43 results on '"Komori, Takashi"'
Search Results
2. The predominance of “astrocytic” intranuclear inclusions in neuronal intranuclear inclusion disease manifesting encephalopathy‐like symptoms: A case series with brain biopsy
3. Altered properties of amyloidogenic prion protein in genetic Creutzfeldt–Jakob disease with PRNP V180I mutation in response to pentosan polysulfate
4. A case of “genetically defined” radiation‐induced glioma: 29 years after surgery and radiation for pilocytic astrocytoma
5. Expanded ischemic lesion due to herniation leads to axonal injury in a site remote to the primary lesion on autopsy brain with acute focal cerebral ischemia
6. Recurrent high‐grade astrocytoma with somatic mosaicism of isocitrate dehydrogenase gene mutation
7. Synthesis, Structures, and Complexation with Phenolic Guests of Acridone‐Incorporated Arylene–Ethynylene Macrocyclic Compounds
8. Iterative synthesis, structures, and properties of acyclic and cyclic acridone oligomers
9. Distribution of amyloid‐β precursor protein‐immunoreactive axons differs according to the severity of cerebral ischemia in autopsy brains
10. Tufted astrocyte‐like glia in two autopsy cases of multiple system atrophy: Is it a concomitant neurodegenerative disorder with multiple system atrophy and progressive supranuclear palsy?
11. Tumor necrosis factor‐α expression aberration of M1 / M2 macrophages in adult h igh‐functioning autism spectrum disorder
12. Implementation of evidence‐based intervention for suicidal patients admitted to the emergency department: Implications from our real‐world experience of assertive case management
13. Retrospective analysis of heroin detoxification with buprenorphine in a psychiatric hospital in Japan
14. cIMPACT‐NOW update 6: new entity and diagnostic principle recommendations of the cIMPACT‐Utrecht meeting on future CNS tumor classification and grading
15. The Self‐Construal Scale: A Potential Tool for Predicting Subjective Well‐Being of Individuals With Autism Spectrum Disorder
16. Social status and modern‐type depression: A review
17. Chemistry of Anthracene−Acetylene Oligomers XXVII. Iterative Synthesis, Structures, and Properties of Anthracene−Diacetylene Cyclic Oligomers with 10‐Mesitylanthracene‐1,8‐diyl Units
18. An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid
19. Brainstem astroblastoma with MN1 translocation
20. Gliosarcoma arising from oligodendroglioma, IDH mutant and 1p/19q codeleted
21. Pathology of oligodendroglia: An overview
22. Comprehensive genetic characterization of rosette-forming glioneuronal tumors: independent component analysis by tissue microdissection
23. A Japanese familial ALS patient with autonomic failure and a p.Cys146Arg mutation in the gene for SOD1 (SOD1)
24. Frequent globular neuronal cytoplasmic inclusions in the medial temporal region as a possible characteristic feature in multiple system atrophy with dementia
25. Early disintegration of myonuclear fibrous lamina in inclusion body myositis: Ultrastructural and immunohistochemical studies
26. Multinodular and vacuolating neuronal tumor affecting amygdala and hippocampus: A quasi-tumor?
27. A 12-year-old boy with a mass located at the left parietal lobe involving the left lateral ventricle
28. Medial temporal regional argyrophilic grain as a possible important factor affecting dementia in Parkinson's disease
29. A Japanese patient with familial ALS and a p.K510M mutation in the gene for FUS (FUS) resulting in the totally locked-in state
30. ChemInform Abstract: Copper‐Mediated Aryl Amination: In situ Generation of an Active Copper(I) Species.
31. Glial cytoplasmic inclusions and tissue injury in multiple system atrophy: A quantitative study in white matter (olivopontocerebellar system) and gray matter (nigrostriatal system)
32. Diagnostic surgical neuropathology of intractable epilepsy
33. An immunocytologic and ultrastructural study of oligodendroglial tumors with respect to chromosome 1p deletion
34. Stromal cells in hemangioblastoma: Neuroectodermal differentiation and morphological similarities to ependymoma
35. Peculiar form of cerebral microdysgenesis characterized by white matter neurons with perineuronal and perivascular glial satellitosis: A study using a variety of human autopsied brains
36. Tau‐positive dial Inclusions in Progressive Supranuclear Palsy, Corticobasal Degeneration and Pick's Disease
37. An autopsy case of sporadic amyotrophic lateral sclerosis with 16-year survival without artificial ventilation
38. Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20 week fetus
39. Argyrophilic meshwork structures in the cerebral cortex of patients with progressive supranuclear palsy
40. Plaque-like structures in the cerebral cortex of corticobasal degeneration: A histopathologic marker?
41. Simple cerebral atrophy of non‐Alzheimer type: A comprehensive category for non‐specific cortical degeneration
42. Reply
43. Rapidly progressive aphasic dementia and motor neuron disease
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