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- W2397525518 abstract "Familial hypokalaemic periodic paralysis is an autosomal dominant muscle disease which has been linked to point mutations in the skeletal muscle L-type calcium channel alpha 1 subunit (alpha 1 s). It consists of muscular weakness episodes due to hypokalaemia caused by intracellular shifting of potassium. We describe the case of a young man of Kurdish origin, with a history of Graves' disease, who was admitted to the emergency room with hypotonic tetraplegia associated with severe hypokalaemia." @default.
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- W2397525518 date "2000-11-04" @default.
- W2397525518 modified "2023-09-23" @default.
- W2397525518 title "Hypokalaemic periodic paralysis associated with controlled thyrotoxicosis." @default.
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