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CpG demethylation enhances alpha-synuclein expression and affects the pathogenesis of Parkinson's disease

PloS one, 2010-11, Vol.5 (11), p.e15522

2010

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Dentatorubropallidoluysian Atrophy with Prominent Autonomic Dysfunction

Internal Medicine, 2023/03/15, Vol.62(6), pp.889-892

2023

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Ventral Variant Posterior Cortical Atrophy with Occipito-temporal Accumulation of Tau Proteins/Astrocyte Gliosis

Internal Medicine, 2024, pp.2844-23

2024

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An Ocular Form of Myasthenia Gravis with a High Titer of Anti-MuSK Antibodies during a Long-term Follow-up

Internal Medicine, 2012, Vol.51(21), pp.3077-3079

2012

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Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases

Brain & development (Tokyo. 1979), 2016-03, Vol.38 (3), p.293-301

2016

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Mutation-induced loss of APP function causes GABAergic depletion in recessive familial Alzheimer's disease: analysis of Osaka mutation-knockin mice

Acta neuropathologica communications, 2017-07, Vol.5 (1), p.59-59, Article 59

2017

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Amyloid beta peptide-induced cerebral neuronal loss is mediated by caspase-3 in vivo

Journal of neuropathology and experimental neurology, 2004-03, Vol.63 (3), p.255-261

2004

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TDP-43 M337V Mutation in Familial Amyotrophic Lateral Sclerosis in Japan

Internal Medicine, 2010, Vol.49(4), pp.331-334

2010

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Fluorescent Arc/Arg3.1 indicator mice: A versatile tool to study brain activity changes in vitro and in vivo

Journal of neuroscience methods, 2009-10, Vol.184 (1), p.25-36

2009

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Frontal allographic agraphia in a patient with behavioral variant frontotemporal dementia

Neurocase, 2024-02, Vol.30 (1), p.32-38

2024

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Sixth nerve palsy associated with obstruction in Dorello's canal, accompanied by nodular type muscular sarcoidosis

Journal of the neurological sciences, 2014-08, Vol.343 (1), p.203-205

2014

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Isoforms changes of tau protein during development in various species

Brain research. Developmental brain research, 2003-05, Vol.142 (2), p.121-127

2003

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A unique mouse model for investigating the properties of amyotrophic lateral sclerosis-associated protein TDP-43, by in utero electroporation

Neuroscience research, 2013-12, Vol.77 (4), p.234-241

2013

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Altered CpG methylation in sporadic Alzheimer's disease is associated with APP and MAPT dysregulation

Human molecular genetics, 2014-02, Vol.23 (3), p.648-656

2014

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A mouse model of amyloid beta oligomers: their contribution to synaptic alteration, abnormal tau phosphorylation, glial activation, and neuronal loss in vivo

The Journal of neuroscience, 2010-04, Vol.30 (14), p.4845-4856

2010

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A new amyloid β variant favoring oligomerization in Alzheimer's-type dementia

Annals of neurology, 2008-03, Vol.63 (3), p.377-387

2008

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E22Δ Mutation in Amyloid β-Protein Promotes β-Sheet Transformation, Radical Production, and Synaptotoxicity, But Not Neurotoxicity

International journal of alzheimer's disease, 2011, Vol.2011 (1), p.431320

2011

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Radiological findings in siblings with dysferlin mutation with diverse phenotype

Journal of the neurological sciences, 2020-02, Vol.409, p.116579, Article 116579

2020

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Dentatorubropallidoluysian Atrophy with Prominent Autonomic Dysfunction

Internal Medicine, 2022, pp.9616-22

2022

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Neurodegenerative Disorder FTDP-17–Related Tau Intron 10 +16C→T Mutation Increases Tau Exon 10 Splicing and Causes Tauopathy in Transgenic Mice

The American journal of pathology, 2013-07, Vol.183 (1), p.211-225

2013

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Third nerve palsy due to local inflammation associated with vascular compression: A case series

Journal of the neurological sciences, 2016-08, Vol.367, p.365-367

2016

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Hereditary diffuse leukoencephalopathy with neuroaxonal spheroids (HDLS) in early-onset dementia

Rinsho shinkeigaku = Clinical neurology, 2012, Vol.52 (11), p.1390

2012

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CpG demethylation enhances alpha-synuclein expression and affects the pathogenesis of Parkinson's disease

The Src/c-Abl pathway is a potential therapeutic target in amyotrophic lateral sclerosis

Drug screening for ALS using patient-specific induced pluripotent stem cells

Dentatorubropallidoluysian Atrophy with Prominent Autonomic Dysfunction

Ventral Variant Posterior Cortical Atrophy with Occipito-temporal Accumulation of Tau Proteins/Astrocyte Gliosis

An Ocular Form of Myasthenia Gravis with a High Titer of Anti-MuSK Antibodies during a Long-term Follow-up

Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases

Mutation-induced loss of APP function causes GABAergic depletion in recessive familial Alzheimer's disease: analysis of Osaka mutation-knockin mice

Amyloid beta peptide-induced cerebral neuronal loss is mediated by caspase-3 in vivo

TDP-43 M337V Mutation in Familial Amyotrophic Lateral Sclerosis in Japan

Fluorescent Arc/Arg3.1 indicator mice: A versatile tool to study brain activity changes in vitro and in vivo

Frontal allographic agraphia in a patient with behavioral variant frontotemporal dementia

Sixth nerve palsy associated with obstruction in Dorello's canal, accompanied by nodular type muscular sarcoidosis

Isoforms changes of tau protein during development in various species

A unique mouse model for investigating the properties of amyotrophic lateral sclerosis-associated protein TDP-43, by in utero electroporation

Altered CpG methylation in sporadic Alzheimer's disease is associated with APP and MAPT dysregulation

Response to comment on "Drug screening for ALS using patient-specific induced pluripotent stem cells"

A mouse model of amyloid beta oligomers: their contribution to synaptic alteration, abnormal tau phosphorylation, glial activation, and neuronal loss in vivo

A new amyloid β variant favoring oligomerization in Alzheimer's-type dementia

E22Δ Mutation in Amyloid β-Protein Promotes β-Sheet Transformation, Radical Production, and Synaptotoxicity, But Not Neurotoxicity

Radiological findings in siblings with dysferlin mutation with diverse phenotype

Dentatorubropallidoluysian Atrophy with Prominent Autonomic Dysfunction

Neurodegenerative Disorder FTDP-17–Related Tau Intron 10 +16C→T Mutation Increases Tau Exon 10 Splicing and Causes Tauopathy in Transgenic Mice

Third nerve palsy due to local inflammation associated with vascular compression: A case series

Hereditary diffuse leukoencephalopathy with neuroaxonal spheroids (HDLS) in early-onset dementia

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