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Isaacs' Syndrome Associated With Acetylcholine Receptor Antibodies Developed After Removal of Malignant Thymoma

Seo JY, Shin BS, Seo MW, Kim YH, Oh SY

  • KMID: 2184980
  • J Korean Neurol Assoc.
  • 2010 Aug;28(3):203-205.
Isaacs' syndrome is a rare and heterogeneous syndrome of continuous muscle fiber activity that originates from peripheral nerves. We report a 56-year-old male patient who showed symptoms of Isaacs' syndrome...
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Anesthetic experience using total intravenous anesthesia in a patient with Isaacs' syndrome: A case report

Kim YM, Lee SH, Han CS, Choi EM, Choi YR, Chung MH

We report on an anesthetic experience with a 74-year-old female with Isaacs' syndrome, who underwent elective surgery for open rotator cuff repair. Isaacs' syndrome is a rare peripheral motor neuron...
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A Case of Isaacs' Syndrome

Kang JK, Lee SA, Kim KK, Lee MC, Choe GY

  • KMID: 1957366
  • J Korean Neurol Assoc.
  • 1993 Dec;11(4):592-598.
A case of Isaacs syndrome with Trousseau s phenomenon wac studied electrophysiologically and histologically. The needle electromyography showed typical neuromyotonic discharges of spontaneous recurrent high-frequency(150-300Hz) bursts of motor unit activity...
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A Case of Morvan Syndrome

Kim SG, Kwon SB, Kwon KH, Jung S, Hwang SH

  • KMID: 1636116
  • J Korean Neurol Assoc.
  • 2006 Dec;24(6):585-588.
Neuromyotonia, or Isaacs' syndrome, consists of continuous muscle fiber activity caused by hyperexcitability of the peripheral nerves. Rarely, these patients also develop CNS symptoms characterized by confusion, insomnia, hallucinations, and...
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A Case of Isaacs' Syndrome Associated with Small Cell Lung Cancer

Hong JK, Choi NC, Jeon SC, Gwak J, Lee YH, Park KJ, Kwon OY, Lim BH

  • KMID: 2342844
  • J Korean Neurol Assoc.
  • 2000 Jul;18(4):499-502.
Isaacs' syndrome consists of spontaneously occurring muscle activity of peripheral nerve origins. This syndrome arises in association with/without polyneuropathy and rarely with malignancy. A 63-year-old man was admitted to our...
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Ocular Neuromyotonia in a Patient with Orbital Metastasis

Ahn KM, Lee SY, Hwang JY, Lee SH, Ha SW, Han JH, Cho EK, Kim DE

  • KMID: 2065774
  • J Korean Neurol Assoc.
  • 2011 Feb;29(1):59-61.
No abstract available.
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Channelopathies

Kim JB

Channelopathies are a heterogeneous group of disorders resulting from the dysfunction of ion channels located in the membranes of all cells and many cellular organelles. These include diseases of the...
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A Case of Idiopathic Ocular Neuromyotonia

Lee JM, Kim JI, Kang BW, Park SP, Suh CK

  • KMID: 2195082
  • J Korean Neurol Assoc.
  • 2003 Jun;21(3):315-317.
Ocular neuromyotonia (ONM) is an episodic involuntary contraction of one or more extraocular muscles, resulting from spontaneous neural discharges of ocular motor nerves. Previous radiation therapy to pituitary or other...
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Myasthenia in Acquired Neuromyotonia

Byun JI, Moon HJ, Hong YH

  • KMID: 2400179
  • J Clin Neurol.
  • 2014 Jan;10(1):69-71.
BACKGROUND: Acquired neuromyotonia (NMT) forms part of the spectrum of acquired peripheral nerve hyperexcitability syndrome, and is thought to be caused by antibodies to voltage-gated potassium channels (VGKC). Exertional weakness...
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The Diagnosis and Treatment of Autoimmune Encephalitis

Lancaster

Autoimmune encephalitis causes subacute deficits of memory and cognition, often followed by suppressed level of consciousness or coma. A careful history and examination may show early clues to particular autoimmune...
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Oculomotor Neuromyotonia with Lid Lag

Yun DJ, Shin HY, Choi KD, Oh SY, Park SH, Hwang JM, Kim JS

  • KMID: 1957684
  • J Korean Neurol Assoc.
  • 2006 Feb;24(1):89-91.
A 52-year-old woman developed episodic diplopia during a period of six months. Between the episodes, depression of the right eye was mildly impaired and lid lag was evident in the...
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