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Progressive Muscular Atrophy with Hypokalemic Periodic Paralysis: A Case Report

Bae YK, Lee JH, Sim YJ, Jeong HJ, Kim GC

Progressive muscular atrophy (PMA) is a rare disease involving lower motor neuron degeneration. Hypokalemic periodic paralysis (HypoPP) is a genetic disorder that causes temporary muscle paralysis due to decreased serum...
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Persistent Hypokalemic Paralysis in a Patient with Graves’ Disease and Gitelman Syndrome

Jeong JW, Yu TY

Thyrotoxic periodic paralysis (TPP) is a potentially life-threatening condition. Graves’ disease accounts for the majority of cases of TPP. However, another diagnosis should be considered when repeated hypokalemic paralysis occurs...
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Hypokalemic Paralysis: A Report of Two Different Cases

Jeong EJ, Lee HI, Yoo HJ, Kwon HK, Lee HJ, Pyun SB

Hypokalemic paralysis is a cause of acute paralysis that can be classified as primary (familial) or secondary according to its etiology. Routine electrodiagnostic examinations can be normal between attacks, potentially...
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Hypokalemic Periodic Paralysis Developed in a Patient with Neurogenic Diabetes Insipidus

Hwang J, Sung JH, Kim YE, Kim K, Kim SH, Park YB, Baek SH

Hypokalemic periodic paralysis one of the channelopathy disorders with low serum potassium level, clinically presenting as acute onset extremity weakness. In most cases, the cause of the hypokalemia is familial,...
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Confirming Genetic Abnormalities of Hypokalemic Periodic Paralysis Using Next-Generation Sequencing: A Case Report and Literature Review

Kim HR, Jeon JW, Lee EJ, Ham YR, Na KR, Lee KW, Park KH, Kim SY, Choi DE

Hypokalemic periodic paralysis (hypoPP) is a disorder characterized by episodic, short-lived, and hypo-reflexive skeletal muscle weakness. HypoPP is a rare disease caused by genetic mutations related to expression of sodium...
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Perioperative Management of a Patient with Hypokalemic Periodic Paralysis: A Case Report

Bae SI, Hwang Y, Kim J, Tak S, Sohn JT

Potassium imbalances can be life-threatening and must be identified and corrected prior to surgery. Patients with hypokalemic periodic paralysis (hypoKPP) experience recurrent muscle weakness or paralysis due to hypokalemia. We...
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Acetazolamide-Induced Type II Renal Tubular Acidosis and Muscle Weakness

Bin CH, Kim JH

No abstract available.
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A Case Report of Thyrotoxic Periodic Paralysis; Serial Nerve Conduction Studies before and after Recovery

Kim MS, Park JA, Seok JI

No abstract available.
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Glucocorticoid Triggers an Attack of Periodic Hypokalemic Paralysis during Treatment for Diffuse Large B-cell Lymphoma

Ha KS, Park YJ, Park SS, Lee JY, Kim JH, Jang I, Byun JH

Hypokalemic periodic paralysis is a rare disorder characterized by sudden onset of weakness and low serum potassium levels. We report a case provoked by combination chemotherapy including prednisolone. A 23-yr-man,...
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The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis

Kim JB, Kim SJ, Kang SY, Yi JW, Kim SM

PURPOSE: Familial hypokalemic periodic paralysis (HOKPP) is an autosomal dominant channelopathy characterized by episodic attacks of muscle weakness and hypokalemia. Mutations in the calcium channel gene, CACNA1S, or the sodium...
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Etiology of Hypokalemic Paralysis in Korea: Data from a Single Center

Wi JK, Lee HJ, Kim EY, Cho JH, Chin SO, Rhee SY, Moon JY, Lee SH, Jeong KH, Ihm CG, Lee TW

Recognizing the underlying causes of hypokalemic paralysis seems to be essential for the appropriate management of affected patients and their prevention of recurrent attacks. There is, however, a paucity of...
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Thyrotoxic Periodic Paralysis Associated with Transient Thyrotoxicosis Due to Painless Thyroiditis

Oh SB, Ahn J, Oh MY, Choi BG, Kang JH, Jeon YK, Kim SS, Kim BH, Kim YK, Kim IJ

Thyrotoxic periodic paralysis (TPP) is a rare manifestation of hyperthyroidism characterized by muscle weakness and hypokalemia. All ethnicities can be affected, but TPP typically presents in men of Asian descent....
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A Case of Thyrotoxic Periodic Paralysis in a 16-Year-Old Adolescent

Ahn MB, Jung YJ, Lee MH, Cho WK, Suh BK

Thyrotoxic periodic paralysis (TPP) is a transient illness characterized by muscle weakness often associated with hypokalemia during thyrotoxic state. Hypokalemia is induced by thyroid hormone excess through stimulation of Na-K...
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An Arg528His Mutation of the CACNL1A3 Gene in a Korean Family with Hypokalemic Periodic Paralysis

Kim KR, Suh ES, Lee YM

  • KMID: 2043932
  • J Korean Child Neurol Soc.
  • 2012 Mar;20(1):28-32.
Familial hypokalemic periodic paralysis (HOPP) is an autosomal dominant disorder characterized by episodic attacks of muscle weakness with concomitant hypokalemia (
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A Case of Thyrotoxic Periodic Paralysis in Adolescent with Graves' Disease

Oh KW, Jeong JY, Kim JS

Thyrotoxic periodic paralysis (TPP) is a rare complication of hyperthyroidism characterized by recurrent paralysis of skeletal muscle and hypokalemia caused by a massive intracellular shift of potassium. TPP mainly affects...
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Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations

Kim H, Hwang H, Cheong HI, Park HW

Primary hypokalemic periodic paralysis (HOKPP) is an autosomal dominant disorder manifesting as recurrent periodic flaccid paralysis and concomitant hypokalemia. HOKPP is divided into type 1 and type 2 based on...
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An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene SCN4A

Park YH, Kim JB

Familial hypokalemic periodic paralysis is an autosomal-dominant channelopathy characterized by episodic muscle weakness with hypokalemia. The respiratory and cardiac muscles typically remain unaffected, but we report an atypical case of...
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A case of type 2 diabetes manifested by hypokalemic periodic paralysis

Yeom DH, Kim HY, Park BH, Cho CG

  • KMID: 2305835
  • Korean J Med.
  • 2009 Apr;76(4):499-501.
Hypokalemic periodic paralysis may be precipitated by stress, rest after exercise, or events that lower serum potassium levels, such as carbohydrate ingestion or the use of insulin or diuretics. In...
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An Arg1239His mutation of the CACNL1A3 gene in a Korean family with hypokalemic periodic paralysis

Yeo CY, Kim YO, Kim MK, Kim JY, Cho YK, Kim CJ, Woo YJ

Familial hypokalemic periodic paralysis (hypoPP) is a rare inherited channelopathy that often presents with episodic weakness accompanied by hypokalemia. Thus far, mutations in the gene encoding two ion channels (CACNL1A3,...
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The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis

Kim JB, Kim MH, Lee SJ, Kim DJ, Lee BC

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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