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2. Conventional magnetic resonance imaging key features for distinguishing pathologically confirmed corticobasal degeneration from its mimics: a retrospective analysis of the J-VAC study

3. Heteromeric amyloid filaments of ANXA11 and TDP-43 in FTLD-TDP type C

7. Pure argyrophilic grain disease revisited: independent effects on limbic, neocortical, and striato-pallido-nigral degeneration and the development of dementia in a series with a low to moderate Braak stage

8. Neurofibrillary tangle-predominant dementia followed by amyloid β pathology: a clinico-radio-pathological case providing insights into current disease-modifying therapeutic strategy

11. LATE-NC staging in routine neuropathologic diagnosis: an update

13. Imaging α-synuclein pathologies in animal models and patients with Parkinson’s and related diseases

20. Structures of α-synuclein filaments from human brains with Lewy pathology

24. LATE to the PART-y

27. Age-dependent formation of TMEM106B amyloid filaments in human brains

29. A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics

30. Clinicopathological study of dementia with grains presenting with parkinsonism compared with a typical case.

31. Tau Protein and Frontotemporal Dementias

34. An autopsy case of type A FTLD‐TDP with a GRN mutation presenting with the logopenic variant of primary progressive aphasia at onset and with corticobasal syndrome subsequently

40. Structure-based classification of tauopathies

46. Corticobasal degeneration with visual hallucination as an initial symptom: A case report.

47. Structure of NFT: Biochemical Approach

48. Exposure to bacterial endotoxin generates a distinct strain of α-synuclein fibril

49. Tau filaments from amyotrophic lateral sclerosis/parkinsonism-dementia complex adopt the CTE fold

50. The new missense G376V-TDP-43 variant induces late-onset distal myopathy but not amyotrophic lateral sclerosis

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