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Glycosaminoglycan and versican deposits in taxane‐induced sclerosis

British journal of dermatology (1951), 2015-10, Vol.173 (4), p.1054-1058

2015

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Granulocyte and monocyte apheresis can control juvenile generalized pustular psoriasis with mutation of IL36RN

British journal of dermatology (1951), 2017-12, Vol.177 (6), p.1732-1736

2017

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Multifaceted array‐based keloidal gene expression profiling reveals specific MDFI upregulation in keloid lesions

Clinical and experimental dermatology, 2021-10, Vol.46 (7), p.1255-1261

2021

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First‐genetic analysis of atypical phenotype of pseudoxanthoma elasticum with ocular manifestations in the absence of characteristic skin lesions

Journal of the European Academy of Dermatology and Venereology, 2018-04, Vol.32 (4), p.e147-e149

2018

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Corrigendum to "Familial primary localized cutaneous amyloidosis in a Japanese family" [J. Dermatol. Sci. 83 (2016) 162–164]

Journal of dermatological science, 2018-01, Vol.89 (1), p.100-100

2018

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Rhizomucor variabilis infection in human cutaneous mucormycosis

Clinical and experimental dermatology, 2011-04, Vol.36 (3), p.312-314

2011

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Pemphigoid without mucosal involvement showing autoantibodies against laminin-332 γ2 subunit

British journal of dermatology (1951), 2010-11, Vol.163 (5), p.1120-1122

2010

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Symmetrical pigmented sclerosis enclosed by pruritic erythema: a new variant of morphoea?

British journal of dermatology (1951), 2009-09, Vol.161 (3), p.703-706

2009

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Two cases of dyshidrosiform pemphigoid with different presentations

Clinical and experimental dermatology, 2009-07, Vol.34 (5), p.e151-e153

2009

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Periorbital milia-like calcinosis

Clinical and experimental dermatology, 2012-10, Vol.37 (7), p.787-788

2012

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Fibrous hamartoma of infancy in a patient with Williams syndrome

British journal of dermatology (1951), 2007-05, Vol.156 (5), p.1052-1055

2007

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Familial case of piebaldism with regression of white forelock

Clinical and experimental dermatology, 2008-07, Vol.33 (4), p.511-512

2008

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Scleredema with diffuse pigmentation

Journal of the European Academy of Dermatology and Venereology, 2010-01, Vol.24 (1), p.100-101

2010

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Occupation-related pigmented macules on the sole with parallel-ridge pattern on dermatoscopy

Clinical and experimental dermatology, 2009-07, Vol.34 (5), p.e31-e33

2009

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Sudden onset of calciphylaxis: painful violaceous livedo in a patient with peritoneal dialysis

Clinical and experimental dermatology, 2009-07, Vol.34 (5), p.622-624

2009

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Intralymphatic histiocytosis associated with rheumatoid arthritis

Clinical and experimental dermatology, 2008-07, Vol.33 (4), p.516-518

2008

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Severe muscle weakness to necessitate rehabilitation in a case of trichorhinophalangeal syndrome type II

Journal of the European Academy of Dermatology and Venereology, 2009-06, Vol.23 (6), p.710-712

2009

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Multiple dermatomal daughter lesions of postzoster granuloma

British journal of dermatology (1951), 2007-06, Vol.156 (6), p.1369-1370

2007

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Anetoderma accompanying microscopic panniculitis in a patient with antiphospholipid syndrome and systemic lupus erythematosus

Clinical and experimental dermatology, 2009-03, Vol.34 (2), p.259-261

2009

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Malignant melanoma derived from cerebriform intradermal naevus

Clinical and experimental dermatology, 2009-12, Vol.34 (8), p.e840-e842

2009

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Primary essential cutis verticis gyrata with hyaluronic acid deposition

British journal of dermatology (1951), 2007-10, Vol.157 (4), p.806-807

2007

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A case of complex regional pain syndrome : an underdiagnosed condition in dermatology

Acta dermato-venereologica, 2007, Vol.87 (5), p.440-441

2007

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Collagenoma in Down syndrome

British journal of dermatology (1951), 2003-03, Vol.148 (3), p.596-597

2003

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The expression of nectin-1α in normal human skin and various skin tumours

British journal of dermatology (1951), 2003-04, Vol.148 (4), p.755-762

2003

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Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-κB activation: common genetic etiology with Blau syndrome

Blood, 2005-02, Vol.105 (3), p.1195-1197

2005

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Glycosaminoglycan and versican deposits in taxane‐induced sclerosis

Granulocyte and monocyte apheresis can control juvenile generalized pustular psoriasis with mutation of IL36RN

Multifaceted array‐based keloidal gene expression profiling reveals specific MDFI upregulation in keloid lesions

First‐genetic analysis of atypical phenotype of pseudoxanthoma elasticum with ocular manifestations in the absence of characteristic skin lesions

Corrigendum to "Familial primary localized cutaneous amyloidosis in a Japanese family" [J. Dermatol. Sci. 83 (2016) 162–164]

Rhizomucor variabilis infection in human cutaneous mucormycosis

Pemphigoid without mucosal involvement showing autoantibodies against laminin-332 γ2 subunit

Symmetrical pigmented sclerosis enclosed by pruritic erythema: a new variant of morphoea?

Two cases of dyshidrosiform pemphigoid with different presentations

Periorbital milia-like calcinosis

Fibrous hamartoma of infancy in a patient with Williams syndrome

Familial case of piebaldism with regression of white forelock

Scleredema with diffuse pigmentation

Occupation-related pigmented macules on the sole with parallel-ridge pattern on dermatoscopy

Sudden onset of calciphylaxis: painful violaceous livedo in a patient with peritoneal dialysis

Intralymphatic histiocytosis associated with rheumatoid arthritis

Severe muscle weakness to necessitate rehabilitation in a case of trichorhinophalangeal syndrome type II

Multiple dermatomal daughter lesions of postzoster granuloma

Anetoderma accompanying microscopic panniculitis in a patient with antiphospholipid syndrome and systemic lupus erythematosus

Malignant melanoma derived from cerebriform intradermal naevus

Primary essential cutis verticis gyrata with hyaluronic acid deposition

A case of complex regional pain syndrome : an underdiagnosed condition in dermatology

Collagenoma in Down syndrome

The expression of nectin-1α in normal human skin and various skin tumours

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-κB activation: common genetic etiology with Blau syndrome

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