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Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

Emily A. Christopher; Yvette Christopher-de Vries; Anitha Devadoss; Laurens D.B. Mandemaker; Jeske van Boxel; Helena M. Copsey; Hanna M. Dusza; Juliette Legler; Florian Meirer; Jane Muncke; Tim S. Nawrot; Nelly D. Saenen; Barbara M. Scholz-Böttcher; Lang Tran; Bert M. Weckhuysen; Runyu Zou; Lisa Zimmermann; Karen S. Galea; Roel Vermeulen; Matthew S. P. Boyles

Microplastics and Nanoplastics, Vol 4, Iss 1, Pp 1-28 (2024)

Xiang Yu; Nina S. Genz; Rafael G. Mendes; Xinwei Ye; Florian Meirer; Maarten Nachtegaal; Matteo Monai; Bert M. Weckhuysen

Nature Communications, Vol 15, Iss 1, Pp 1-12 (2024)

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Epilepsia, vol 63, iss 3
Epilepsia : the journal of the International League Against Epilepsy 63(3), 723-735 (2022). doi:10.1111/epi.17166

Vonck K; Department Neurology - 4Brain, Ghent University Hospital, Ghent, Belgium.; Bodart O; Neurology Department, University Hospital of Liège, Liège, Belgium.; Weckhuysen S; Neurology Department, University Hospital Antwerp, Antwerp, Belgium.; Tanghe A; Hict NV, Ghent, Belgium.; Callebaut B; Hict NV, Ghent, Belgium.; Verdonck C; Hict NV, Ghent, Belgium.; Van den Bergh L; Angelini Pharma, Paris, France.; Legros B; Neurology Department, HUB-Hôpital Erasme, Brussels, Belgium.

Publisher: Taylor & Francis Country of Publication: England NLM ID: 9892255 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1941-837X (Electronic) Linking ISSN: 13696998 NLM ISO Abbreviation: J Med Econ Subsets: MEDLINE

Hadermann A; Global Health Institute, University of Antwerp, Antwerp, Belgium.; Bhwana D; National Institute for Medical Research, Tanga Research, Tanga, Tanzania.; Mhina AD; National Institute for Medical Research, Tanga Research, Tanga, Tanzania.; Amaral LJ; Global Health Institute, University of Antwerp, Antwerp, Belgium.; Siewe Fodjo JN; Global Health Institute, University of Antwerp, Antwerp, Belgium.; Emonds MP; Histocompatibility and Immunogenetics Laboratory, Belgian Red Cross-Flanders, Mechelen, Belgium.; Weckhuysen S; Department of Neurology, University Hospital Antwerp, Belgium.; VIB-Center for Molecular Neurology, VIB, University of Antwerp, Belgium.; Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; Mmbando BP; National Institute for Medical Research, Tanga Research, Tanga, Tanzania.; Colebunders R; Global Health Institute, University of Antwerp, Antwerp, Belgium.

Publisher: Public Library of Science Country of Publication: United States NLM ID: 101291488 Publication Model: eCollection Cited Medium: Internet ISSN: 1935-2735 (Electronic) Linking ISSN: 19352727 NLM ISO Abbreviation: PLoS Negl Trop Dis Subsets: MEDLINE

N. Dirkx; Wout J. Weuring; E. De Vriendt; N. Smal; J. van de Vondervoort; Ruben van ’t Slot; M. Koetsier; N. Zonnekein; Tim De Pooter; S. Weckhuysen; B. P. C. Koeleman

BMC Biology, Vol 21, Iss 1, Pp 1-15 (2023)

Serpieri V; Department of Molecular Medicine, University of Pavia, 27100 Pavia, Italy.; Vezain-Mouchard M; Univ Rouen Normandie, INSERM U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, 76000 Rouen, France.; Orsi A; Department of Molecular Medicine, University of Pavia, 27100 Pavia, Italy.; Lecointre M; Univ Rouen Normandie, INSERM U1245, 76000 Rouen, France.; Mazzotta C; Department of Molecular Medicine, University of Pavia, 27100 Pavia, Italy.; Marguet F; Univ Rouen Normandie, INSERM U1245 and CHU Rouen, Department of Pathology, 76000 Rouen, France.; Garbelli A; Institute of Molecular Genetics 'Luigi Luca Cavalli-Sforza', National Research Council (IGM-CNR), 27100 Pavia, Italy.; Marcorelles P; CHU Brest, Department of Pathology, 29200 Brest, France.; Celli L; Institute of Molecular Genetics 'Luigi Luca Cavalli-Sforza', National Research Council (IGM-CNR), 27100 Pavia, Italy.; Goldenberg A; Univ Rouen Normandie, INSERM U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, 76000 Rouen, France; CH Le Havre, Department of Genetics, 76600 Le Havre, France.; De Mori R; Induced Pluripotent Stem Cells and Organoids Unit, IRCCS Santa Luicia Foundation, 00179 Rome, Italy.; Drouot N; Univ Rouen Normandie, INSERM U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, 76000 Rouen, France.; Petrizzelli F; Bioinformatics Laboratory, IRCSS Casa Sollievo Della Sofferenza, 71013 S. Giovanni Rotondo (FG), Italy.; Janin F; Univ Rouen Normandie, INSERM U1245, 76000 Rouen, France.; Nicolas G; Univ Rouen Normandie, INSERM U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, 76000 Rouen, France.; Smal N; Translational Epilepsy Genomics Group, VIB Center for Molecular Neurology, VIB, 2610 Antwerp, Belgium.; Condoluci C; Developmental Disabilities and Rehabilitation, IRCCS San Raffaele Roma, 00166 Rome, Italy.; Marini C; Child Neurology and Psychiatric Unit, G. Salesi Pediatric Hospital, Azienda Ospedaliera-Universitaria Delle Marche, 60126 Ancona, Italy.; Tran-Mau-Them F; Unité Fonctionnelle Innovation en Diagnostic Génomique des maladies rares, CHU Dijon Bourgogne, and INSERM UMR1231 GAD, 21079 Dijon, France.; Ruault V; Reference Center for Rare Diseases Developmental Anomaly and Malformative Syndromes, Genetics Department, Montpellier Hospital, 34000 Montpellier, France.; Micalizzi A; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy; Medical Genetics Unit, San Pietro Fatebenefratelli Hospital, 00189 Rome, Italy.; Bione S; Institute of Molecular Genetics 'Luigi Luca Cavalli-Sforza', National Research Council (IGM-CNR), 27100 Pavia, Italy.; Mazza T; Computational Biology and Bioinformatics Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, 00168 Rome, Italy.; Pichiecchio A; Department of Brain and Behavioral Sciences, University of Pavia, 27100 Pavia, Italy; Neuroradiology Department, IRCCS Mondino Foundation, 27100 Pavia, Italy.; Ginevrino M; Parkinson and Movement Disorders Unit, Study Center on Neurodegeneration (CESNE), Department of Neurosciences, University of Padua, 35121 Padua, Italy.; Weckhuysen S; Translational Epilepsy Genomics Group, VIB Center for Molecular Neurology, VIB, 2610 Antwerp, Belgium; Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, 2610 Antwerp, Belgium; Department of Neurology, University Hospital, 2650 Antwerp, Belgium.; Bedois A; Service de Génétique, Eurofins Biomnis, Lyon, France.; Desnous B; Department of Pediatric Neurology, Aix-Marseille University, Marseille, France.; Hermitte L; Neuroradiology Department at Timone Hospital, Aix-Marseille University, Marseille, France.; Rabie G; Hereditary Research Laboratory, Bethlehem University, Bethlehem, Palestine.; Kanaan M; Hereditary Research Laboratory, Bethlehem University, Bethlehem, Palestine.; Gonzalez BJ; Univ Rouen Normandie, INSERM U1245, 76000 Rouen, France.; Sabbioneda S; Institute of Molecular Genetics 'Luigi Luca Cavalli-Sforza', National Research Council (IGM-CNR), 27100 Pavia, Italy.; Laquerrière A; Univ Rouen Normandie, INSERM U1245 and CHU Rouen, Department of Pathology, 76000 Rouen, France.; Saugier-Veber P; Univ Rouen Normandie, INSERM U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, 76000 Rouen, France.; Valente EM; Department of Molecular Medicine, University of Pavia, 27100 Pavia, Italy; Neurogenetics Research Center, IRCCS Mondino Foundation, 27100 Pavia, Italy. Electronic address: enzamaria.valente@unipv.it.

Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Wolking S.; Moreau C.; McCormack M.; Krause R.; Krenn M.; Berkovic S.; Cavalleri G. L.; Delanty N.; Depondt C.; Johnson M. R.; Koeleman B. P. C.; Kunz W. S.; Lerche H.; Marson A. G.; O'Brien T. J.; Petrovski S.; Sander J. W.; Sills G. J.; Striano P.; Zara F.; Zimprich F.; Sisodiya S. M.; Girard S. L.; Cossette P.; Avbersek A.; Leu C.; Heggeli K.; Demurtas R.; Willis J.; Speed D.; Sargsyan N.; Chinthapalli K.; Borghei M.; Coppola A.; Gambardella A.; Becker F.; Rau S.; Hengsbach C.; Weber Y. G.; Berghuis B.; Campbell E.; Gudmundsson L. J.; Ingason A.; Stefansson K.; Schneider R.; Balling R.; Auce P.; Francis B.; Jorgensen A.; Morris A.; Langley S.; Srivastava P.; Brodie M.; Todaro M.; Hutton J.; Muhle H.; Klein K. M.; Moller R. S.; Nikanorova M.; Weckhuysen S.; Rener-Primec Z.; Craig J.; Stefansson H.

Ann Clin Transl Neurol
Annals of Clinical and Translational Neurology, Vol 8, Iss 7, Pp 1376-1387 (2021)
info:eu-repo/grantAgreement/EC/FP7/279062
Annals of Clinical and Translational Neurology 8(7), 1376-1387 (2021). doi:10.1002/acn3.51374

Millevert C; VIB Center for Molecular Neurology, Translational Epilepsy Genomics Group, VIB 2610, Antwerp, Belgium.; Department of Neurology, University Hospital of Antwerp, Antwerp 2650, Belgium.; μNEURO Research Centre of Excellence, University of Antwerp, Antwerp 2610, Belgium.; Kan ASH; Brain and Mind Centre, School of Medical Sciences, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2050, Australia.; Hanke M; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, member of European Reference Network EpiCARE, University of Tübingen, Tübingen 72076, Germany.; Koko M; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, member of European Reference Network EpiCARE, University of Tübingen, Tübingen 72076, Germany.; Omidvar ME; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, member of European Reference Network EpiCARE, University of Tübingen, Tübingen 72076, Germany.; Hedrich UBS; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, member of European Reference Network EpiCARE, University of Tübingen, Tübingen 72076, Germany.; Wuttke TV; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, member of European Reference Network EpiCARE, University of Tübingen, Tübingen 72076, Germany.; Department of Neurosurgery, University of Tübingen, Tübingen 72074, Germany.; Barišić N; University Hospital Centre Split, School of Medicine, University of Zagreb, Zagreb 10000, Croatia.; Lagae L; Department of Development and Regeneration, Section Pediatric Neurology, University Hospital KU Leuven, Leuven 3000, Belgium.; Aledo-Serrano Á; Epilepsy and Neurogenetics Program, Vithas Madrid La Milagrosa University Hospital, Vithas Hospital Group, Madrid 28010, Spain.; Niehoff EM; Centre for Child and Adolescent Health, Helios Klinikum Krefeld (HKK), Krefeld 47805, Germany.; Platzer K; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig 04103, Germany.; Zacher P; Epilepsy Center Kleinwachau, Dresden-Radeberg 01454, Germany.; Department for Psychiatry and Psychotherapy II, LVR-Hospital Bonn, Bonn 53111, Germany.; Polster T; Bethel Epilepsy Center, Klinik Mara I, Bielefeld 33617, Germany.; Dilena R; Neurophysiopathology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan 20122, Italy.; Monfrini E; Neurology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan 20122, Italy.; Dino Ferrari Center, Dept. of Pathophysiology and Transplantation, University of Milan, Milan 20122, Italy.; Geneviève D; Service de Neuropédiatire, CHU Montpellier, INM, INSERM U 1298, Montpellier 34295, France.; Reference Center for Malformative Syndrome, Department of Genetics, Montpellier Hospital, Montpellier 34295, France.; Roubertie A; Reference Center for Malformative Syndrome, Department of Genetics, Montpellier Hospital, Montpellier 34295, France.; Bruel AL; Laboratoire de Génomique Médicale-Centre NEOMICS, CHU Dijon Bourgogne, Dijon 21000, France.; INSERM, Genetics of Developmental Anomalies, Université de Bourgogne, Dijon 21000, France.; Mau-Them FT; Laboratoire de Génomique Médicale-Centre NEOMICS, CHU Dijon Bourgogne, Dijon 21000, France.; INSERM, Genetics of Developmental Anomalies, Université de Bourgogne, Dijon 21000, France.; Dasouki M; Department of Pediatric Genetics, AdventHealth Medical Group, Orlando, FL 32804, USA.; Cohen S; Division of Translational Medicine and Human Genetics, Hospital of University of Pennsylvania, Philadelphia, PA 19104, USA.; Genetic Diagnostic Laboratory, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.; Helbig I; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Neurology, University of Pennsylvania, Philadelphia, PA 19104, USA.; The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Harrison AG; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Ellis C; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Neurology, University of Pennsylvania, Philadelphia, PA 19104, USA.; Dubbs HA; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Marsh ED; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Lebon S; Pediatric Neurology and Neurorehabilitation Unit, Dept. Woman-Mother-Child, Lausanne University Hospital and University of Lausanne, Lausanne 1011, Switzerland.; He N; Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, the Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, China.; Meng H; Department of Neurology, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.; Chebib M; Brain and Mind Centre, School of Medical Sciences, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2050, Australia.; Møller RS; Department of Epilepsy Genetics and Personalized Treatment, Danish Epilepsy Center Filadelfia, member of European Reference Network EpiCARE, Dianalund 4293, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense 5230, Denmark.; Marini C; Child Neurology and Psychiatric Unit, G. Salesi Pediatric Hospital, Azienda Ospedaliero Universitaria Delle Marche, Ancona 60123, Italy.; Ahring PK; Brain and Mind Centre, School of Medical Sciences, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2050, Australia.; Lerche H; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, member of European Reference Network EpiCARE, University of Tübingen, Tübingen 72076, Germany.; Weckhuysen S; VIB Center for Molecular Neurology, Translational Epilepsy Genomics Group, VIB 2610, Antwerp, Belgium.; Department of Neurology, University Hospital of Antwerp, Antwerp 2650, Belgium.; μNEURO Research Centre of Excellence, University of Antwerp, Antwerp 2610, Belgium.; Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, Antwerp 2610, Belgium.

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

Perucca P.; Anderson A.; Jazayeri D.; Hitchcock A.; Graham J.; Todaro M.; Tomson T.; Battino D.; Perucca E.; Ferri M. M.; Rochtus A.; Lagae L.; Canevini M. P.; Zambrelli E.; Campbell E.; Koeleman B. P. C.; Scheffer I. E.; Berkovic S. F.; Kwan P.; Sisodiya S. M.; Goldstein D. B.; Petrovski S.; Craig J.; Vajda F. J. E.; O'Brien T. J.; Leu C.; Wolking S.; Peter S.; Weber Y. G.; Weckhuysen S.; Moller R. S.; Nikanorova M.; Muhle H.; Avbersek A.; Heggeli K.; Striano P.; Gambardella A.; Langley S. R.; Krenn M.; Klein K. M.; McCormack M.; Borghei M.; Willis J.; Berghuis B.; Jorgensen A.; Auce P.; Francis B.; Srivastava P.; Sonsma A. C. M.; Sander JW.; Zimprich F.; Depondt C.; Johnson M. M.; Marson A. G.; Sills G. J.; Kunz W. S.; Cavalleri G. L.; Delanty N.; Zara F.; Krause R.; Lerche H.; Andrade D.; Sen A.; Bazil C. W.; Boland M.; Cavalleri G.; Choi H.; Colombo S.; Costello D.; Devinsky O.; Doherty C. P.; Dugan P.; Frankel W.; Heinzen E.; Johnson M.; Marson T.; Mikati M.; Ottman R.; Pandolfo M.; Radtke R.; Rees M.; Sadoway T.; Valley N.; Walley N.; Wood N.; Zuberi S.

Annals of Neurology. 87:897-906

Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Eoli A; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Krey I; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.; Popp B; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Strehlow V; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Wittekind DA; Department of Psychiatry and Psychotherapy, University of Leipzig Medical Center, Leipzig, Germany.; Institue for Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University of Leipzig Medical Center, Leipzig, Germany.; Vuorinen AL; Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.; Faculty of Social Sciences, Unit of Health Sciences, Tampere University, Tampere, Finland.; Aldhalaan HM; Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.; Baer S; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; de Saint Martin A; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; Hammer TB; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Herman I; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Hornemann F; Department of Pediatrics, Klinikum Chemnitz, Chemnitz, Germany.; Ingebrigtsen T; National Centre for Epilepsy, Oslo University Hospital, Oslo, Norway.; Lederer D; Centre de Génétique Humaine, Institut de Pathologie et Génétique (IPG), Charleroi (Gosselies), Belgium.; Lesca G; Department of Medical Genetics, University Hospital of Lyon, Claude Bernard University Lyon 1, Lyon, France.; Marafie D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Faculty of Medicine, Kuwait University, Safat, Kuwait.; Mathot M; Neuropediatric Unit, CHU UCL-Namur, Namur, Belgium.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Baylor Genetics Laboratory, Houston, TX, USA.; Møller RS; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.; Schelhaas HJ; Department of Neurology, Stichting Epilepsie Instellingen Nederland, SEIN, Zwolle, The Netherlands.; Stillman C; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Orsini A; Section of Pediatric Neurology, Division of Pediatrics, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.; Patel AD; Division of Pediatric Neurology, Nationwide Children's Hospital, Department of Pediatrics, The Ohio State College of Medicine, Columbus, OH, USA.; Piard J; Centre de Génétique Humaine, Centre Hospitalier Universitaire, Université de Franche-Comté, Besançon, France.; UMR 1231 GAD, Inserm, Université de Bourgogne, Dijon, France.; Veggiotti P; Neuroscience Research Center, Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.; Pediatric Neurology Unit, Buzzi Children's Hospital, Milan, Italy.; Vlaskamp DRM; Department of Genetics and Department of Neurology, University Medical Center Groningen, Groningen, The Netherlands.; Weckhuysen S; VIB-Center for Molecular Neurology, VIB, Antwerp, Belgium.; Department of Neurology, University Hospital Antwerp, Antwerp, Belgium.; Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; Traynelis SF; Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.; Center for the Functional Evaluation of Rare Variants (CFERV), Emory University School of Medicine, Atlanta, GA, USA.; Benke TA; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Heyne HO; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany. Henrike.Heyne@hpi.de.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Henrike.Heyne@hpi.de.; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland. Henrike.Heyne@hpi.de.; Syrbe S; Heidelberg University, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Clinic 1, Division of Pediatric Epileptology, Heidelberg, Germany.

Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE; In Process

Ortiz S; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Filadelfia, Member of the European Reference Network EpiCARE, Dianalund, Denmark.; Department of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark, Odense, Denmark.; Affronte L; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Filadelfia, Member of the European Reference Network EpiCARE, Dianalund, Denmark.; Child Neuropsychiatry, IRCCS, Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.; Bagliani C; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Filadelfia, Member of the European Reference Network EpiCARE, Dianalund, Denmark.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.; Child Neuropsychiatry Unit, IRCCS, Istituto Giannina Gaslini, Full Member of the European Reference Network EpiCARE, Genoa, Italy.; El-Kamand S; School of Medical Sciences, Faculty of Medicine and Health, Brain and Mind Centre, The University of Sydney, Sydney, New South Wales, Australia.; Kan ASH; School of Medical Sciences, Faculty of Medicine and Health, Brain and Mind Centre, The University of Sydney, Sydney, New South Wales, Australia.; Kristoffersen IT; School of Medical Sciences, Faculty of Medicine and Health, Brain and Mind Centre, The University of Sydney, Sydney, New South Wales, Australia.; Dahl RS; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Filadelfia, Member of the European Reference Network EpiCARE, Dianalund, Denmark.; Department of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark, Odense, Denmark.; Højte AF; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Filadelfia, Member of the European Reference Network EpiCARE, Dianalund, Denmark.; Auvin S; INSERM NeuroDiderot, DMU Innov-RDB, Neurologie Pédiatrique, AP-HP, Hôpital Robert-Debré, Member of European Reference Network EpiCARE, Université de Paris, Paris, France.; Bouman A; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.; Zeidler S; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.; Kluger G; Center for Pediatric Neurology, Neurorehabilitation, and Epileptology, Schoen-Clinic, Vogtareuth, Germany.; Children's Hospital Salzburg, Research Institute 'Rehabilitation, Transition and Palliation' PMU Salzburg, Salzburg, Austria.; Lesca G; Genetics Department, Hospices Civils de Lyon, Member of ERN EpiCARE, Lyon, France.; Neuromyogene Institute, Pathology and Genetics of Neuron and Muscle, CNRS UMR 5261 INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.; Chatron N; Genetics Department, Hospices Civils de Lyon, Member of ERN EpiCARE, Lyon, France.; Goke-Samar Z; Department of Pediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, Hôpital Femme Mère Enfant, Member of ERN EpiCARE, University Hospitals of Lyon (HCL), Lyon, France.; Papadopoulou MT; Department of Pediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, Hôpital Femme Mère Enfant, Member of ERN EpiCARE, University Hospitals of Lyon (HCL), Lyon, France.; CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, EDUWELL, Université Claude Bernard Lyon 1, Bron, France.; Terzi MAP; Department of Pediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, Hôpital Femme Mère Enfant, Member of ERN EpiCARE, University Hospitals of Lyon (HCL), Lyon, France.; Schaefer E; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace, Strasbourg, France.; de Saint Martin A; Department of Neuropediatrics, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Institute for Genetics and Molecular and Cellular Biology (IGBMC), CNRS UMR7104, INSERM U1258, University of Strasbourg, Illkirch, France.; French Reference Center for Rare Epilepsies (CréER), ERN EpiCARE, France.; Baer S; Department of Neuropediatrics, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Institute for Genetics and Molecular and Cellular Biology (IGBMC), CNRS UMR7104, INSERM U1258, University of Strasbourg, Illkirch, France.; Al Owain M; Department of Medical Genomics, Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; Takroni S; Department of Medical Genomics, Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; Al-Dhalaan H; Department of Neuroscience, Center for Autism Research, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Bonanni P; Epilepsy and Clinical Neurophysiology Unit, Scientific Institute for Research, Hospitalization and Healthcare, IRCCS, E. Medea, IRCCS Eugenio Medea, Conegliano, Italy.; Rossi A; Epilepsy and Clinical Neurophysiology Unit, Scientific Institute for Research, Hospitalization and Healthcare, IRCCS, E. Medea, IRCCS Eugenio Medea, Conegliano, Italy.; Zanotta N; Unit of Clinical Neurophysiology and Epilepsy Centre, IRCCS E. Medea, Lecco, Italy.; Trivisano M; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network EpiCARE, Rome, Italy.; Specchio N; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network EpiCARE, Rome, Italy.; de Dominicis A; Neurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network EpiCARE, Rome, Italy.; Striano P; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, Full Member of the European Reference Network EpiCARE, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Orsini A; Pediatric Neurology, University Hospital of Pisa, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.; Mancardi MM; Unit of Child Neuropsychiatry, Full Member ERN EpiCARE, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Neuens S; Department of Genetics, Hôpital Universitaire Des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.; Jennesson-Lyver M; Department of Pediatric Neurology, American Memorial Hospital, CHU Reims, Reims, France.; Benkel-Herrenbrueck I; Sana-Krankenhaus Düsseldorf-Gerresheim, Academic Teaching Hospital der Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.; Genevieve D; Department of Clinical Genetics, Inserm U1183, Centre de Référence «Anomalies du Développement et Syndromes Malformatifs», University Hospital of Montpellier, Montpellier University, Montpellier, France.; Sidlow R; Department of Medical Genetics and Metabolism, Valley Children's Hospital, Madera, California, USA.; Tezcan K; Department of Genetics, Kaiser Permanente, Sacramento, California, USA.; Krey I; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Platzer K; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Lederer D; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.; Talvik I; Tallin Children's Hospital, Tallin, Estonia.; Vaher U; Children's Clinic, Tartu University Hospital, Tartu, Estonia.; Braun KPJ; Department of Child Neurology and Neurosurgery, University Medical Center, Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Guerrot AM; Department of Genetics and Reference Center for Developmental Disorders, Inserm U1245 and CHU Rouen, Univ Rouen Normandie, Normandie Univ, Rouen, France.; More R; Département de Pédiatrie Néonatale Réanimation Pédiatrique, Centre Hospitalier Universitaire de Rouen, Rouen, France.; De Wachter M; Department of Pediatric Neurology, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.; Weckhuysen S; Department of Neurology, Antwerp University Hospital, Antwerp, Belgium.; VIB Center for Molecular Neurology, Antwerp, Belgium.; Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; Carapancea E; Institute of Neuroscience, Université Catholique de Louvain, Brussels, Belgium.; Division of Pediatric Neurology, Department of Pediatrics, Saint-Luc University Hospital, Université Catholique de Louvain, Brussels, Belgium.; Cilio MR; Institute of Neuroscience, Université Catholique de Louvain, Brussels, Belgium.; Division of Pediatric Neurology, Department of Pediatrics, Saint-Luc University Hospital, Université Catholique de Louvain, Brussels, Belgium.; Jacobs J; Hotchkiss Brain Institute and Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.; Sterbova K; Department of Paediatric Neurology, Second Faculty of Medicine, Charles University and Motol Epilepsy Center, University Hospital Motol, Prague, Czech Republic.; Balestrini S; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.; Neuroscience Department, Meyer Children's Hospital, European Reference Network ERN EpiCARE, Florence, Italy.; Chalfont Centre for Epilepsy, London, UK.; Guerrini R; Neuroscience Department, Meyer Children's Hospital, European Reference Network ERN EpiCARE, Florence, Italy.; Child and Adolescent Psychiatry Unit, Neuroscience and Human Genetics Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Peroni G; Neuroscience Department, Meyer Children's Hospital, European Reference Network ERN EpiCARE, Florence, Italy.; Mero IL; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.; ElNaggar W; Department of Pediatrics, Faculty of Medicine, Cairo University, Giza, Egypt.; Elkhateeb N; Department of Clinical Genetics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.; Schmetz A; Institute of Human Genetics, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University, Düsseldorf, Germany.; Chan DL; Neurology Department, Sydney Children's Hospital, Sydney, New South Wales, Australia.; School of Women's and Children's Health, UNSW Medicine, UNSW Sydney, Sydney, New South Wales, Australia.; Mirzaa GM; Norcliffe Foundation Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, USA.; Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA.; Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, Washington, USA.; Chaumette B; INSERM U1266, Institute of Psychiatry and Neuroscience of Paris, Université Paris Cité, Paris, France.; Legrand A; GHU PARIS Psychiatrie et Neurosciences, Sainte-Anne Hospital, Paris, France.; McTague A; Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health, London, UK.; Department of Neurology, Great Ormond Street Hospital, London, UK.; Stödberg T; Division of Pediatric Neurology, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.; Section of Pediatric Neurology, Astrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.; Harris RV; Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.; Berkovic SF; Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.; Scheffer IE; Epilepsy Research Centre, Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.; Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, Royal Children's Hospital, The University of Melbourne, Parkville, Victoria, Australia.; Florey Institute of Neuroscience and Mental Health, Heidelberg, Victoria, Australia.; Chebib M; School of Medical Sciences, Faculty of Medicine and Health, Brain and Mind Centre, The University of Sydney, Camperdown, New South Wales, Australia.; Gardella E; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Filadelfia, Member of the European Reference Network EpiCARE, Dianalund, Denmark.; Department of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark, Odense, Denmark.; Ahring PK; School of Medical Sciences, Faculty of Medicine and Health, Brain and Mind Centre, The University of Sydney, Sydney, New South Wales, Australia.; Absalom NL; School of Medical Sciences, Faculty of Medicine and Health, Brain and Mind Centre, The University of Sydney, Sydney, New South Wales, Australia.; School of Science, Western Sydney University, Penrith, New South Wales, Australia.; Behaviour and Development, MARCS Institute for Brain, Westmead, New South Wales, Australia.; Møller RS; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre, Filadelfia, Member of the European Reference Network EpiCARE, Dianalund, Denmark.; Department of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark, Odense, 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

Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany. johannes.lemke@medizin.uni-leipzig.de.; Eoli A; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Krey I; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.; Popp B; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Strehlow V; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Wittekind DA; Department of Psychiatry and Psychotherapy, University of Leipzig Medical Center, Leipzig, Germany.; Institue for Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University of Leipzig Medical Center, Leipzig, Germany.; Vuorinen AL; Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.; Faculty of Social Sciences, Unit of Health Sciences, Tampere University, Tampere, Finland.; Aldhalaan HM; Department of Neuroscience Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.; Baer S; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; de Saint Martin A; Department of Pediatric Neurology, University Hospitals of Strasbourg, Strasbourg, France.; Hammer TB; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Herman I; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Hornemann F; Department of Pediatrics, Klinikum Chemnitz, Chemnitz, Germany.; Ingebrigtsen T; National Centre for Epilepsy, Oslo University Hospital, Oslo, Norway.; Lederer D; Centre de Génétique Humaine, Institut de Pathologie et Génétique (IPG), Charleroi (Gosselies), Belgium.; Lesca G; Department of Medical Genetics, University Hospital of Lyon, Claude Bernard University Lyon 1, Lyon, France.; Marafie D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Faculty of Medicine, Kuwait University, Safat, Kuwait.; Mathot M; Neuropediatric Unit, CHU UCL-Namur, Namur, Belgium.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Baylor Genetics Laboratory, Houston, TX, USA.; Møller RS; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Centre, Dianalund, Denmark.; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.; Schelhaas HJ; Department of Neurology, Stichting Epilepsie Instellingen Nederland, SEIN, Zwolle, The Netherlands.; Stillman C; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Orsini A; Section of Pediatric Neurology, Division of Pediatrics, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.; Patel AD; Division of Pediatric Neurology, Nationwide Children's Hospital, Department of Pediatrics, The Ohio State College of Medicine, Columbus, OH, USA.; Piard J; Centre de Génétique Humaine, Centre Hospitalier Universitaire, Université de Franche-Comté, Besançon, France.; UMR 1231 GAD, Inserm, Université de Bourgogne, Dijon, France.; Veggiotti P; Neuroscience Research Center, Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.; Pediatric Neurology Unit, Buzzi Children's Hospital, Milan, Italy.; Vlaskamp DRM; Department of Genetics and Department of Neurology, University Medical Center Groningen, Groningen, The Netherlands.; Weckhuysen S; VIB-Center for Molecular Neurology, VIB, Antwerp, Belgium.; Department of Neurology, University Hospital Antwerp, Antwerp, Belgium.; Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; Traynelis SF; Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.; Center for the Functional Evaluation of Rare Variants (CFERV), Emory University School of Medicine, Atlanta, GA, USA.; Benke TA; Section of Child Neurology, Department of Pediatrics, University of Colorado, Aurora, CO, USA.; Heyne HO; Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam, Germany. Henrike.Heyne@hpi.de.; Windreich Department of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Henrike.Heyne@hpi.de.; Finnish Institute for Molecular Medicine (FIMM), University of Helsinki, Helsinki, Finland. Henrike.Heyne@hpi.de.; Syrbe S; Heidelberg University, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Clinic 1, Division of Pediatric Epileptology, Heidelberg, Germany.

Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE

Moya-Mendez ME; Department of Pediatrics, Division of Pediatric Cardiology, Duke University School of Medicine, Durham, North Carolina.; Bidzimou MT; Department of Pediatrics, Division of Pediatric Cardiology, Duke University School of Medicine, Durham, North Carolina.; Muralidharan P; Department of Pediatrics, Division of Pediatric Cardiology, Duke University School of Medicine, Durham, North Carolina.; Zhang Z; Department of Pediatrics, Division of Pediatric Cardiology, Duke University School of Medicine, Durham, North Carolina.; Ezekian JE; Department of Pediatrics, Division of Pediatric Cardiology, Duke University School of Medicine, Durham, North Carolina.; Division of Pediatric Cardiology, Department of Pediatrics, University of Texas Southwestern, Dallas.; Perelli RM; Department of Cell Biology, Duke University School of Medicine, Durham, North Carolina.; Parker LE; Department of Pediatrics, Division of Pediatric Cardiology, Duke University School of Medicine, Durham, North Carolina.; Prange L; Department of Pediatrics, Division of Neurology, Duke University School of Medicine, Durham, North Carolina.; Boggs A; Department of Pediatrics, Division of Neurology, Duke University School of Medicine, Durham, North Carolina.; Kim JJ; Department of Pediatrics, Section of Cardiology, Baylor College of Medicine, Houston, Texas.; Howard TS; Department of Pediatrics, Section of Cardiology, Baylor College of Medicine, Houston, Texas.; Word TA; Cardiovascular Research Institute, Baylor College of Medicine, Houston, Texas.; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas.; Wehrens XHT; Department of Pediatrics, Section of Cardiology, Baylor College of Medicine, Houston, Texas.; Cardiovascular Research Institute, Baylor College of Medicine, Houston, Texas.; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas.; Reyes Valenzuela G; Hospital Nacional de Pediatría Juan P. Garrahan, Buenos Aires, Argentina.; Caraballo R; Hospital Nacional de Pediatría Juan P. Garrahan, Buenos Aires, Argentina.; Garone G; Division of Neurology, Bambino Gesù Children's Hospital, Rome, Italy.; Vigevano F; Division of Neurology, Bambino Gesù Children's Hospital, Rome, Italy.; Weckhuysen S; Department of Neurology, Antwerp University Hospital, Antwerp, Belgium.; Applied and Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; Millevert C; Department of Neurology, Antwerp University Hospital, Antwerp, Belgium.; Applied and Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Troncoso M; Child Neurology Service, Hospital San Borja Arriarán, University of Chile, Santiago, Chile.; Matamala M; Child Neurology Service, Hospital San Borja Arriarán, University of Chile, Santiago, Chile.; Balestrini S; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.; Neuroscience Department, Meyer Children's Hospital, European Reference Network ERN EpiCARE, Florence, Italy.; Chalfont Centre for Epilepsy, London, United Kingdom.; Sisodiya SM; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.; Chalfont Centre for Epilepsy, London, United Kingdom.; Poole J; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, United Kingdom.; Chalfont Centre for Epilepsy, London, United Kingdom.; Zucca C; Clinical Neurophysiology Unit, IRCCS Eugenio Medea, Bosisio Parini, Italy.; Panagiotakaki E; Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, University Hospitals of Lyon, Lyon, France.; Papadopoulou MT; Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, University Hospitals of Lyon, Lyon, France.; Tchaicha S; Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, University Hospitals of Lyon, Lyon, France.; Zawadzka M; Department of Developmental Neurology, Medical University of Gdansk, Gdansk, Poland.; Mazurkiewicz-Beldzinska M; Department of Developmental Neurology, Medical University of Gdansk, Gdansk, Poland.; Fons C; Pediatric Neurology Department, Hospital Sant Joan de Déu, Barcelona University, Institut de Recerca Sant Joan de Déu, Barcelona, Spain.; Anticona J; Pediatric Neurology Department, Hospital Sant Joan de Déu, Barcelona University, Institut de Recerca Sant Joan de Déu, Barcelona, Spain.; De Grandis E; Child Neuropsychiatry Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Cordani R; Child Neuropsychiatry Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Pisciotta L; Unit of Child Neuropsychiatry, ASST Fatebenefratelli Sacco, Milan, Italy.; Groppa S; Clinic of Neurology, Johannes Gutenberg University of Mainz, Mainz, Germany.; Paryjas S; Clinic of Neurology, Johannes Gutenberg University of Mainz, Mainz, Germany.; Ragona F; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.; ERN EpiCARE, Milan, Italy.; Mangia E; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.; ERN EpiCARE, Milan, Italy.; Granata T; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.; ERN EpiCARE, Milan, Italy.; Megvinov A; Informatics Department, Euro-Mediterranean Institute of Science and Technology, Palermo, Italy.; Pavlicek M; French Alternating Hemiplegia of Childhood Association, Issou, France.; Ess K; Children's Hospital Colorado, Aurora.; Simmons CQ; Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.; George AL Jr; Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.; Vavassori R; Informatics Department, Euro-Mediterranean Institute of Science and Technology, Palermo, Italy.; IAHCRC International Consortium for the Research on Alternating Hemiplegia of Childhood and Other ATP1A3 Related Diseases, Palermo, Italy.; European Patient Advocacy Group, ERN EpiCARE, Palermo, Italy.; Association AHC18+ eV, Bischofsheim, Germany.; Mikati MA; Department of Pediatrics, Division of Neurology, Duke University School of Medicine, Durham, North Carolina.; Landstrom AP; Department of Pediatrics, Division of Pediatric Cardiology, Duke University School of Medicine, Durham, North Carolina.; Department of Cell Biology, Duke University School of Medicine, Durham, North Carolina.

Publisher: American Medical Association Country of Publication: United States NLM ID: 101589544 Publication Model: Print Cited Medium: Internet ISSN: 2168-6211 (Electronic) Linking ISSN: 21686203 NLM ISO Abbreviation: JAMA Pediatr Subsets: MEDLINE