Search Results - "Choi, Kyoung Gyu"
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Clinical predictors of seizure recurrence after the first post-ischemic stroke seizure
Published in BMC neurology (05-11-2016)“…The number of patients suffering post-stroke seizure after ischemic stroke (PSSi) is quite considerable, especially because ischemic stroke is more prevalent…”
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2
Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth Disease
Published in Human mutation (01-11-2012)“…Charcot–Marie–Tooth disease (CMT) is one of the most common inherited neuropathies and is a genetically and clinically heterogeneous disorder with variable…”
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3
Interaction of motor training and intermittent theta burst stimulation in modulating motor cortical plasticity: influence of BDNF Val66Met polymorphism
Published in PloS one (25-02-2013)“…Cortical physiology in human motor cortex is influenced by behavioral motor training (MT) as well as repetitive transcranial magnetic stimulation protocol such…”
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A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14
Published in Human mutation (01-06-2011)“…Both peripheral neuropathy and distal myopathy are well‐established inherited neuromuscular disorders characterized by progressive weakness and atrophy of the…”
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T1-weighted axial visual rating scale for an assessment of medial temporal atrophy in Alzheimer's disease
Published in Journal of Alzheimer's disease (01-01-2014)“…The most-widely used visual rating scale (VRS) for medial temporal atrophy is the T1-weighted (T1W) coronal VRS developed by Scheltens et al. However, it is…”
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Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot-Marie-Tooth neuropathy patients
Published in Human mutation (01-08-2004)“…We examined CMT1A duplication of 17p11.2‐p12, mutations of PMP22, MPZ (P0), GJB1 (Cx32), EGR2 and NEFL genes in 57 Korean families with patients diagnosed as…”
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A novel GDAP1 Q218E mutation in autosomal dominant Charcot-Marie-Tooth disease
Published in Journal of human genetics (01-04-2008)“…A wide range of phenotypes have been reported in autosomal recessive (AR) Charcot-Marie-Tooth disease (CMT) patients carrying mutations in the…”
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Motor Cortical Excitability in Patients with Poststroke Epilepsy
Published in Epilepsia (Copenhagen) (01-01-2008)“…Summary Purpose: To gain insight into the mechanisms underlying poststroke epilepsy (PSE), we evaluated motor cortical function in chronic stroke patients with…”
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Sleep Related Problems as a Nonmotor Symptom of Dentatorubropallidoluysian Atrophy
Published in Journal of Korean medical science (2018)Get full text
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10
A 6-month longitudinal study of bone mineral density with antiepileptic drug monotherapy
Published in Epilepsy & behavior (01-03-2007)“…Abstract Antiepileptic drugs (AEDs) can affect bone metabolism, but the exact mechanisms or differences in individual drugs are still unknown. The purpose of…”
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SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3
Published in Neurology (09-07-2013)“…OBJECTIVE:To identify the genetic cause of an autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4B (CMT4B) family. METHODS:We enrolled 14…”
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NEUROPSYCHIATRIC SYMPTOMS IN EARLY VERSUS LATE-ONSET AMNESTIC MILD COGNITIVE IMPAIRMENT: THREE-YEAR LONGITUDINAL STUDY
Published in Alzheimer's & dementia (01-07-2017)Get full text
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13
A survey of sleep deprivation patterns and their effects on cognitive functions of residents and interns in Korea
Published in Sleep medicine (01-04-2011)“…Abstract Objective To investigate the effects of sleep deprivation on physical health, cognition, and work performance in residents and interns who suffer from…”
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14
Effect of Individual and District-level Socioeconomic Disparities on Cognitive Decline in Community-dwelling Elderly in Seoul
Published in Journal of Korean medical science (01-09-2017)“…This study was to investigate the effects of individual and district-level socioeconomic status (SES) on the development of cognitive impairment among the…”
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15
Individual Therapeutic Singing Program for Vocal Quality and Depression in Parkinson’s Disease
Published in Journal of movement disorders (01-09-2018)“…Objective Patients with Parkinson’s disease (PD) frequently experience depression associated with voice problems. Singing involves the use of similar muscles…”
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Erratum to: Clinical predictors of seizure recurrence after the first post-ischemic stroke seizure
Published in BMC neurology (04-05-2017)“…After publication of the original article [1], it came to the authors’ attention that there was an error in the abstract under the Methods heading. The first…”
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Multiplex analysis of cytokines in the serum and cerebrospinal fluid of patients with Alzheimer's disease by color-coded bead technology
Published in Journal of clinical neurology (Seoul, Korea) (01-06-2008)“…The availability and promise of effective treatments for neurodegenerative disorders are increasing the importance of early diagnosis. Having molecular and…”
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MPZ mutation in an early-onset Charcot-Marie-Tooth disease type 1B family by genome-wide linkage analysis
Published in International journal of molecular medicine (01-09-2011)“…Charcot-Marie-Tooth disease (CMT) is a clinically and genetically heterogeneous peripheral neuropathy. The objective of this study was to find the causative…”
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Encephalopathy in an Elderly Patient Following Oral Ingestion of Topical Methyl Salicylate
Published in Journal of neurocritical care (01-06-2016)“…Background: Methyl salicylate overdose is usually caused by frequent topical applications or accidental ingestion, especially in children. Case Report: A…”
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Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication
Published in Journal of clinical neurology (Seoul, Korea) (01-06-2012)“…Charcot-Marie-Tooth disease (CMT) type 1A (CMT1A) is the demyelinating form of CMT that is significantly associated with PMP22 duplication. Some studies have…”
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