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A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms
Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Journal article › Research › peer-review
- Marisol Sampedro Castañeda, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
, - Edmar Zanoteli, Universidade de Sao Paulo
, - Renata S. Scalco, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
, - Vinicius Scaramuzzi, Universidade de Sao Paulo
, - Vitor Marques Caldas, Universidade de Sao Paulo
, - Umbertina Conti Reed, Universidade de Sao Paulo
, - Andre Macedo Serafim da Silva, Universidade de Sao Paulo
, - Benjamin O'Callaghan, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
, - Rahul Phadke, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
, - Enrico Bugiardini, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
, - Richa Sud, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
, - Samuel McCall, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
, - Michael G. Hanna, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
, - Hanne Poulsen
- Roope Männikkö, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
, - Emma Matthews, Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London
Original language | English |
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Journal | Brain : a journal of neurology |
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Volume | 141 |
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Issue | 12 |
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Pages (from-to) | 3308-3318 |
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Number of pages | 11 |
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ISSN | 0006-8950 |
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DOIs | |
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Publication status | Published - 1 Dec 2018 |
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Citationformats
ID: 138771002