- The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis
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Kim JB, Kim MH, Lee SJ, Kim DJ, Lee BC
- KMID: 1785751
- J Korean Med Sci.
- 2007 Dec;22(6):946-951.
- doi: 10.3346/jkms.2007.22.6.946
Familial hypokalemic periodic paralysis (HOPP) is a rare autosomal-dominant disease characterized by reversible attacks of muscle weakness occurring with episodic hypokalemia. Mutations in the skeletal muscle calcium (CACNA1S) and sodium... -
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- Familial Hemiplegic Migraine with Prolonged Coma and Cerebellar Atrophy: CACNA1A T666M Mutation in a Korean Family
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Choi KH, Kim JS, Lee SY, Ryu SW, Kim SS, Lee SH, Kim S, Park HK
- KMID: 1782151
- J Korean Med Sci.
- 2012 Sep;27(9):1124-1127.
- doi: 10.3346/jkms.2012.27.9.1124
We report the first Korean patient with familial hemiplegic migraine type 1, with clinical and multimodal imaging findings. A 43-yr-old man was admitted for right hemianopia and aphasia, followed by... -
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