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A Case of Levetiracetam-induced Rhabdomyolysis

Kim H, Lee H, Kim H, Sung E, Kim YS

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Differential Diagnosis of Middle Cerebellar Peduncle Signal Changes on Brain MRI

Jang SH, Chae S, Yun DM, Lim SM, Yoon SJ

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Multiple Cerebral Infarction Associated with Microscopic Polyangiitis

Kim H, Sung E, Lee H, Koh SH, Lee KY, Choi H

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Pulsatile Tinnitus Caused by Engorged Persistent Stapedial Artery with Dural Arteriovenous Fistula

Han SK, Hyung SW, Lee JY, Sunwoo M, Yu HJ

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Neurological Manifestations of MTHFR-related Hyperhomocysteinemia

Kang M, Ahn JW, Kim S, Seok HY, Park JS

Methylene-tetrahydrofolate reductase (MTHFR) is a homocysteine metabolism-related enzyme and defects of MTHFR is a risk factor for hyperhomocysteinemia and related various neurological disease. Among them, 665C>T polymorphism is the most...
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Focal Clonic Seizure Manifested in Diabetic Ketoacidosis

Park SM, Lee JJ, Yoo I, Kim YS, Kang K, Lee WW, Kim BK

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High Attenuate CT Crescent Sign in Basilar Artery Dissection Patient

Lee CJ, Lee DK, Lee MA, Hwang BW, Kim JH, Moon HS, Ahn SH

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Disseminated Cryptococcosis Mimicking Multiple Metastatic Malignancy

Kim GY, Lee SH, Kim KT

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Clinical Reasoning: A 62-year-old Woman Presenting with Ptosis and Diplopia

Kim YS, Lee HS

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Cytotoxic Lesions of the Splenium of Corpus Callosum (CLOCC) Induced by Hyponatremia

Ha J, Hwang S, Choi MY, Kim SJ, Cho EB, Jeong H, Jung S, Yang TW

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Bilateral Thalamic Infarction Related to Artery of Percheron with Microembolic Signal

Lee HL, Kim YL, Shin BS, Kang HG

The artery of Percheron (AOP) is an uncommon variant of the posterior cerebral artery that supplies blood to the paramedian thalamus and rostral midbrain. AOP is often difficult to recognize...
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Anti-N-methyl-D-aspartate Receptor Encephalitis in Illicit Substance Use

Sung E, Kang IM, Kim H, Lee H, Park J

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a neuroinflammatory disease mediated by autoantibodies against the NMDAR, typically presenting with psychiatric symptoms, cognitive dysfunction, and motor dysfunction. These neuropsychiatric symptoms may be mimicked...
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A Familial Case Presented with Various Clinical Manifestations Caused by OPA1 Mutation

Lee JH, Kang J, Seo Yd, Eun JI, Hwang H, Ryu S, Jang J, Park J

Ataxia is presented by various etiologies, including acquired, genetic and degenerative disorders. Although hereditary ataxia is suspected when typical symptom of ataxia with concurrent is identified, it is sometimes difficult...
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Calcified Neurocysticercosis that Invaded the Subarachnoid Space Presenting as Focal Status Epilepticus

Lee JY, Han Sk, Hyung SW, Kim DY, Seong MJ

Neurocysticercosis is the most common parasitic infection of the nervous system. However, the improvement in public health made the prevalence of neurocysticercosis low. Neurocysticercosis may have symptoms such as seizures,...
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Reversible Gait Disturbance Due to Vitamin B12 Deficiency

Yun DM, Chae S, Kim JO, Choi K, Moon Y

Vitamin B12 deficiency causes a variety of symptoms in the hematologic, gastrointestinal tract, and neurologic deficit. We report a rare case of progressive gait disturbance, bradykinesia and dysarthria which was...
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The Etiology of Acute Stroke with Experience of Repeated Upper Extremity Deep Vein Thrombosis

Lee CJ, Lee DK, Lee MA, Hwang BW, Kim JH, Moon HS, Lim SC, Ahn SH

In stroke patients, upper extremity deep vein thrombosis (UEDVT) is uncommon compared with lower extremity. Unlike the blood stasis in lower extremity, UEDVT has been developed by secondary cause. We...
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Reversible Burst-suppression Pattern of Acute Hyperammonemic Encephalopathy

Yoon JE, Kim Hj, Kang MK, Cho S, Lee D, Park JM, Kwon Oh, Yoon BW, Lee HY, Hong YH

Acute hyperammonemic encephalopathy is generally associated with severe liver disease, manifesting with neuropsychiatric symptoms including confusion, lethargy, seizure, coma, and even death. Electroencephalogram (EEG) is a proven diagnostic, prognostic, and...
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A Case of Inclusion Body Myositis with Clinical, Pathological and Serological Consideration

Park YE, Kang M, Shin JH, Kim DS

Inclusion body myositis is a rare condition of idiopathic inflammatory myopathy. Prior criteria for the diagnosis of inclusion body myositis essentially required pathological features of rimmed vacuoles, tubulofilamentous inclusions, and...
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A Case of Anterior Communicating Artery Aneurysm Impending Rupture Presenting with Isolated Painful Adduction Palsy Mimicking Ischemic Internuclear Ophthalmoplegia

Ko J, Kim M, Kang SY, Kang JH, Oh JH, Choi JC, Lee JS, Song SK, Kang CH, Kim HJ, Rhim JK, Kim JG

Anterior communicating artery (ACoA) aneurysms may rarely lead to oculomotor nerve palsy. We present here interesting cases in which isolated unilateral adduction paresis mimicking internuclear ophthalmoplegia (INO) was one of...
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The Effect of Cognitive Programs on Cognitive Functions of the Elderly with Normal Cognitive Functions in the Community: Based on the Program 'Connect Memories'

Background: This study aims to develop a well-founded program for the elderly in the community to provide a guide to continuous practice and to be used as basic data for...
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