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Two cases of the intermediate phenotype of recessive dystrophic epidermolysis bullosa harboring the novel COL7A1 mutation c.3570G>A

Journal of dermatological science, 2022-06, Vol.106 (3), p.193-195

2022

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Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Testing Mutation Consequences in Dystrophic Epidermolysis Bullosa

International journal of molecular sciences, 2021-12, Vol.22 (24), p.13369

2021

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Eruptive melanocytic nevi associated with encorafenib and cetuximab combination therapy

Journal of dermatology, 2023-05, Vol.50 (5), p.e173-e174

2023

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Three cases of drug‐induced hypersensitivity syndrome associated with mRNA‐based coronavirus disease 2019 vaccines

Journal of dermatology, 2022-06, Vol.49 (6), p.652-655

2022

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Overview of epidermolysis bullosa

Journal of dermatology, 2010-03, Vol.37 (3), p.214-219

2010

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Clarithromycin for the treatment of pyoderma gangrenosum associated with myelodysplastic syndrome

Journal of dermatology, 2022-04, Vol.49 (4), p.e131-e132

2022

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Role of phlebotomy in the treatment of liver damage related to erythropoietic porphyria

Scientific reports, 2022-04, Vol.12 (1), p.6100-6100, Article 6100

2022

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Ultraviolet B irradiation leads to the development of experimental bullous pemphigoid targeting BPAG1e

Journal of dermatological science, 2022-11, Vol.108 (2), p.112-115

2022

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Novel mutation in the UROS gene causing congenital erythropoietic porphyria in an elderly Japanese female

Journal of dermatology, 2022-06, Vol.49 (6), p.e215-e216

2022

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Clinical practice guide for the treatment of perforating dermatosis

Journal of dermatology, 2020-12, Vol.47 (12), p.1374-1382

2020

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Widespread kerosene dermatitis associated with rhabdomyolysis

Journal of dermatology, 2021-08, Vol.48 (8), p.e386-e387

2021

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Characterizing the main and epistatic effects and interactions of germination-related quantitative trait loci of tomato using a backcross inbred line population and near-isogenic lines

Scientia horticulturae, 2020-02, Vol.261, p.109028, Article 109028

2020

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Pyoderma gangrenosum triggered by switching from adalimumab to secukinumab

Journal of dermatology, 2019-03, Vol.46 (3), p.e108-e109

2019

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Benign neonatal hemangiomatosis with early regression of skin lesions: A case report and review of the published work

Journal of dermatology, 2020-08, Vol.47 (8), p.911-916

2020

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Protein Adsorption of Ultrafine Metal Oxide and Its Influence on Cytotoxicity toward Cultured Cells

Chemical research in toxicology, 2009-03, Vol.22 (3), p.543-553

2009

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Author reply to “WNT10A variant and severe scoliosis?”

Journal of dermatology, 2022-11, Vol.49 (11), p.e424-e425

2022

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Japanese case of Papillon–Lefèvre syndrome with novel compound heterozygous mutations

Journal of dermatology, 2020-08, Vol.47 (8), p.e293-e295

2020

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Novel nonsense mutation in the SLC39A4 gene in a Japanese boy with mild acrodermatitis enteropathica

Journal of dermatology, 2021-12, Vol.48 (12), p.e602-e603

2021

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Partial spontaneous regression of pediatric large fibroblastic connective tissue nevus

Journal of dermatology, 2020-06, Vol.47 (6), p.e232-e234

2020

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A mild case of acute generalized exanthematous pustulosis caused by gemcitabine

Journal of dermatology, 2022-08, Vol.49 (8), p.e261-e263

2022

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Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene

Journal of dermatological science, 2020-11, Vol.100 (2), p.156-159

2020

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Paraneoplastic syndrome associated with chronic myelogenous leukemia mimicking adult‐onset Still's disease

Journal of dermatology, 2020-02, Vol.47 (2), p.e67-e69

2020

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Atypical eosinophilic annular erythema clinically resembling granuloma annulare

International journal of dermatology, 2021-10, Vol.60 (10), p.e416-e417

2021

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Two novel mutations in the ATP2C1 gene found in Japanese patients with Hailey–Hailey disease

Journal of dermatology, 2022-06, Vol.49 (6), p.656-660

2022

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Pedunculated aneurysmal fibrous histiocytoma with increased 18F‐fluorodeoxyglucose uptake on positron emission tomography/computed tomography

Journal of dermatology, 2020-03, Vol.47 (3), p.e100-e102

2020

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Two cases of the intermediate phenotype of recessive dystrophic epidermolysis bullosa harboring the novel COL7A1 mutation c.3570G>A

Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Testing Mutation Consequences in Dystrophic Epidermolysis Bullosa

Eruptive melanocytic nevi associated with encorafenib and cetuximab combination therapy

Three cases of drug‐induced hypersensitivity syndrome associated with mRNA‐based coronavirus disease 2019 vaccines

Overview of epidermolysis bullosa

Clarithromycin for the treatment of pyoderma gangrenosum associated with myelodysplastic syndrome

Role of phlebotomy in the treatment of liver damage related to erythropoietic porphyria

Ultraviolet B irradiation leads to the development of experimental bullous pemphigoid targeting BPAG1e

Novel mutation in the UROS gene causing congenital erythropoietic porphyria in an elderly Japanese female

Clinical practice guide for the treatment of perforating dermatosis

Widespread kerosene dermatitis associated with rhabdomyolysis

Characterizing the main and epistatic effects and interactions of germination-related quantitative trait loci of tomato using a backcross inbred line population and near-isogenic lines

Pyoderma gangrenosum triggered by switching from adalimumab to secukinumab

Benign neonatal hemangiomatosis with early regression of skin lesions: A case report and review of the published work

Protein Adsorption of Ultrafine Metal Oxide and Its Influence on Cytotoxicity toward Cultured Cells

Author reply to “WNT10A variant and severe scoliosis?”

Japanese case of Papillon–Lefèvre syndrome with novel compound heterozygous mutations

Novel nonsense mutation in the SLC39A4 gene in a Japanese boy with mild acrodermatitis enteropathica

Partial spontaneous regression of pediatric large fibroblastic connective tissue nevus

A mild case of acute generalized exanthematous pustulosis caused by gemcitabine

Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene

Paraneoplastic syndrome associated with chronic myelogenous leukemia mimicking adult‐onset Still's disease

Atypical eosinophilic annular erythema clinically resembling granuloma annulare

Two novel mutations in the ATP2C1 gene found in Japanese patients with Hailey–Hailey disease

Pedunculated aneurysmal fibrous histiocytoma with increased 18F‐fluorodeoxyglucose uptake on positron emission tomography/computed tomography

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