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

Brain (London, England : 1878), 2022-04, Vol.145 (3), p.1139-1150

2022

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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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Plasmablasts as migratory IgG-producing cells in the pathogenesis of neuromyelitis optica

PloS one, 2013-12, Vol.8 (12), p.e83036-e83036

2013

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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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GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy

Annals of neurology, 2019-12, Vol.86 (6), p.962-968

2019

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Transmission experiments verify sporadic V2 prion in a patient with E200K mutation

Acta neuropathologica, 2024-06, Vol.147 (1), p.89, Article 89

2024

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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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White matter hyperintensities on MRI in dementia with Lewy bodies, Parkinson's disease with dementia, and Alzheimer's disease

Journal of the neurological sciences, 2018-02, Vol.385, p.99-104

2018

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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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Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes

JAMA neurology, 2021-07, Vol.78 (7), p.853

2021

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CCR2(+)CCR5(+) T cells produce matrix metalloproteinase-9 and osteopontin in the pathogenesis of multiple sclerosis

The Journal of immunology (1950), 2012-11, Vol.189 (10), p.5057-5065

2012

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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

2021

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An Aerodynamic Study of Phonations in Patients With Parkinson Disease (PD)

Journal of voice, 2015-05, Vol.29 (3), p.273-280

2015

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

Characterization of IgG4 anti‐neurofascin 155 antibody‐positive polyneuropathy

Plasmablasts as migratory IgG-producing cells in the pathogenesis of neuromyelitis optica

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?

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy

Transmission experiments verify sporadic V2 prion in a patient with E200K mutation

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

White matter hyperintensities on MRI in dementia with Lewy bodies, Parkinson's disease with dementia, and Alzheimer's disease

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

Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes

CCR2(+)CCR5(+) T cells produce matrix metalloproteinase-9 and osteopontin in the pathogenesis of multiple sclerosis

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

An Aerodynamic Study of Phonations in Patients With Parkinson Disease (PD)

Prevention of prion disease transmission

Ataxic phenotype with altered Ca V 3.1 channel property in a mouse model for spinocerebellar ataxia 42

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

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