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Cutaneous Manifestations in Dermatomyositis: Key Clinical and Serological Features—a Comprehensive Review

Clinical Reviews in Allergy & Immunology, 2016-12, Vol.51 (3), p.293-302

2016

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The Majority of Generalized Pustular Psoriasis without Psoriasis Vulgaris Is Caused by Deficiency of Interleukin-36 Receptor Antagonist

Journal of investigative dermatology, 2013-11, Vol.133 (11), p.2514-2521

2013

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Long‐term risk of cancer development among anti‐Th/To antibody–positive systemic sclerosis patients: comment on the article by Mecoli et al

Arthritis & rheumatology (Hoboken, N.J.), 2022-02, Vol.74 (2), p.368-369

2022

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Deep Phenotyping of Superficial Epidermolytic Ichthyosis due to a Recurrent Mutation in KRT2

International journal of molecular sciences, 2022-07, Vol.23 (14), p.7791

2022

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Initial predictors of poor survival in myositis-associated interstitial lung disease: a multicentre cohort of 497 patients

Rheumatology (Oxford, England), 2018-07, Vol.57 (7), p.1212-1221

2018

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Comment on: Disease evolution in a long-term follow-up of 104 undifferentiated connective tissue disease patients

Clinical and experimental rheumatology, 2023-01, Vol.41 (1), p.195

2023

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Low prevalence of anti-small ubiquitin-like modifier activating enzyme antibodies in dermatomyositis patients

Autoimmunity (Chur, Switzerland), 2013-06, Vol.46 (4), p.279-284

2013

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Whole‐exome sequencing reveals a retinitis pigmentosa‐causative PRPH2 variant as a secondary finding in a patient with pseudoxanthoma elasticum

Journal of dermatology, 2023-02, Vol.50 (2), p.e85-e86

2023

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Case of ichthyosis with confetti caused by KRT10 mutation, complicated with multiple malignant melanomas

Journal of dermatology, 2022-07, Vol.49 (7), p.e228-e229

2022

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Ceramide Analysis in Combination With Genetic Testing May Provide a Precise Diagnosis for Self-Healing Collodion Babies

Journal of lipid research, 2022-12, Vol.63 (12), p.100308-100308, Article 100308

2022

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Immune recognition of lysyl-tRNA synthetase and isoleucyl-tRNA synthetase by anti-OJ antibody-positive sera

Journal of autoimmunity, 2021-08, Vol.122, p.102680, Article 102680

2021

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Extremely mild dominant dystrophic epidermolysis bullosa: Genotype information from whole‐exome sequencing of salivary gDNA predicts disease severity

Journal of dermatology, 2022-08, Vol.49 (8), p.e276-e277

2022

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Darier’s disease with epilepsy in an elderly patient after surgery for aortic dissection

Journal of dermatology, 2021-04, Vol.48 (4), p.e169-e170

2021

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Autoantibodies to Su/Argonaute 2 in Japanese patients with inflammatory myopathy

Clinica chimica acta, 2017-08, Vol.471, p.304-307

2017

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A heterozygous SERPINB7 mutation is a possible modifying factor for epidermolytic palmoplantar keratoderma

Journal of dermatological science, 2020-11, Vol.100 (2), p.148-151

2020

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Development of severe fingertip ulcers, pulmonary hypertension, and scleroderma renal crisis in a patient with systemic sclerosis and anti‐PL12 antibodies

Journal of cutaneous immunology and allergy, 2023-02, Vol.6 (1), p.32-34

2023

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UVB-Induced Skin Autoinflammation Due to Nlrp1b Mutation and Its Inhibition by Anti-IL-1β Antibody

Frontiers in immunology, 2022-06, Vol.13, p.876390-876390

2022

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Paradoxical Reaction in a Patient with Hidradenitis Suppurativa Undergoing Adalimumab Treatment

Acta dermato-venereologica, 2021-06, Vol.101 (6), p.adv00484-adv00484

2021

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Epidemiologic study of clinically amyopathic dermatomyositis and anti-melanoma differentiation-associated gene 5 antibodies in central Japan

Arthritis research & therapy, 2011-01, Vol.13 (6), p.R214-R214

2011

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Eosinophilic granulomatosis with polyangiitis complicated with idiopathic thrombocytopenic purpura and sclerosing cholangitis showing eosinophilic infiltration

Journal of dermatology, 2022-08, Vol.49 (8), p.e270-e271

2022

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Brief Report: Autoantibodies to DNA Mismatch Repair Enzymes in Polymyositis/Dermatomyositis and Other Autoimmune Diseases: A Possible Marker of Favorable Prognosis

Arthritis & Rheumatology, 2014-12, Vol.66 (12), p.3457-3462

2014

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Autoantibodies against the plakin family proteins as a novel marker for chronic graft-versus-host disease of the lung

Bone marrow transplantation (Basingstoke), 2021-09, Vol.56 (9), p.2291-2294

2021

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Autoinflammatory Keratinization Disease With Hepatitis and Autism Reveals Roles for JAK1 Kinase Hyperactivity in Autoinflammation

Frontiers in immunology, 2022-01, Vol.12, p.737747-737747

2022

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Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists

Journal of dermatology, 2019-01, Vol.46 (1), p.e1-e18

2019

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Cutaneous Manifestations in Dermatomyositis: Key Clinical and Serological Features—a Comprehensive Review

2019 Diagnostic criteria for mixed connective tissue disease (MCTD): From the Japan research committee of the ministry of health, labor, and welfare for systemic autoimmune diseases

The Majority of Generalized Pustular Psoriasis without Psoriasis Vulgaris Is Caused by Deficiency of Interleukin-36 Receptor Antagonist

Long‐term risk of cancer development among anti‐Th/To antibody–positive systemic sclerosis patients: comment on the article by Mecoli et al

Deep Phenotyping of Superficial Epidermolytic Ichthyosis due to a Recurrent Mutation in KRT2

Initial predictors of poor survival in myositis-associated interstitial lung disease: a multicentre cohort of 497 patients

Comment on: Disease evolution in a long-term follow-up of 104 undifferentiated connective tissue disease patients

Low prevalence of anti-small ubiquitin-like modifier activating enzyme antibodies in dermatomyositis patients

Whole‐exome sequencing reveals a retinitis pigmentosa‐causative PRPH2 variant as a secondary finding in a patient with pseudoxanthoma elasticum

Case of ichthyosis with confetti caused by KRT10 mutation, complicated with multiple malignant melanomas

Ceramide Analysis in Combination With Genetic Testing May Provide a Precise Diagnosis for Self-Healing Collodion Babies

Immune recognition of lysyl-tRNA synthetase and isoleucyl-tRNA synthetase by anti-OJ antibody-positive sera

Extremely mild dominant dystrophic epidermolysis bullosa: Genotype information from whole‐exome sequencing of salivary gDNA predicts disease severity

Darier’s disease with epilepsy in an elderly patient after surgery for aortic dissection

Autoantibodies to Su/Argonaute 2 in Japanese patients with inflammatory myopathy

A heterozygous SERPINB7 mutation is a possible modifying factor for epidermolytic palmoplantar keratoderma

Development of severe fingertip ulcers, pulmonary hypertension, and scleroderma renal crisis in a patient with systemic sclerosis and anti‐PL12 antibodies

UVB-Induced Skin Autoinflammation Due to Nlrp1b Mutation and Its Inhibition by Anti-IL-1β Antibody

Paradoxical Reaction in a Patient with Hidradenitis Suppurativa Undergoing Adalimumab Treatment

Epidemiologic study of clinically amyopathic dermatomyositis and anti-melanoma differentiation-associated gene 5 antibodies in central Japan

Eosinophilic granulomatosis with polyangiitis complicated with idiopathic thrombocytopenic purpura and sclerosing cholangitis showing eosinophilic infiltration

Brief Report: Autoantibodies to DNA Mismatch Repair Enzymes in Polymyositis/Dermatomyositis and Other Autoimmune Diseases: A Possible Marker of Favorable Prognosis

Autoantibodies against the plakin family proteins as a novel marker for chronic graft-versus-host disease of the lung

Autoinflammatory Keratinization Disease With Hepatitis and Autism Reveals Roles for JAK1 Kinase Hyperactivity in Autoinflammation

Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists

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