370 results on '"Kim, Yun Joong"'
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102. Ataxia with Oculomotor Apraxia Type 1 without Oculomotor Apraxia: A Case Report
103. Development of an Acquisition and Visualization of Forearm Tremors and Pronation/Supination Motor Activities in a Smartphone based Environment for an Early Diagnosis of Parkinson’s Disease
104. Quantitative Assessment of Forearm Pronation/Supination Motor functions using a Smartphone Accelerometer for an early Diagnosis of Parkinson’s Disease
105. A Visual Rating Scale for the Hummingbird Sign with Adjustable Diagnostic Validity
106. Genetics of Progressive Supranuclear Palsy
107. Overlap of autism spectrum disorder and glucose transporter 1 deficiency syndrome associated with a heterozygous deletion at the 1p34.2 region
108. Apolipoprotein E4 Affects Topographical Changes in Hippocampal and Cortical Atrophy in Alzheimer's Disease Dementia: A Five-Year Longitudinal Study
109. Cognitive Dysfunction in Drug-induced Parkinsonism Caused by Prokinetics and Antiemetics
110. Erratum: Analysis of Dosage Mutation inPARK2among Korean Patients with Early-Onset or Familial Parkinson's Disease
111. Utility of the Midbrain Tegmentum Diameter in the Differential Diagnosis of Progressive Supranuclear Palsy from Idiopathic Parkinson's Disease
112. Asymmetrical changes of the pedunculopontine nucleus in a case of freezing of gait after carbon monoxide intoxication
113. SCA in Korea and its regional distribution: A multicenter analysis
114. P4-145: BRAINSTEM MICROBLEEDS AFFECT MOTOR DEFICITS IN SUBCORTICAL VASCULAR COGNITIVE IMPAIRMENT
115. Analysis of Dosage Mutation inPARK2among Korean Patients with Early-Onset or Familial Parkinson's Disease
116. Reduction of Continuous Theta Burst Stimulation-Induced Motor Plasticity in Healthy Elderly With COMT Val158Met Polymorphism
117. Serotonin transporter gene polymorphisms may be associated with poststroke neurological recovery after escitalopram use
118. Fatigue in Drug-Naïve Parkinson's Disease
119. Gray and white matter changes linking cerebral small vessel disease to gait disturbances.
120. Prodromal Dementia With Lewy Bodies Manifesting as Sertraline-induced Parkinsonism
121. Association of mutations in the glucocerebrosidase gene with Parkinson disease in a Korean population
122. A Comparison of the Prospective Memory among College Students, Normal Elderly, and Parkinson's Disease Patients
123. Analysis of mutations and the association between polymorphisms in the cerebral dopamine neurotrophic factor (CDNF) gene and Parkinson disease
124. Ipsilateral Tilt and Contralateral Sensory Change of Neck in Cortical Infarction
125. Dura Mater Graft-Associated Creutzfeldt-Jakob Disease: The First Case in Korea
126. A Case of Painful Hemimasticatory Spasm with Masseter Muscle Hypertrophy Responsive to Botulinum Toxin
127. Ipsilateral Wallerian Degeneration of the Distal Optic Radiations After Infarction at Their Root
128. Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia
129. Klotho is a genetic risk factor for ischemic stroke caused by cardioembolism in Korean females
130. Sequence variants of ACE, AGT, AT1R, and PAI-1 as genetic risk factors for vascular dementia
131. Outcome of Surgical Angioplasty for Isolated Coronary Ostial Stenosis
132. Odour identification test and its relation to cardiac 123I-metaiodobenzylguanidine in patients with drug induced parkinsonism.
133. Odour identification test and its relation to cardiac 123l-metaiodobenzylguanidine in patients with drug induced parkinsonism.
134. Is the cingulate island sign a marker for early dementia conversion in Parkinson's disease?
135. Differential Implications of Cerebral Hypoperfusion and Hyperperfusion in Parkinson's Disease.
136. Association between choroid plexus volume and cognition in Parkinson disease.
137. Corticobasal syndrome associated with antiphospholipid syndrome without cerebral infarction.
138. SYNERGISTIC EFFECTS OF AMYLOID AND VASCULAR CHANGES ON THE LOBAR MICROBLEEDS: A THREE-YEAR LONGITUDINAL STUDY IN PATIENTS WITH SUBCORTICAL VASCULAR MILD COGNITIVE IMPAIRMENT.
139. Patterns of striatal dopamine depletion and motor deficits in de novo Parkinson's disease.
140. Identifying the white matter structural network of motor reserve in early Parkinson's disease.
141. Patterns of regional cerebral hypoperfusion in early Parkinson's disease: Clinical implications.
142. Different patterns of β-amyloid deposition in patients with Alzheimer's disease according to the presence of mild parkinsonism.
143. Upregulation of immunoproteasome PSMB8 is associated with Parkinson's disease.
144. Genome-wide association study of copy number variations in Parkinson's disease.
145. Association of Body Mass Index and Parkinson Disease: A Bidirectional Mendelian Randomization Study.
146. The First East Asian Patient With Parkinson's Disease Caused by the A53E SNCA Mutation With Early Progression to Dementia.
147. Hypoperfusion in Alzheimer's Disease-Prone Regions and Dementia Conversion in Parkinson's Disease.
148. Comparing Montreal Cognitive Assessment Performance in Parkinson's Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning.
149. Primary Familial Brain Calcification With XPR1 Mutation Presenting With Cognitive Dysfunction.
150. Mitochondrial-Membrane-Protein-Associated Neurodegeneration in Longitudinal Magnetic Resonance Imaging Over 11 Years of Follow-Up.
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