Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

66 results
Display

Repetitive Transcranial Magnetic Stimulation for Limb-Kinetic Apraxia in Parkinson's Disease

Park JE

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Apraxia of Eyelid Closure and Motor Impersistence of Eyelid in a Patient with Amyotrophic Lateral Sclerosis

Shin DI, Lee SH, Lee SS

  • KMID: 2343274
  • J Korean Neurol Assoc.
  • 2007 Aug;25(3):434-437.
No abstract available
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Apraxia of Eyelid Opening Caused by Lithium

Kim SE, Lee SH, Lee SY, Yeo MJ, Choi KH, Kim SH, Lee KU

  • KMID: 2343388
  • J Korean Neurol Assoc.
  • 2010 Nov;28(4):329-331.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Apraxia of Eyelid Opening Secondary to Right Thalamic Infarction

Koh SB, Kim BJ, Park MK, Park KW, Lee DH

  • KMID: 2342994
  • J Korean Neurol Assoc.
  • 2002 Jul;20(4):394-396.
Apraxia of eyelid opening is nonparalytic inability to open the eyes at will in the absence of visible contraction of the orbicularis oculi muscle. It is known that apraxia of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Ataxia with Oculomotor Apraxia Type 1 without Oculomotor Apraxia: A Case Report

Lee M, Kim NY, Huh JY, Kim YE, Kim YJ

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Reliability and Validity of Korean Version of Apraxia Screen of TULIA (K-AST)

Kim SJ, Yang YN, Lee JW, Lee JY, Jeong E, Kim BR, Lee J

OBJECTIVE: To evaluate the reliability and validity of Korean version of AST (K-AST) as a bedside screening test of apraxia in patients with stroke for early and reliable detection. METHODS: AST...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Novel APTX Variant and Ataxia with Oculomotor Apraxia Type 1

Manzoor H, Bukhari I, Wajid M, Zhang Y, Zhang H, Brüggemann N, Klein C, Shi Q, Naz S

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Joubert Syndrome Presented with Ocular Motor Apraxia

Cho EH, Kim YS, Jin YH

  • KMID: 2205192
  • J Korean Ophthalmol Soc.
  • 1995 Dec;36(12):2276-2281.
Agenesis of the cerebellar vermis, episodic hyperpnea alternating with apnea, abnormal eye movement, ataxia, and psychomotor retardation are shown in Joubert syndrome. This rare syndrome is inherited as an autosomal...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pure Apraxia of Speech after the Left Insular Infarction

Cho KH, Lee JH, Kwon SU, Song HS, Kwon M

  • KMID: 2065611
  • J Korean Neurol Assoc.
  • 2006 Oct;24(5):479-482.
Apraxia of speech (AOS) is a disorder in programming the speech musculature to produce the correct sounds of words in the proper sequence. Pure AOS without other speech-language deficit is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Sporadic Congenital Oculomotor Apraxia Associated with Ataxia

Hong S, Han S, Lee J

  • KMID: 2207852
  • J Korean Ophthalmol Soc.
  • 2005 Aug;46(8):1368-1373.
PURPOSE: To evaluate the natural clinical course of sporadic congenital oculomotor apraxia associated with ataxia. METHODS: In a retrospective study from June 1994 to March 2004, 3 patients with sporadic...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical and EMG Characteristics of Pretarsal Motor Persistence

Joo US, Lee PH, Lee JH, Yong SW

  • KMID: 1626995
  • J Korean Neurol Assoc.
  • 2005 Feb;23(1):128-131.
Pretarsal motor persistence (PMP), a subtype of apraxia of the eyelid opening, is characterized by the inability to open the eyelids at will due to persistent activity of orbicularis oculi...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of ataxia telangiectasia

Kang DW, Ahn SS, Jeon BS

  • KMID: 2016258
  • J Korean Neurol Assoc.
  • 1997 Aug;15(4):895-899.
Ataxia telangiectasia is an autosomal recessive disorder characterized by progressive cerebellar degeneration, cancer predisposition, immune defects, radiosensitivity and genetic instability. Ataxia telangiectasia is rare and has not been reported in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Congenital Ocular Motor Apraxia

Kim WJ, Chang BL

  • KMID: 1950056
  • J Korean Ophthalmol Soc.
  • 1992 Mar;33(3):263-267.
Congenital ocular motor apraxia (COA), first described by Cogan in 1953, is a rare disorder which shows characteristic defect of horizontal voluntary saccades and head thrust. Until now, most cases...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Unilateral congenital ocular motor apraxia: a case report

Kim WJ, Chang BL

Congenital ocular motor apraxia (COA), first described by Cogan in 1953, is a rare disorder which shows characteristic defects of the horizontal voluntary saccades, and compensatory head thrust. Until now,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Bedside Evaluation of Neurobehavioral Disorders

Jeong Y, Na DL

  • KMID: 2342985
  • J Korean Neurol Assoc.
  • 2002 Jul;20(4):325-338.
This article provides clinical practice guidelines for neurologists in the assessment of neurobehavioral and neurocognitive deficits. It has been known that cognitive functions lie mainly in the cortex and that...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Crossed Aphasia in a Dextral

Lee SK, Kim JW, Ha KM

  • KMID: 2016120
  • J Korean Neurol Assoc.
  • 1992 Jun;10(2):219-223.
A strictly right handed patient showed aphasia and left hemiplegia following a deep infarct of the right hemisphere. He had no personal or family history o{ left-handedness. His aphasia was...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Apraxia of Eyelid Closing and Unilateral Meige's Syndrome Complicating Left Middle Cerebral Artery Infarction

Kim JW, Yeo SH, Yong SW, Lee PH

  • KMID: 2343273
  • J Korean Neurol Assoc.
  • 2007 Aug;25(3):430-433.
Apraxia of eyelid closure is an uncommon condition characterized by difficulties in voluntary eye closing with preserved normal blinking. Meige's syndrome is a disorder of adults, and is characterized by...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Two Cases of Congenital Ocular Motor Apraxia Associated With Cerebellar Vermian Dysplasia

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

  • KMID: 2181878
  • J Korean Bal Soc.
  • 2008 Jun;7(1):63-67.
Congenital ocular motor apraxia is a rare syndrome characterized by rotational head thrusts that attempt to compensate for the lack of voluntary eye movements. We describe the clinical, oculographic and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Ocular Motor Apraxia after Sequential Bilateral Striatal Infarctions

Chung PW, Moon HS, Song HS, Kim YB

Ocular motor apraxia has been reported in bilateral frontoparietal lesions. We report a case of ocular motor apraxia after bilateral striatal infarctions. The patient had impaired voluntary saccades and smooth...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Apraxia: Review and Update

Park JE

Praxis, the ability to perform skilled or learned movements is essential for daily living. Inability to perform such praxis movements is defined as apraxia. Apraxia can be further classified into...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr