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Cerebral white matter tau-positive granular glial pathology as a characteristic pathological feature in long survivors of multiple system atrophy

Journal of the neurological sciences, 2020-09, Vol.416, p.117010-117010, Article 117010

2020

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Leucine-rich Glioma-inactivated 1 Encephalitis Followed by Isaacs Syndrome: Alternating Presence of Pathogenic Autoantibodies to Leucine-rich Glioma-inactivated 1 and Contactin-associated Protein-like 2

Internal Medicine, 2023/06/01, Vol.62(11), pp.1659-1663

2023

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Tufted astrocyte‐like glia in two autopsy cases of multiple system atrophy: Is it a concomitant neurodegenerative disorder with multiple system atrophy and progressive supranuclear palsy?

Neuropathology, 2022-02, Vol.42 (1), p.74-81

2022

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Case report: MRI-negative myelitis following COVID-19 with SEP abnormalities: a case series and literature review

Frontiers in neurology, 2023-10, Vol.14

2023

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Myoclonic Epilepsy with Ragged-red Fibers with Intranuclear Inclusions

Internal Medicine, 2022/02/15, Vol.61(4), pp.547-552

2022

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Effects of oral care on prolonged viral shedding in coronavirus disease 2019 (COVID‐19)

Special care in dentistry, 2020-09, Vol.40 (5), p.470-474

2020

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An Autopsy Case of Elderly Onset Brainstem Acute Disseminated Encephalomyelitis

Case reports in neurology, 2023-01, Vol.15 (1), p.31-40

2023

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Aging-induced degradation in tracking performance in three-dimensional movement

SICE Journal of Control, Measurement, and System Integration, 2024-12, Vol.17 (1), p.239-246

2024

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Immunoglobulin G4-related Disease Accompanied by Peripheral Neuropathy: A Report of Two Cases

Internal Medicine, 2021/06/15, Vol.60(12), pp.1941-1947

2021

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Differential immunophenotypes of neuronal cytoplasmic inclusions in the dentate gyrus of multiple system atrophy and their association with clinicopathological features

Journal of neuropathology and experimental neurology, 2023-04, Vol.82 (4), p.302-311

2023

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Dopa-responsive dystonia in spinocerebellar ataxia 6: A case report

Clinical neurology and neurosurgery, 2023-06, Vol.229, p.107721, Article 107721

2023

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Spinal Segmental Myoclonus during Postural Maintenance in a Patient with Cervical Spondylosis: A Case Report

Internal Medicine, 2011, Vol.50(17), pp.1839-1841

2011

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Association of dysphagia severity in multiple system atrophy with the specific binding ratio on dopamine transporter SPECT

Journal of the neurological sciences, 2024-08, Vol.463, p.123116, Article 123116

2024

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A Variant Form of Nasogastric Tube Syndrome

Internal Medicine, 2005, Vol.44(12), pp.1286-1290

2005

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Leucine-rich Glioma-inactivated 1 Encephalitis Followed by Isaacs Syndrome: Alternating Presence of Pathogenic Autoantibodies to Leucine-rich Glioma-inactivated 1 and Contactin-associated Protein-like 2

Internal Medicine, 2023, pp.9670-22

2023

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Chronic demyelinating neuropathy with anti-myelin-associated glycoprotein antibody without any detectable M-protein

Neurological sciences, 2017-12, Vol.38 (12), p.2165-2169

2017

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Central nervous system involvement in patients with critical illness polyneuropathy

Journal of the neurological sciences, 2019-01, Vol.396, p.216-218

2019

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Clinical characteristics of children and adults with anti-N-methyl-D-aspartate receptor encephalitis

Clinical neurology and neurosurgery, 2020-09, Vol.196, p.106015-106015, Article 106015

2020

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Headache as a manifestation of SAPHO syndrome with a lesion extending to the dura mater, parietal bone, and temporal muscle

Rinsho shinkeigaku = Clinical neurology, 2012, Vol.52 (2), p.106

2012

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Saccharopinuria accompanied by hyperammonemia and hypercitrullinemia presented with elderly-onset epilepsy, progressive cognitive decline, and gait ataxia

Intractable & Rare Diseases Research, 2021/05/31, Vol.10(2), pp.126-130

2021

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Prevalence and clinical characteristics of corticobasal syndrome with an initial symptom outside of the upper limb

Neurological sciences, 2017-05, Vol.38 (5), p.783-787

2017

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Treatment With Cyclosporine A for Statin-Naïve Anti-HMGCR Antibody-Associated Necrotizing Myopathy

Journal of clinical rheumatology, 2019-08, Vol.25 (5), p.e72

2019

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Early-onset dysphagia predicts short survival in multiple system atrophy

Journal of neurology, 2024-08

2024

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Immunoglobulin G4-related Disease Accompanied by Peripheral Neuropathy: A Report of Two Cases

Internal Medicine, 2021, pp.6461-20

2021

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Cerebral white matter tau-positive granular glial pathology as a characteristic pathological feature in long survivors of multiple system atrophy

Leucine-rich Glioma-inactivated 1 Encephalitis Followed by Isaacs Syndrome: Alternating Presence of Pathogenic Autoantibodies to Leucine-rich Glioma-inactivated 1 and Contactin-associated Protein-like 2

Tufted astrocyte‐like glia in two autopsy cases of multiple system atrophy: Is it a concomitant neurodegenerative disorder with multiple system atrophy and progressive supranuclear palsy?

Case report: MRI-negative myelitis following COVID-19 with SEP abnormalities: a case series and literature review

Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2

Myoclonic Epilepsy with Ragged-red Fibers with Intranuclear Inclusions

Effects of oral care on prolonged viral shedding in coronavirus disease 2019 (COVID‐19)

An Autopsy Case of Elderly Onset Brainstem Acute Disseminated Encephalomyelitis

Aging-induced degradation in tracking performance in three-dimensional movement

Immunoglobulin G4-related Disease Accompanied by Peripheral Neuropathy: A Report of Two Cases

Differential immunophenotypes of neuronal cytoplasmic inclusions in the dentate gyrus of multiple system atrophy and their association with clinicopathological features

Dopa-responsive dystonia in spinocerebellar ataxia 6: A case report

Spinal Segmental Myoclonus during Postural Maintenance in a Patient with Cervical Spondylosis: A Case Report

Association of dysphagia severity in multiple system atrophy with the specific binding ratio on dopamine transporter SPECT

A Variant Form of Nasogastric Tube Syndrome

Leucine-rich Glioma-inactivated 1 Encephalitis Followed by Isaacs Syndrome: Alternating Presence of Pathogenic Autoantibodies to Leucine-rich Glioma-inactivated 1 and Contactin-associated Protein-like 2

Chronic demyelinating neuropathy with anti-myelin-associated glycoprotein antibody without any detectable M-protein

Central nervous system involvement in patients with critical illness polyneuropathy

Clinical characteristics of children and adults with anti-N-methyl-D-aspartate receptor encephalitis

Headache as a manifestation of SAPHO syndrome with a lesion extending to the dura mater, parietal bone, and temporal muscle

Saccharopinuria accompanied by hyperammonemia and hypercitrullinemia presented with elderly-onset epilepsy, progressive cognitive decline, and gait ataxia

Prevalence and clinical characteristics of corticobasal syndrome with an initial symptom outside of the upper limb

Treatment With Cyclosporine A for Statin-Naïve Anti-HMGCR Antibody-Associated Necrotizing Myopathy

Early-onset dysphagia predicts short survival in multiple system atrophy

Immunoglobulin G4-related Disease Accompanied by Peripheral Neuropathy: A Report of Two Cases

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