362 results on '"Furuya, Hirokazu"'
Search Results
2. Association of right precuneus compression with apathy in idiopathic normal pressure hydrocephalus: a pilot study
3. Relationship between tongue pressure and functional oral intake scale diet type in patients with neurological and neuromuscular disorders
4. Longitudinal Changes of Tongue Thickness and Tongue Pressure in Neuromuscular Disorders
5. A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia
6. A case of non-thymomatous refractory anti-AChR, Kv1.4 and titin antibodies positive generalized myasthenia gravis successfully treated by extended thymectomy
7. A polymorphism in CCR1/CCR3 is associated with narcolepsy
8. SCA8 RAN polySer protein preferentially accumulates in white matter regions and is regulated by eIF3F
9. Association of right precuneus compression with apathy in idiopathic normal pressure hydrocephalus: A case control study
10. Tailor-made RNAi knockdown against triplet repeat disease-causing alleles
11. Immediate Effects of Sit up Practice for Parkinson’s Disease Patients: Effect of Intervention with Step by Step Difficulty Adjustment on Motion Time
12. Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses
13. Structure and Expression of mRNA for the Mouse Homolog of Alzheimer Amyloid Beta Protein Precursor
14. Efficacy and Safety of Ultrahigh-Dose Methylcobalamin in Early-Stage Amyotrophic Lateral Sclerosis
15. Effects of cyclodextrins on GM1-gangliosides in fibroblasts from GM1-gangliosidosis patients
16. New susceptibility variants to narcolepsy identified in HLA class II region
17. An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene
18. Impaired Food Transportation in Parkinson’s Disease Related to Lingual Bradykinesia
19. Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation
20. Amyloid-β accumulation caused by chloroquine injections precedes ER stress and autophagosome formation in rat skeletal muscle
21. Transactivation response DNA‐binding protein of 43 kDa proteinopathy and lysosomal abnormalities in spastic paraplegia type 11
22. An iPSC-based neural model of sialidosis uncovers glycolytic impairment-causing presynaptic dysfunction and deregulation of Ca2+ dynamics
23. Molecular Cloning and Structural Analysis of the Human Amyloid ß Protein Precursor Gene
24. Endoplasmic reticulum stress in myotonic dystrophy type 1 muscle
25. Erratum: Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses
26. Symmetrical glial hyperplasia in the brainstem of fibrodysplasia ossificans progressiva
27. Longitudinal Changes of Tongue Thickness and Tongue Pressure in Neuromuscular Disorders
28. Dysferlin expression in tubular aggregates: their possible relationship to endoplasmic reticulum stress
29. Involvement of cathepsin B in the motor neuron degeneration of amyotrophic lateral sclerosis
30. Specific HLA types are associated with antiepileptic drug-induced Stevens–Johnson syndrome and toxic epidermal necrolysis in Japanese subjects
31. Dysphagia in duchenne muscular dystrophy versus myotonic dystrophy type 1
32. Disease progression and phenotypes of non‐motor symptoms in Parkinson’s disease
33. Identification of a pre‐possible multiple system atrophy phase
34. Novel Drug Candidates Improve Ganglioside Accumulation and Neural Dysfunction in GM1 Gangliosidosis Models with Autophagy Activation
35. Narcolepsy-like excessive daytime sleepiness associated with moyamoya disease: case report
36. Management of Dysphagia in Patients with Parkinson's Disease and Related Disorders
37. HLA-B*1511 is a risk factor for carbamazepine-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients
38. Erratum: FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion
39. Sleep- and Non-Sleep-Related Hallucinations—Relationship to Ghost Tales and Their Classifications
40. Neurological signs and symptoms in patients with chronic PCB poisoning (Yusho accident) for more than 36 years
41. HLA-B locus in Japanese patients with anti-epileptics and allopurinol-related Stevens–Johnson syndrome and toxic epidermal necrolysis
42. A unique case of fibrodysplasia ossificans progressiva with an ACVR1 mutation, G356D, other than the common mutation (R206H)
43. Adrenoleukodystrophy: subcellular localization and degradation of adrenoleukodystrophy protein (ALDP/ABCD1) with naturally occurring missense mutations
44. Some flavonoids and DHEA-S prevent the cis-effect of expanded CTG repeats in a stable PC12 cell transformant
45. Therapeutic effects of normal cells on ABCD1 deficient cells in vitro and hematopoietic cell transplantation in the X-ALD mouse model
46. A novel mutation (L250V) in the presenilin 1 gene in a Japanese familial Alzheimer's disease with myoclonus and generalized convulsion
47. Myelitis with atopic diathesis: a nationwide survey of 79 cases in Japan
48. Longitudinal Changes of Tongue Thickness and Tongue Pressure in Neuromuscular Disorders.
49. Transient thyrotoxicosis‐aggravated attacks of paralysis in a patient with hereditary hypokalemic periodic paralysis type 2
50. Atypical Familial Amyotrophic Lateral Sclerosis with Slowly Progressing Lower Extremities-predominant Late-onset Muscular Weakness and Atrophy
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