216 results on '"Sasaki, Ryogen"'
Search Results
2. Endemic parkinsonism: clusters, biology and clinical features
3. Reply to: Questioning the cycad theory of Kii ALS–PDC causation
4. An immigrant family with Kii amyotrophic lateral sclerosis/parkinsonism–dementia complex
5. Mutation spectrum and health status in skeletal muscle channelopathies in Japan
6. Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patients
7. Functional analysis of a double-point mutation in the KCNJ2 gene identified in a family with Andersen-Tawil syndrome
8. Chronic cerebral hypoperfusion upregulates leptin receptor expression in astrocytes and tau phosphorylation in tau transgenic mice
9. Teaching Video NeuroImage: Carbamazepine Improves Gait Initiation in Autosomal Recessive Myotonia Congenita
10. Tau filaments from amyotrophic lateral sclerosis/parkinsonism-dementia complex adopt the CTE fold
11. Proteomic Profiling of Exosomal Proteins for Blood-based Biomarkers in Parkinson's Disease
12. Comparison of Premortem Magnetic Resonance Imaging and Postmortem Autopsy Findings of a Cortical Microinfarct
13. Thomsen disease with ptosis and abnormal MR findings
14. Tau filaments from amyotrophic lateral sclerosis/parkinsonism-dementia complex adopt the CTE fold.
15. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
16. APOE Alleles With Tau and Aβ Pathology in Patients With Amyotrophic Lateral Sclerosis and Parkinsonism-Dementia Complex in the Kii Peninsula
17. Chronic cerebral ischemia induces redistribution and abnormal phosphorylation of transactivation-responsive DNA-binding protein-43 in mice
18. Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS
19. Amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula of Japan (Kii ALS/PDC) may be a familial tauopathy. Epidemiological trends, clinical features, neuropathology and molecular genetics
20. Astrocytic neuroprotection through induction of cytoprotective molecules; a proteomic analysis of mutant P301S tau-transgenic mouse
21. Effect of Standard vs Intensive Blood Pressure Control on the Risk of Recurrent Stroke A Randomized Clinical Trial and Meta-analysis
22. An immigrant family with Kii amyotrophic lateral sclerosis/parkinsonism–dementia complex
23. Teaching Video NeuroImage: Carbamazepine Improves Gait Initiation in Autosomal Recessive Myotonia Congenita
24. Reversible stenosis of large cerebral arteries in a patient with combined Sjögren’s syndrome and neuromyelitis optica spectrum disorder
25. Alleles With Tau and Aβ Pathology in Patients With Amyotrophic Lateral Sclerosis and Parkinsonism-Dementia Complex in the Kii Peninsula.
26. VPS35 Mutation in Japanese Patients with Typical Parkinsonʼs Disease
27. Initial Result of Stroke Care at the Stroke Center in a New Hospital Opened by the Merger of Three Facilities with Different Management Bases: Effect of Stroke Center on Mechanical Thrombectomy
28. Expression of Mutant Ubiquitin and Proteostasis Impairment in Kii Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex Brains
29. Paramyotonia Congenita with Persistent Distal and Facial Muscle Weakness: A Case Report with Literature Review
30. EF hand‐like motif mutations of Nav1.4 C‐terminus cause myotonic syndrome by impairing fast inactivation
31. NEW MUTATION OF THE NA CHANNEL IN THE SEVERE FORM OF POTASSIUM-AGGRAVATED MYOTONIA
32. Mouse Model of Multiple System Atrophy α-Synuclein Expression in Oligodendrocytes Causes Glial and Neuronal Degeneration
33. Mutation analyses in amyotrophic lateral sclerosis/parkinsonism–dementia complex of the Kii peninsula, Japan
34. Expression of Mutant Ubiquitin and Proteostasis Impairment in Kii Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex Brains
35. Mutation spectrum and health status in skeletal muscle channelopathies in Japan
36. Biochemical and Ultrastructural Study of Neurofibrillary Tangles in Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex in the Kii Peninsula of Japan
37. Somatosensory evoked potential recovery in Kii amyotrophic lateral sclerosis/parkinsonism–dementia complex (Kii ALS/PDC)
38. Induction of IL-10-producing regulatory T cells with TCR diversity by epitope-specific immunotherapy in pollinosis
39. Myotonic Mutations of Nav1.4 Located At EF Hand-Like Motif in C-Terminus Impair Fast Inactivation
40. A Novel Mutation in the Gene for the Adult Skeletal Muscle Sodium Channel alpha-Subunit (SCN4A) That Causes Paramyotonia Congenita of von Eulenburg
41. Mutational Analysis and Genotype-Phenotype Correlation of 29 Unrelated Japanese Patients With X-linked Adrenoleukodystrophy
42. Paramyotonia congenita with persistent distal and facial muscle weakness: A case report with literature review
43. A novel de novo point mutation in the GTP cyclohydrolase I gene in a Japanese patients with hereditary progressive and dopa responsive dystonia
44. Widespread expression of α-synuclein and τ immunoreactivity in Hallervorden–Spatz syndrome with protracted clinical course
45. Paramyotonia congenita with persistent distal and facial muscle weakness: A case report with literature review
46. Hyperkalemic periodic paralysis and paramyotonia congenita – A novel sodium channel mutation –
47. Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotonia
48. Clinical significance of cortical lesions in patients with multiple sclerosis: A neuropsychological and neuroimaging study
49. EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population
50. Dopaminergic Positron Emission Tomography Study on Amyotrophic Lateral Sclerosis/Parkinsonism–Dementia Complex in Kii, Japan
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