Movement disorders in genetically confirmed mitochondrial disease and the putative role of the cerebellum-Reference-Cited by-同舟云学术

Movement disorders in genetically confirmed mitochondrial disease and the putative role of the cerebellum

Published:2017-09-13 Issue:1 Volume:33 Page:146-155
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Schreglmann Sebastian R.¹²³^ORCID,Riederer Franz²⁴,Galovic Marian³⁵⁶,Ganos Christos¹⁷,Kägi Georg³,Waldvogel Daniel²,Jaunmuktane Zane⁸,Schaller Andre⁹,Hidding Ute⁷,Krasemann Ernst¹⁰,Michels Lars¹¹,Baumann Christian R.²,Bhatia Kailash¹,Jung Hans H.²

Affiliation:

1. Sobell Department of Motor Neuroscience and Movement Disorders; University College London (UCL) Institute of Neurology; Queen Square London UK

2. Department of Neurology; University Hospital Zurich; Zurich Switzerland

3. Department of Neurology; Kantonsspital St. Gallen; St. Gallen Switzerland

4. Neurological Center Rosenhuegel and Karl Landsteiner Institute for Epilepsy Research and Cognitive Neurology; Vienna Austria

5. UK National Institute for Health Research; University College London Hospitals Biomedical Research Centre

6. Department of Clinical and Experimental Epilepsy, University College London (UCL) Institute of Neurology, London, UK; Epilepsy Society; Chalfont St. Peter UK

7. Department of Neurology; University Medical Center Hamburg-Eppendorf; Hamburg Germany

8. Department of Molecular Neuroscience; University College London (UCL) Institute of Neurology and Division of Neuropathology, The National Hospital for Neurology and Neurosurgery; London UK

9. Department of Genetics; Inselspital Bern; Bern Switzerland

10. Department of Human Genetics; Medizinisches Versorgungszentrum (MVZ) Labor Fenner GmbH; Hamburg Germany

11. Clinic of Neuroradiology; University Hospital Zurich; Zurich Switzerland

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference47 articles.

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4. Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study;Luoma;Lancet,2004

5. Familial parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase twinkle;Baloh;Arch Neurol,2007

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