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PIGN encephalopathy: Characterizing the epileptology.
Bayat, Allan; de Valles-Ibáñez, Guillem; Pendziwiat, Manuela; Knaus, Alexej; Alt, Kerstin; Biamino, Elisa; Bley, Annette; Calvert, Sophie; Carney, Patrick; Caro-Llopis, Alfonso; Ceulemans, Berten; Cousin, Janice; Davis, Suzanne; des Portes, Vincent; Edery, Patrick; England, Eleina; Ferreira, Carlos; Freeman, Jeremy; Gener, Blanca; Gorce, Magali; Heron, Delphine; Hildebrand, Michael S; Jezela-Stanek, Aleksandra; Jouk, Pierre-Simon; Keren, Boris; Kloth, Katja; Kluger, Gerhard; Kuhn, Marius; Lemke, Johannes R; Li, Hong; Martinez, Francisco; Maxton, Caroline; Mefford, Heather C; Merla, Giuseppe; Mierzewska, Hanna; Muir, Alison; Monfort, Sandra; Nicolai, Joost; Norman, Jennifer; O'Grady, Gina; Oleksy, Barbara; Orellana, Carmen; Orec, Laura Elena; Peinhardt, Charlotte; Pronicka, Ewa; Rosello, Monica; Santos-Simarro, Fernando; Schwaibold, Eva Maria Christina; Stegmann, Alexander P A; Stumpel, Constance T.
Affiliation
  • Bayat A; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.
  • de Valles-Ibáñez G; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.
  • Pendziwiat M; Department of Paediatrics and Child Health, University of Otago, Wellington, New Zealand.
  • Knaus A; Department of Neuropediatrics, University Medical Center Schleswig-Holstein, Christian Albrecht University, Kiel, Germany.
  • Alt K; Institute of Clinical Molecular Biology, Christian Albrecht University of Kiel, Kiel, Germany.
  • Biamino E; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rhenish Friedrich Wilhelm University of Bonn, Bonn, Germany.
  • Bley A; Center for Human Genetics, Neu-Ulm, Germany.
  • Calvert S; Department of Pediatrics, Regina Margherita Children's Hospital, Turin, Italy.
  • Carney P; University Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Caro-Llopis A; Center for Rare Diseases, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Ceulemans B; Department of Neurosciences, Queensland Children's Hospital, South Brisbane, Queensland, Australia.
  • Cousin J; Department of Medicine, University of Melbourne, Parkville, Victoria, Australia.
  • Davis S; Genomics Unit, University and Polytechnic Hospital La Fe, Valencia, Spain.
  • des Portes V; Department of Pediatric Neurology, Antwerp University Hospital, Edegem, Belgium.
  • Edery P; Section of Human Biochemical Genetics, National Human Genome Research Institute, Bethesda, Maryland, USA.
  • England E; Department of Paediatrics and Child Health, University of Otago, Wellington, New Zealand.
  • Ferreira C; Department of Neuropediatrics, Lyon University Hospital, Lyon, France.
  • Freeman J; Department of Medical Genetics, University Hospital of Lyon, Lyon, France.
  • Gener B; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, Massachusetts, USA.
  • Gorce M; National Human Genome Research Institute, Bethesda, Maryland, USA.
  • Heron D; Royal Children's Hospital, Parkville, Victoria, Australia.
  • Hildebrand MS; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Jezela-Stanek A; Department of Genetics, Cruces University Hospital, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
  • Jouk PS; Angers University Hospital, Angers, France.
  • Keren B; Department of Genetics, Intellectual Disability and Autism Clinical Research Group, Pierre and Marie Curie University, Pitié-Salpêtrière Hospital, Public Hospital Network of Paris, Paris, France.
  • Kloth K; Royal Children's Hospital, Florey institute and Murdoch Children's Research Institute, Melbourne, Victoria, Australia.
  • Kluger G; Epilepsy Research Centre, Department of Medicine (Austin Health), University of Melbourne, Heidelberg, Victoria, Australia.
  • Kuhn M; Department of Genetics and Clinical Immunology, National Institute of Tuberculosis and Lung Diseases, Warsaw, Poland.
  • Lemke JR; Inserm U1209, Grenoble Alpes University Hospital Center, University of Grenoble Alpes, Grenoble, France.
  • Li H; Department of Genetics, Intellectual Disability and Autism Clinical Research Group, Pierre and Marie Curie University, Pitié-Salpêtrière Hospital, Public Hospital Network of Paris, Paris, France.
  • Martinez F; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Maxton C; Center for Human Genetics, Neu-Ulm, Germany.
  • Mefford HC; Center for Human Genetics, Neu-Ulm, Germany.
  • Merla G; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
  • Mierzewska H; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.
  • Muir A; Emory University School of Medicine, Atlanta, Georgia, USA.
  • Monfort S; Genomics Unit, University and Polytechnic Hospital La Fe, Valencia, Spain.
  • Nicolai J; Clinic for Pediatric Neurology, Hamburg, Germany.
  • Norman J; Center for Pediatric Neurological Disease Research, Department of Cell and Molecular Biology, St, Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • O'Grady G; Department of Pediatrics, Regina Margherita Children's Hospital, Turin, Italy.
  • Oleksy B; Department of Child and Adolescent Neurology, Institute of Mother and Child, Warsaw, Poland.
  • Orellana C; Center for Pediatric Neurological Disease Research, Department of Cell and Molecular Biology, St, Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Orec LE; Department of Neurology, Maastricht University Medical Center, Maastricht, the Netherlands.
  • Peinhardt C; Department of Neurology, Maastricht University Medical Center, Maastricht, the Netherlands.
  • Pronicka E; INTEGRIS Pediatric Neurology, Oklahoma City, Oklahoma, USA.
  • Rosello M; Starship Children's Hospital, Auckland, New Zealand.
  • Santos-Simarro F; Center for Child and Adolescent Medicine, Pediatric Neurology, Heidelberg University Hospital, Heidelberg, Germany.
  • Schwaibold EMC; Department of Neurology, Maastricht University Medical Center, Maastricht, the Netherlands.
  • Stegmann APA; Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland.
  • Stumpel CT; Emory University School of Medicine, Atlanta, Georgia, USA.
Epilepsia ; 63(4): 974-991, 2022 04.
Article in En | MEDLINE | ID: mdl-35179230
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Drug Resistant Epilepsy / Intellectual Disability Type of study: Prognostic_studies Limits: Female / Humans Language: En Journal: Epilepsia Year: 2022 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Drug Resistant Epilepsy / Intellectual Disability Type of study: Prognostic_studies Limits: Female / Humans Language: En Journal: Epilepsia Year: 2022 Document type: Article Affiliation country: