1,007 results on '"Itoyama, Yasuto"'
Search Results
202. Alteration of familial ALS-linked mutant SOD1 solubility with disease progression: Its modulation by the proteasome and Hsp70
203. Activity in the Lateral Prefrontal Cortex Reflects Multiple Steps of Future Events in Action Plans
204. α-Synuclein facilitates the toxicity of oxidized catechol metabolites: Implications for selective neurodegeneration in Parkinson's disease
205. Loss of Aquaporin-4 in Active Perivascular Lesions in Neuromyelitis Optica: A Case Report
206. Disease progression of human SOD1 (G93A) transgenic ALS model rats
207. MRI Findings from a Case of Fulminating Adult-onset Measles Encephalitis
208. Establishment of a New Sensitive Assay for Anti-Human Aquaporin-4 Antibody in Neuromyelitis Optica
209. Relapsing Focal Myositis
210. Altered populations of natural killer cell and natural killer T cell subclasses in myasthenia gravis
211. Periodic episodes of aphasia as an unusual manifestation of partial status epilepticus
212. Transethmoidal intranasal meningoencephalocele in an adult with recurrent meningitis
213. Erythropoietin prevents spinal cord damage and affecting enzyme levels of brain-derived neurotrophic factor after transient spinal cord ischemia in rabbits
214. Endoplasmic reticulum stress induced by spinal cord ischemia in rabbits: Induction of Grp78 and caspase12 in motor neurons
215. Expression profiling with progression of dystrophic change in dysferlin-deficient mice (SJL)
216. Chemokine profile in the cerebrospinal fluid and serum of Vogt–Koyanagi–Harada disease
217. Motoneuron degeneration after facial nerve avulsion is exacerbated in presymptomatic transgenic rats expressing human mutant Cu/Zn superoxide dismutase
218. Ibudilast, a nonselective phosphodiesterase inhibitor, regulates Th1/Th2 balance and NKT cell subset in multiple sclerosis
219. Heme Catabolism and Heme Oxygenase in Neurodegenerative Disease
220. MCI-186 reduces oxidative cellular damage and increases DNA repair function in the rabbit spinal cord after transient ischemia
221. Accelerated α-synuclein aggregation after differentiation of SH-SY5Y neuroblastoma cells
222. Th1/Th2 balance and HTLV-I proviral load in HAM/TSP patients treated with interferon-α
223. Arg(184)his mutant GTP cyclohydrolase I, causing recessive hyperphenylalaninemia, is responsible for dopa-responsive dystonia with parkinsonism: A case report
224. Histochemical features of stress-induced aggregates in α-synuclein overexpressing cells
225. Novel dysferlin mutations and characteristic muscle atrophy in late-onset Miyoshi myopathy
226. Interferon-α significantly reduces cerebrospinal fluid CD4 cell subsets in HAM/TSP
227. Association between a polymorphism ofbrain-derived neurotrophic factor gene and sporadic Parkinson's disease
228. Intradermal doxorubicin reduces ganglionic reactivation of latent herpes simplex virus in mice after pretreatment with hypertonic saline
229. Cell cycle protein expression in proliferating microglia and astrocytes following transient global cerebral ischemia in the rat
230. Complementarity-Determining Region 3 Spectratyping Analysis of the TCR Repertoire in Multiple Sclerosis
231. Mutant SOD1 linked to familial amyotrophic lateral sclerosis, but not wild-type SOD1, induces ER stress in COS7 cells and transgenic mice
232. Familial Inclusion Body Myositis: A Report on Two Japanese Sisters
233. Impaired chemosensitivity to hypoxia is a marker of multiple system atrophy
234. Expression of OX40 in muscles of polymyositis and granulomatous myopathy
235. Functional MRI and optical topography for the assessment of poststroke functional recovery
236. Hypoperfusion in the supplementary motor area, dorsolateral prefrontal cortex and insular cortex in Parkinson's disease
237. Rats Expressing Human Cytosolic Copper–Zinc Superoxide Dismutase Transgenes with Amyotrophic Lateral Sclerosis: Associated Mutations Develop Motor Neuron Disease
238. Decrement of N20 Amplitude of the Median Nerve Somatosensory Evoked Potential in Creutzfeldt-Jakob Disease Patients
239. Neuroprotective effect of riluzole in MPTP-treated mice
240. Marked reduction of the Cu/Zn superoxide dismutase polypeptide in a case of familial amyotrophic lateral sclerosis with the homozygous mutation
241. Dementia in Parkinson's Disease: Its Incidence and a Possible Relationship with Dopa-refractory Symptoms
242. Severe Sequelae of Group B Streptococcal (Streptococcus Agalactiae) Meningitis in an 82‐year‐old Man
243. Lambert-Eaton myasthenic syndrome associated with an anterior mediastinal small cell carcinoma
244. Nitric oxide synthase inhibitors cause motor deficits in mice
245. Clinical and physiological significance of abnormally prolonged central motor conduction time in HAM/TSP
246. Chemokine receptor expression on T cells in blood and cerebrospinal fluid at relapse and remission of multiple sclerosis: imbalance of Th1/Th2-associated chemokine signaling
247. Pure Anarthria with Predominantly Sequencing Errors in Phoneme Articulation: A Case Report
248. Increased Production of β-Amyloid and Vulnerability to Endoplasmic Reticulum Stress by an Aberrant Spliced Form of Presenilin 2
249. Biochemical and immunohistological changes in the brain of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-treated mouse
250. Differential Expression of Three Sialidase Genes in Rat Development
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