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Reappraisal of the anatomical spreading and propagation hypothesis about TDP‐43 aggregation in amyotrophic lateral sclerosis and frontotemporal lobar degeneration

Neuropathology, 2020-10, Vol.40 (5), p.426-435

Riku, Yuichi

2020

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Exosome secretion is a key pathway for clearance of pathological TDP-43

Brain (London, England : 1878), 2016-12, Vol.139 (Pt 12), p.3187-3201

2016

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Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration

Brain (London, England : 1878), 2022-08, Vol.145 (8), p.2769-2784

2022

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TDP-43 Proteinopathy and Tauopathy: Do They Have Pathomechanistic Links?

International journal of molecular sciences, 2022-12, Vol.23 (24), p.15755

2022

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Pathway from TDP-43-Related Pathology to Neuronal Dysfunction in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration

International journal of molecular sciences, 2021-04, Vol.22 (8), p.3843

2021

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A novel monoclonal antibody generated by immunization with granular tau oligomers binds to tau aggregates at 423-430 amino acid sequence

Scientific reports, 2024-07, Vol.14 (1), p.16391-13, Article 16391

2024

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The hot cross bun sign in corticobasal degeneration

Neuropathology, 2021-10, Vol.41 (5), p.376-380

2021

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Nuclear Expression of TDP-43 Is Linked with Morphology and Ubiquitylation of Cytoplasmic Aggregates in Amyotrophic Lateral Sclerosis

International journal of molecular sciences, 2023-07, Vol.24 (15), p.12176

2023

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Altered Tau Isoform Ratio Caused by Loss of FUS and SFPQ Function Leads to FTLD-like Phenotypes

Cell reports (Cambridge), 2017-01, Vol.18 (5), p.1118-1131

2017

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Macroscopic diagnostic clue for parkinsonism

Neuropathology, 2022-10, Vol.42 (5), p.394-419

2022

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Involvement of the Precuneus/Posterior Cingulate Cortex Is Significant for the Development of Alzheimer's Disease: A PET (THK5351, PiB) and Resting fMRI Study

Frontiers in aging neuroscience, 2018-10, Vol.10, p.304-304

2018

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Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosis

Neuropathology, 2021-12, Vol.41 (6), p.457-467

2021

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Identification of intracerebral hemorrhage in the early‐phase of MM1+2C‐type sporadic Creutzfeldt–Jakob disease: A case report

Neuropathology, 2020-08, Vol.40 (4), p.399-406

2020

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Pathological observations of a long spinal cord lesion in a patient with multiple sclerosis

Neuropathology, 2022-06, Vol.42 (3), p.212-217

2022

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Pathologic Involvement of Glutamatergic Striatal Inputs From the Cortices in TAR DNA-Binding Protein 43 kDa-Related Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

Journal of neuropathology and experimental neurology, 2017-09, Vol.76 (9), p.759-768

2017

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Marked Involvement of the Striatal Efferent System in TAR DNA-Binding Protein 43 kDa-Related Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

Journal of neuropathology and experimental neurology, 2016-08, Vol.75 (8), p.801-811

2016

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Neuropathological investigation of patients with prolonged anorexia nervosa

Psychiatry and clinical neurosciences, 2022-05, Vol.76 (5), p.187-194

2022

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Neurolymphomatosis in follicular lymphoma: an autopsy case report

Neuropathology, 2022-08, Vol.42 (4), p.295-301

2022

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NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment

Acta neuropathologica communications, 2023-05, Vol.11 (1), p.71-71, Article 71

2023

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Effects of a polymorphism in the GFAP promoter on the age of onset and ambulatory disability in late-onset Alexander disease

Journal of human genetics, 2013-09, Vol.58 (9), p.635-638

2013

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HMGCR antibody-associated myopathy as a paraneoplastic manifestation of esophageal carcinoma

Neurology, 2016-08, Vol.87 (8), p.841

2016

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Clinical and Imaging Features of Multiple System Atrophy: Challenges for an Early and Clinically Definitive Diagnosis

Journal of movement disorders, 2018-09, Vol.11 (3), p.107-120

2018

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Autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease with spongiform changes of the cerebral cortex

Neuropathology, 2019-12, Vol.39 (6), p.452-460

2019

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Semantic deficits in ALS related to right lingual/fusiform gyrus network involvement

EBioMedicine, 2019-09, Vol.47, p.506-517

2019

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Actin-binding protein filamin-A drives tau aggregation and contributes to progressive supranuclear palsy pathology

Science advances, 2022-05, Vol.8 (21), p.eabm5029-eabm5029

2022

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Reappraisal of the anatomical spreading and propagation hypothesis about TDP‐43 aggregation in amyotrophic lateral sclerosis and frontotemporal lobar degeneration

Exosome secretion is a key pathway for clearance of pathological TDP-43

Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration

TDP-43 Proteinopathy and Tauopathy: Do They Have Pathomechanistic Links?

Pathway from TDP-43-Related Pathology to Neuronal Dysfunction in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration

A novel monoclonal antibody generated by immunization with granular tau oligomers binds to tau aggregates at 423-430 amino acid sequence

The hot cross bun sign in corticobasal degeneration

Nuclear Expression of TDP-43 Is Linked with Morphology and Ubiquitylation of Cytoplasmic Aggregates in Amyotrophic Lateral Sclerosis

Altered Tau Isoform Ratio Caused by Loss of FUS and SFPQ Function Leads to FTLD-like Phenotypes

Macroscopic diagnostic clue for parkinsonism

Involvement of the Precuneus/Posterior Cingulate Cortex Is Significant for the Development of Alzheimer's Disease: A PET (THK5351, PiB) and Resting fMRI Study

Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosis

Identification of intracerebral hemorrhage in the early‐phase of MM1+2C‐type sporadic Creutzfeldt–Jakob disease: A case report

Pathological observations of a long spinal cord lesion in a patient with multiple sclerosis

Pathologic Involvement of Glutamatergic Striatal Inputs From the Cortices in TAR DNA-Binding Protein 43 kDa-Related Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

Marked Involvement of the Striatal Efferent System in TAR DNA-Binding Protein 43 kDa-Related Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

Neuropathological investigation of patients with prolonged anorexia nervosa

Neurolymphomatosis in follicular lymphoma: an autopsy case report

NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment

Effects of a polymorphism in the GFAP promoter on the age of onset and ambulatory disability in late-onset Alexander disease

HMGCR antibody-associated myopathy as a paraneoplastic manifestation of esophageal carcinoma

Clinical and Imaging Features of Multiple System Atrophy: Challenges for an Early and Clinically Definitive Diagnosis

Autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease with spongiform changes of the cerebral cortex

Semantic deficits in ALS related to right lingual/fusiform gyrus network involvement

Actin-binding protein filamin-A drives tau aggregation and contributes to progressive supranuclear palsy pathology

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