129 results on '"Koike, Ryoko"'
Search Results
2. Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy
3. Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial
4. Characteristics of spinopelvic alignment in Parkinson's disease: Comparison with adult spinal deformity
5. Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy
6. Array comparative genomic hybridization analysis discloses chromosome copy number alterations as indicators of patient outcome in lymph node-negative breast cancer
7. Characteristics and exacerbating factors of chronic low back pain in Parkinson’s disease
8. Development of a Novel Nutrition-Related Multivariate Biomarker for Mild Cognitive Impairment Based on the Plasma Free Amino Acid Profile
9. Neuropsychological and regional cerebral blood flow of posterior parietal area features in patients with Parkinson’s disease with mild cognitive impairment
10. Parkinson's disease and parkinsonism: Clinicopathological discrepancies on diagnosis in three patients
11. Small Vessel Diseases: 3D Characteristics of the Vasculature and White Matter
12. Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity
13. A fatal neuromuscular disease in an adult patient after poliomyelitis in early childhood: Consideration of the pathology of post-polio syndrome
14. Mutational analysis of X-linked adrenoleukodystrophy gene
15. Primary lateral sclerosis: Upper-motor-predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration – immunohistochemical and biochemical analyses of TDP-43
16. Evaluating the Angiogenetic Properties of Ovarian Cancer Stem-Like Cells using the Three-Dimensional Co-Culture System, NICO-1
17. Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: A correlation with CAG repeat length
18. Adult onset globoid cell leukodystrophy (Krabbe disease): analysis of galactosylceramidase cDNA from four Japanese patients
19. Mutational Analysis and Genotype-Phenotype Correlation of 29 Unrelated Japanese Patients With X-linked Adrenoleukodystrophy
20. The proteasome deubiquitinase inhibitor bAP15 downregulates TGF-β/Smad signaling and induces apoptosis via UCHL5 inhibition in ovarian cancer
21. Successful twin pregnancy in a patient with parkin-associated autosomal recessive juvenile parkinsonism
22. Co-existence of spastic paraplegia-30 with novel KIF1A mutation and spinocerebellar ataxia 31 with intronic expansion of BEAN and TK2 in a family
23. Abstract TP269: Distinct Molecular Mechanisms of Htra1 Mutants in Manifesting Heterozygotes With Carasil
24. Distinct molecular mechanisms ofHTRA1mutants in manifesting heterozygotes with CARASIL
25. Co-Existence of Novel KIF1A Mutation (SPG30) and Intronic Expansion of BEAN (SCA31) in a Family: Clinical and Genetic Characterization (P5.390)
26. A serial MRI study in a patient with progressive supranuclear palsy with cerebellar ataxia
27. Effect of sodium pyruvate on exercise intolerance and muscle weakness due to mitochondrial myopathy: a case report
28. Multifocal hits for propagation of prion protein in sporadic Creutzfeldt-Jakob disease
29. Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL.
30. A fatal neuromuscular disease in an adult patient after poliomyelitis in early childhood: Consideration of the pathology of post-polio syndrome
31. Primary lateral sclerosis: Upper-motor-predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration - immunohistochemical and biochemical analyses of TDP-43
32. Successful twin pregnancy in a patient with parkin-associated autosomal recessive juvenile parkinsonism
33. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene
34. Distinct molecular mechanisms of HTRA1mutants in manifesting heterozygotes with CARASIL
35. Adrenoleukodystrophyにおける脂肪酸鎖長延長活性の役割ならびに単価不飽和脂肪酸による治療効果のメカニズムについて
36. A Japanese family with adrenoleukodystrophy with a codon 291 deletion: a clinical, biochemical, pathological, and genetic report
37. Adrenoleukodystrophy with involvement of the cerebral cortex
38. CT and MR Findings of Neuroacanthocytosis
39. Partial deletions of putative adrenoleukodystrophy (ALD) gene in Japanese ALD patients
40. Effect of intravenous immunoglobulin in Lambert-Eaton myasthenic syndrome with small-cell lung cancer: Correlation with the titer of anti-voltage-gateo calcium channel antibody
41. Letters to the editor
42. Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity.
43. Physiological significance of fatty acid elongation system in adrenoleukodystrophy
44. Inhibition of erythropoiesis by human parvovirus‐containing serum from a patient with hereditary spherocytosis in aplastic crisis
45. Biochemical analysis of decreased ornithine transport activity in the liver mitochondria from patients with hyperornithinemia, hyperammonemia and homocitrullinuria
46. Infection with human parvovirus (B19), aplasia of the bone marrow and a rash in hereditary spherocytosis
47. EPIDEMIC OF APLASTIC CRISIS IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS IN JAPAN
48. [Clinical and neuropsychological features and changes to regional cerebral blood flow in patients with Parkinson's disease dementia].
49. [Burnout in Japanese neurologists: comparison of male and female physicians].
50. [Current and future strategies for burnout in Japanese neurologists].
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