Browsing by Yonsei Author : Choi, Young Chul

eperson profile image
Name:
Choi, Young Chul [최영철]
orcid http://orcid.org/0000-0001-5525-6861
Department :
College of Medicine (의과대학) - Dept. of Neurology (신경과학교실)
Scopus ID :
Scopus (7404776179)

Keyword Cloud

Researcher Network

Showing results 1 to 50 of 214

This table browses all dspace content
Issue DateTitleJournal Title
2023Transcriptome analysis of skeletal muscle in dermatomyositis, polymyositis, and dysferlinopathy, using a bioinformatics approach FRONTIERS IN NEUROLOGY
2023Novel Pathogenic Variant in PIEZO4 in a Korean Patient with Distal Arthrogryposis Journal of Electrodiagnosis and Neuromuscular Diseases
2023Clinical significance of anti-NT5c1A autoantibody in Korean patients with inflammatory myopathies PLOS ONE
2023Anti-titin antibodies are associated with myocarditis in patients with myasthenia gravisJOURNAL OF NEUROLOGY
2023Transcriptome profiling of skeletal muscles from Korean patients with Bethlem myopathy MEDICINE
2022Serum uric acid level predicts the progression of amyotrophic lateral sclerosis following treatment with edaravone REDOX REPORT
2022Validation of the Individualized Neuromuscular Quality of Life Questionnaire in Korean Patients With Genetic Neuromuscular Diseases JOURNAL OF CLINICAL NEUROLOGY
2022Clinical and Pathological Findings of Korean Patients with Selenoprotein N-Related Myopathy Journal of the Korean Association of EMG-Electrodiagnostic Medicine
2022The avalglucosidase alfa phase 3 COMET trial in late-onset Pompe disease patients: Efficacy and safety results after 97 weeksMOLECULAR GENETICS AND METABOLISM
2022Incidence, Disability, and Mortality in Patients With Guillain-Barré Syndrome in Korea: A Nationwide Population-Based Study JOURNAL OF CLINICAL NEUROLOGY
2021Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trialLANCET NEUROLOGY
2021A Compound Heterozygous Pathogenic Variant in B4GALNT1 Is Associated With Axonal Charcot-Marie-Tooth Disease JOURNAL OF CLINICAL NEUROLOGY
2021Evaluating an In-House Cell-Based Assay for Detecting Antibodies Against Muscle-Specific Tyrosine Kinase in Myasthenia Gravis JOURNAL OF CLINICAL NEUROLOGY
2021Predicting Insignificant Prostate Cancer: Analysis of the Pathological Outcomes of Candidates for Active Surveillance according to the Pre-International Society of Urological Pathology (Pre-ISUP) 2014 Era Versus the Post-ISUP2014 Era WORLD JOURNAL OF MENS HEALTH
2021Clinical and genetic spectra in patients with dystrophinopathy in Korea: A single-center study PLOS ONE
2021진단되지 않은 근육병 환자를 대상으로 시행한 늦은 발병 폼페병의 다기관 표적집단선별검사 Journal of the Korean Neurological Association(대한신경과학회지)
2021Clinical Features and Brain MRI Findings in Korean Patients with AGel Amyloidosis YONSEI MEDICAL JOURNAL
2021근육병 환자의 평가를 위한 임상 척도 Journal of the Korean Neurological Association(대한신경과학회지)
2021Null variants in DYSF result in earlier symptom onsetCLINICAL GENETICS
2021Nogo-A Is Critical for Pro-Inflammatory Gene Regulation in Myocytes and Macrophages CELLS
2021Nogo-A regulates myogenesis via interacting with Filamin-C CELL DEATH DISCOVERY
2021Two Cases of Facioscapulohumeral Muscular Dystrophy 2 in Korea YONSEI MEDICAL JOURNAL
2020First Case of TARDBP-Related Amyotrophic Lateral Sclerosis in Korea JOURNAL OF CLINICAL NEUROLOGY
2020Prevalence, Mortality, and Cause of Death in Charcot-Marie-Tooth Disease in Korea: A Nationwide, Population-Based StudyNEUROEPIDEMIOLOGY
2020Olaparib monotherapy for Asian patients with a germline BRCA mutation and HER2-negative metastatic breast cancer: OlympiAD randomized trial subgroup analysis SCIENTIFIC REPORTS
2020Hereditary Spastic Paraplegia with Axonal Sensorimotor Polyneuropathy in a Korean Family Caused by Pathogenic Variant of KIF5A (c.611G>A) JOURNAL OF CLINICAL NEUROLOGY
2020LGMD2E with a novel nonsense variant in SGCB gene: a case of LGMD2E with a novel variant Annals of Clinical Neurophysiology
2020Gender Differences Influence Over Insomnia in Korean Population: A Cross-Sectional Study PLOS ONE
2020Proteomic Analysis of the Skeletal Muscles From Dysferlinopathy PatientsJOURNAL OF CLINICAL NEUROSCIENCE
2019Prevalence and Socioeconomic Status of Patients with Genetic Myopathy in Korea: A Nationwide, Population-Based StudyNEUROEPIDEMIOLOGY
2019Clinical and Radiographic Characteristics of Neuro-Behçet's Disease in South Korea JOURNAL OF CLINICAL NEUROLOGY
2019Progression of GNE Myopathy Based on the Patient-Reported Outcome Journal of Clinical Neurology
2019Unusual cortical involvement in aquaporin-4 antibody-positive patients: An analysis with double inversion recovery and phase-sensitive inversion recovery imagingMultiple Sclerosis and Related Disorders
2019Effect of thymectomy in elderly patients with non-thymomatous generalized myasthenia gravisJournal of Neurology
2019Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort st Scientific Reports
2019호흡곤란으로 인한 의식저하가 발생한 Tropomyosin 3 (TPM3) 유전자 돌연변이에 의한 선천근섬유형불균형 1가계 Journal of the Korean Neurological Association (대한신경과학회지)
2019Comparative transcriptome analysis of skeletal muscle in ADSSL1 myopathyNEUROMUSCULAR DISORDERS
2019Neurological Manifestations of Myeloneuropathy in Patients with Nitrous Oxide Intoxication JOURNAL OF CLINICAL NEUROLOGY
2018Henoch-Schönlein Purpura Presenting as Mononeuritis Multiplex JOURNAL OF CLINICAL NEUROLOGY
2018Two Korean Families with Limb-Girdle Muscular Dystrophy Type 1D Associated with DNAJB6 Mutations YONSEI MEDICAL JOURNAL
2018Lower-extremity magnetic resonance imaging in patients with hyperkalemic periodic paralysis carrying the SCN4A mutation T704M: 30-month follow-up of seven patients.NEUROMUSCULAR DISORDERS
2018Risk factors for osteoporosis in chronic inflammatory demyelinating polyradiculoneuropathy.MUSCLE & NERVE
2018선천성 혈소판감소증을 동반한 GNE 근육병증 Korean Journal of Neuromuscular Disorders (대한신경근육질환학회지)
2018Clinical and laboratory features of patients with osteomalacia initially presenting with neurological manifestationsOSTEOPOROSIS INTERNATIONAL
2018Pathogenic Variant of REEP1 in a Korean Family with Autosomal-Dominant Hereditary Spastic Paraplegia JOURNAL OF CLINICAL NEUROLOGY
2018Partial Conduction Block as an Early Nerve Conduction Finding in Neurolymphomatosis JOURNAL OF CLINICAL NEUROLOGY
2018FAT1 Gene Alteration in Facioscapulohumeral Muscular Dystrophy Type 1 YONSEI MEDICAL JOURNAL
2018Clinical and Pathologic Findings of Korean Patients with RYR1-Related Congenital Myopathy JOURNAL OF CLINICAL NEUROLOGY
2017Identification of FASTKD2 compound heterozygous mutations as the underlying cause of autosomal recessive MELAS-like syndromeMITOCHONDRION
2017Long-Term Outcome of Amyotrophic Lateral Sclerosis in Korean Subjects Annals of Rehabilitation Medicine

Browse

Links