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Cranial Nerve Involvement and Dysautonomia in Post-COVID-19 Guillain-Barré Syndrome

Internal Medicine, 2021/11/01, Vol.60(21), pp.3477-3480

2021

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Isolated Paravermal Hyperintensities in Neuronal Intranuclear Inclusion Disease

Neurology, 2022-05, Vol.98 (22), p.938-939

2022

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Inflammatory myopathies associated with anti-mitochondrial antibodies

Brain (London, England : 1878), 2012-06, Vol.135 (Pt 6), p.1767-1777

2012

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Response to: Calpainopathy Can Manifest Itself in Not Only Skeletal Muscle but Also the Brain and Myocardium

Internal Medicine, 2024, pp.3974-24

2024

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A Case of a Patient with Calpainopathy Carrying Compound Heterozygous Mutations of a de novo Pathogenic Variant of c.1333G>A and a Novel Variant of c.1331C>T in CAPN3

Internal Medicine, 2024, pp.3435-23

2024

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Increased 18F-THK5351 Uptake at Bilateral Primary Motor Cortex in Patients with Progressive Pseudobulbar Palsy

Acta neurologica Scandinavica, 2024-03, Vol.2024, p.1-6

2024

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Cancer association as a risk factor for anti-HMGCR antibody-positive myopathy

Neurology : neuroimmunology & neuroinflammation, 2016-12, Vol.3 (6), p.e290-e290

2016

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Alanine transaminase is predominantly increased in the active phase of anti-HMGCR myopathy

Neuromuscular disorders : NMD, 2022-01, Vol.32 (1), p.25-32

2022

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Severe finger necrosis in antisynthetase syndrome with positive anti‐OJ antibodies

Clinical case reports, 2024-06, Vol.12 (6), p.e8990-n/a

2024

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Anti-Ku antibody-positive myositis presenting as a wide range of axial myopathies and myocarditis: A case report and review of the literature

Modern rheumatology case reports, 2022-01, Vol.6 (1), p.64-68

2022

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Anti‐nuclear matrix protein 2 antibody‐positive dermatomyositis with gastrointestinal ulcers: A case report

International journal of rheumatic diseases, 2023-12, Vol.26 (12), p.2572-2575

2023

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Serum Cytokine Analysis in Idiopathic Inflammatory Myopathies Diagnosed on the Basis of Pathological Findings (P3.301)

Neurology, 2014-04, Vol.82 (10_supplement)

Maeda, Meiko

2014

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The effect of immunosuppressive therapy on cardiac involvements in anti‐mitochondrial antibody‐positive myositis

ESC Heart Failure, 2022-12, Vol.9 (6), p.4112-4119

2022

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Anti-mitochondrial antibody: Potential marker of myositis with chronic clinical course, muscle atrophy, cardiac involvement and granulomatous inflammation in muscle biopsy

Clinical & experimental neuroimmunology, 2013-06, Vol.4 (1), p.18-18

2013

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Prevalence and risk surveillance of anti-mitochondrial antibody-positive myositis: Outcomes of a nationwide survey

Journal of the neurological sciences, 2024-10, p.123287, Article 123287

2024

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Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth disease

Annals of neurology, 2012-01, Vol.71 (1), p.84-92

2012

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Vertebral artery dissection due to the C6 transverse process and laryngeal cartilage associated with vertebral artery anomaly

Rinsho shinkeigaku = Clinical neurology, 2014, Vol.54 (7), p.589

2014

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Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy

American journal of human genetics, 2020-06, Vol.106 (6), p.793-804

2020

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Idiopathic Inflammatory Myopathy and Anti-aminoacyl-tRNA Synthetase Antibody

Brain and nerve = Shinkei kenkyū no shinpo, 2018-04, Vol.70 (4), p.439

Maeda, Meiko Hashimoto

2018

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Clinicopathologic features of myositis patients with CD8-MHC-1 complex pathology

Neurology, 2017-09, Vol.89 (10), p.1060-1068

2017

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Clinicopathological Features of Anti-NT5c1A Positive Patients in the Group of Myositis Patients with CD8-MHC-1 Complex Pathology (P5.030)

Neurology, 2016-04, Vol.86 (16_supplement)

2016

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Sporadic late‐onset nemaline myopathy as a rare cause of slowly progressive muscle weakness with young adult onset

Muscle & nerve, 2015-05, Vol.51 (5), p.772-774

2015

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Clinicopathological features of patients with neuromuscular disease showing CD8-MHC-1 complex pathology (P5.065)

Neurology, 2015-04, Vol.84 (14_supplement)

2015

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Cranial Nerve Involvement and Dysautonomia in Post-COVID-19 Guillain-Barré Syndrome

Internal Medicine, 2021, pp.7355-21

2021

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Cranial Nerve Involvement and Dysautonomia in Post-COVID-19 Guillain-Barré Syndrome

Isolated Paravermal Hyperintensities in Neuronal Intranuclear Inclusion Disease

Inflammatory myopathies associated with anti-mitochondrial antibodies

Response to: Calpainopathy Can Manifest Itself in Not Only Skeletal Muscle but Also the Brain and Myocardium

A Case of a Patient with Calpainopathy Carrying Compound Heterozygous Mutations of a de novo Pathogenic Variant of c.1333G>A and a Novel Variant of c.1331C>T in CAPN3

Increased 18F-THK5351 Uptake at Bilateral Primary Motor Cortex in Patients with Progressive Pseudobulbar Palsy

Cancer association as a risk factor for anti-HMGCR antibody-positive myopathy

Alanine transaminase is predominantly increased in the active phase of anti-HMGCR myopathy

Severe finger necrosis in antisynthetase syndrome with positive anti‐OJ antibodies

Anti-Ku antibody-positive myositis presenting as a wide range of axial myopathies and myocarditis: A case report and review of the literature

Anti‐nuclear matrix protein 2 antibody‐positive dermatomyositis with gastrointestinal ulcers: A case report

Serum Cytokine Analysis in Idiopathic Inflammatory Myopathies Diagnosed on the Basis of Pathological Findings (P3.301)

The effect of immunosuppressive therapy on cardiac involvements in anti‐mitochondrial antibody‐positive myositis

Anti-mitochondrial antibody: Potential marker of myositis with chronic clinical course, muscle atrophy, cardiac involvement and granulomatous inflammation in muscle biopsy

Prevalence and risk surveillance of anti-mitochondrial antibody-positive myositis: Outcomes of a nationwide survey

Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth disease

Vertebral artery dissection due to the C6 transverse process and laryngeal cartilage associated with vertebral artery anomaly

Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy

Idiopathic Inflammatory Myopathy and Anti-aminoacyl-tRNA Synthetase Antibody

Clinicopathologic features of myositis patients with CD8-MHC-1 complex pathology

Anti-TIF1-γ antibody and cancer-associated myositis: A clinicohistopathologic study

Clinicopathological Features of Anti-NT5c1A Positive Patients in the Group of Myositis Patients with CD8-MHC-1 Complex Pathology (P5.030)

Sporadic late‐onset nemaline myopathy as a rare cause of slowly progressive muscle weakness with young adult onset

Clinicopathological features of patients with neuromuscular disease showing CD8-MHC-1 complex pathology (P5.065)

Cranial Nerve Involvement and Dysautonomia in Post-COVID-19 Guillain-Barré Syndrome

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