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YUHSpace1. College of Medicine (의과대학)Dept. of Neurology (신경과학교실)

1. Journal Papers

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Issue DateTitleJournal Title
2025Intensive blood pressure lowering in acute stroke with intracranial stenosis post-thrombectomy: A secondary analysis of the OPTIMAL-BP trialINTERNATIONAL JOURNAL OF STROKE
2025Is motor reserve associated with a rapid progression of Parkinson disease?JOURNAL OF PARKINSONS DISEASE
2025Inverse association of obesity with bout periodicity in episodic cluster headache: a multicenter cross-sectional study JOURNAL OF HEADACHE AND PAIN
2025TMEM14A Gene Affects Hippocampal Sclerosis in Mesial Temporal Lobe Epilepsy JOURNAL OF CLINICAL MEDICINE
2025Nitrous oxide abuse unmasking anti-phospholipid syndrome in a 24-year-old male with cerebral venous thrombosis and pulmonary thromboembolism: a case report BMC NEUROLOGY
2018Characteristics of South Korean Patients with Hereditary Transthyretin Amyloidosis JOURNAL OF CLINICAL NEUROLOGY
2013Decremental Responses to Repetitive Nerve Stimulation in X-Linked Bulbospinal Muscular Atrophy JOURNAL OF CLINICAL NEUROLOGY
2012A Case of Lambert-Eaton Myasthenic Syndrome with Small-Cell Lung Cancer and Transient Increase in Anti-Acetylcholine-Receptor-Binding Antibody Titer JOURNAL OF CLINICAL NEUROLOGY
2012Altered fast and slow inactivation of the N440K Nav1.4 mutant in a periodic paralysis syndromeNEUROLOGY
2012Comparison between Clinical Disabilities and Electrophysiological Values in Charcot-Marie-Tooth 1A Patients with PMP22 Duplication JOURNAL OF CLINICAL NEUROLOGY
2011Serial electrophysiological changes in uraemic patients with tetrodotoxin intoxicationCLINICAL NEUROPHYSIOLOGY
2011Neurogenic muscle hypertrophy in type III spinal muscular atrophyJOURNAL OF THE NEUROLOGICAL SCIENCES
2011Compound mutations of PEO1 and TYMP in a progressive external ophthalmoplegia patient with incomplete mitochondrial neurogastrointestinal encephalomyopathy phenotypeGENES & GENOMICS
2009Brain abnormalities in Sjogren syndrome with recurrent CNS manifestations: association with neuromyelitis opticaMULTIPLE SCLEROSIS
2007CCR2-64I and CCR5Delta32 Polymorphisms in Korean Patients with Myasthenia Gravis JOURNAL OF CLINICAL NEUROLOGY
2007Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean familiesJOURNAL OF HUMAN GENETICS
2005CMT 환자들에서 Neurofilament Light Chain (NEFL) 유전자 돌연변이 분석 Journal of the Korean Neurological Association
2004Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion EXPERIMENTAL AND MOLECULAR MEDICINE
2003Critical illness myopathy 1예 Journal of the Korean Neurological Association(대한신경과학회지)
2003Listeria monocytogenes에 의한 다발성 뇌농양 1예 Journal of the Korean Neurological Association(대한신경과학회지)
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