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Pericarditis due to Campylobacter coli infection: a case report

BMC infectious diseases, 2023-05, Vol.23 (1), p.316-316, Article 316

2023

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The Current State of Hospital Staff ’s Awareness and Practice in Advance Care Planning

Palliative Care Research, 2020, Vol.15(3), pp.251-258

2020

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The Current State of Hospital Staff ’s Awareness and Practice in Advance Care Planning

Palliative care research, 2020, Vol.15 (3), p.251-258

2020

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アドバンス・ケア・プランニングに関する病院職員の意識と実践の状況

Palliative Care Research, 2020, Vol.15(3), pp.251-258

2020

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Metabolism of Naphthalene in Bacterial Strains Isolated from Oil Well Soils

Journal of Japan Society on Water Environment, 2000, Vol.23(11), pp.731-736

2000

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原油湧出土から単離した菌株によるナフタレンの代謝

水環境学会誌, 2000, Vol.23(11), pp.731-736

2000

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Aggresome formation and liquid-liquid phase separation independently induce cytoplasmic aggregation of TAR DNA-binding protein 43

Cell death & disease, 2020-10, Vol.11 (10), p.909-909, Article 909

2020

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Clinicopathological characteristics of subtypes of chronic inflammatory demyelinating polyradiculoneuropathy

Journal of neurology, neurosurgery and psychiatry, 2019-09, Vol.90 (9), p.988

2019

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Schwann cell and endothelial cell damage in transthyretin familial amyloid polyneuropathy

Neurology, 2016-11, Vol.87 (21), p.2220

2016

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Widespread Cardiac and Vasomotor Autonomic Dysfunction in Non-Val30Met Hereditary Transthyretin Amyloidosis

Internal Medicine, 2018/12/01, Vol.57(23), pp.3365-3370

2018

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Paranodal dissection in chronic inflammatory demyelinating polyneuropathy with anti-neurofascin-155 and anti-contactin-1 antibodies

Journal of neurology, neurosurgery and psychiatry, 2017-06, Vol.88 (6), p.465

2017

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Demyelinating Neuropathy with Markedly Elevated Serum IgG4 Levels and Anti-Contactin 1 IgG4 Antibody

Internal Medicine, 2023/05/01, Vol.62(9), pp.1341-1344

2023

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The morphology of amyloid fibrils and their impact on tissue damage in hereditary transthyretin amyloidosis: An ultrastructural study

Journal of the neurological sciences, 2018-11, Vol.394, p.99-106

2018

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Cardiac and peripheral vasomotor autonomic functions in late-onset transthyretin Val30Met familial amyloid polyneuropathy

Journal of neurology, 2017-11, Vol.264 (11), p.2293-2302

2017

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Restoration of a Conduction Block after the Long-term Treatment of CIDP with Anti-neurofascin 155 Antibodies: Follow-up of a Case over 23 Years

Internal Medicine, 2018/07/15, Vol.57(14), pp.2061-2066

2018

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Alcoholic Myelopathy and Nutritional Deficiency

Internal Medicine, 2017/01/01, Vol.56(1), pp.105-108

2017

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Complement deposition and macrophage-induced demyelination in CIDP with anti-LM1 antibodies

Journal of the neurological sciences, 2020-01, Vol.408, p.116509, Article 116509

2020

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A Case of Demyelinating Neuropathy with Markedly Elevated Serum IgG4 Levels and Anti-Contactin 1 IgG4 Antibody

Internal Medicine, 2022, pp.9286-21

2022

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Estrogen Inhibits Transforming Growth Factor β Signaling by Promoting Smad2/3 Degradation

The Journal of biological chemistry, 2010-05, Vol.285 (19), p.14747-14755

2010

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Vasculitic neuropathy with anti‐phosphatidylserine/prothrombin complex antibody

Muscle & nerve, 2019-06, Vol.59 (6), p.E44-E46

2019

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Common clinicopathological features in late-onset hereditary transthyretin amyloidosis (Ala97Gly, Val94Gly and Val30Met)

Amyloid, 2019-03, Vol.26 (sup1), p.24-25

2019

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Cardiovascular autonomic functions in late-onset hereditary transthyretin amyloidosis with Val30Met mutation

Amyloid, 2019-03, Vol.26 (sup1), p.6-6

2019

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Cardiac and peripheral vasomotor autonomic functions in hereditary transthyretin amyloidosis with non-Val30Met mutation

Amyloid, 2019-03, Vol.26 (sup1), p.13-14

2019

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Evolution of amyloid fibrils in hereditary transthyretin amyloidosis: an ultrastructural study

Amyloid, 2019-03, Vol.26 (sup1), p.26-26

2019

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Systemic angiopathy and axonopathy in hereditary transthyretin amyloidosis with Ala97Gly (p. Ala117Gly) mutation: a post-mortem analysis

Amyloid, 2018-04, Vol.25 (2), p.141-142

2018

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Pericarditis due to Campylobacter coli infection: a case report

The Current State of Hospital Staff ’s Awareness and Practice in Advance Care Planning

The Current State of Hospital Staff ’s Awareness and Practice in Advance Care Planning

アドバンス・ケア・プランニングに関する病院職員の意識と実践の状況

Metabolism of Naphthalene in Bacterial Strains Isolated from Oil Well Soils

原油湧出土から単離した菌株によるナフタレンの代謝

Aggresome formation and liquid-liquid phase separation independently induce cytoplasmic aggregation of TAR DNA-binding protein 43

Clinicopathological characteristics of subtypes of chronic inflammatory demyelinating polyradiculoneuropathy

Schwann cell and endothelial cell damage in transthyretin familial amyloid polyneuropathy

Widespread Cardiac and Vasomotor Autonomic Dysfunction in Non-Val30Met Hereditary Transthyretin Amyloidosis

Paranodal dissection in chronic inflammatory demyelinating polyneuropathy with anti-neurofascin-155 and anti-contactin-1 antibodies

Demyelinating Neuropathy with Markedly Elevated Serum IgG4 Levels and Anti-Contactin 1 IgG4 Antibody

The morphology of amyloid fibrils and their impact on tissue damage in hereditary transthyretin amyloidosis: An ultrastructural study

Cardiac and peripheral vasomotor autonomic functions in late-onset transthyretin Val30Met familial amyloid polyneuropathy

Restoration of a Conduction Block after the Long-term Treatment of CIDP with Anti-neurofascin 155 Antibodies: Follow-up of a Case over 23 Years

Alcoholic Myelopathy and Nutritional Deficiency

Complement deposition and macrophage-induced demyelination in CIDP with anti-LM1 antibodies

A Case of Demyelinating Neuropathy with Markedly Elevated Serum IgG4 Levels and Anti-Contactin 1 IgG4 Antibody

Estrogen Inhibits Transforming Growth Factor β Signaling by Promoting Smad2/3 Degradation

Vasculitic neuropathy with anti‐phosphatidylserine/prothrombin complex antibody

Common clinicopathological features in late-onset hereditary transthyretin amyloidosis (Ala97Gly, Val94Gly and Val30Met)

Cardiovascular autonomic functions in late-onset hereditary transthyretin amyloidosis with Val30Met mutation

Cardiac and peripheral vasomotor autonomic functions in hereditary transthyretin amyloidosis with non-Val30Met mutation

Evolution of amyloid fibrils in hereditary transthyretin amyloidosis: an ultrastructural study

Systemic angiopathy and axonopathy in hereditary transthyretin amyloidosis with Ala97Gly (p. Ala117Gly) mutation: a post-mortem analysis

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