23 results on '"Aoki Masashi"'
Search Results
2. Associations between neuromyelitis optica spectrum disorder, Sjögren's syndrome, and conditions with electrolyte disturbances
3. Repeated follow-up of AQP4-IgG titer by cell-based assay in neuromyelitis optica spectrum disorders (NMOSD)
4. Preoperative risks of post-operative myasthenic crisis (POMC): A meta-analysis
5. Follow-up of retinal thickness and optic MRI after optic neuritis in anti-MOG antibody-associated disease and anti-AQP4 antibody-positive NMOSD
6. Occurrence of basophilic inclusions and FUS-immunoreactive neuronal and glial inclusions in a case of familial amyotrophic lateral sclerosis
7. Neuronal NOS is dislocated during muscle atrophy in amyotrophic lateral sclerosis
8. Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis
9. Severe symptoms of 16q-ADCA coexisting with SCA8 repeat expansion
10. Radiological findings in siblings with dysferlin mutation with diverse phenotype
11. A juvenile sporadic amyotrophic lateral sclerosis case with P525L mutation in the FUS gene: A rare co-occurrence of autism spectrum disorder and tremor
12. Five-year history of dysphagia as a sole initial symptom in inclusion body myositis
13. Longitudinal study of cognitive and cerebral metabolic changes in Parkinson's disease
14. A mismatch between MRI lesions and SPECT hypoperfusion in tacrolimus-related encephalopathy
15. Altered white matter metabolism in delayed neurologic sequelae after carbon monoxide poisoning: A proton magnetic resonance spectroscopic study
16. Recurrent cerebral infarction synchronous with menorrhagia caused by endometrial stromal sarcoma
17. Heparin-responsive angiopathy in the central nervous system caused by intravascular large B-cell lymphoma
18. Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations
19. Familial spinal arachnoiditis with secondary syringomyelia: clinical studies and MRI findings
20. Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics
21. Analysis of the McLeod syndrome gene in three patients with neuroacanthocytosis
22. Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease
23. Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in superoxide dismutase gene: A possible new subtype of familial ALS
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