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A Case of Early Onset Cerebellar Ataxia with Retained Tendon Reflexes

Lee JB, Lee HY, Yang JS, Lim BK

  • KMID: 2024068
  • J Korean Pediatr Soc.
  • 1997 Jan;40(1):129-133.
Early onset cerebellar ataxia with retained tendon reflexes is clinical syndrome characterized by progressive cerebelar ataxia of unknown etiology with an onset within the first two decades. This disorder was...
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Spinocerebellar Ataxia Type 2 with Only Clinical Feature of Memory Impairment: Case Report

Joo J, Han SW, Ha SW, Han JH, Kim DE, Yang Y

Spinocerebellar ataxia (SCA) is one of a group of genetic disorders characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements....
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Otogenic Brain Abscess Presenting with Gait Ataxia

Cho SH, Park MK, Lee JD, Hwang CS

Although the occurrence of otogenic brain abscess has been considerably reduced through improvements to antibiotics, brain abscesses remains one of the most significant life threatening complications of chronic otitis media....
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Episodic Ataxia Type 2 with Downbeating Nystagmus Caused by Mutation in the CACNA1A: A Case Report

Yun S, Chang YJ, Jung SC, Kwon JW, Lee GH, Lee CM, Song YM, Kim JI

  • KMID: 1626918
  • J Korean Neurol Assoc.
  • 2005 Jun;23(3):399-401.
Episodic ataxia type 2 (EA 2) is a rare disorder characterized by intermittent episodes of ataxia with interictal nystagmus. The authors report a patient with EA 2, who presented with...
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Vestibular Dysfunction in Acute Cerebellar Ataxia

Lee CM

Acute cerebellar ataxia is described as a clinical syndrome of acute onset of cerebellar dysfunction with a good long-term prognosis. The pathogenesis of acute cerebellar ataxia remains unclear. A 55-year-old...
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Acquired Hepatocerebral Degeneration Presenting with Downbeat Nystagmus and Ataxia: A Case Report

Lee CM, Yu HJ, Ryu JA, Kim JI

  • KMID: 2185264
  • J Korean Neurol Assoc.
  • 2007 Feb;25(1):101-104.
Nystagmus or ataxia is a rare manifestation of acquired hepatocerebral degeneration (AHCD). A 49-year-old woman presented with downbeat nystagmus and limb and gait ataxia. She was diagnosed as primary biliary...
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A Case of Familial Spinocerebellar Ataxia Type 8

Lee SH, Ki CS, Cho HI, Lee PW, Kim JW, Lee WY

  • KMID: 2343123
  • J Korean Neurol Assoc.
  • 2004 Dec;22(6):659-662.
Spinocerebellar ataxia type 8 (SCA8), originally described in a family characterized by pure cerebellar ataxia, is caused by the expansion of combined CTA/CTG repeats on chromosome 13q21. We experienced a...
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Ataxia in Thalamic Stroke

Yoon SS, Chang DI, Chung KC

  • KMID: 2066045
  • J Korean Neurol Assoc.
  • 1996 Mar;14(1):69-73.
BACKGROUND & PURPOSE: Of thalamic stroke syndrome, according to previous reports, the syndrome of hemiataxia and hemisensory loss (thalamic ataxia syndrome) is known to have localizing value confined to the...
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Ataxic Form of Central Pontine Myelinolysis Developed during Alcohol Withdrawal in a Chronic Alcoholic

Shin DS, Jeong D, Yang KI, Park HK, Oh HG

Central pontine myelinolysis (CPM) is well-recognized osmotic demyelination syndrome that is related to various conditions such as rapid correction of hyponatremia and chronic alcoholism. Acute ataxia as a sole clinical...
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Wernicke's Syndrome Induced by Hyperemesis Gravidarum

Kim YH, Lee SJ, Yoon JK, Hong WP

  • KMID: 2205981
  • J Korean Ophthalmol Soc.
  • 2001 Mar;42(3):538-541.
PURPOSE: Wernicke's syndrome, which is characterized by nystagmus, abducent and conjugate gaze palsies, ataxia, mental confusion, and amnesia, is caused by a deficiency in levels of thiamine and is observed...
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Lithium-Induced Downbeat Nystagmus with Reversible Splenial Lesion

Kim DU, Lee SH, Jung HJ, Kang KW

  • KMID: 2328962
  • J Korean Bal Soc.
  • 2007 Dec;6(2):150-154.
Lithium is recognized as a cause of reversible or permanent downbeat nystagmus. Many patients who were treated with lithium for psychiatric illness developed downbeat nystagmus and other neurological manifestations. Reversible...
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Four Cases of Wernicke's Encephalopathy with Impaired Horizontal Vestibular Ocular Reflexes

Jang HS, Shin BS, Seo MW, Oh SY

Wernicke's encephalopathy (WE) is a neurological disorder induced by a dietary vitamin B1 (thiamine) deficiency which is characterized by encephalopathy, gait ataxia, and variant ocular motor dysfunction. In addition to...
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Acute-Onset Chronic Inflammatory Demyelinating Polyradiculoneuropathy Mimicking Miller-Fisher Syndrome

Baek HS, Bin CH, Park MS

A 77-year-old man developed diplopia, gait ataxia, and paresthesia. A clinical examination also revealed ophthalmoplegia, facial palsy, ataxia of the limbs and trunk, and reduced deep tender reflexes. Laboratory and...
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A Family of Dentatorubropallidoluysian Atrophy

Chung JY, Park MY, Lee J, Yoon JP, Park HJ

  • KMID: 2320174
  • Yeungnam Univ J Med.
  • 2006 Jun;23(1):118-123.
Dentatorubropallidoluysian atrophy (DRPLA) is a rare neurodegenerative disorder usually inherited in an autosomal dominant pattern. DRPLA has been shown to be associated with expansion of an unstable cytosine-adenine-guanine (CAG) trinucleotide...
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Wernicke's Encephalopathy Associated with Hyperthyoidism in Hyperemesis Gravidrum

Han JE, Kang TJ, Kim YJ, Ahn JJ, Woo BH

A case report is presented on a patient with Wernicke's encephalopathy secondary to hyperemesis gravidarum. The 30-year-old woman was admitted with a severe dehydrated state, ataxia, dizziness at 17 weeks....
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A Case of Ramsay Hunt Syndrome Complicated by Cerebellitis

Park HK, Lee JH

Cerebellitis associated with herpes zoster has rarely been observed. We report here a 76-year-old man who had a history of anterior resection for sigmoid colon cancer and presented during chemotherapy...
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Two Cases of Acute Cerebellitis

Nam HS, Lee KY, Jung YK, Lee BI, Kim WC, Kim WJ, Choi YC, Chung WK

  • KMID: 1812898
  • J Korean Neurol Assoc.
  • 1999 May;17(3):403-406.
Acute cerebellitis occurrs in the absence of cerebral hemispheric involvement and is exceptionally rare. It is charac-terized by an acute onset of cerebellar dysfunction following a respiratory, gastrointesitnal infection or...
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A Clinical Study of 38 Cases of Olivopontocerebellar Atrophy

Kim BJ, Kim JW, Kim KK, Rho JK, lee SB, Myung HJ

  • KMID: 2065893
  • J Korean Neurol Assoc.
  • 1989 Dec;7(2):244-251.
Olivopontocerebellar atrophy (OPCA) is a form of degenerative disease associated with neuronal degeneration in the cerebellar cortex, pons, and inferior olives. The authors have reviewed 38 cases, clinically diagnosed as...
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A Case of Sjogren's Syndrome Presented with Vertigo as a Initial Manifestation

Park JY, Lee JD, Lee TK, Sung KB

  • KMID: 2316772
  • Res Vestib Sci.
  • 2009 Jun;8(1):70-73.
Sjogren's syndrome (SS) can shows various neurologic symptoms as it involves the central, peripheral and autonomic nervous system. However, CNS involvement as a initial manifestation is rare. We report a...
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Non-systemic Vasculitic Neuropathy Presenting as Ascending Paralysis

Yu HS, Kim SM, Kwon KH, Lee BC, Shin JH, Kang IS

  • KMID: 1539431
  • J Korean Geriatr Soc.
  • 1999 Dec;3(4):56-61.
Typical vasculitic neuropathy commonly manifests as a subacute multiple mononeuropathy, symmetrical or asymmetrical sensori-motor polyneuropathy. Various clinical presentations of peripheral neuropathy may confuse the diagnostic approach sometimes. A 76-year old...
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