1,494 results on '"Aoki Masashi"'
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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. Dysregulation of SNX1-retromer axis in pharmacogenetic models of Parkinson’s disease
4. Anti-aquaporin-4 immune complex stimulates complement-dependent Th17 cytokine release in neuromyelitis optica spectrum disorders
5. Case Report: An Adult Case of Poretti-Boltshauser Syndrome Diagnosed by Medical Checkup
6. Impact of sex, age at onset, and anti-cN1A antibodies on sporadic inclusion body myositis
7. LONRF2 is a protein quality control ubiquitin ligase whose deficiency causes late-onset neurological deficits
8. Efficacy confirmation study of aceneuramic acid administration for GNE myopathy in Japan
9. White blood cell count profiles in anti-aquaporin-4 antibody seropositive neuromyelitis optica spectrum disorder and anti-myelin oligodendrocyte glycoprotein antibody-associated disease
10. Stochastic models for the onset and disease course of multiple sclerosis
11. Dynamic changes in patient admission and their disabilities in multiple sclerosis and neuromyelitis optica: A Japanese nationwide administrative data study
12. Genetics of amyotrophic lateral sclerosis: seeking therapeutic targets in the era of gene therapy
13. Suppression of dynamin GTPase decreases α-synuclein uptake by neuronal and oligodendroglial cells: a potent therapeutic target for synucleinopathy
14. Efficacy and Safety of Bimagrumab in Sporadic Inclusion Body Myositis: Long-term Extension of RESILIENT.
15. The necessity to improve disaster preparedness among patients with amyotrophic lateral sclerosis and their families
16. Referral odyssey plot to visualize causes of surgical delay in mesial temporal lobe epilepsy with hippocampal sclerosis
17. Associations between neuromyelitis optica spectrum disorder, Sjögren's syndrome, and conditions with electrolyte disturbances
18. CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis
19. Efficacy of oligodendrocyte precursor cells as delivery vehicles for single-chain variable fragment to misfolded SOD1 in ALS rat model
20. Safety and efficacy of aceneuramic acid in GNE myopathy: open-label extension study
21. Reduced histone H3K4 trimethylation in oral mucosa of patients with DYT-KMT2B
22. “Caterpillar sign” in corpus callosum associated with curvilinear pericallosal lipoma in MRI: A case report
23. Relapse activity in the chronic phase of anti-myelin-oligodendrocyte glycoprotein antibody-associated disease
24. SQSTM1, a protective factor of SOD1-linked motor neuron disease, regulates the accumulation and distribution of ubiquitinated protein aggregates in neuron
25. Mutation screening of the DNAJC7 gene in Japanese patients with sporadic amyotrophic lateral sclerosis
26. Randomized phase 2 study of perampanel for sporadic amyotrophic lateral sclerosis
27. RSPO3 is a novel contraction-inducible factor identified in an “in vitro exercise model” using primary human myotubes
28. Long-term outcomes after surgery to prevent aspiration for patients with amyotrophic lateral sclerosis
29. Upregulated complement receptors correlate with Fc gamma receptor 3A-positive natural killer and natural killer-T cells in neuromyelitis optica spectrum disorder
30. Feeder-supported in vitro exercise model using human satellite cells from patients with sporadic inclusion body myositis
31. Humanized-Aquaporin-4-Expressing Rat Created by Gene-Editing Technology and Its Use to Clarify the Pathology of Neuromyelitis Optica Spectrum Disorder.
32. High prevalence of serum anti-NH2-terminal of α-enolase antibodies in patients with multiple system atrophy and corticobasal syndrome
33. Improved Activities of Daily Living With Adjunctive Intravenous Steroids in Bacterial Meningitis: A Nationwide, Population-Based Medical Database Study
34. Genome-wide association analysis identifies PLA2G4C as a susceptibility locus for Multiple System Atrophy
35. A web-based questionnaire survey on the influence of coronavirus disease-19 on the care of patients with muscular dystrophy
36. A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathy
37. Impact of comorbid Sjögren syndrome in anti-aquaporin-4 antibody-positive neuromyelitis optica spectrum disorders
38. CH50 as a putative biomarker of eculizumab treatment in neuromyelitis optica spectrum disorder
39. Patulous Eustachian Tube Patients With Oculopharyngeal Muscular Dystrophy
40. Seasonal variation of onset in patients with anti-aquaporin-4 antibodies and anti-myelin oligodendrocyte glycoprotein antibody
41. Hybrid Assistive Limb® for sporadic inclusion body myositis: A case series
42. Alpha‐synuclein promotes PRMT5‐mediated H4R3me2s histone methylation by interacting with the BAF complex.
43. An Amyotrophic Lateral Sclerosis-Associated Mutant of C21ORF2 Is Stabilized by NEK1-Mediated Hyperphosphorylation and the Inability to Bind FBXO3
44. Repeated follow-up of AQP4-IgG titer by cell-based assay in neuromyelitis optica spectrum disorders (NMOSD)
45. Case report: An adult case of Poretti-Boltshauser syndrome diagnosed by medical checkup.
46. Establishment of a novel amyotrophic lateral sclerosis patient-derived blood-brain barrier model: Investigating barrier dysfunction and immune cell interaction
47. Amyotrophic Lateral Sclerosis with a Priority Request for a Postmortem Kidney Donation to a Relative
48. A Reduction in the Number of Hospitalized Cases of Acute Meningitis during the COVID-19 Pandemic in Japan
49. Myelin oligodendrocyte glycoprotein antibody‐associated disorders: An overview
50. Dynamic Changes in Patient Admission and Their Disabilities in Multiple sclerosis and Neuromyelitis Optica: A Japanese Nationwide Administrative Data Study
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