- Reliability and Validity of the Comprehensive Limb and Oral Apraxia Test: Standardization and Clinical Application in Korean Patients With Stroke
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Pyun SB, Hwang YM, Jo SY, Ha JW
- KMID: 2463702
- Ann Rehabil Med.
- 2019 Oct;43(5):544-554.
- doi: 10.5535/arm.2019.43.5.544
OBJECTIVE: To develop and standardize the Limb and Oral Apraxia Test (LOAT) for Korean patients and investigate its reliability, validity, and clinical usefulness for patients with stroke. METHODS: We developed the... -
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- Neuroanatomical Predictors of Dysphagia after Stroke: Voxel-Based Lesion Symptom Mapping Study
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Pyun SB, Yoo HJ, Jung Y, Tae WS
- KMID: 2455053
- J Korean Dysphagia Soc.
- 2019 Jul;9(2):68-76.
- doi: 10.34160/jkds.2019.9.2.003
OBJECTIVE: Dysphagia is a common consequence of stroke with a negative effect on the clinical outcome. Given these potential outcomes, it is important to identify the precursors to dysphagia after... -
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- Crossed Aphasia after Right Corpus Callosum Infarction: a Case Report
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Yoo HS, Kim HS
- KMID: 2469636
- Brain Neurorehabil.
- 2019 Mar;12(1):e6.
- doi: 10.12786/bn.2019.12.e6
Crossed aphasia (CA) is defined as language impairment following right-hemispheric brain lesion in right-handed person. Exact mechanism responsible for CA is ambiguous, and recently several brain lesions have been proposed... -
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- A Novel Homozygous Variant of SETX Causes Ataxia with Oculomotor Apraxia Type 2
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Tariq H, Imran R, Naz S
- KMID: 2424178
- J Clin Neurol.
- 2018 Oct;14(4):498-504.
- doi: 10.3988/jcn.2018.14.4.498
BACKGROUND AND PURPOSE: Autosomal recessive cerebellar ataxias constitute a highly heterogeneous group of neurodegenerative disorders. This study was carried out to determine the clinical and genetic causes of ataxia in... -
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- Association of Brain Lesions and Videofluoroscopic Dysphagia Scale Parameters on Patients With Acute Cerebral Infarctions
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Mo SJ, Jeong HJ, Han YH, Hwang K, Choi JK
- KMID: 2420048
- Ann Rehabil Med.
- 2018 Aug;42(4):560-568.
- doi: 10.5535/arm.2018.42.4.560
OBJECTIVE: To investigate the characteristics and risk factors of dysphagia using the videofluoroscopic dysphagia scale (VDS) with a videofluoroscopic swallowing study (VFSS) in patients with acute cerebral infarctions. METHODS: In this... -
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- Repetitive Transcranial Magnetic Stimulation for Limb-Kinetic Apraxia in Parkinson's Disease
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Park JE
- KMID: 2399610
- J Clin Neurol.
- 2018 Jan;14(1):110-111.
- doi: 10.3988/jcn.2018.14.1.110
No abstract available. -
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- Posterior Type of Alzheimer's Dementia Presenting with Homonymous Hemianopsia
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Park Y, Park KW, Lee CN
- KMID: 2442730
- Dement Neurocogn Disord.
- 2017 Dec;16(4):128-131.
- doi: 10.12779/dnd.2017.16.4.128
BACKGROUND: Alzheimer's disease is a chronic neurodegenerative condition, mostly affecting the medial temporal lobe and associated neocortical structures. In this report, we present a rare clinical manifestation of this disease. CASE... -
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- Neuroanatomical Mechanism of Cerebellar Mutism After Stroke
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Lee S, Na YH, Moon HI, Tae WS, Pyun SB
- KMID: 2400293
- Ann Rehabil Med.
- 2017 Dec;41(6):1076-1081.
- doi: 10.5535/arm.2017.41.6.1076
Cerebellar mutism (CM) is a rare neurological condition characterized by lack of speech due to cerebellar lesions. CM is often reported in children. We describe a rare case of CM... -
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- Apraxia: Review and Update
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Park JE
- KMID: 2392126
- J Clin Neurol.
- 2017 Oct;13(4):317-324.
- doi: 10.3988/jcn.2017.13.4.317
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... -
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- Three Cases of Gait Improvement after Rehabilitation Management in Corticobasal Syndrome
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Bang MH, Kwon J, Kim HS
- KMID: 2390160
- Brain Neurorehabil.
- 2017 Sep;10(2):e16.
- doi: 10.12786/bn.2017.10.e16
Corticobasal syndrome (CBS) is characterized by asymmetric dystonia, and myoclonus accompanied by higher cortical features including apraxia, alien limb phenomena, cortical sensory loss. Here, we report treatment course of 3... -
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- A Novel APTX Variant and Ataxia with Oculomotor Apraxia Type 1
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Manzoor H, Bukhari I, Wajid M, Zhang Y, Zhang H, Brüggemann N, Klein C, Shi Q, Naz S
- KMID: 2391678
- J Clin Neurol.
- 2017 Jul;13(3):303-305.
- doi: 10.3988/jcn.2017.13.3.303
No abstract available. -
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- A Case Report of a 37-Year-Old Alzheimer's Disease Patient with Prominent Striatum Amyloid Retention
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Um YH, Choi WH, Jung WS, Park YH, Lee CU, Lim HK
- KMID: 2387146
- Psychiatry Investig.
- 2017 Jul;14(4):521-524.
- doi: 10.4306/pi.2017.14.4.521
With recent advancement in amyloid imaging, diagnostic application of this new modality has become a great interest among researchers. New ligands, such as 18F- florbetaben, florbetapir and flutemetamol, have been... -
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- Corticobasal Syndrome Initially Presenting with Apraxia of Speech
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Suh J, Jung YJ, Shin CW, Kim YK, Lee JY
- KMID: 2359454
- J Korean Neurol Assoc.
- 2016 Nov;34(5):375-379.
- doi: 10.17340/jkna.2016.4.17
Apraxia of speech is a disorder of speech programming and planning. We report a 64-year-old woman presenting with progressive apraxia of speech that evolved into right-side-dominant akinesia-rigidity syndrome over a... -
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- Reliability and Validity of Korean Version of Apraxia Screen of TULIA (K-AST)
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Kim SJ, Yang YN, Lee JW, Lee JY, Jeong E, Kim BR, Lee J
- KMID: 2382908
- Ann Rehabil Med.
- 2016 Oct;40(5):769-778.
- doi: 10.5535/arm.2016.40.5.769
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... -
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- Corticobasal Degeneration Presenting as Non-Fluent/Agrammatic Primary Progressive Aphasia: A Case Report
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Kim JS, Lee GB, Hong YJ, Park KW
- KMID: 2442857
- Dement Neurocogn Disord.
- 2016 Jun;15(2):55-58.
- doi: 10.12779/dnd.2016.15.2.55
BACKGROUND: Non-fluent agrammatic primary progressive aphasia (naPPA) is characterized by progressive non-fluent speech disorder and might be associated with taupathy such as corticobasal degeneration (CBD) and progressive supranuclear palsy. We... -
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- Ataxia with Oculomotor Apraxia Type 1 without Oculomotor Apraxia: A Case Report
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Lee M, Kim NY, Huh JY, Kim YE, Kim YJ
- KMID: 2364933
- J Clin Neurol.
- 2016 Jan;12(1):126-128.
- doi: 10.3988/jcn.2016.12.1.126
No abstract available. -
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- Genetic studies on speech and language disorders
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Kang C
- KMID: 2169087
- J Biomed Res.
- 2015 Sep;16(3):77-83.
- doi: 10.12729/jbr.2015.16.3.077
Speech and language are uniquely human-specific traits that have contributed to humans becoming the predominant species on earth from an evolutionary perspective. Disruptions in human speech and language function may... -
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- Recent advances in genetic studies of stuttering
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Kang C
- KMID: 2055585
- J Genet Med.
- 2015 Jun;12(1):19-24.
- doi: 10.5734/JGM.2015.12.1.19
Speech and language are uniquely human-specific traits, which contributed to humans becoming the predominant species on earth. Disruptions in the human speech and language function may result in diverse disorders.... -
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- Apraxia of Eyelid Opening After Brain Injury: A Case Report
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Kim MJ, Kim SJ, Kim BR, Lee J
- KMID: 2267097
- Ann Rehabil Med.
- 2014 Dec;38(6):847-851.
- doi: 10.5535/arm.2014.38.6.847
Apraxia of eyelid opening (AEO) is a syndrome characterized by the patient's difficulty in initiating eyelid elevation spontaneously. Most of the reported cases were associated with extrapyramidal diseases. We report... -
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- A Case of Acquired Ocular Motor Apraxia Accompanied with Esotropia due to Multiple Brain Infarcts
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Kim YD, Kim SJ
- KMID: 2217129
- J Korean Ophthalmol Soc.
- 2014 Sep;55(9):1396-1400.
- doi: 10.3341/jkos.2014.55.9.1396
PURPOSE: We present a case of acquired ocular motor apraxia accompanied with esotropia due to multiple brain infarcts. CASE SUMMARY: A 59-year-old male was referred for diplopia that started 9 years... -
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