UnKyu Yun

ORCID: 0000-0001-6469-5874
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Muscle Physiology and Disorders
  • Neurogenetic and Muscular Disorders Research
  • Intracerebral and Subarachnoid Hemorrhage Research
  • Neurosurgical Procedures and Complications
  • Brain Metastases and Treatment
  • Genetic Syndromes and Imprinting
  • Healthcare and Venom Research
  • Cardiomyopathy and Myosin Studies
  • Venous Thromboembolism Diagnosis and Management
  • Traumatic Brain Injury and Neurovascular Disturbances
  • Memory and Neural Mechanisms
  • Intracranial Aneurysms: Treatment and Complications
  • Herpesvirus Infections and Treatments
  • Long-Term Effects of COVID-19
  • Peripheral Neuropathies and Disorders
  • Meningioma and schwannoma management
  • Pathogenesis and Treatment of Hiccups
  • Intensive Care Unit Cognitive Disorders
  • Parkinson's Disease Mechanisms and Treatments
  • Genomics and Rare Diseases
  • Glioma Diagnosis and Treatment
  • Neuroscience and Neuropharmacology Research
  • Cardiac tumors and thrombi
  • Diabetic Foot Ulcer Assessment and Management
  • Neurological and metabolic disorders

Sejong General Hospital
2021-2022

Gangnam Severance Hospital
2020

Yonsei University
2020

Seoul Veterans Hospital
2017-2019

Seoul Medical Center
2018

Dystrophinopathy is a group of inherited phenotypes arising from pathogenic variants in DMD . We evaluated the clinical and genetic characteristics Korean patients with genetically confirmed dystrophinopathy. retrospectively reviewed medical records (January 2004-September 2020) myopathy database maintained at study hospital found 227 218 unrelated families Clinical included 120 (53%) Duchenne muscular dystrophy (DMD) cases, 20 (9%) intermediate phenotype (IMD) 65 (29%) Becker (BMD) 18 (8%)...

10.1371/journal.pone.0255011 article EN cc-by PLoS ONE 2021-07-23

We investigated the clinical, laboratory, and genetic spectra in Korean patients with dysferlinopathy to clarify its genotype-phenotype correlation. retrospectively reviewed 101 from 96 unrelated families pathogenic variants of DYSF. The most common initial phenotype was Miyoshi myopathy 50 patients. Median ages at examination symptom onset were 23 [interquartile range (IQR): 18-30] 36 years [IQR: 27-48], respectively. observed 38 variants, including nine novel variants. Four (c.2494C > T,...

10.1111/cge.13887 article EN Clinical Genetics 2020-11-20

Transient global amnesia (TGA) is defined by a sudden onset of anterograde and retrograde that lasts up to 24 h.The clinical feature this syndrome has been discussed in recent studies.Several etiological factors, such as epileptic phenomena, migraine-related mechanisms, focal ischemia, venous flow abnormalities, have implicated its pathophysiology. 1 A 68-year-old male visited our emergency room with temporary memory loss.He was taking medications for hypertension benign prostate...

10.12779/dnd.2017.16.4.132 article EN Dementia and Neurocognitive Disorders 2017-01-01

Zoster-associated limb paresis is a relatively uncommon complication of herpes zoster that characterized by focal motor weakness. Awareness this disorder important to avoid unnecessary invasive investigations and ensure appropriate treatment. We report case involving the femoral nerve.

10.14253/acn.2019.21.1.44 article EN Annals of Clinical Neurophysiology 2019-01-01

뇌경색에서 출혈변환(hemorrhagic transformation)의 위험인자로 는 고령, 고혈압, 심장성색전증에 의한 경우 항혈전제 치료 등이

10.17340/jkna.2019.1.20 article EN Journal of the Korean Neurological Association 2019-02-01
Coming Soon ...