2,836 results on '"Kuwabara, Satoshi"'
Search Results
102. Meningitis-retention syndrome: Clinical features, frequency and prognosis
103. Safety and efficacy of eculizumab in Guillain-Barré syndrome: a multicentre, double-blind, randomised phase 2 trial
104. Soluble CD40 ligand disrupts the blood–brain barrier and exacerbates inflammation in experimental autoimmune encephalomyelitis
105. MR findings in the substantia nigra on phase difference enhanced imaging in neurodegenerative parkinsonism
106. Validation of the Modified Fatigue Impact Scale and the relationships among fatigue, pain and serum interleukin-6 levels in patients with neuromyelitis optica spectrum disorder
107. Idiopathic cerebellar ataxia (IDCA): Diagnostic criteria and clinical analyses of 63 Japanese patients
108. Genetic and transcriptional landscape of plasma cells in POEMS syndrome
109. Isolated paravermal T2 high-intensity lesions in dentatorubral–pallidoluysian atrophy
110. 'Dense Inverted Triangle Sign' in Cerebral Venous Thrombosis
111. Spinal Arachnoid Web Probably Associated with Systemic Inflammation
112. Two Cases of Encephalitis without Anti-N-methyl-D-aspartate Receptor Antibody Successfully Treated with Ovarian Teratoma Resection and Immunotherapy
113. Unilateral Wing-Beating Tremor in Neuronal Intranuclear Inclusion Disease
114. Different Patterns of Gray Matter Volume Reduction in Early-onset and Late-onset Alzheimer Disease
115. POEMS Syndrome
116. Characterizing restless legs syndrome and leg motor restlessness in patients with Parkinson's disease: A multicenter case-controlled study
117. Optimizing the electrodiagnostic accuracy in Guillain-Barré syndrome subtypes: Criteria sets and sparse linear discriminant analysis
118. Soluble CD40 ligand contributes to blood–brain barrier breakdown and central nervous system inflammation in multiple sclerosis and neuromyelitis optica spectrum disorder
119. Serum soluble Talin-1 levels are elevated in patients with multiple sclerosis, reflecting its disease activity
120. Association between Aβ and tau accumulations and their influence on clinical features in aging and Alzheimer's disease spectrum brains: A [11C]PBB3-PET study
121. Electrophysiology in Fisher syndrome
122. A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis
123. Vertical pons hyperintensity and hot cross bun sign in cerebellar-type multiple system atrophy and spinocerebellar ataxia type 3
124. Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy
125. Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke: Case Report and Literature Review
126. ALS is a multistep process in South Korean, Japanese, and Australian patients
127. Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment
128. Japanese multicenter database of healthy controls for [123I]FP-CIT SPECT
129. Serum anti-JCV antibody indexes in Japanese patients with multiple sclerosis: elevations along with fingolimod treatment duration
130. Clinical and magnetic resonance imaging features of elderly onset dentatorubral–pallidoluysian atrophy
131. International Delphi Consensus on the Management of AQP4-IgG+ NMOSD
132. Isolated contralateral spinothalamic sensory loss below thoracic level due to lateral medullary infarction
133. Genetic factors affecting survival in Japanese patients with sporadic amyotrophic lateral sclerosis: a genome-wide association study and verification in iPSC-derived motor neurons from patients
134. Genome-wide association study identifies a new susceptibility locus inPLA2G4Cfor Multiple System Atrophy
135. Cerebrospinal Fluid Findings in Relation to Clinical Characteristics, Subtype, and Disease Course in Patients With Guillain-Barré Syndrome
136. Cardiovascular autonomic dysfunction induced by mechanical insufflation‐exsufflation in Guillain–Barré syndrome
137. Cerebral cortex swelling in V180I genetic Creutzfeldt–Jakob disease: comparative imaging study between sporadic and V180I genetic Creutzfeldt–Jakob disease in the early stage
138. Epidemiological and clinical characteristics of myelin oligodendrocyte glycoprotein antibody-associated disease in a nationwide survey
139. Association between Cognitive Impairment and Hippocampal Subfield Volumes in Multiple System Atrophy
140. Genetic and functional analysis of KIF5A variants in Japanese patients with sporadic amyotrophic lateral sclerosis
141. Awaji criteria improves the diagnostic sensitivity in amyotrophic lateral sclerosis: A systematic review using individual patient data
142. Prevalence, clinical profiles, and prognosis of POEMS syndrome in Japanese nationwide survey
143. Ultrasound-based radiomic analysis of the peripheral nerves for differentiation between CIDP and POEMS syndrome.
144. Delayed Appearance of Brain Magnetic Resonance Imaging Abnormalities in a Patient with Glial Fibrillary Acidic Protein Astrocytopathy
145. Role of soluble forms of follicular helper T-cell membrane molecules in the pathogenesis of myasthenia gravis
146. Effectiveness of early cycles of fast-acting treatment in generalised myasthenia gravis
147. Utility of movement disorder society-unified Parkinson's disease rating scale for evaluating effect of subthalamic nucleus deep brain stimulation
148. Autoantibodies against vinculin in patients with chronic inflammatory demyelinating polyneuropathy
149. Altered axonal excitability properties and nerve edema in POEMS syndrome
150. Effects of low frequency filtering on distal compound muscle action potential duration for diagnosis of CIDP: A Japanese–European multicenter prospective study
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