hospital, Turku, Finland.; Hoyer J; Friedrich-Alexander-Universität Erlangen Nürnberg, Institute of Human Genetics, Erlangen, Germany.; Hurst ACE; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.; Kallish S; Division of Translational Medicine and Human Genetics, Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Karkare SN; Division of Pediatric Neurology, Department of Pediatrics, Cohen Children's Medical Center, New Hyde Park, New York, USA.; Khan A; Department of Zoology, Faculty of Biological Sciences, University of Lakki Marwat, Lakki Marwat, Pakistan.; Institute for Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Kleinendorst L; Department of Human Genetics, Amsterdam University Medical Center (UMC), University of Amsterdam, Amsterdam, the Netherlands.; Emma Center for Personalized Medicine, Amsterdam University Medical Center (UMC), University of Amsterdam, Amsterdam, the Netherlands.; Koch J; University Children's Hospital, Paracelsus Medical University, Salzburg, Austria.; Kothare SV; Division of Pediatric Neurology, Department of Pediatrics, Cohen Children's Medical Center, New Hyde Park, New York, USA.; Koudijs SM; Department of Neurology, Erasmus Medical Center (MC) Sophia Children's Hospital, Rotterdam, the Netherlands.; Erfelijke Neuro-Cognitieve Ontwikkelingsstoornissen, Rotterdam, Erasmus Medical Center (ENCORE)-GRIN Expertise Center, Rotterdam, the Netherlands.; Lagae L; Department of Development and Regeneration, Section Paediatric Neurology, member of the European Reference Network EpiCARE, University Hospitals Leuven, Leuven, Belgium.; Lakeman P; Department of Human Genetics, Amsterdam University Medical Center (UMC), University of Amsterdam, Amsterdam, the Netherlands.; Leppig KA; Genetic Services, Kaiser Permanente of Washington, Seattle, Washington, USA.; Lesca G; Service de Genetique, Hospices Civils de Lyon, Bron, France.; Institute NeuroMyoGène, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, Centre National de la recherche scientifique (CNRS) Unité mixte de recherche (UMR) 5261- L'Institut national de la santé et de la recherche médicale (INSERM) U1315, Université de Lyon-Université Claude Bernard Lyon 1, Lyon, France.; Lopergolo D; Department of Medicine, Surgery, and Neurosciences, University of Siena, Siena, Italy.; Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Stella Maris Foundation, Pisa, Italy.; Lusk L; Division of Neurology, Epilepsy Neurogenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Mackenzie A; Research Institute, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.; Mei D; Neuroscience Department, Meyer Children's Hospital IRCCS (Istituto di Ricovero e Cura a Carattere Scientifico), member of the European Reference Network EpiCARE, Florence, Italy.; Møller RS; Department of Epilepsy Genetics and Precision Medicine, Danish Epilepsy Center Filadelfia, member of the European Reference Network EpiCARE, Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.; Pereira EM; Division of Clinical Genetics, Department of Pediatrics, Columbia University Vagelos College of Physicians and Surgeons and New York-Presbyterian Morgan Stanley Children's Hospital, New York, New York, USA.; Platzer K; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Quelin C; Department of Medical Genetics, CHU de Rennes, Rennes, France.; Revah-Politi A; Institute for Genomic Medicine, Columbia University Irving Medical Center, New York, New York, USA.; Rheims S; Department of Functional Neurology and Epileptology, member of the European Reference Network EpiCARE, Hospices Civils de Lyon and Lyon 1 University, Lyon, France.; Rodríguez-Palmero A; Paediatric Neurology Unit, Department of Pediatrics, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, Barcelona, Spain.; Grupo de Investigación Biomédica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Rossi A; Unit of Child Neurology and Psychiatry, Azienda Socio Sanitaria Territoriale (ASST) Spedali Civili of Brescia, Brescia, Italy.; Santorelli F; Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Stella Maris Foundation, Pisa, Italy.; Seinfeld S; Department of Pediatric Neurology, Neuroscience Center, Joe DiMaggio Children's Hospital, Hollywood, Florida, USA.; Sell E; Division of Neurology, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Stephenson D; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Szczaluba K; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.; Center of Excellence for Rare and Undiagnosed Diseases, Medical University of Warsaw, Warsaw, Poland.; Trinka E; Department of Neurology, Neurointensive Care and Neurorehabilitation, Christian Doppler University Hospital, member of the European Reference Network EpiCARE, Paracelsus Medical University, Center for Cognitive Neuroscience, Salzburg, Austria.; Neuroscience Institute, Christian Doppler University Hospital, member of the European Reference Network EpiCARE, Paracelsus Medical University, Center for Cognitive Neuroscience, Salzburg, Austria.; Umair M; Medical Genomics Research Department, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.; Department of Life Sciences, School of Science, University of Management and Technology, Lahore, Pakistan.; Van Esch H; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.; van Haelst MM; Department of Human Genetics, Amsterdam University Medical Center (UMC), University of Amsterdam, Amsterdam, the Netherlands.; Emma Center for Personalized Medicine, Amsterdam University Medical Center (UMC), University of Amsterdam, Amsterdam, the Netherlands.; Veenma DCM; Erfelijke Neuro-Cognitieve Ontwikkelingsstoornissen, Rotterdam, Erasmus Medical Center (ENCORE)-GRIN Expertise Center, Rotterdam, the Netherlands.; Department of Pediatrics, Erasmus Medical Center (MC)-Sophia Hospital, Rotterdam, the Netherlands.; Weber S; Service de Génétique, Centre Hospitalier Universitaire (CHU) de Caen-Normandie, Caen, France.; Service de Neurologie, Centre Hospitalier Universitaire (CHU) de Caen-Normandie, Caen, France.; Weckhuysen S; Applied and Translational Neurogenomics Group, Vlaams Instituut voor Biotechnologie (VIB) Center for Molecular Neurology, Antwerp, Belgium.; Department of Neurology, Antwerp University Hospital, Antwerp, Belgium.; Zacher P; Center for Adults with Disability (MZEB), Epilepsy Center Kleinwachau, Radeberg, Germany.; Tümer Z; Department of Clinical Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.; Rubboli G; Department of Epilepsy Genetics and Precision Medicine, Danish Epilepsy Center Filadelfia, member of the European Reference Network EpiCARE, Dianalund, Denmark.; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

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

Kassabian, Benedetta; Duhring Fenger, Christina; Willems, Marjolaine; Aledo-Serrano, Angel; Linnankivi, Tarja; Pojomovsky McDonnell, Pamela; Lusk, Laina; Jepsen, Birgit Susanne; Bayat, Michael; Kattentidt, Anja; Abuli Vidal, Anna; Valero-Lopez, Gabriel; Alarcon-Martinez, Helena; Goodspeed, Kimberly; van Slegtenhorst, Marjon; Barakat, Stefan; Moller, Rikke S.; Johannesen, Katrine M.; Rubboli, Guido

Kassabian , B , Duhring Fenger , C , Willems , M , Aledo-Serrano , A , Linnankivi , T , Pojomovsky McDonnell , P , Lusk , L , Jepsen , B S , Bayat , M , Kattentidt , A , Abuli Vidal , A , Valero-Lopez , G , Alarcon-Martinez , H , Goodspeed , K , van Slegtenhorst , M , Barakat , S , Moller , R S , Johannesen , K M & Rubboli , G 2023 , ' Intrafamilial variability in SLC6A1-related neurodevelopmental disorders ' , Frontiers in Neuroscience , vol. 17 , 1219262 , pp. 01-11 .