Works matching AU Ikeuchi, Takeshi
Results: 178
A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review.
- Published in:
- 2017
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- Publication type:
- journal article
An early-onset case of adult-onset autosomal dominant leukodystrophy.
- Published in:
- 2024
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- Publication type:
- Letter
Mutational Analysis in Early-Onset Familial Dementia in the Japanese Population.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2008, v. 26, n. 1, p. 43, doi. 10.1159/000141483
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- Publication type:
- Article
Cell-free generation of the Notch1 intracellular domain (NICD) and APP-CTFγ.
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- NeuroMolecular Medicine, 2002, v. 1, n. 1, p. 43, doi. 10.1385/NMM:1:1:43
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- Publication type:
- Article
Initial symptoms of early‐onset dementia in Japan: nationwide survey.
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- Psychogeriatrics, 2023, v. 23, n. 3, p. 422, doi. 10.1111/psyg.12949
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- Publication type:
- Article
Involvement of inflammation in the medial temporal region in the development of agitation in Alzheimer's disease: an in vivo positron emission tomography study.
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- Psychogeriatrics, 2023, v. 23, n. 1, p. 126, doi. 10.1111/psyg.12915
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- Publication type:
- Article
Prevalence and subtype distribution of early‐onset dementia in Japan.
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- Psychogeriatrics, 2020, v. 20, n. 6, p. 817, doi. 10.1111/psyg.12596
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- Publication type:
- Article
Remarkable behavioural signs and progressive non‐fluent aphasia in a patient with adult‐onset leucoencephalopathy with axonal spheroids and pigmented glia.
- Published in:
- 2019
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- Publication type:
- Case Study
A rare functional variant of SHARPIN attenuates the inflammatory response and associates with increased risk of late-onset Alzheimer's disease.
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- Molecular Medicine, 2019, v. 25, n. 1, p. N.PAG, doi. 10.1186/s10020-019-0090-5
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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- Article
USP10 is a critical factor for Tau-positive stress granule formation in neuronal cells.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47033-7
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- Publication type:
- Article
Correction: Polygenic effects on the risk of Alzheimer's disease in the Japanese population.
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- 2024
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- Publication type:
- Correction Notice
Combining plasma Aβ and p-tau217 improves detection of brain amyloid in non-demented elderly.
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- Alzheimer's Research & Therapy, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13195-024-01469-w
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- Publication type:
- Article
Polygenic effects on the risk of Alzheimer's disease in the Japanese population.
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- Alzheimer's Research & Therapy, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13195-024-01414-x
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- Publication type:
- Article
Adult-onset leukoencephalopathy with axonal spheroids and pigmental glia with diffuse cerebral microbleeds: case report.
- Published in:
- 2023
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- Publication type:
- Letter
Switched Aβ43 generation in familial Alzheimer's disease with presenilin 1 mutation.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01684-1
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- Publication type:
- Article
Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01272-3
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- Publication type:
- Article
Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01272-3
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- Publication type:
- Article
Switched Aβ43 generation in familial Alzheimer's disease with presenilin 1 mutation.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01684-1
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- Publication type:
- Article
Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01272-3
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- Publication type:
- Article
Higher longitudinal brain white matter atrophy rate in aquaporin-4 IgG-positive NMOSD compared with healthy controls.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-38893-1
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- Publication type:
- Article
Higher longitudinal brain white matter atrophy rate in aquaporin-4 IgG-positive NMOSD compared with healthy controls.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-38893-1
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- Publication type:
- Article
Frequent Germline and Somatic Single Nucleotide Variants in the Promoter Region of the Ribosomal RNA Gene in Japanese Lung Adenocarcinoma Patients.
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- Cells (2073-4409), 2020, v. 9, n. 11, p. 2409, doi. 10.3390/cells9112409
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- Publication type:
- Article
Systematic review and meta-analysis of Japanese familial Alzheimer's disease and FTDP-17.
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- Journal of Human Genetics, 2015, v. 60, n. 5, p. 281, doi. 10.1038/jhg.2015.15
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- Publication type:
- 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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- Publication type:
- Article
Multiple γ-secretase product peptides are coordinately increased in concentration in the cerebrospinal fluid of a subpopulation of sporadic Alzheimer's disease subjects.
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- Molecular Neurodegeneration, 2012, v. 7, n. 1, p. 16, doi. 10.1186/1750-1326-7-16
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- Publication type:
- 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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- Publication type:
- Article
Globular Glial Mixed Four Repeat Tau and TDP-43 Proteinopathy with Motor Neuron Disease and Frontotemporal Dementia.
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- Brain Pathology, 2016, v. 26, n. 1, p. 82, doi. 10.1111/bpa.12262
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- Publication type:
- Article
Urinary Apolipoprotein C3 Is a Potential Biomarker for Alzheimer's Disease.
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- Dementia & Geriatric Cognitive Disorders Extra, 2020, v. 10, n. 3, p. 94, doi. 10.1159/000509561
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- Publication type:
- Article
Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients.
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- Dementia & Geriatric Cognitive Disorders Extra, 2019, v. 9, n. 1, p. 53, doi. 10.1159/000496100
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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- Article
Evidence for a Common Founder and Clinical Characteristics of Japanese Families with the MAPT R406W Mutation.
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- Dementia & Geriatric Cognitive Disorders Extra, 2011, v. 1, n. 1, p. 267, doi. 10.1159/000331243
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- Publication type:
- Article
Four Swedish cases of CSF1R‐related leukoencephalopathy: Visualization of clinical phenotypes.
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- Acta Neurologica Scandinavica, 2022, v. 145, n. 5, p. 599, doi. 10.1111/ane.13589
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- Publication type:
- Article
Reduced CSF Water Influx in Alzheimer’s Disease Supporting the β-Amyloid Clearance Hypothesis.
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- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0123708
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- Publication type:
- 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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- Publication type:
- Article
A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees.
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- Annals of Neurology, 2002, v. 52, n. 4, p. 516, doi. 10.1002/ana.10341
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- Publication type:
- Article
Impaired insulin signal transduction in neurons may be involved in β-amyloid-induced hyperphosphorylation of tau
- Published in:
- 2011
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- Publication type:
- Abstract
Analysis of an Aβ-like peptide in CSF to reveal whether and how the cleavage precision of presenilin/γ-secretase is altered in AD patients
- Published in:
- 2009
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- Publication type:
- Abstract
O4-03-01: Evidence that RER1 is the limiting cellular factor for the ER retrieval of gamma-secretase complex
- Published in:
- 2008
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- Publication type:
- Abstract
Correlated levels of cerebrospinal fluid pathogenic proteins in drug-naïve Parkinson's disease.
- Published in:
- 2019
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- Publication type:
- journal article
Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease.
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- Neurogenetics, 2015, v. 16, n. 4, p. 265, doi. 10.1007/s10048-015-0451-3
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- Publication type:
- Article
A possible variant of neuro-Behçet disease presenting chronic progressive ataxia without mucocutaneo-ocular symptoms.
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- Rheumatology International, 2006, v. 27, n. 1, p. 61, doi. 10.1007/s00296-006-0171-y
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- Publication type:
- Article
Low serum 25-hydroxyvitamin D increases cognitive impairment in elderly people.
- Published in:
- 2019
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- Publication type:
- journal article
A patient with neuronal intranuclear inclusion disease developed encephalitis‐like symptoms after cerebral angiography.
- Published in:
- 2025
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- Publication type:
- Case Study
Sporadic Japanese case of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia caused by a de novo p.Phe849del mutation in CSF1R.
- Published in:
- Neurology & Clinical Neuroscience, 2020, v. 8, n. 2, p. 96, doi. 10.1111/ncn3.12367
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- Publication type:
- Article
Sporadic case of young‐onset rapidly progressive dementia with a novel frameshift mutation in exon 3 of CSF1R.
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- Neurology & Clinical Neuroscience, 2019, v. 7, n. 2, p. 103, doi. 10.1111/ncn3.12259
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- Publication type:
- Article
A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variant.
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- Human Genome Variation, 2024, v. 11, n. 1, p. 1, doi. 10.1038/s41439-024-00265-0
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- Publication type:
- Article