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Seizure. 2019 Mar;66:1-3. doi: 10.1016/j.seizure.2019.01.029. Epub 2019 Jan 30.

Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier.

Author information

1
Department of Epileptology, University of Bonn Hospital, Bonn, Germany.
2
Department of Neurology, University Hospital of Bonn, Bonn, Germany; Center for Rare Diseases Bonn (ZSEB), University Hospital of Bonn, Bonn, Germany.
3
Department of Epileptology, University of Bonn Hospital, Bonn, Germany; Institute of Experimental Epileptology and Cognition Research, University Bonn, Bonn, Germany.
4
Department of Opthalmology, University of Bonn Hospital, Bonn, Germany.
5
Department of Neuropathology, University of Bonn Hospital, Bonn, Germany.
6
Department of Nuclear Medicine, University of Bonn Hospital, Bonn, Germany.
7
Department of Radiology, University of Bonn Hospital, Bonn, Germany.
8
Department of Epileptology, University of Bonn Hospital, Bonn, Germany; Department of Neurology, Section of Epileptology, University Hospital RWTH Aachen, Aachen, Germany.
9
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.

KEYWORDS:

Mitochondrial retinoencephalopathy; OPA-1; Occipital lobe epilepsy

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