1,089 results on '"Osame, Mitsuhiro"'
Search Results
152. Use of Tiotropium Bromide for Pre-operative Treatment in Chronic Obstructive Pulmonary Disease Patients: Comparison with Oxitropium Bromide
153. Increased serum vascular endothelial growth factor levels in microscopic poly angiitis with pulmonary involvement
154. Zidovudine plus lamivudine in Human T-Lymphotropic Virus type-I-associated myelopathy: a randomised trial
155. Specific inhibition of nonsense-mediated mRNA decay components, SMG-1 or Upf1, rescues the phenotype of ullrich disease fibroblasts
156. Association of AKT1 haplotype with the risk of schizophrenia in Iranian population
157. In Replay: Renin-Angiotensin System Blockade and COPD
158. RETRACTED: Discoidin Domain Receptor 1 Contributes to the Survival of Lung Fibroblast in Idiopathic Pulmonary Fibrosis
159. Desert hedgehog-patched 2 expression in peripheral nerves during Wallerian degeneration and regeneration
160. Chronic progressive sensory ataxic neuropathy associated with limited systemic sclerosis
161. RETRACTED: Increased Serum Vascular Endothelial Growth Factor Level in Churg-Strauss Syndrome
162. n-hexane polyneuropathy presenting with CIDP-like features.
163. RETRACTED: Effects of Omega-3 Polyunsaturated Fatty Acids on Inflammatory Markers in COPD
164. Killer Cell Immunoglobulin-Like Receptor Genotype and HTLV-1 Associated Disease’s Susceptibilities.
165. Activation of Discoidin Domain Receptor 1 on CD14-Positive Bronchoalveolar Lavage Fluid Cells Induces Chemokine Production in Idiopathic Pulmonary Fibrosis
166. Differences in viral and host genetic risk factors for development of human T-cell lymphotropic virus type 1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis between Iranian and Japanese HTLV-1-infected individuals
167. Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency
168. Hermansky-Pudlak Syndrome with a Novel Mutation
169. Hyponatremia Upon Resumption of Paroxetine Therapy
170. Living-donor Lobar Lung Transplantation in Sauropus androgynus-associated Bronchiolitis Obliterans in Japan
171. Human T Cell Lymphotropic Virus Type I (HTLV-I) p12IIs Dispensable for HTLV-I Transmission and Maintenance of Infection in Vivo
172. Mechanism of action of voltage‐gated K+ channel antibodies in acquired neuromyotonia
173. TNF-related apoptosis-inducing ligand is involved in neutropenia of systemic lupus erythematosus
174. Clinical features of asthmatic patients with increased urinary leukotriene E4 excretion (hyperleukotrienuria)Involvement of chronic hyperplastic rhinosinusitis with nasal polyposis
175. Pulmonary Dirofilariasis with Serologic Study on Familial Infection with Dirofilaria immitis
176. Pleural Cryptococcosis with Idiopathic CD4 Positive T-lymphocytopenia
177. Inhibition of nonsense-mediated mRNA decay rescues the phenotype in Ullrich's disease
178. A case of adult-onset Alexander disease with Arg416Trp human glial fibrillary acidic protein gene mutation
179. Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiency
180. Degenerate specificity of HTLV-1–specific CD8+ T cells during viral replication in patients with HTLV-1–associated myelopathy (HAM/TSP)
181. Mitochondrial DNA mutation correlates with stage progression and prognosis in non-small cell lung cancer
182. Predictive Value of Serial Platelet Count and VEGF Determination for the Management of DIC in the Crow-Fukase (POEMS) Syndrome
183. A Case of Cutaneous T-cell Lymphoma Associated with Paraneoplastic Cerebellar Degeneration
184. Fibronectin receptor reduction in skin and fibroblasts of patients with Ullrich's disease
185. Failure to Detect HTLV Type 1 DNA from HTLV Type 1-Seronegative Patients with Chronic Progressive Spastic Paraparesis in Kagoshima
186. Targeted Deletion of Both Thymidine Phosphorylase and Uridine Phosphorylase and Consequent Disorders in Mice
187. Selective matrix metalloproteinase inhibitor, N-biphenyl sulfonyl phenylalanine hydroxamic acid, inhibits the migration of CD4+ T lymphocytes in patients with HTLV-I-associated myelopathy
188. Cerebrovascular disorders and genetic polymorphisms: mitochondrial DNA5178C is predominant in cerebrovascular disorders
189. Autosomal dominant palatal myoclonus and spinal cord atrophy
190. Diagnosis of dystrophinopathy by skin biopsy
191. Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations
192. A Patient with Acute-Onset HAM/TSP after Blood Transfusion Complicated with Pseudopseudohypoparathyroidism.
193. Adult T-cell Leukemia (ATL) Cells which Express Neural Cell Adhesion Molecule (NCAM) and Infiltrate into the Central Nervous System.
194. Expression of Midkine in Regenerating Skeletal Muscle Fibers and Cultured Myoblasts of Human Skeletal Muscle
195. Logistic Model Analysis of Neurological Findings in Minamata Disease and the Predicting Index.
196. Isaacs' syndrome as a potassium channelopathy of the nerve
197. Multifocal Relapsing-remitting Myelitis in a Patient with Atopic Dermatitis: Multiple Sclerosis or Atopic Myelitis?
198. A Clinical Study of Adult Human Parvovirus B19 Infection.
199. Cross-Sectional Analysis of Neurological Findings among Healthy Elderly: Study in a Remote Island in Kagoshima, Japan
200. Frameshift mutation in the collagen VI gene causes Ullrich's disease
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