923 results on '"Kitamoto, Tetsuyuki"'
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2. Involvement of the nigrostriatal system in Gerstman–Sträussler–Scheinker disease with the PRNP-P102L mutation
3. Genetic Creutzfeldt‒Jakob disease with 5-octapeptide repeats presented as frontotemporal dementia
4. A point mutation in GPI-attachment signal peptide accelerates the development of prion disease
5. Vacuoles related to tissue neuron-astrocyte ratio and infiltration of macrophages/monocytes contribute to hyperintense brain signals on diffusion-weighted magnetic resonance imaging in sporadic Creutzfeldt-Jakob disease
6. Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics
7. Preventive or promotive effects of PRNP polymorphic heterozygosity on the onset of prion disease
8. Specific electroencephalogram features in the very early phases of sporadic Creutzfeldt–Jakob disease
9. Potential for transmission of sporadic Creutzfeldt–Jakob disease through peripheral routes
10. Accumulation Area of a Japanese PRNP P102L Variant: The Ariake PRNP P102L Variant
11. Diffusion-weighted magnetic resonance imaging in dura mater graft-associated Creutzfeldt-Jakob disease
12. Correlating diffusion-weighted MRI intensity with type 2 pathology in mixed MM-type sporadic Creutzfeldt-Jakob disease
13. Two distinct conformers of PrPD type 1 of sporadic Creutzfeldt–Jakob disease with codon 129VV genotype faithfully propagate in vivo
14. Characterization of Sporadic Creutzfeldt-Jakob Disease and History of Neurosurgery to Identify Potential Iatrogenic Cases
15. A Novel Combination of Prion Strain Co-Occurrence in Patients with Sporadic Creutzfeldt-Jakob Disease
16. Ganglioside Synthase Knockout Reduces Prion Disease Incubation Time in Mouse Models
17. In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrPV180I Mutation
18. An autopsy case of variably protease‐sensitive prionopathy with Met/Met homogeneity at codon 129
19. Bilateral tonic–clonic seizure and focal cortical hyperexcitability in familial Creutzfeldt‐Jakob disease with E200K mutation of the prion protein
20. V180I genetic Creutzfeldt‐Jakob disease: Severe degeneration of the inferior olivary nucleus in an autopsied patient with identification of the M2T prion strain
21. Cerebral cortex swelling in V180I genetic Creutzfeldt–Jakob disease: comparative imaging study between sporadic and V180I genetic Creutzfeldt–Jakob disease in the early stage
22. Vascular Variant of Prion Protein Cerebral Amyloidosis with τ -Positive Neurofibrillary Tangles: The Phenotype of the Stop Codon 145 Mutation in PRNP
23. Age at onset in genetic prion disease and the design of preventive clinical trials
24. Iatrogenic Creutzfeldt–Jakob disease
25. The characterization of AD/PART co-pathology in CJD suggests independent pathogenic mechanisms and no cross-seeding between misfolded Aβ and prion proteins
26. Protective effect of [Val.sub.129]-PrP against bovine spongiform encephalopathy but not variant Creutzfeldt-Jakob disease
27. Propagation of Diffusion-Weighted MRI Abnormalities in the Preclinical Stage of Sporadic Creutzfeldt-Jakob Disease
28. 18F-THK5351 positron emission tomography imaging for Gerstmann-Sträussler-Scheinker disease
29. An autopsy case of Creutzfeldt‐Jakob disease with a prion protein gene codon 180 mutation presenting with pathological laughing and an exaggerated startle reaction
30. MM1‐type sporadic Creutzfeldt‐Jakob disease with 1‐month total disease duration and early pathologic indicators
31. MM2 type sporadic Creutzfeldt-Jakob disease: clinicoradiologic features and clinical diagnosis
32. PrPres deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD)
33. Neuroimaging-pathological correlations of [18F]THK5351 PET in progressive supranuclear palsy
34. Creutzfeldt-Jakob disease with Alzheimer pathology, presenting with status epilepticus following repeated partial seizures: a case report and literature review
35. An autopsy case of MV2K ‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings
36. Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases
37. An autopsied case of MM1 + MM2‐cortical with thalamic‐type sporadic Creutzfeldt‐Jakob disease presenting with hyperintensities on diffusion‐weighted MRI before clinical onset
38. The influence of PRNP polymorphisms on human prion disease susceptibility: an update
39. Correction to: In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrPV180I Mutation
40. Early Diagnosis of V180I Genetic Creutzfeldt-Jakob Disease at the Preserved Cognitive Function Stage
41. Significant association of cadaveric dura mater grafting with subpial Aβ deposition and meningeal amyloid angiopathy
42. Co-Occurrence of Types 1 and 2 PrP res in Sporadic Creutzfeldt-Jakob Disease MM1
43. Molecular barriers to zoonotic transmission of prions
44. Neuropathological and biochemical criteria to identify acquired Creutzfeldt‐Jakob disease among presumed sporadic cases
45. Sporadic Creutzfeldt–Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties
46. Efficient propagation of variant Creutzfeldt-Jakob disease prion protein using the cell-protein misfolding cyclic amplification technique with samples containing plasma and heparin
47. Propagation of Diffusion-Weighted MRI Abnormalities in the Preclinical Stage of Sporadic Creutzfeldt-Jakob Disease.
48. Optic nerve atrophy and visual disturbance following PRNP Y162X truncation mutation
49. Early clinical and radiological diagnosis of sporadic Creuzfeldt-Jakob’s disease (sCJD) — a case study of pathologically-proved sCJD MV2 —
50. Familial Creutzfeldt-Jakob disease with a point mutation (Met to Arg) at codon 232: two different phenotypes
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