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Successful treatment of multicentric Castleman's disease associated with dystrophic epidermolysis bullosa using anti‐interleukin‐6 receptor antibody

Journal of dermatology, 2024-08, Vol.51 (8), p.e268-e269

2024

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Bone marrow transplant with post‐transplant cyclophosphamide for recessive dystrophic epidermolysis bullosa expands the related donor pool and permits tolerance of nonhaematopoietic cellular grafts

British journal of dermatology (1951), 2019-12, Vol.181 (6), p.1238-1246

2019

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Immunological mechanisms underlying progression of chronic wounds in recessive dystrophic epidermolysis bullosa

Experimental dermatology, 2021-12, Vol.30 (12), p.1724-1733

2021

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Pembrolizumab for Treatment of a Patient With Multiple Cutaneous Squamous Cell Carcinomas and Recessive Dystrophic Epidermolysis Bullosa

JAMA dermatology (Chicago, Ill.), 2020-06, Vol.156 (6), p.708

2020

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High Local Concentrations of Intradermal MSCs Restore Skin Integrity and Facilitate Wound Healing in Dystrophic Epidermolysis Bullosa

Molecular therapy, 2015-08, Vol.23 (8), p.1368-1379

2015

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High concordance between clinical diagnosis of epidermolysis bullosa and immunofluorescence with a small, well‐matched antibody panel

Australasian journal of dermatology, 2018-02, Vol.59 (1), p.73-76

2018

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De Novo Anti-Type VII Collagen Antibodies in Patients with Recessive Dystrophic Epidermolysis Bullosa

Journal of investigative dermatology, 2014-04, Vol.134 (4), p.1138-1140

2014

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Pseudosyndactyly - an inflammatory and fibrotic wound healing disorder in recessive dystrophic epidermolysis bullosa

Journal der Deutschen Dermatologischen Gesellschaft, 2015-12, Vol.13 (12), p.1257-1266

2015

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Immune reactivity to type VII collagen: implications for gene therapy of recessive dystrophic epidermolysis bullosa

Gene therapy, 2010-07, Vol.17 (7), p.930-937

2010

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Immunofluorescence Mapping for Diagnosis of Congenital Epidermolysis Bullosa

Actas dermo-sifiliográficas (English ed.), 2010-10, Vol.101 (8), p.673-682

2010

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Common IL-31 Gene Haplotype Associated with Non-atopic Eczema is Not Implicated in Epidermolysis Bullosa Pruriginosa

Acta dermato-venereologica, 2010-01, Vol.90 (6), p.631-632

2010

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High frequency of the 425A→G splice-site mutation and novel mutations of the COL7A1 gene in central Europe: significance for future mutation detection strategies in dystrophic epidermolysis bullosa

British journal of dermatology (1951), 2005-05, Vol.152 (5), p.879-886

2005

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Autoimmunity to Type VII Collagen: Epidermolysis Bullosa Acquisita

Current directions in autoimmunity, 2008, Vol.10, p.195-205

2008

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Dystrophic epidermolysis bullosa pruriginosa with autoantibodies against collagen VII

EJD. European journal of dermatology, 2012-07, Vol.22 (4), p.541-542

2012

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Immunofluorescence studies using skin sections of recessive dystrophic epidermolysis bullosa patients indicated that the antigen of anti-p200 pemphigoid is not a fragment of type VII collagen

Journal of dermatological science, 2003-08, Vol.32 (2), p.125-129

2003

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Reduced anchoring fibril formation and collagen VII immunoreactivity in feline dystrophic epidermolysis bullosa

Veterinary pathology, 1999-11, Vol.36 (6), p.616-618

1999

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Atopic dermatitis: therapeutic challenge in an infant with dystrophic epidermolysis bullosa

British journal of dermatology (1951), 2002-08, Vol.147 (2), p.350-352

2002

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Diminished expression of the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) in the epidermal basement membrane of patients with generalized atrophic benign epidermolysis bullosa

Experimental dermatology, 1995-08, Vol.4 (4), p.199-206

1995

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Altered expression of a new antigen of the dermal-epidermal junction (NU-T2 DEJ Ag) in junctional epidermolysis bullosa

Archives of Dermatological Research, 1995, Vol.287 (8), p.699-704

1995

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Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiency

Archives of dermatology (1960), 1996-02, Vol.132 (2), p.145

1996

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Impaired secretory immunity in dystrophic epidermolysis bullosa

Oral microbiology and immunology, 1999-10, Vol.14 (5), p.316-320

1999

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Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosa

Archives of dermatology (1960), 1990-12, Vol.126 (12), p.1587

1990

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HLA and epidermolysis bullosa. Association between the HLA complex and recessive dystrophic epidermolysis bullosa

Archives of dermatology (1960), 1991-10, Vol.127 (10), p.1524

1991

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Peripheral blood mononuclear cell subsets in patients with severe inherited forms of epidermolysis bullosa

Archives of dermatology (1960), 1992-02, Vol.128 (2), p.201

1992

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The clinical efficacy and safety of anti‐IgE therapy in recessive dystrophic epidermolysis bullosa

Clinical genetics, 2022-01, Vol.101 (1), p.110-115

2022

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Successful treatment of multicentric Castleman's disease associated with dystrophic epidermolysis bullosa using anti‐interleukin‐6 receptor antibody

Bone marrow transplant with post‐transplant cyclophosphamide for recessive dystrophic epidermolysis bullosa expands the related donor pool and permits tolerance of nonhaematopoietic cellular grafts

Immunological mechanisms underlying progression of chronic wounds in recessive dystrophic epidermolysis bullosa

Pembrolizumab for Treatment of a Patient With Multiple Cutaneous Squamous Cell Carcinomas and Recessive Dystrophic Epidermolysis Bullosa

High Local Concentrations of Intradermal MSCs Restore Skin Integrity and Facilitate Wound Healing in Dystrophic Epidermolysis Bullosa

High concordance between clinical diagnosis of epidermolysis bullosa and immunofluorescence with a small, well‐matched antibody panel

De Novo Anti-Type VII Collagen Antibodies in Patients with Recessive Dystrophic Epidermolysis Bullosa

Pseudosyndactyly - an inflammatory and fibrotic wound healing disorder in recessive dystrophic epidermolysis bullosa

Immune reactivity to type VII collagen: implications for gene therapy of recessive dystrophic epidermolysis bullosa

Immunofluorescence Mapping for Diagnosis of Congenital Epidermolysis Bullosa

Common IL-31 Gene Haplotype Associated with Non-atopic Eczema is Not Implicated in Epidermolysis Bullosa Pruriginosa

High frequency of the 425A→G splice-site mutation and novel mutations of the COL7A1 gene in central Europe: significance for future mutation detection strategies in dystrophic epidermolysis bullosa

Autoimmunity to Type VII Collagen: Epidermolysis Bullosa Acquisita

Dystrophic epidermolysis bullosa pruriginosa with autoantibodies against collagen VII

Immunofluorescence studies using skin sections of recessive dystrophic epidermolysis bullosa patients indicated that the antigen of anti-p200 pemphigoid is not a fragment of type VII collagen

Reduced anchoring fibril formation and collagen VII immunoreactivity in feline dystrophic epidermolysis bullosa

Atopic dermatitis: therapeutic challenge in an infant with dystrophic epidermolysis bullosa

Diminished expression of the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) in the epidermal basement membrane of patients with generalized atrophic benign epidermolysis bullosa

Altered expression of a new antigen of the dermal-epidermal junction (NU-T2 DEJ Ag) in junctional epidermolysis bullosa

Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiency

Impaired secretory immunity in dystrophic epidermolysis bullosa

Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosa

HLA and epidermolysis bullosa. Association between the HLA complex and recessive dystrophic epidermolysis bullosa

Peripheral blood mononuclear cell subsets in patients with severe inherited forms of epidermolysis bullosa

The clinical efficacy and safety of anti‐IgE therapy in recessive dystrophic epidermolysis bullosa

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