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Difference between the MRI Findings for Neuro-Behçet Disease and Neuro-Sweet Disease

Internal Medicine, 2022/09/01, Vol.61(17), pp.2701-2701

2022

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Association of autoantibodies to muscarinic acetylcholine receptors with gastrointestinal symptoms and disease severity in patients with postural orthostatic tachycardia syndrome

Immunologic research, 2022-04, Vol.70 (2), p.197-207

2022

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Iliopsoas Hematomas in a Patient with Progressive Encephalomyelitis with Rigidity and Myoclonus

Internal Medicine, 2021/08/01, Vol.60(15), pp.2475-2477

2021

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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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G protein-coupled receptors related to autoimmunity in postural orthostatic tachycardia syndrome

Immunological medicine, 2024-06, p.1-8

2024

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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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Two distinct degenerative types of nigrostriatal dopaminergic neuron in the early stage of parkinsonian disorders

Clinical parkinsonism & related disorders, 2024, Vol.10, p.100242-100242, Article 100242

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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Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes

Internal Medicine, 2017/01/01, Vol.56(1), pp.95-99

2017

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Neuromelanin-sensitive magnetic resonance imaging： a promising technique for depicting tissue characteristics containing neuromelanin

Neural regeneration research, 2014-04, Vol.9 (7), p.759-760

2014

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Difference between the MRI Findings for Neuro-Behçet Disease and Neuro-Sweet Disease

Internal Medicine, 2022, pp.9127-21

2022

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Rimmed Vacuoles in Myositis Associated with Antimitochondrial Antibody

Journal of Clinical Neurology, 2020, 16(3), , pp.510-512

2020

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Quantitative connection between polyglutamine aggregation kinetics and neurodegenerative process in patients with Huntington's disease

Molecular neurodegeneration, 2012-05, Vol.7 (1), p.20-20

2012

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Nucleation of protein aggregation kinetics as a basis for genotype-phenotype correlations in polyglutamine diseases

Molecular neurodegeneration, 2009-07, Vol.4 (1), p.29-29

2009

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Reversible encephalopathy with focal brain edema in patients with neuronal intranuclear inclusion disease

Neurology and clinical neuroscience, 2017-11, Vol.5 (6), p.198-200

2017

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Minocycline-associated rimmed vacuolar myopathy in a patient with rheumatoid arthritis

BMC neurology, 2012-11, Vol.12 (1), p.140-140, Article 140

2012

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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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Polyglutamine expansion mutation yields a pathological epitope linked to nucleation of protein aggregate: determinant of Huntington's disease onset

PloS one, 2007-07, Vol.2 (7), p.e635

2007

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Degeneration of nigrostriatal dopaminergic neurons in the early to intermediate stage of dementia with Lewy bodies and Parkinson's disease

Journal of the neurological sciences, 2023-06, Vol.449, p.120660-120660, Article 120660

2023

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Hypertrophic pachymeningitis and encephalitis in a patient with relapsing polychondritis

Neurology and clinical neuroscience, 2015-01, Vol.3 (1), p.42-43

2015

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Hashimoto Encephalopathy Presenting with Acute Psychosis and Inappropriate Secretion of Antidiuretic Hormone: A Rare Case Responding to Steroid Therapy

The American journal of case reports, 2023-12, Vol.24, p.e942297-e942297

2023

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Iliopsoas Hematomas in a Patient with Progressive Encephalomyelitis with Rigidity and Myoclonus

Internal Medicine, 2021, pp.6604-20

2021

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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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Early-onset dysphagia predicts short survival in multiple system atrophy

Journal of neurology, 2024-08

2024

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Isolated mitochondrial stroke‐like episodes in an elderly patient with the MT‐ND3 gene mutation

Neurology and clinical neuroscience, 2015-07, Vol.3 (4), p.153-156

2015

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Difference between the MRI Findings for Neuro-Behçet Disease and Neuro-Sweet Disease

Association of autoantibodies to muscarinic acetylcholine receptors with gastrointestinal symptoms and disease severity in patients with postural orthostatic tachycardia syndrome

Iliopsoas Hematomas in a Patient with Progressive Encephalomyelitis with Rigidity and Myoclonus

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

G protein-coupled receptors related to autoimmunity in postural orthostatic tachycardia syndrome

Myoclonic Epilepsy with Ragged-red Fibers with Intranuclear Inclusions

Two distinct degenerative types of nigrostriatal dopaminergic neuron in the early stage of parkinsonian disorders

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

Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes

Neuromelanin-sensitive magnetic resonance imaging： a promising technique for depicting tissue characteristics containing neuromelanin

Difference between the MRI Findings for Neuro-Behçet Disease and Neuro-Sweet Disease

Rimmed Vacuoles in Myositis Associated with Antimitochondrial Antibody

Quantitative connection between polyglutamine aggregation kinetics and neurodegenerative process in patients with Huntington's disease

Nucleation of protein aggregation kinetics as a basis for genotype-phenotype correlations in polyglutamine diseases

Reversible encephalopathy with focal brain edema in patients with neuronal intranuclear inclusion disease

Minocycline-associated rimmed vacuolar myopathy in a patient with rheumatoid arthritis

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

Polyglutamine expansion mutation yields a pathological epitope linked to nucleation of protein aggregate: determinant of Huntington's disease onset

Degeneration of nigrostriatal dopaminergic neurons in the early to intermediate stage of dementia with Lewy bodies and Parkinson's disease

Hypertrophic pachymeningitis and encephalitis in a patient with relapsing polychondritis

Hashimoto Encephalopathy Presenting with Acute Psychosis and Inappropriate Secretion of Antidiuretic Hormone: A Rare Case Responding to Steroid Therapy

Iliopsoas Hematomas in a Patient with Progressive Encephalomyelitis with Rigidity and Myoclonus

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

Early-onset dysphagia predicts short survival in multiple system atrophy

Isolated mitochondrial stroke‐like episodes in an elderly patient with the MT‐ND3 gene mutation

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