1,190 results on '"Itoyama Y"'
Search Results
152. 2-30-06 Striatal fluorodopa uptake and dopamine D2 receptor bindings in early and late onset of Parkinson's disease studied by positron emission tomography
153. Marked improvement of delayed methotrexate-induced leukoencephalopathy treated with high-dose folinic acid
154. Amelioration of brain edema by topical application of glial cell line-derived neurotrophic factor in reperfused rat brain
155. In vivo adenovirus-mediated gene transfer and the expression in ischemic and reperfused rat brain
156. Expressions of P-selectin- and HSP72-like immunoreactivities in rat brain after transient middle cerebral artery occlusion
157. Postischemic expression of P-selectin immunoreactivity in rat brain
158. Upregulation of protein-tyrosine nitration in the anterior horn cells of amyotrophic lateral sclerosis
159. Protective effect of a novel free radical scavenger, OPC-14117, on wobbler mouse motor neuron disease
160. A presenilin‐1 mutation in a Japanese family with Alzheimer's disease and distinctive abnormalities on cranial MRI
161. Dissociative expression of adenoviral-mediated E. coli LacZ gene between ischemic and reperfused rat brains
162. Age-related Changes in [3H]Nimodipine and [3H]Rolipram Binding in the Rat Brain
163. Expression of tumor necrosis factor-α in muscles of polymyositis
164. A novel missense point mutation (S134N) of the Cu/Zn superoxide dismutase gene in a patient with familal motor neuron disease
165. Inductions of Cu/Zn superoxide dismutase- and nitric oxide synthase-like immunoreactivities in rabbit spinal cord after transient ischemia
166. A Japanese family of autosomal dominant hypokalemic periodic paralysis with a CACNL1A3 gene mutation
167. Molecular and clinical analysis on muscle wasting in patients with spinocerebellar ataxia type 1
168. Interferon-alpha is effective in HTLV-I-associated myelopathy
169. Clinical characteristics of familial amyotrophic lateral sclerosis with superoxide dismutase gene mutations
170. Variable clinical symptoms in familial amyotrophic lateral sclerosis with a novel point mutation in the Cu/Zn superoxide dismutase gene
171. A Japanese family with Machado-Joseph disease characterized by initial emaciation and myoclonus
172. Induction of nitrotyrosine-like immunoreactivity in the lower motor neuron of amyotrophic lateral sclerosis
173. Induction of heparin-binding growth-associated molecule expression in reactive astrocytes following hippocampal neuronal injury
174. A family with mild clinical manifestations of spinocerebellar ataxia type 1 (SCA1): correlation with smaller CAG repeats
175. A clinical variance in familial amyotrophic lateral sclerosis with a point mutation in Cu/Zn superoxide dismutase gene
176. An immunohistochemical study of heat shock protein-27 in the hippocampus in a gerbil model of cerebral ischemia and ischemic tolerance
177. Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan
178. Expresgions of nerve growth factor and p75 low affinity receptor after transient forebrain ischemia in gerbil hippocampal CA1 neurons
179. Differential diagnosis of early stage Huntington's disease from dentatorubral‐pallidoluysian atrophy by DNA analysis
180. Rapid and semiquantitative analysis of HSP72 and HSC73 heat shock mRNAs by mimic RT-PCR
181. Brain-gut gene expression of heat shock protein 70 and heat shock cognate protein 70 by psychophysiological stress in rats
182. Endothelin Receptors in Ischemic Rat Brain and Alzheimer Brain
183. ATP responses in the embryo chick ciliary ganglion cells
184. Early immunohistochemical changes of microtubule based motor proteins in gerbil hippocampus after transient ischemia
185. A novel point mutation in the Cu/Zn superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis
186. Glycine response in acutely dissociated ventromedial hypothalamic neuron of the rat: new approach with gramicidin perforated patch-clamp technique
187. Detection of human T lymphotrophic virus type I (HTLV-I) proviral DNA and analysis of T cell receptor V beta CDR3 sequences in spinal cord lesions of HTLV-I-associated myelopathy/tropical spastic paraparesis.
188. The protective effect of L-threo-3,4-dihydroxyphenylserine on ischemic hippocampal neuronal death in gerbils.
189. TNF-beta produced by human T lymphotropic virus type I-infected cells influences the proliferation of human endothelial cells and fibroblasts.
190. Reduction of nerve growth factor receptor immunoreactivity in ischaemic gerbil hippocampal CA1 neurons after treatment with L-threo-3,4-dihydroxyphenylserine (DOPS)
191. Expression of cytokines in brain lesions in subacute sclerosing panencephalitis
192. Multiple neutralizing B-cell epitopes of human T-cell leukemia virus type 1 (HTLV-1) identified by human monoclonal antibodies. A basis for the design of an HTLV-1 peptide vaccine.
193. Neutralizing antibodies against HTLV-I in HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP) patients and asymptomatic carriers
194. Identification of new epitopes recognized by human monoclonal antibodies with neutralizing and antibody-dependent cellular cytotoxicity activities specific for human T cell leukemia virus type 1.
195. HAM/TSP attributable to blood transfusion.
196. Linear antigenic regions of the structural proteins of human T-cell lymphotropic virus type I detected by enzyme-linked immunosorbent assays using synthetic peptides as antigens
197. In vivo visualization of alpha-synuclein deposition by carbon-11-labelled 2-[2-(2-dimethylaminothiazol-5-yl)ethenyl]-6-[2-(fluoro)ethoxy]benzoxazole positron emission tomography in multiple system atrophy.
198. Clustering of three cases of Creutzfeldt-Jakob disease near Fukuoka City, Japan
199. Temporal changes and geographical differences in multiple sclerosis phenotypes in Japanese: nationwide survey results over 30 years.
200. Mechanisms of neuronal death in synucleinopathy.
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