783 results on '"Iwasaki, Yasushi"'
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2. Ultrasensitive detection of TDP-43 and amyloid-β protein aggregates using micelle-assisted seed amplification assay
3. Detection limitations of prion seeding activities in blood samples from patients with sporadic prion disease
4. Correlation between clinical and neuropathological subtypes of progressive supranuclear palsy
5. Clinical characteristics of Japanese patients with corticobasal degeneration
6. Identical tau filaments in subacute sclerosing panencephalitis and chronic traumatic encephalopathy
7. NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment
8. Neurogenic intermittent claudication caused by vasculitis in the cauda equina: an autopsy case report
9. A point mutation in GPI-attachment signal peptide accelerates the development of prion disease
10. CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis
11. Clinical diagnosis sensitivity of neuropathologically established multiple system atrophy in Japan
12. Age-Related Pathology in Corticobasal Degeneration
13. Diffusion-weighted magnetic resonance imaging in dura mater graft-associated Creutzfeldt-Jakob disease
14. Topoisomerase IIβ immunoreactivity (IR) co-localizes with neuronal marker-IR but not glial fibrillary acidic protein-IR in GLI3-positive medulloblastomas: an immunohistochemical analysis of 124 medulloblastomas from the Japan Children’s Cancer Group
15. Degeneration of olivospinal tract in the upper cervical spinal cord of multiple system atrophy patients: Reappraisal of Helweg's triangular tract.
16. Correlating diffusion-weighted MRI intensity with type 2 pathology in mixed MM-type sporadic Creutzfeldt-Jakob disease
17. The importance of neuropathological evaluation for accurately diagnosing sporadic creutzfeldt-Jakob disease
18. Factors influencing the survival period in patients with V180I genetic Creutzfeldt-Jakob disease
19. Severe argyrophilic grain disease in a centenarian with severe dementia who did not show the “sloping shoulders sign”
20. Degeneration of olivospinal tract in the upper cervical spinal cord of multiple system atrophy patients: Reappraisal of Helweg's triangular tract
21. Correction to: FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report
22. Tyrosine 136 phosphorylation of α-synuclein aggregates in the Lewy body dementia brain: involvement of serine 129 phosphorylation by casein kinase 2
23. Essential roles of plexin-B3+ oligodendrocyte precursor cells in the pathogenesis of Alzheimer’s disease
24. FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report
25. Publisher Correction: Essential roles of plexin-B3+ oligodendrocyte precursor cells in the pathogenesis of Alzheimer’s disease
26. Brain Pathology in Myotonic Dystrophy
27. A Novel Combination of Prion Strain Co-Occurrence in Patients with Sporadic Creutzfeldt-Jakob Disease
28. Neuropathological substrate of incident dementia in older patients with schizophrenia: A clinicopathological study
29. Detection Limitations of Prion Seeding Activities in Blood Samples from Patients with Sporadic Prion Disease
30. Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation
31. Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease
32. Nuclear Expression of TDP-43 Is Linked with Morphology and Ubiquitylation of Cytoplasmic Aggregates in Amyotrophic Lateral Sclerosis
33. An autopsy case of copper deficiency myelopathy and selenium deficiency-associated central nervous system disorder after total parenteral nutrition
34. Unclassified four-repeat tauopathy associated with familial parkinsonism and progressive respiratory failure
35. Neuropathological substrate of incident dementia in older patients with schizophrenia: A clinicopathological study.
36. Prion-Like Seeding of Misfolded α-Synuclein in the Brains of Dementia with Lewy Body Patients in RT-QUIC
37. Late‐onset panic disorder as the initial presentation in autopsy‐confirmed dementia with Lewy bodies
38. Identical Tau Filaments in Subacute Sclerosing Panencephalitis and Chronic Traumatic Encephalopathy
39. An autopsy case of schizophrenia comorbid with argyrophilic grain disease
40. TDP-43 Proteinopathy and Tauopathy: Do They Have Pathomechanistic Links?
41. Amyloid β-related angiitis of the central nervous system occurring after COVID-19 vaccination: A case report
42. Neurogenic intermittent claudication caused by vasculitis in the cauda equina: an autopsy case report
43. Severe cerebrovascular pathology of the first supercentenarian to be autopsied in the world
44. Additional file 1 of Identical tau filaments in subacute sclerosing panencephalitis and chronic traumatic encephalopathy
45. Non-motor multiple system atrophy associated with sudden death: pathological observations of autonomic nuclei
46. Clinicopathological features of progressive supranuclear palsy with asymmetrical atrophy of the superior cerebellar peduncle
47. Macroscopic differentiation as a fundamental strategy to activate clinicians, education and research — Back to the primitive observation!
48. Macroscopic diagnostic clue for parkinsonism
49. An autopsy case of Creutzfeldt‐Jakob disease with a prion protein gene codon 180 mutation presenting with pathological laughing and an exaggerated startle reaction
50. An autopsied case of corticobasal degeneration presenting with frontotemporal dementia followed by myoclonus
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