- Electrophysiological Changes by Exercise and Cold Provocation Test in a Patient with Hyperkalemic Periodic Paralysis
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Kim GS, Choo MK, Oh YM, Kim SM, Sunwoo IN
- KMID: 2065467
- J Korean Neurol Assoc.
- 2000 Sep;18(5):665-668.
Hyperkalemic periodic paralysis and paramyotona congenita share common clinical manifestations, such as autosomal dominant diseases with missense mutations at a gene encoding alpha-subunit of skeletal muscle voltage sensitive sodium channel... -
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- A Case of Hyperkalemic Periodic Paralysis Induced by Diabetic Nephropathy
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Lee CS, Park JM, Kim MS, Lee JH, Kim DY, Lim YB, Lee YK
- KMID: 2258893
- Korean J Med.
- 2011 Jun;80(Suppl 2):S227-S232.
Hyperkalemic periodic paralysis is characterized by episodic flaccid paralysis of the skeletal muscles due to an increase in serum potassium concentrations. Primary hyperkalemic periodic paralysis is caused by point mutations... -
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- Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A
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Han JY, Kim JB
- KMID: 1506498
- Korean J Pediatr.
- 2011 Nov;54(11):470-472.
- doi: 10.3345/kjp.2011.54.11.470
Familial hyperkalemic periodic paralysis (HYPP) is an autosomaldominant channelopathy characterized by transient and recurrent episodes of paralysis with concomitant hyperkalemia. Mutations in the skeletal muscle voltage-gated sodium channel gene SCN4A... -
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- A family with hyperkalemic periodic paralysis
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Kim J, Kim JM
- KMID: 2016264
- J Korean Neurol Assoc.
- 1997 Aug;15(4):931-936.
We report clinical characteristics of seven members in a family with hyper kalemic periodic paralysis (HYPP). Duration of periodic paralysis were noted for 3 to 7 days in adult patients,... -
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- A Case of Addison's Disease Accompanied by Painless Thyroiditis and Hyperkalemic Periodic Paralysis
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Koh MJ, Seo HM, Kim YU, Kim S, Lee SA, Yoo WS, Kim SM
- KMID: 2269131
- Korean J Med.
- 2015 Apr;88(4):442-446.
- doi: 10.3904/kjm.2015.88.4.442
In cases of hyperkalemia with preserved renal function, the differential diagnoses that should be considered are drug-related disorders, primary tubular disease, and hormonal diseases including primary adrenal insufficiency. Addison's disease... -
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- Genetics of Channelopathy: Familial Periodic Paralysis
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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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- Electrodiagnostic Findings and Clinical Characteristics of Familial Hyperkalemic Periodic Paralysis With a SCN4A Met1592Val Mutation
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Lee JY, Kim JY, Kim JG, Kang JH, Choi JC, Lee JS, Kang SY
- KMID: 2184978
- J Korean Neurol Assoc.
- 2010 Aug;28(3):186-191.
BACKGROUND: Hyperkalemic periodic paralysis (HYPP) is characterized by episodic flaccid paralysis of skeletal muscles that is exacerbated by the consumption of potassium-containing foods, fasting, or rest following exercise. HYPP is... -
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- A Case of Adynamia Episodica Hereditaria
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Hu K, Choi IS, Kim KH
- KMID: 1957588
- J Korean Neurol Assoc.
- 1983 Jun;1(1):101-105.
Four members of a family suffering from frequent attacks of flaccid paralysis with asymptomatic myotonia were evaluated. There was an autosomal dominant pattern of inheritance and their earliest symptoms were... -
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- Clinical Diversity of SCN4A-Mutation-Associated Skeletal Muscle Sodium Channelopathy
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Lee SC, Kim HS, Park YE, Choi YC, Park KH, Kim DS
- KMID: 2287648
- J Clin Neurol.
- 2009 Dec;5(4):186-191.
- doi: 10.3988/jcn.2009.5.4.186
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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- Whole-Body Muscle MRI in Patients with Hyperkalemic Periodic Paralysis Carrying the SCN4A Mutation T704M: Evidence for Chronic Progressive Myopathy with Selective Muscle Involvement
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Lee YH, Lee HS, Lee HE, Hahn S, Nam TS, Shin HY, Choi YC, Kim SM
- KMID: 2179752
- J Clin Neurol.
- 2015 Oct;11(4):331-338.
- doi: 10.3988/jcn.2015.11.4.331
BACKGROUND AND PURPOSE: Hyperkalemic periodic paralysis (hyperKPP) is a muscle sodium-ion channelopathy characterized by recurrent paralytic attacks. A proportion of affected individuals develop fixed or chronic progressive weakness that results... -
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- A Case of Adynamia Episodica Hereditaria
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Lee SS, Lee MS, Kim WT, Choi IS
- KMID: 2065860
- J Korean Neurol Assoc.
- 1988 Jun;6(1):122-126.
This is a case report of 32 year-old man with adynamia episodica hereditaria. Adynamia episodica hereditaria is a rare disorder characterized by episodic atacks of muscle weakness occuring in association... -
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