104 results on '"Hasegawa, Masato"'
Search Results
2. Corticobasal degeneration with visual hallucination as an initial symptom: A case report
3. Atypical TDP‐43 proteinopathy clinically presenting with progressive nonfluent aphasia: A case report
4. Cryo‐EM structures of tau filaments from SH‐SY5Y cells seeded with brain extracts from cases of Alzheimer's disease and corticobasal degeneration
5. Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathy
6. An autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau
7. An autopsy case of progressive supranuclear palsy. Pallido‐nigro‐luysian type with argyrophilic grains clinically presenting with personality and behavioral changes
8. TDP‐43 Proteinopathy Presenting with Typical Symptoms of Parkinson's Disease
9. An autopsy case of MV2K ‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings
10. Pathologically Verified Corticobasal Degeneration Mimicking Richardson's Syndrome Coexisting with Clinically and Radiologically Shunt‐Responsive Normal Pressure Hydrocephalus
11. Independent distribution between tauopathy secondary to subacute sclerotic panencephalitis and measles virus: An immunohistochemical analysis in autopsy cases including cases treated with aggressive antiviral therapies
12. Neuropathological investigation of patients with prolonged anorexia nervosa
13. An autopsy case of Alzheimer's disease with amygdala‐predominant Lewy pathology presenting with frontotemporal dementia‐like psychiatric symptoms
14. The hot cross bun sign in corticobasal degeneration
15. Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrus
16. An autopsy case of corticobasal degeneration with inferior olivary hypertrophy
17. Progression of phosphorylated α‐synuclein in Macaca fuscata
18. Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases
19. Seeded assembly in vitro does not replicate the structures of α‐synuclein filaments from multiple system atrophy
20. An autopsy case of corticobasal syndrome due to asymmetric degeneration of the motor cortex and substantia nigra with TDP ‐43 proteinopathy, associated with Alzheimer's disease pathology
21. Asparagine residue 368 is involved in Alzheimer’s disease tau strain‐specific aggregation
22. Globular glial tauopathy Type I presenting with behavioral variant frontotemporal dementia
23. Experimental models of prion‐like protein propagation
24. Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases
25. Corticobasal degeneration with deep white matter lesion diagnosed by brain biopsy
26. Structurally Distinct α‐Synuclein Fibrils Induce Robust Parkinsonian Pathology
27. O3‐01‐02: TAU‐RELATED DYSFUNCTION OF BRCA1 LEADS TO REDUCED NEURONAL PLASTICITY IN ALZHEIMER'S DISEASE
28. An autopsy case of globular glial tauopathy presenting with clinical features of motor neuron disease with dementia and iron deposition in the motor cortex
29. Unusual tau pathology of the cerebellum in patients with amyotrophic lateral sclerosis/parkinsonism-dementia complex from the Kii Peninsula, Japan
30. Frontotemporal dementia with trans-activation response DNA-binding protein 43 presenting with catatonic syndrome
31. Molecular mechanisms of the co-deposition of multiple pathological proteins in neurodegenerative diseases
32. Pathological and immunoblot analysis of phosphorylated TDP-43 in sporadic amyotrophic lateral sclerosis with pallido-nigro-luysian degeneration
33. Pick's disease with neuronal four-repeat tau accumulation in the basal ganglia, brain stem nuclei and cerebellum
34. FTLD-TDP-43 AND FTLD-FUS
35. Laparoscopic-endoscopic cooperative surgery for a duodenal neuroendocrine tumor: A case report
36. P3-300: Phosphorylated TAU and Alpha-Synuclein Accumulation in Familial Granulin Mutation Cases
37. P4-088: C9Orf72 Dipeptide Repeat Proteins Cause Intracellular Aggregation of Phosphorylated TDP-43
38. Cerebellar neuronal loss in amyotrophic lateral sclerosis cases with ATXN2 intermediate repeat expansions
39. An autopsied case of unclassifiable sporadic four-repeat tauopathy presenting with parkinsonism and speech disturbances
40. The Relationship Between Development of Neuronal and Astrocytic Tau Pathologies in Subcortical Nuclei and Progression of Argyrophilic Grain Disease
41. An autopsy case of familial amyotrophic lateral sclerosis with aTARDBPQ343R mutation
42. Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions inC9ORF72gene
43. C9ORF72repeat-associated non-ATG-translated polypeptides are distributed independently of TDP-43 in a Japanese patient with c9ALS
44. P4-019: PHOSPHORYLATION OF TDP-43 BY CASEIN KINASE 1 DELTA FACILITATES MISLOCALIZATION AND INTRACELLULAR AGGREGATE FORMATION OF TDP-43
45. P3-061: TREATMENT OF CELLS EXPRESSING AMYLOID PRECURSOR PROTEIN WITH TAU FIBRILS INDUCES INTRACELLULAR AGGREGATE FORMATION OF TAU
46. P4-045: Truncated tau causes microtubule disassembly with aging in tauopathy model mice
47. P2-227: Tau pathology in the parahippocampal region is related to delusion in the elderly: Neuropathological study of two autopsy cases
48. P2-225: Pathological and biochemical study of the nucleus accumbens in tangle-predominant dementia
49. P4-050: Insoluble TDP-43 prepared from diseased brains has prion-like properties
50. P3-331: Methylene blue reduced tau phosphorylation and aggregation in P301L tau transgenic mice
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