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Eosinophilic annular erythema is clinically characterized by central pigmentation reflecting basal melanosis: a clinicopathological study of 10 cases

Journal of the European Academy of Dermatology and Venereology, 2017-11, Vol.31 (11), p.1916-1923

2017

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Intravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study

Journal of the European Academy of Dermatology and Venereology, 2021-08, Vol.35 (8), p.e528-e531

2021

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Functional analysis of keratin filament network formation indicates clinical severity of epidermolysis bullosa simplex

Journal of the European Academy of Dermatology and Venereology, 2020-10, Vol.34 (10), p.e613-e616

2020

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Intracytoplasmic abnormality of corneocytes in circumscribed palmar or plantar hypokeratosis: ultrastructural observations

Journal of the European Academy of Dermatology and Venereology, 2020-11, Vol.34 (11), p.e709-e711

2020

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Amino acid charge and epidermolysis bullosa simplex severity: genotype‐phenotype correlations

Journal of the European Academy of Dermatology and Venereology, 2020-02, Vol.34 (2), p.e87-e90

2020

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Pregnancy‐triggered atypical extrapalmoplantar erythematous hyperkeratotic lesions in palmoplantar keratoderma with mitochondrial mutations

Journal of the European Academy of Dermatology and Venereology, 2021-04, Vol.35 (4), p.e269-e272

2021

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Genetic analysis of a novel splice-site mutation in TMC8 reveals the in vivo importance of the transmembrane channel-like domain of TMC8

British journal of dermatology (1951), 2016-10, Vol.175 (4), p.803-806

2016

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A severe case of X‐linked ichthyosis showing palmar hyperlinearity without FLG mutations

Journal of the European Academy of Dermatology and Venereology, 2017-02, Vol.31 (2), p.e119-e120

2017

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Mucocutaneous pyoderma gangrenosum due to trisomy 8 neutrophilic infiltrates in a patient with myelodysplastic syndrome

British journal of dermatology (1951), 2016-01, Vol.174 (1), p.239-241

2016

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Appearance of antidesmocollin 1 autoantibodies leading to a vegetative lesion in a patient with pemphigus vulgaris

British journal of dermatology (1951), 2018-01, Vol.178 (1), p.294-295

2018

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Circulating IgA and IgE autoantibodies in antilaminin-332 mucous membrane pemphigoid

British journal of dermatology (1951), 2010-03, Vol.162 (3), p.513-517

2010

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Skipped exon in COL7A1 determines the clinical phenotypes of dystrophic epidermolysis bullosa

British journal of dermatology (1951), 2015-04, Vol.172 (4), p.1141-1144

2015

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The first familial cases of epidermolysis bullosa simplex, generalized severe with p.Asn176Ser in KRT5 revealing the clinical chronology

Journal of the European Academy of Dermatology and Venereology, 2017-05, Vol.31 (5), p.e251-e253

2017

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Thymoma‐associated multi‐organ autoimmunity: two cases and a review of the literature

Journal of the European Academy of Dermatology and Venereology, 2017-07, Vol.31 (7), p.e324-e326

2017

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Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood

Journal of the European Academy of Dermatology and Venereology, 2013-09, Vol.27 (9), p.1182-1184

2013

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Dystrophic epidermolysis bullosa: a review

Clinical, cosmetic and investigational dermatology, 2015-01, Vol.8 (default), p.275-284

Shinkuma, Satoru

2015

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Extensive Erythema and Hyperkeratosis on the Extremities and Lumbar Area as an Unusual Mani-festation of Nagashima-type Palmoplantar Keratosis

Acta dermato-venereologica, 2016-08, Vol.96 (6), p.856-858

2016

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915 Acneiform eruptions caused by EGFR inhibitors may result from reduced expression of human β-defensin-3 induced by S. epidermidis

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S157-S157

2023

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054 Combination of thymus and activation-regulated chemokine and soluble OX40 as a diagnostic biomarker for DIHS/DRESS

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S189-S189

2022

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Mucous membrane pemphigoid with generalized blisters: IgA and IgG autoantibodies target both laminin‐332 and type XVII collagen

British journal of dermatology (1951), 2012-05, Vol.166 (5), p.1116-1120

2012

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858 Genotype-phenotype correlation of porokeratosis

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S147-S147

2023

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Possible modifier effects of keratin 17 gene mutation on keratitis-ichthyosis-deafness syndrome

British journal of dermatology (1951), 2012-04, Vol.166 (4), p.903-905

2012

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Advances in Engineering and Information Science Toward Smart City and Beyond

1st ed. 2023., 2023

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878 CRISPR/Cas9 targeting an intronic region retrieving protein expression in a compound heterozygous model mice via inducing revertant mosaicism pathways

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S150-S150

2023

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Childhood subepidermal blistering disease with autoantibodies to type VII collagen and laminin-332

British journal of dermatology (1951), 2011-02, Vol.164 (2), p.452-454

2011

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Eosinophilic annular erythema is clinically characterized by central pigmentation reflecting basal melanosis: a clinicopathological study of 10 cases

Intravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study

Functional analysis of keratin filament network formation indicates clinical severity of epidermolysis bullosa simplex

Intracytoplasmic abnormality of corneocytes in circumscribed palmar or plantar hypokeratosis: ultrastructural observations

Amino acid charge and epidermolysis bullosa simplex severity: genotype‐phenotype correlations

Pregnancy‐triggered atypical extrapalmoplantar erythematous hyperkeratotic lesions in palmoplantar keratoderma with mitochondrial mutations

Genetic analysis of a novel splice-site mutation in TMC8 reveals the in vivo importance of the transmembrane channel-like domain of TMC8

A severe case of X‐linked ichthyosis showing palmar hyperlinearity without FLG mutations

Mucocutaneous pyoderma gangrenosum due to trisomy 8 neutrophilic infiltrates in a patient with myelodysplastic syndrome

Appearance of antidesmocollin 1 autoantibodies leading to a vegetative lesion in a patient with pemphigus vulgaris

Circulating IgA and IgE autoantibodies in antilaminin-332 mucous membrane pemphigoid

Skipped exon in COL7A1 determines the clinical phenotypes of dystrophic epidermolysis bullosa

The first familial cases of epidermolysis bullosa simplex, generalized severe with p.Asn176Ser in KRT5 revealing the clinical chronology

Thymoma‐associated multi‐organ autoimmunity: two cases and a review of the literature

Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood

Dystrophic epidermolysis bullosa: a review

Extensive Erythema and Hyperkeratosis on the Extremities and Lumbar Area as an Unusual Mani-festation of Nagashima-type Palmoplantar Keratosis

915 Acneiform eruptions caused by EGFR inhibitors may result from reduced expression of human β-defensin-3 induced by S. epidermidis

054 Combination of thymus and activation-regulated chemokine and soluble OX40 as a diagnostic biomarker for DIHS/DRESS

Mucous membrane pemphigoid with generalized blisters: IgA and IgG autoantibodies target both laminin‐332 and type XVII collagen

858 Genotype-phenotype correlation of porokeratosis

Possible modifier effects of keratin 17 gene mutation on keratitis-ichthyosis-deafness syndrome

Advances in Engineering and Information Science Toward Smart City and Beyond

878 CRISPR/Cas9 targeting an intronic region retrieving protein expression in a compound heterozygous model mice via inducing revertant mosaicism pathways

Childhood subepidermal blistering disease with autoantibodies to type VII collagen and laminin-332

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