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Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series.
Dzinovic, Ivana; Skorvánek, Matej; Necpál, Ján; Boesch, Sylvia; Svantnerová, Jana; Wagner, Matias; Havránková, Petra; Pavelekova, Petra; Han, Vladimír; Janzarik, Wibke G; Berweck, Steffen; Diebold, Isabel; Kuster, Alice; Jech, Robert; Winkelmann, Juliane; Zech, Michael.
Affiliation
  • Dzinovic I; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.
  • Skorvánek M; Department of Neurology, P.J. Safarik University, Kosice, Slovak Republic; Department of Neurology, University Hospital of L. Pasteur, Kosice, Slovak Republic.
  • Necpál J; Department of Neurology, Zvolen Hospital, Slovakia.
  • Boesch S; Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.
  • Svantnerová J; Second Department of Neurology, Faculty of Medicine, Comenius University, University Hospital Bratislava, Bratislava, Slovakia.
  • Wagner M; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Technical University of Munich, Munich, Germany; School of Medicine, Institute of Human Genetics.
  • Havránková P; Department of Neurology, Charles University, 1st Faculty of Medicine and General University Hospital in Prague, Prague, Czech Republic.
  • Pavelekova P; Department of Neurology, P.J. Safarik University, Kosice, Slovak Republic; Department of Neurology, University Hospital of L. Pasteur, Kosice, Slovak Republic.
  • Han V; Department of Neurology, P.J. Safarik University, Kosice, Slovak Republic; Department of Neurology, University Hospital of L. Pasteur, Kosice, Slovak Republic.
  • Janzarik WG; Department of Neuropediatrics and Muscle Disorders, University Medical Center, Faculty of Medicine, University of Freiburg, Germany.
  • Berweck S; Ludwig Maximilian University of Munich, Munich, Germany; Hospital for Neuropediatrics and Neurological Rehabilitation, Centre of Epilepsy for Children and Adolescents, Schoen Klinik Vogtareuth, Vogtareuth, Germany.
  • Diebold I; MGZ - Medical Genetics Center Munich, Munich, Germany; Department of Pediatrics, Technical University of Munich School of Medicine, Munich, Germany.
  • Kuster A; Inborn Errors of Metabolism, Pediatric Intensive Care Unit, University Hospital of Nantes, Nantes, France.
  • Jech R; Department of Neurology, Charles University, 1st Faculty of Medicine and General University Hospital in Prague, Prague, Czech Republic.
  • Winkelmann J; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Technical University of Munich, Munich, Germany; School of Medicine, Institute of Human Genetics; Lehrstuhl für Neurogenetik, Technische Universität München, Munich, Germany; Munich Cluster for Systems Neurology, SyNergy, Munich
  • Zech M; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany; Technical University of Munich, Munich, Germany; School of Medicine, Institute of Human Genetics. Electronic address: michael.zech@mri.tum.de.
Parkinsonism Relat Disord ; 90: 73-78, 2021 09.
Article in En | MEDLINE | ID: mdl-34399161
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases / Dystonia / Neurodevelopmental Disorders / Epileptic Syndromes Type of study: Prognostic_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Parkinsonism Relat Disord Journal subject: NEUROLOGIA Year: 2021 Type: Article Affiliation country: Germany
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases / Dystonia / Neurodevelopmental Disorders / Epileptic Syndromes Type of study: Prognostic_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Parkinsonism Relat Disord Journal subject: NEUROLOGIA Year: 2021 Type: Article Affiliation country: Germany