The clinical and genetic heterogeneity of paroxysmal dyskinesias

Brain - Tập 138 Số 12 - Trang 3567-3580 - 2015
A. Gardiner1,2, Fatima Jaffer1,2, Russell C. Dale3, Robyn Labrum4, Roberto Erro5, Esther Meyer6, Georgia Xiromerisiou1,7, María Stamelou5,8,9, Matthew C. Walker10, Dimitri M. Kullmann10, Thomas T. Warner1, Paul Jarman5, Michael G. Hanna2, Manju A. Kurian11,6, Kailash P. Bhatia5, Henry Houlden1,2,4
1Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK
2MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK
3Paediatrics and Child Health, Children's Hospital, Westmead, University of Sydney, Australia
4Neurogenetics Laboratory, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK
5Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK
6Developmental Neurosciences, UCL Institute of Child Health, London WC1N 3JH, UK
7Department of Neurology, Papageorgiou Hospital, Thessaloniki University of Athens, Greece
8Department of Neurology, University of Athens, Greece
9Department of Neurology, Philipps University, Marburg, Germany
10Department of Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK
11Department of Neurology, Great Ormond Street Hospital, London WC1N, UK

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Brain

Tập 138 Số 12

3567-3580

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