| 2018 | 3,4 diaminopyridine for the treatment of myasthenia gravis with electrophysiological patterns of Lambert-Eaton myasthenic syndrome | JOURNAL OF CLINICAL NEUROSCIENCE |
| 2012 | A case of acute polyneuropathy with nephrotic syndrome showing transient proximal sensory conduction defects
| YONSEI MEDICAL JOURNAL |
| 2008 | A novel GDAP1 Q218E mutation in autosomal dominant Charcot-Marie-Tooth disease | JOURNAL OF HUMAN GENETICS |
| 2005 | An aggressive form of familial amyloid polyneuropathy caused by a Glu54Gly mutation in the transthyretin gene | EUROPEAN JOURNAL OF NEUROLOGY |
| 2013 | Analysis of high-voltage electrical spinal cord injury using diffusion tensor imaging | JOURNAL OF NEUROLOGY |
| 2009 | Anatomic variation of the innervation of the flexor digitorum profundus muscle and its clinical implications | MUSCLE & NERVE |
| 2009 | Characteristics and the fate of intraluminal thrombus of the intracranial and extracranial cerebral arteries in acute ischemic stroke patients | EUROPEAN NEUROLOGY |
| 2006 | Charcot-Marie-Tooth 2A 환자들의 전기생리학적 특성
| Journal of the Korean Association of EMG-Electrodiagnostic Medicine |
| 2013 | Clinical and electromyographic features of radiation-induced lower cranial neuropathy | CLINICAL NEUROPHYSIOLOGY |
| 2014 | Clinical and Electrophysiologic Responses to Acetylcholinesterase Inhibitors in MuSK-Antibody-Positive Myasthenia Gravis: Evidence for Cholinergic Neuromuscular Hyperactivity
| JOURNAL OF CLINICAL NEUROLOGY |
| 2014 | Clinical and Genetic Aspects in Twelve Korean Patients with Adrenomyeloneuropathy
| YONSEI MEDICAL JOURNAL |
| 2018 | Clinical and laboratory features of patients with osteomalacia initially presenting with neurological manifestations | OSTEOPOROSIS INTERNATIONAL |
| 2018 | Clinical and Pathologic Findings of Korean Patients with RYR1-Related Congenital Myopathy
| JOURNAL OF CLINICAL NEUROLOGY |
| 2017 | Clinical and Pathological Findings of a Korean Family with Pathogenic Variants of the TTN Gene
| JOURNAL OF CLINICAL NEUROLOGY |
| 2016 | Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations
| YONSEI MEDICAL JOURNAL |
| 2019 | Clinical and Radiographic Characteristics of Neuro-Behçet's Disease in South Korea
| JOURNAL OF CLINICAL NEUROLOGY |
| 2009 | Clinical characteristics and outcomes of juvenile and adult dermatomyositis.
| JOURNAL OF KOREAN MEDICAL SCIENCE |
| 2010 | Clinical heterogeneity in Korean patients with nemaline myopathy
| YONSEI MEDICAL JOURNAL |
| 2016 | Clinical Significance of Repetitive Compound Muscle Action Potentials in Patients with Myasthenia Gravis: A Predictor for Cholinergic Side Effects of Acetylcholinesterase Inhibitors
| JOURNAL OF CLINICAL NEUROLOGY |
| 2013 | Clinical, immunohistochemical, Western blot, and genetic analysis in dystrophinopathy | JOURNAL OF CLINICAL NEUROSCIENCE |
| 2017 | Clinical, Pathologic, and Genetic Features of Collagen VI-Related Myopathy in Korea
| JOURNAL OF CLINICAL NEUROLOGY |
| 2019 | Comparative transcriptome analysis of skeletal muscle in ADSSL1 myopathy | NEUROMUSCULAR DISORDERS |
| 2009 | Comparison of the characteristics for in-hospital and out-of-hospital ischaemic strokes | EUROPEAN JOURNAL OF NEUROLOGY |
| 2004 | Cx32 유전자 돌연변이를 보인 CMTX와 PMP22 유전자 중복을 보인 CMT1A 환자들의 임상 및 전기생리학적 특성 비교
| Journal of the Korean Neurological Association |
| 2004 | Cx32 유전자에서 새로이 발견된 돌연변이 V136A와 EGR2 유전자 돌연변이 R359W를 보인 Charcot-Marie-Tooth 환자
| Journal of the Korean Neurological Association |
| 2008 | Different clinical and magnetic resonance imaging features between Charcot-Marie-Tooth disease type 1A and 2A | NEUROMUSCULAR DISORDERS |
| 2010 | Diffuse large B-cell lymphoma presenting as piriformis syndrome | MUSCLE & NERVE |
| 2017 | Discovery of pathogenic variants in a large Korean cohort of inherited muscular disorders | CLINICAL GENETICS |
| 2017 | Distal myopathy with ADSSL1 mutations in Korean patients | NEUROMUSCULAR DISORDERS |
| 2006 | Early onset severe and late-onset mild Charcot–Marie–Tooth disease with mitofusin 2 (MFN2) mutations
| BRAIN |
| 2008 | Early-onset stroke associated with a mutation in mitofusin 2 | NEUROLOGY |
| 2019 | Effect of thymectomy in elderly patients with non-thymomatous generalized myasthenia gravis | Journal of Neurology |
| 2008 | ENMC 진단기준을 이용한 다발성근염의 임상적, 병리학적 특성
| Journal of the Korean Rheumatism Association (대한류마티스학회지) |
| 2021 | Evaluating an In-House Cell-Based Assay for Detecting Antibodies Against Muscle-Specific Tyrosine Kinase in Myasthenia Gravis
| JOURNAL OF CLINICAL NEUROLOGY |
| 2018 | FAT1 Gene Alteration in Facioscapulohumeral Muscular Dystrophy Type 1
| YONSEI MEDICAL JOURNAL |
| 2016 | First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy
| JOURNAL OF CLINICAL NEUROLOGY |
| 2004 | Hereditary neuropathy with liability to pressure palsies와 Charcot-Marie-Tooth1A 환자군의 신경전도검사 소견의 비교
| Journal of the Korean Neurological Association |
| 2012 | Heterogeneous characteristics of Korean patients with dysferlinopathy
| JOURNAL OF KOREAN MEDICAL SCIENCE |
| 2012 | Insulin resistance is independently associated with peripheral and autonomic neuropathy in Korean type 2 diabetic patients | ACTA DIABETOLOGICA |
| 2004 | Isolated Lateropulsion by a Lesion of the Dorsal Spinocerebellar Tract | CEREBROVASCULAR DISEASES |
| 2016 | Juvenile Myasthenia Gravis in Korea: Subgroup Analysis According to Sex and Onset Age | JOURNAL OF CHILD NEUROLOGY |
| 2005 | Kennedy 병의 신경전도검사
| Journal of the Korean Association of EMG-Electrodiagnostic Medicine |
| 2012 | Leprotic neuropathy misdiagnosed as chronic inflammatory demyelinating polyneuropathy.
| LEPROSY REVIEW |
| 2019 | Long-Term Safety and Efficacy of Tacrolimus in Myasthenia Gravis
| Yonsei Medical Journal |
| 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 |
| 2012 | Mechanism of medullary infarction based on arterial territory involvement
| JOURNAL OF CLINICAL NEUROLOGY |
| 2007 | MFN2 유전자 돌연변이가 발견된 축삭형 charcot-marie-tooth 환자들의 하지 MRI 특성
| Journal of the Korean Neurological Association |
| 2006 | Mitofusin 2 (MFN2) 유전자 돌연변이가 있는 Charcot-Marie-Tooth 2A 환자들의 임상 및 유전학적 특성
| Journal of the Korean Neurological Association |
| 2015 | Molecular Genetic Diagnosis of a Bethlem Myopathy Family with an Autosomal-Dominant COL6A1 Mutation, as Evidenced by Exome Sequencing
| JOURNAL OF CLINICAL NEUROLOGY |
| 2008 | NEFL Pro22Arg mutation in Charcot-Marie-Tooth disease type 1 | JOURNAL OF HUMAN GENETICS |
| 2005 | Neurofilament light chain (NEFL) 유전자 돌연변이 CMT 환자들의 전기생리학적 특성
| Journal of the Korean Association of EMG-Electrodiagnostic Medicine |
| 2011 | NMO-IgG 양성 환자에서 숨뇌 병변에 의하여 발생된 난치성 구토 1예
| Journal of Multiple Sclerosis (대한다발성경화증학회지) |
| 2021 | Null variants in DYSF result in earlier symptom onset | CLINICAL GENETICS |
| 2009 | O’Sullivan-McLeod 증후군 1례
| Journal of the Korean Association of EMG-Electrodiagnostic Medicine |
| 2011 | Parkinsonism associated with glucocerebrosidase mutation
| JOURNAL OF CLINICAL NEUROLOGY |
| 2018 | Partial Conduction Block as an Early Nerve Conduction Finding in Neurolymphomatosis
| JOURNAL OF CLINICAL NEUROLOGY |
| 2021 | Postganglionic Sudomotor Dysfunction and Brain Glucose Hypometabolism in Patients with Multiple System Atrophy | JOURNAL OF PARKINSONS DISEASE |
| 2015 | Predictive factors for myasthenic crisis after videoscopic thymectomy in patients with myasthenia gravis | MUSCLE & NERVE |
| 2016 | Predictive model for recovery of visual field after surgery of pituitary adenoma | JOURNAL OF NEURO-ONCOLOGY |
