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Case Report: Extremely Early Detection of Preclinical Magnetic Resonance Imaging Abnormality in Creutzfeldt–Jakob Disease With the V180I Mutation

Frontiers in neurology, 2021-10, Vol.12

2021

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Characterization of IgG4 anti‐neurofascin 155 antibody‐positive polyneuropathy

Annals of clinical and translational neurology, 2015-10, Vol.2 (10), p.960-971

2015

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Relationship between motor learning and gambling propensity in Parkinson's disease

Journal of clinical and experimental neuropsychology, 2022-01, Vol.44 (1), p.50-61

2022

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Rapid and comprehensive diagnostic method for repeat expansion diseases using nanopore sequencing

Npj genomic medicine, 2022-10, Vol.7 (1), p.62-62, Article 62

2022

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Neural mechanisms of foreign accent syndrome: Lesion and network analysis

NeuroImage clinical, 2021-01, Vol.31, p.102760-102760, Article 102760

2021

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Adjustment of Subthalamic Deep Brain Stimulation Parameters Improves Wheeze and Dyspnea in Parkinson's Disease

Frontiers in neurology, 2019-12, Vol.10, p.1317

2019

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Reduced likelihood of the Poggendorff illusion in cerebellar strokes: a clinical and neuroimaging study

Brain communications, 2023-03, Vol.5 (2), p.fcad053-fcad053

2023

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The advances in the early and accurate diagnosis of Creutzfeldt-Jakob disease and other prion diseases: where are we today?

Expert review of neurotherapeutics, 2023-09, Vol.23 (9), p.1-817

2023

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Lung adenocarcinoma with Lambert-Eaton myasthenic syndrome indicated by voltage-gated calcium channel: a case report

Journal of medical case reports, 2012-09, Vol.6 (1), p.281-281, Article 281

2012

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Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment

Brain (London, England : 1878), 2021-05, Vol.144 (4), p.1103-1117

2021

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Intracerebroventricular delivery of dominant negative prion protein in a mouse model of iatrogenic Creutzfeldt-Jakob disease after dura graft transplantation

Neuroscience letters, 2006-07, Vol.402 (3), p.222-226

2006

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Erratum to: Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment

Brain (London, England : 1878), 2021-09, Vol.144 (8), p.e67-e67

2021

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Autopsy case of Creutzfeldt–Jakob disease with Met/Val heterozygosity at codon 129 and type 1 protease‐resistant prion protein presenting some florid‐type plaques and many Kuru plaques in the cerebellum

Neuropathology, 2006-08, Vol.26 (4), p.313-317

2006

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Qualitative Deficits in Verbal Fluency in Parkinson's Disease with Mild Cognitive Impairment: A Clinical and Neuroimaging Study

Journal of Parkinson's disease, 2021-01, Vol.11 (4), p.2005-2016

2021

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Prevention of prion disease transmission

Nihon rinshō, 2007-08, Vol.65 (8), p.1454

2007

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Plasmablasts as Migratory IgG-Producing Cells in the Pathogenesis of Neuromyelitis Optica: e83036

PloS one, 2013-12, Vol.8 (12)

2013

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Case Report: Autopsy case of Creutzfeldt-Jakob disease with Met-Val heterozygosity at codon 129 and type 1 protease-resistant prion protein presenting some florid-type plaques and many Kuru plaques in the cerebellum

Neuropathology, 2006-08, Vol.26 (4), p.313-317

2006

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Anti-MuSK antibody positive myasthenia gravis with HIV infection successfully treated with cyclosporin: a case report

Rinshō shinkeigaku, 2008, Vol.48 (9), p.666-669

2008

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Non-glycosylphosphatidylinositol (GPI)-anchored recombinant prion protein with dominant-negative mutation inhibits PrP^sup Sc^ replication in vitro

Amyloid, 2004-03, Vol.11 (1), p.14

2004

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Inherited Creutzfeldt-Jakob disease

Nihon rinshō, 2004-01, Vol.62 Suppl, p.261

2004

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Kuru

Nihon rinshō, 2004-01, Vol.62 Suppl, p.257

2004

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Three-repeat Tau 69 is a major tau isoform in laser-microdissected Pick bodies

Amyloid, 2006-03, Vol.13 (1), p.1-5

2006

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Non-glycosylphosphatidylinositol (GPI)-anchored recombinant prion protein with dominant-negative mutation inhibits PrPSc replication in vitro

Amyloid, 2004-03, Vol.11 (1), p.14-20

2004

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Repeat conformation heterogeneity in cerebellar ataxia, neuropathy, vestibular areflexia syndrome

Case Report: Extremely Early Detection of Preclinical Magnetic Resonance Imaging Abnormality in Creutzfeldt–Jakob Disease With the V180I Mutation

Characterization of IgG4 anti‐neurofascin 155 antibody‐positive polyneuropathy

Relationship between motor learning and gambling propensity in Parkinson's disease

Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42

Rapid and comprehensive diagnostic method for repeat expansion diseases using nanopore sequencing

Neural mechanisms of foreign accent syndrome: Lesion and network analysis

Adjustment of Subthalamic Deep Brain Stimulation Parameters Improves Wheeze and Dyspnea in Parkinson's Disease

Reduced likelihood of the Poggendorff illusion in cerebellar strokes: a clinical and neuroimaging study

The advances in the early and accurate diagnosis of Creutzfeldt-Jakob disease and other prion diseases: where are we today?

Lung adenocarcinoma with Lambert-Eaton myasthenic syndrome indicated by voltage-gated calcium channel: a case report

Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment

Intracerebroventricular delivery of dominant negative prion protein in a mouse model of iatrogenic Creutzfeldt-Jakob disease after dura graft transplantation

Erratum to: Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment

Autopsy case of Creutzfeldt–Jakob disease with Met/Val heterozygosity at codon 129 and type 1 protease‐resistant prion protein presenting some florid‐type plaques and many Kuru plaques in the cerebellum

Qualitative Deficits in Verbal Fluency in Parkinson's Disease with Mild Cognitive Impairment: A Clinical and Neuroimaging Study

Prevention of prion disease transmission

Plasmablasts as Migratory IgG-Producing Cells in the Pathogenesis of Neuromyelitis Optica: e83036

Case Report: Autopsy case of Creutzfeldt-Jakob disease with Met-Val heterozygosity at codon 129 and type 1 protease-resistant prion protein presenting some florid-type plaques and many Kuru plaques in the cerebellum

Anti-MuSK antibody positive myasthenia gravis with HIV infection successfully treated with cyclosporin: a case report

Non-glycosylphosphatidylinositol (GPI)-anchored recombinant prion protein with dominant-negative mutation inhibits PrP^sup Sc^ replication in vitro

Inherited Creutzfeldt-Jakob disease

Kuru

Three-repeat Tau 69 is a major tau isoform in laser-microdissected Pick bodies

Non-glycosylphosphatidylinositol (GPI)-anchored recombinant prion protein with dominant-negative mutation inhibits PrPSc replication in vitro

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