348 results on '"Arimura, Kimiyoshi"'
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2. Guidelines for single fiber EMG
3. Intraepidermal nerve fiber density and nerve conduction study parameters correlate with clinical staging of diabetic polyneuropathy
4. Reference values for voluntary and stimulated single-fibre EMG using concentric needle electrodes: A multicentre prospective study
5. Polymorphism in the Interleukin-10 Promoter Affects Both Provirus Load and the Risk of Human T Lymphotropic Virus Type I-Associated Myelopathy/Tropical Spastic Paraparesis
6. A multicentre prospective study of Guillain-Barré Syndrome in Japan: a focus on the incidence of subtypes
7. Metabolic syndrome-related markers in obese university students in Kagoshima, Japan: Implications of uric acid and plasminogen activator inhibitor type-1
8. Diagnostic value of serum peptidome analyses for protease activated pathological conditions beyond cancer diagnosis
9. A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy
10. Reduced Foxp3 expression with increased cytomegalovirus-specific CTL in HTLV-I-associated myelopathy
11. Increased frequency of CD4+T cells expressing fractalkine receptor CX3CR1 in patients with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP), but its AIDS susceptible polymorphisms are not associated with the disease
12. Median neuropathy at the wrist as an early manifestation of diabetic neuropathy
13. ARE MULTIFOCAL MOTOR NEUROPATHY PATIENTS UNDERDIAGNOSED? AN EPIDEMIOLOGICAL SURVEY IN JAPAN
14. Accumulation of human T-lymphotropic virus type I (HTLV-I)-infected cells in the cerebrospinal fluid during the exacerbation of HTLV-I-associated myelopathy
15. Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?
16. Safety and efficacy of interferon-α in 167 patients with human T-cell lymphotropic virus type 1-associated myelopathy
17. Abnormalities of spinal magnetic resonance images implicate clinical variability in human T-cell lymphotropic virus type I-associated myelopathy
18. Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene
19. Clinical symptoms and the odds of human T-cell lymphotropic virus type 1-associated myelopathy/ tropical spastic paraparesis (HAM/TSP) in healthy virus carriers: Application of best-fit logistic regression equation based on host genotype, age, and provirus load
20. Genetic variability in the extracellular matrix protein as a determinant of risk for developing HTLV-I-associated neurological disease
21. Different pattern of HSP47 expression in skeletal muscle of patients with neuromuscular diseases
22. Effects of thymectomy on late-onset myasthenia gravis without thymoma
23. Serum VEGF—As a prognostic factor of atherosclerosis
24. Discoidin domain receptor 1 contributes to eosinophil survival in an NF-κB–dependent manner in Churg-Strauss syndrome
25. Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families
26. Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency
27. Does suppression of VEGF alone lead to clinical recovery in POEMS syndrome?
28. Diagnostic spectrum of multifocal motor neuropathy
29. Skeletal muscle abnormalities in two patients with dystonia
30. Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease
31. HTLV-I proviral load correlates with progression of motor disability in HAM/TSP: Analysis of 239 HAM/TSP patients including 64 patients followed up for 10 years
32. Increased serum vascular endothelial growth factor levels in microscopic poly angiitis with pulmonary involvement
33. MRI studies of spinal visceral larva migrans syndrome
34. Flow cytometry evaluation of the T-cell receptor Vβ repertoire among human T-cell lymphotropic virus type-1 (HTLV-1) infected individuals: Effect of interferon alpha therapy in HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP)
35. Discoidin Domain Receptor 1 Contributes to the Survival of Lung Fibroblast in Idiopathic Pulmonary Fibrosis
36. Chapter 36 Immune-mediated potassium channelopathies
37. Microvascular endothelial abnormality in skeletal muscle from a patient with gastric cancer without dermatomyositis
38. Early recognition of POEMS syndrome: what is the role of clinical neurophysiology?
39. Multiple episodes of thrombosis in a patient with Becker muscular dystrophy with marked expression of utrophin on the muscle cell membrane
40. Polyneuropathy with minifascicle formation in a patient with 46XY mixed gonadal dysgenesis
41. A new mitochondria-related disease showing myopathy with episodic hyper-creatine kinase-emia
42. Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case
43. Histopathological and ultrastructural features of feline hereditary cerebellar cortical atrophy: a novel animal model of human spinocerebellar degeneration
44. Different manners of sarcoglycan expression in genetically proven α-sarcoglycan deficiency and γ-sarcoglycan deficiency
45. The origin of spontaneous discharges in acquired neuromyotonia. A Macro EMG study
46. A prospective uncontrolled trial of fermented milk drink containing viable Lactobacillus casei strain Shirota in the treatment of HTLV-1 associated myelopathy/tropical spastic paraparesis
47. ApaI polymorphism of vitamin D receptor gene is associated with susceptibility to HTLV-1-associated myelopathy/tropical spastic paraparesis in HTLV-1 infected individuals
48. Comparative electrophysiological study of response to botulinum toxin type B in Japanese and Caucasians
49. Inclusion Body Myositis Associated With Human T-Lymphotropic Virus-Type I Infection: Eleven Patients From an Endemic Area in Japan
50. Muscle membrane excitability after exercise in thyrotoxic periodic paralysis and thyrotoxicosis without periodic paralysis
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