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Diagnosis and Clinical Features in Autoimmune-Mediated Movement Disorders

Hsieh PC, Wu YR

Movement disorders are common manifestations in autoimmune-mediated encephalitis. This group of diseases is suspected to be triggered by infection or neoplasm. Certain phenotypes correlate with specific autoantibody-related neurological disorders, such...
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Re: Comment on “Parainfectious Anti-Glial Fibrillary Acidic Protein-Associated Meningoencephalitis”

Yoo D, Ahn TB

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Syringomyelia Manifesting With Pseudodystonia: A Case Report

Hwang YS, Lee SH, Jo S, Chung SJ

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Pseudodystonia and Neuropathic Tremor in a Patient With Monomelic Amyotrophy

Lee SH, Hwang YS, Jo S, Chung SJ

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Hand Movement-Induced Eyeblink Bursts in a Patient With Parkinson’s Disease

Yamada G, Horiba M, Toyoda T, Katada E, Matsukawa N

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Validation of the Thai Version of the Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale

Objective This study aims to validate the Thai translation of the Movement Disorder Society-sponsored revision of the Unified Parkinson’s Disease Rating Scale (MDS-UPDRS). Methods The English version was translated into Thai...
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Comment on “Parainfectious Anti-Glial Fibrillary Acidic Protein-Associated Meningoencephalitis”

Ahn BJ, Kwon KY

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Acute Extrapyramidal Side Effects Following Domperidone Intake in a 48-Year-Old Female Patient: The First Genetic Alteration and Drug Interaction Characterized

Thuan ND, Nhung VP, Dung HT, Son ND, Hai Ha N, Ton ND

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Asymmetric Parkinsonism With Progressive Nigrosomal Change Secondary to Kernohan’s Notch Phenomenon

Kim HK, Baek MS, Ahn SJ, Lyoo CH

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A Case of AOA2 With Compound Heterozygous SETX Mutations

Chang HJ, Kim R, Kim M, Moon J, Kim MJ, Kim HJ

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Expanding the Clinical Spectrum of RFC1 Gene Mutations

Kulshreshtha D, Ganguly J, Jog M

Biallelic intronic repeat expansion in the replication factor complex unit 1 (RFC1) gene has recently been described as a cause of late onset ataxia with degeneration of the cerebellum, sensory...
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Effect of Chelation Therapy on a Korean Patient With Brain Manganese Deposition Resulting From a Compound Heterozygous Mutation in the SLC39A14 Gene

Lee JH, Shin JH

Mutations in the manganese transporter gene SLC39A14 lead to inherited disorders of manganese metabolism. Chelation therapy with edetate calcium disodium (CaNa2EDTA) is known to effectively reduce manganese deposition. We describe...
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Long-Term Outcome of Hemimasticatory Spasm

Ray S, Kamble N, Yadav R, Pal PK

Objective This study aims to identify the demographic, clinical, and therapeutic characteristics of four patients with hemimasticatory spasm (HMS) seen in our outpatient department over a period of 20 years. Methods...
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Automatic Measurement of Postural Abnormalities With a Pose Estimation Algorithm in Parkinson’s Disease

Shin JH, Woo KA, Lee CY, Jeon SH, Kim HJ, Jeon B

Objective This study aims to develop an automated and objective tool to evaluate postural abnormalities in Parkinson’s disease (PD) patients. Methods We applied a deep learning-based pose-estimation algorithm to lateral photos...
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Utility of Clinical Exome Sequencing in Dystonia: A Single-Center Study From India

Holla VV, Neeraja K, Stezin A, Prasad S, Surisetti BK, Netravathi M, Kamble N, Yadav R, Pal PK

Objective With the use of next-generation sequencing in clinical practice, several genetic etiologies of dystonia have been identified. This study aimed to ascertain the utility of clinical exome sequencing (CES)...
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Labrune’s Syndrome Presenting With Stereotypy-Like Movements and Psychosis: A Case Report and Review

Sim CY, Mukari SAM, Ngu LH, Loh CY, Remli R, Ibrahim NM

Labrune’s syndrome, or leukoencephalopathy with brain calcifications and cysts (LCC), is a rare genetic syndrome with variable neurological presentations. Psychiatric manifestations and involuntary movements are uncommonly reported. We report the...
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Umami and Other Taste Perceptions in Patients With Parkinson’s Disease

Jagota P, Chotechuang N, Anan C, Kitjawijit T, Boonla C, Bhidayasiri R

Objective Studies of taste perceptions in Parkinson’s disease (PD) patients have been controversial, and none of these studies have assessed umami taste. This study aimed to assess umami, along with...
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Fecal Calprotectin in Parkinson’s Disease and Multiple System Atrophy

Hor JW, Lim SY, Khor ES, Chong KK, Song SL, Ibrahim NM, Teh CSJ, Chong CW, Hilmi IN, Tan AH

Objective Converging evidence suggests that intestinal inflammation is involved in the pathogenesis of neurodegenerative diseases. Previous studies on fecal calprotectin in Parkinson’s disease (PD) were limited by small sample sizes,...
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Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease

Jeon J, Kim K, Baek K, Chung SJ, Yoon J, Kim YJ

Objective The Montreal Cognitive Assessment (MoCA) is recommended for assessing general cognition in Parkinson’s disease (PD). Several cutoffs of MoCA scores for diagnosing PD with cognitive impairment (PD-CI) have been...
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Development of Clinical Milestones in Parkinson’s Disease After Bilateral Subthalamic Deep Brain Stimulation

Ong JNA, Shin JH, Jeon S, Lee CY, Kim HJ, Paek SH, Jeon B

Objective Deep brain stimulation of the subthalamic nucleus (STN-DBS) in Parkinson’s disease (PD) patients does not halt disease progression, as these patients will progress and develop disabling non-levodopa responsive symptoms....
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