Works by Onodera, Osamu
Results: 150
A CARASIL Patient from Americas with Novel Mutation and Atypical Features: Case Presentation and Literature Review.
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- Cerebrovascular Diseases, 2017, v. 44, n. 3/4, p. 135, doi. 10.1159/000477358
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- Article
Mutational Analysis in Early-Onset Familial Dementia in the Japanese Population.
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- Dementia & Geriatric Cognitive Disorders, 2008, v. 26, n. 1, p. 43, doi. 10.1159/000141483
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- Article
Stroke incidence and chronic kidney disease: A hospital‐based prospective cohort study.
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- Nephrology, 2022, v. 27, n. 7, p. 577, doi. 10.1111/nep.14049
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- Article
Polyglutamine Domains Are Substrates of Tissue Transglutaminase: Does Transglutaminase Play a Role in Expanded CAG/Poly-Q Neurodegenerative Diseases?
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- Journal of Neurochemistry, 1997, v. 69, n. 1, p. 431, doi. 10.1046/j.1471-4159.1997.69010431.x
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- Article
Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: A correlation with CAG repeat length.
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- Movement Disorders, 2010, v. 25, n. 11, p. 1694, doi. 10.1002/mds.23167
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- Article
Novel GFAP mutation in patient with adult-onset Alexander disease presenting with spastic ataxia.
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- Movement Disorders, 2009, v. 24, n. 9, p. 1393, doi. 10.1002/mds.22556
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- Article
Sacsin-related ataxia with neither retinal hypermyelination nor spasticity.
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- Movement Disorders, 2007, v. 22, n. 9, p. 1362, doi. 10.1002/mds.21557
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- Article
Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.
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- Movement Disorders, 2007, v. 22, n. 6, p. 857, doi. 10.1002/mds.21443
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- Article
New mutation in the non-gigantic exon of SACS in Japanese siblings.
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- Movement Disorders, 2007, v. 22, n. 5, p. 748, doi. 10.1002/mds.21365
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- Article
Botulinum toxin A injections improve apraxia of eyelid opening without overt blepharospasm associated with neurodegenerative diseases.
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- Movement Disorders, 2007, v. 22, n. 4, p. 597, doi. 10.1002/mds.21367
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- Article
Sacsin-related autosomal recessive ataxia without prominent retinal myelinated fibers in Japan.
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- Movement Disorders, 2005, v. 20, n. 3, p. 380, doi. 10.1002/mds.20315
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- Article
Reduced bowel sounds in Parkinson's disease and multiple system atrophy patients.
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- Clinical Autonomic Research, 2011, v. 21, n. 3, p. 181, doi. 10.1007/s10286-010-0102-6
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- Article
Publisher Correction: A novel therapeutic approach using peripheral blood mononuclear cells preconditioned by oxygen-glucose deprivation.
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- 2019
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- Correction Notice
Missense Variants in COL4A1/2 Are Associated with Cerebral Aneurysms: A Case Report and Literature Review.
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- Neurology International, 2024, v. 16, n. 1, p. 226, doi. 10.3390/neurolint16010015
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- Article
Progressive conus medullaris lesions are suggestive of intravascular large B‐cell lymphoma.
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- European Journal of Neurology, 2023, v. 30, n. 10, p. 3236, doi. 10.1111/ene.15941
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- Article
Partial deletions of putative adrenoleukodystrophy (ALD) gene in Japanese ALD patients.
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- Human Mutation, 1995, v. 6, n. 3, p. 263, doi. 10.1002/humu.1380060314
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- Article
Do patients with multiple system atrophy have decreased nocturnal urinary concentration?
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- 2021
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- Letter
Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage.
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- Journal of Human Genetics, 2012, v. 57, n. 3, p. 202, doi. 10.1038/jhg.2012.5
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- Article
Cerebral small-vessel disease protein HTRA1 controls the amount of TGF-β1 via cleavage of proTGF-β1.
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- Human Molecular Genetics, 2011, v. 20, n. 9, p. 1800, doi. 10.1093/hmg/ddr063
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- Article
Severe neurological phenotypes of Q129 DRPLA transgenic mice serendipitously created by en masse expansion of CAG repeats in Q76 DRPLA mice.
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- Human Molecular Genetics, 2009, v. 18, n. 4, p. 723, doi. 10.1093/hmg/ddn403
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- Article
Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxic.
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- Human Molecular Genetics, 2008, v. 17, n. 3, p. 345, doi. 10.1093/hmg/ddm311
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- Article
Aprataxin, a novel protein that protects against genotoxic stress.
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- Human Molecular Genetics, 2004, v. 13, n. 10, p. 1081, doi. 10.1093/hmg/ddh122
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- Article
Polyglutamine Diseases: Where does Toxicity Come from? What is Toxicity? Where are We Going?
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- Journal of Molecular Cell Biology, 2010, v. 2, n. 4, p. 180, doi. 10.1093/jmcb/mjq005
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- Article
Cataract Surgery and Chronic Kidney Disease: A Hospital-based Prospective Cohort Study.
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- Internal Medicine, 2024, v. 63, n. 9, p. 1207, doi. 10.2169/internalmedicine.2176-23
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- Article
Case Report: A patient with spinocerebellar ataxia type 31 and sporadic Creutzfeldt-Jakob disease.
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- Prion, 2018, v. 12, n. 2, p. 147, doi. 10.1080/19336896.2018.1436926
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- Article
Pathological and Clinical Spectrum of Progressive Supranuclear Palsy: With Special Reference to Astrocytic Tau Pathology.
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- Brain Pathology, 2016, v. 26, n. 2, p. 155, doi. 10.1111/bpa.12265
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- Article
Preclinical Characterization of the Tau PET Tracer [ <sup>18</sup>F]SNFT-1: Comparison of Tau PET Tracers.
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- Journal of Nuclear Medicine, 2023, v. 64, n. 9, p. 1495, doi. 10.2967/jnumed.123.265593
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- Article
Electroclinical features of epilepsy in patients with juvenile type dentatorubral-pallidoluysian atrophy.
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- Epilepsia (Series 4), 2008, v. 49, n. 12, p. 2041, doi. 10.1111/j.1528-1167.2008.01701.x
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- Article
A case report of reversible cerebral vasoconstriction syndrome with thunderclap headache significantly exacerbated in the supine position and alleviated in the standing position.
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- 2023
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- Case Study
Case report: Progressive multifocal leukoencephalopathy co-occurring with neurosarcoidosis: early brain biopsy and appropriate therapy for PML resulted in a favorable prognosis.
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- Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1447992
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- Article
HTRA1 Mutations Identified in Symptomatic Carriers Have the Property of Interfering the Trimer-Dependent Activation Cascade.
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- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00693
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- Article
Modifiable Factors Associated with Cognitive Impairment in 1,143 Japanese Outpatients: The Project in Sado for Total Health (PROST).
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- Dementia & Geriatric Cognitive Disorders Extra, 2016, v. 6, n. 2, p. 341, doi. 10.1159/000447963
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- Article
Elevated C-Reactive Protein Is Associated with Cognitive Decline in Outpatients of a General Hospital: The Project in Sado for Total Health (PROST).
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- Dementia & Geriatric Cognitive Disorders Extra, 2016, v. 6, n. 1, p. 10, doi. 10.1159/000442585
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- Article
Amyotrophic Lateral Sclerosis with Pallidonigroluysian Degeneration: A Clinicopathological Study.
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- 2020
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- journal article
Characteristic microglial features in patients with hereditary diffuse leukoencephalopathy with spheroids.
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- 2016
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- journal article
TDP- 43 mutation in familial amyotrophic lateral sclerosis.
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- Annals of Neurology, 2008, v. 63, n. 4, p. 538, doi. 10.1002/ana.21392
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- Article
A mutant PSEN1 causes dementia with lewy bodies and variant Alzheimer's disease.
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- Annals of Neurology, 2005, v. 57, n. 3, p. 429
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- Article
Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein.
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- Annals of Neurology, 2004, v. 55, n. 2, p. 241
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- Article
SCA17 homozygote showing Huntington's disease-like phenotype.
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- Annals of Neurology, 2004, v. 55, n. 2, p. 281
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- Article
Accuracy of a machine learning method based on structural and locational information from AlphaFold2 for predicting the pathogenicity of TARDBP and FUS gene variants in ALS.
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- BMC Bioinformatics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12859-023-05338-5
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- Article
USP10 Inhibits Aberrant Cytoplasmic Aggregation of TDP-43 by Promoting Stress Granule Clearance.
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- Molecular & Cellular Biology, 2022, v. 42, n. 3, p. 1, doi. 10.1128/mcb.00393-21
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- Article
Quantitative evaluation of brainstem involvement in multiple system atrophy by diffusion-weighted MR imaging.
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- Journal of Neurology, 2004, v. 251, n. 9, p. 1121, doi. 10.1007/s00415-004-0494-0
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- Article
Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes.
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- Neurogenetics, 2011, v. 12, n. 1, p. 41, doi. 10.1007/s10048-010-0253-6
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- Article
Authors' reply.
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- Journal of Bone & Mineral Metabolism, 2022, v. 40, n. 3, p. 537, doi. 10.1007/s00774-022-01315-9
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- Article
Polypharmacy, chronic kidney disease, and incident fragility fracture: a prospective cohort study.
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- Journal of Bone & Mineral Metabolism, 2022, v. 40, n. 1, p. 157, doi. 10.1007/s00774-021-01272-9
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- Article
Low serum 25-hydroxyvitamin D increases cognitive impairment in elderly people.
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- 2019
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- Publication type:
- journal article
A patient with neuronal intranuclear inclusion disease developed encephalitis‐like symptoms after cerebral angiography.
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- 2025
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- Case Study
Reliability study for the Japanese version of the Columbia Muscle Cramp Scale in amyotrophic lateral sclerosis.
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- Neurology & Clinical Neuroscience, 2025, v. 13, n. 1, p. 14, doi. 10.1111/ncn3.12838
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- Article
The Japan MSA registry: A multicenter cohort study of multiple system atrophy.
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- Neurology & Clinical Neuroscience, 2024, v. 12, n. 5, p. 271, doi. 10.1111/ncn3.12809
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- Article
A new Japanese amyotrophic lateral sclerosis family with TARDBP (TDP‐43) mutation.
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- Neurology & Clinical Neuroscience, 2019, v. 7, n. 2, p. 101, doi. 10.1111/ncn3.12250
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- Article