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A case of Hypokalemic Familial Periodic Paralysis

Seo SK, Lee GH, Jeong HY, Kim SW, Kim KH

  • KMID: 1682881
  • J Korean Pediatr Soc.
  • 1989 Jul;32(7):1012-1016.
No abstract available.
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Hypokalemic Familial Periodic Paralysis: A Report of 4 members in a family

Rhee KJ, Yune SH, Chae HK

Hypokalemic familial periodic paralysis is one of the rare familial disease characterized by recurrent and transient attacks of weakness or paralysis of the somatic musculature. Also, this disease is usually...
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A Case of Hypokalemic Familial Periodic Paralysis

Kim KN, Noh JK, Kim YC, Lee SN, Kyung NH, Park LG

A case of hypokalemic familial periodic paralysis is presented and the litures are reviewed. A 15-year-old boy was admitted to Ewha Womans University Hospital with chief complaints of paralysis of...
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Genetics of Channelopathy: Familial Periodic Paralysis

Kim MK

  • KMID: 1852252
  • J Korean Neurol Assoc.
  • 2005 Dec;23(6):737-744.
Familial periodic paralysis (FPP) is inherited as a dominant trait, and the intermittent failure to maintain the skeletal muscle resting potential is due to mutations in the genes coding for...
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Clinical Diversity of SCN4A-Mutation-Associated Skeletal Muscle Sodium Channelopathy

Lee SC, Kim HS, Park YE, Choi YC, Park KH, Kim DS

BACKGROUND AND PURPOSE: Mutations of the skeletal muscle sodium channel gene SCN4A, which is located on chromosome 17q23-25, are associated with various neuromuscular disorders that are labeled collectively as skeletal...
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A Practical Approach to Genetic Hypokalemia

Lin SH, Yang SS, Chau T

Mutations in genes encoding ion channels, transporters, exchangers, and pumps in human tissues have been increasingly reported to cause hypokalemia. Assessment of history and blood pressure as well as the...
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