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Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier.
Nass, Robert Daniel; Hansen, Niels; Quesada, Carlos; Rüber, Theodor; Kornblum, Cornelia; Zsurka, Gábor; Hermann, Philipp; Becker, Albert; Gärtner, Florian; Hattingen, Elke; Block, Wolfgang; Steidl, Eike; Elger, Christian E; Surges, Rainer; Kunz, Wolfram S.
Afiliação
  • Nass RD; Department of Epileptology, University of Bonn Hospital, Bonn, Germany.
  • Hansen N; Department of Epileptology, University of Bonn Hospital, Bonn, Germany.
  • Quesada C; Department of Epileptology, University of Bonn Hospital, Bonn, Germany.
  • Rüber T; Department of Epileptology, University of Bonn Hospital, Bonn, Germany.
  • Kornblum C; Department of Neurology, University Hospital of Bonn, Bonn, Germany; Center for Rare Diseases Bonn (ZSEB), University Hospital of Bonn, Bonn, Germany.
  • Zsurka G; Department of Epileptology, University of Bonn Hospital, Bonn, Germany; Institute of Experimental Epileptology and Cognition Research, University Bonn, Bonn, Germany.
  • Hermann P; Department of Opthalmology, University of Bonn Hospital, Bonn, Germany.
  • Becker A; Department of Neuropathology, University of Bonn Hospital, Bonn, Germany.
  • Gärtner F; Department of Nuclear Medicine, University of Bonn Hospital, Bonn, Germany.
  • Hattingen E; Department of Radiology, University of Bonn Hospital, Bonn, Germany.
  • Block W; Department of Radiology, University of Bonn Hospital, Bonn, Germany.
  • Steidl E; Department of Radiology, University of Bonn Hospital, Bonn, Germany.
  • Elger CE; Department of Epileptology, University of Bonn Hospital, Bonn, Germany.
  • Surges R; Department of Epileptology, University of Bonn Hospital, Bonn, Germany; Department of Neurology, Section of Epileptology, University Hospital RWTH Aachen, Aachen, Germany.
  • Kunz WS; Department of Epileptology, University of Bonn Hospital, Bonn, Germany; Institute of Experimental Epileptology and Cognition Research, University Bonn, Bonn, Germany. Electronic address: wolfram.kunz@ukbonn.de.
Seizure ; 66: 1-3, 2019 Mar.
Article em En | MEDLINE | ID: mdl-30738307
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Epilepsias Parciais / Doenças Mitocondriais / GTP Fosfo-Hidrolases Limite: Adult / Humans / Male Idioma: En Revista: Seizure Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Reino Unido
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Epilepsias Parciais / Doenças Mitocondriais / GTP Fosfo-Hidrolases Limite: Adult / Humans / Male Idioma: En Revista: Seizure Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Reino Unido