2004 | Identification of a Dysferlin Gene Mutation in a Korean Case with Miyoshi Myopathy
| YONSEI MEDICAL JOURNAL |
2017 | Identification of FASTKD2 compound heterozygous mutations as the underlying cause of autosomal recessive MELAS-like syndrome | MITOCHONDRION |
2016 | Impact of smoking on neurodegeneration and cerebrovascular disease markers in cognitively normal men | EUROPEAN JOURNAL OF NEUROLOGY |
2022 | Incidence, Disability, and Mortality in Patients With Guillain-Barré Syndrome in Korea: A Nationwide Population-Based Study
| JOURNAL OF CLINICAL NEUROLOGY |
2004 | Increase in Transglutaminase 2 in Idiopathic Inflammatory Myopathies | EUROPEAN NEUROLOGY |
2001 | Induction of a1-Acid Glycoprotein mRNA by Cytokines and Differentiation in Human Colon Carcinoma Cell
| MOLECULES AND CELLS |
2012 | Insulin resistance is independently associated with peripheral and autonomic neuropathy in Korean type 2 diabetic patients | ACTA DIABETOLOGICA |
2020 | LGMD2E with a novel nonsense variant in SGCB gene: a case of LGMD2E with a novel variant
| Annals of Clinical Neurophysiology |
2017 | Long-Term Outcome of Amyotrophic Lateral Sclerosis in Korean Subjects
| Annals of Rehabilitation Medicine |
2015 | Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumeral muscular dystrophy type 1 | NEUROMUSCULAR DISORDERS |
2018 | Lower-extremity magnetic resonance imaging in patients with hyperkalemic periodic paralysis carrying the SCN4A mutation T704M: 30-month follow-up of seven patients. | NEUROMUSCULAR DISORDERS |
2005 | Magnetic resonance tractography in a patient with alexia without agraphia | EUROPEAN NEUROLOGY |
2004 | Merosin 결핍 선천성근이영양증 1예
| Journal of the Korean Neurological Association |
2005 | Miyoshi형 원위부 근육병증 1례
| Journal of the Korean Association of EMG-Electrodiagnostic Medicine |
2015 | Molecular Genetic Diagnosis of a Bethlem Myopathy Family with an Autosomal-Dominant COL6A1 Mutation, as Evidenced by Exome Sequencing
| JOURNAL OF CLINICAL NEUROLOGY |
2010 | Multiplex Ligation-dependent Probe Amplification (MLPA) 방법에 의한 디스트로핀 유전자 돌연변이 분자학적 진단의 유용성
| Journal of the Korean Neurological Association |
2006 | MuSK antibody-positive, seronegative myasthenia gravis in Korea | JOURNAL OF CLINICAL NEUROSCIENCE |
2005 | MuSK 항체 양성을 보이는 혈청음성 중증근무력증 환자의 임상적 특징
| Journal of the Korean Neurological Association |
2006 | Mutation analysis of the GNE gene in Korean patients with distal myopathy with rimmed vacuoles | JOURNAL OF HUMAN GENETICS |
2019 | Neurological Manifestations of Myeloneuropathy in Patients with Nitrous Oxide Intoxication
| JOURNAL OF CLINICAL NEUROLOGY |
2007 | Neuromyelitis optica with brainstem lesion mistaken for brainstem glioma. Case report. | JOURNAL OF NEUROSURGERY |
2021 | Nogo-A Is Critical for Pro-Inflammatory Gene Regulation in Myocytes and Macrophages
| CELLS |
2021 | Nogo-A regulates myogenesis via interacting with Filamin-C
| CELL DEATH DISCOVERY |
2009 | Novel CLCN1 mutations and clinical features of korean patients with myotonia congenita.
| JOURNAL OF KOREAN MEDICAL SCIENCE |
2017 | Novel Mutation (c.8725T>C) in Two Siblings With Late-Onset LAMA2-Related Muscular Dystrophy
| ANNALS OF LABORATORY MEDICINE |
2023 | Novel Pathogenic Variant in PIEZO4 in a Korean Patient with Distal Arthrogryposis
| Journal of Electrodiagnosis and Neuromuscular Diseases |
2021 | Null variants in DYSF result in earlier symptom onset | CLINICAL GENETICS |
2020 | Olaparib monotherapy for Asian patients with a germline BRCA mutation and HER2-negative metastatic breast cancer: OlympiAD randomized trial subgroup analysis
| SCIENTIFIC REPORTS |
2015 | Pandemic influenza A vaccination and incidence of Guillain-Barré syndrome in Korea | VACCINE |
2018 | Partial Conduction Block as an Early Nerve Conduction Finding in Neurolymphomatosis
| JOURNAL OF CLINICAL NEUROLOGY |
2018 | Pathogenic Variant of REEP1 in a Korean Family with Autosomal-Dominant Hereditary Spastic Paraplegia
| JOURNAL OF CLINICAL NEUROLOGY |
2005 | Phenotypic variability in Kennedy's disease: implication of the early diagnostic features | ACTA NEUROLOGICA SCANDINAVICA |
2005 | Pneumomediastinum Due to Intractable Hiccup as the Presenting Symptom of Multiple Sclerosis
| YONSEI MEDICAL JOURNAL |
2012 | Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect. | CLINICAL GENETICS |
2021 | Predicting 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 |
2003 | Prediction of Early Clinical Severity and Extent of Neuronal Damage in Anterior-Circulation Infarction Using the Initial Serum Neuron-Specific Enolase Level | ARCHIVES OF NEUROLOGY |
2015 | Predictive factors for myasthenic crisis after videoscopic thymectomy in patients with myasthenia gravis | MUSCLE & NERVE |
2019 | Prevalence and Socioeconomic Status of Patients with Genetic Myopathy in Korea: A Nationwide, Population-Based Study | NEUROEPIDEMIOLOGY |
2014 | Prevalence of Anti-Ganglioside Antibodies and Their Clinical Correlates with Guillain-Barre Syndrome in Korea: A Nationwide Multicenter Study
| JOURNAL OF CLINICAL NEUROLOGY |
2020 | Prevalence, Mortality, and Cause of Death in Charcot-Marie-Tooth Disease in Korea: A Nationwide, Population-Based Study | NEUROEPIDEMIOLOGY |
2008 | Prognosis of ocular myasthenia in Korea: a retrospective multicenter analysis of 202 patients | JOURNAL OF THE NEUROLOGICAL SCIENCES |
2019 | Progression of GNE Myopathy Based on the Patient-Reported Outcome
| Journal of Clinical Neurology |
2020 | Proteomic Analysis of the Skeletal Muscles From Dysferlinopathy Patients | JOURNAL OF CLINICAL NEUROSCIENCE |
2016 | Recurrent Episodes of Rhabdomyolysis after Seizures in a Patient with Glycogen Storage Disease Type V
| JOURNAL OF CLINICAL NEUROLOGY |
2018 | Risk factors for osteoporosis in chronic inflammatory demyelinating polyradiculoneuropathy. | MUSCLE & NERVE |
2019 | Risk of osteoporosis in patients with chronic inflammatory neuropathy- a population-based cohort st
| Scientific Reports |
2021 | Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial | LANCET NEUROLOGY |
2005 | Serotonin transporter gene polymorphism and migraine in the Korean population | HEADACHE |
2012 | Serum and cerebrospinal fluid neuron-specific enolase for diagnosis of tuberculous meningitis
| YONSEI MEDICAL JOURNAL |
2008 | Serum BAFF expression in patients with myasthenia gravis | JOURNAL OF NEUROIMMUNOLOGY |
2015 | Serum interleukin-27 expression in patients with myasthenia gravis | JOURNAL OF NEUROIMMUNOLOGY |
2010 | Serum neuron-specific enolase level as a biomarker in differential diagnosis of seizure and syncope | JOURNAL OF NEUROLOGY |
2022 | Serum uric acid level predicts the progression of amyotrophic lateral sclerosis following treatment with edaravone
| REDOX REPORT |
1996 | Sleep related periodic leg movments associated with spinal cord lesion | MOVEMENT DISORDERS |
2016 | Spinal cord involvement in Behçet’s disease | MULTIPLE SCLEROSIS JOURNAL |
2000 | Sporadic inclusion body myositis correlates with increased expression and cross-linking by transglutaminases 1 and 2
| Journal of Biological Chemistry |
2014 | Subdural hemorrhage mimicking peripheral neuropathy.
| JOURNAL OF KOREAN NEUROSURGICAL SOCIETY |
2010 | Superficial siderosis in cervical disc herniation | EUROPEAN NEUROLOGY |
2015 | Targeted next-generation sequencing for the genetic diagnosis of dysferlinopathy | NEUROMUSCULAR DISORDERS |
2017 | Targeted population screening of late onset Pompe disease in unspecified myopathy patients for Korean population | NEUROMUSCULAR DISORDERS |