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Longitudinal expression of type I interferon responsive genes in systemic lupus erythematosus

Lupus, 2009-10, Vol.18 (11), p.980-989

2009

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Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

British journal of dermatology (1951), 2020-10, Vol.183 (4), p.614-627

2020

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Matrix metalloproteinase-7 activates heparin-binding epidermal growth factor-like growth factor in cutaneous squamous cell carcinoma

British journal of dermatology (1951), 2010-10, Vol.163 (4), p.726-735

2010

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Another twist of the allogenic haematopoietic cell transplantation story

British journal of dermatology (1951), 2021-08, Vol.185 (2), p.248-249

Bauer, J.W.

2021

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Expanding the use of allogeneic haematopoietic cell transplantation in dermatology

British journal of dermatology (1951), 2021-06, Vol.184 (6), p.1002-1003

Bauer, J.W.

2021

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Photodynamic therapy using topical methyl 5-aminolevulinate compared with cryotherapy for actinic keratosis: A prospective, randomized study

Journal of the American Academy of Dermatology, 2002-08, Vol.47 (2), p.258-262

2002

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Cytokeratin 8 interacts with clumping factor B: a new possible virulence factor target

Microbiology (Society for General Microbiology), 2010-12, Vol.156 (Pt 12), p.3710-3721

2010

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MicroRNAs: one for all, all for one

British journal of dermatology (1951), 2019-11, Vol.181 (5), p.890-891

2019

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Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab

British journal of dermatology (1951), 2007-08, Vol.157 (2), p.417-419

2007

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Successful allogeneic cord blood transplantation in a patient with Evans syndrome leads to correction of hereditary angioedema type I as secondary effect

Bone marrow transplantation (Basingstoke), 2012-09, Vol.47 (9), p.1259-1261

2012

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Transformation-specific matrix metalloproteinases (MMP)-7 and MMP-13 are expressed by tumour cells in epidermolysis bullosa-associated squamous cell carcinomas

British journal of dermatology (1951), 2008-04, Vol.158 (4), p.778-785

2008

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An ex vivo RNA trans‐splicing strategy to correct human generalized severe epidermolysis bullosa simplex

British journal of dermatology (1951), 2019-01, Vol.180 (1), p.141-148

2019

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Construction and validation of an RNA trans-splicing molecule suitable to repair a large number of COL7A1 mutations

Gene therapy, 2016-11, Vol.23 (11), p.775-784

2016

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Type XVII collagen gene mutations in junctional epidermolysis bullosa and prospects for gene therapy

Clinical and experimental dermatology, 2003-01, Vol.28 (1), p.53-60

2003

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Increased tumour cell PD‐L1 expression, macrophage and dendritic cell infiltration characterise the tumour microenvironment of ulcerated primary melanomas

Journal of the European Academy of Dermatology and Venereology, 2019-04, Vol.33 (4), p.667-675

2019

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Metformin shows anti‐neoplastic properties by inhibition of oxidative phosphorylation and glycolysis in epidermolysis bullosa‐associated aggressive cutaneous squamous cell carcinoma

Journal of the European Academy of Dermatology and Venereology, 2024-01, Vol.38 (1), p.112-123

2024

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Phenotypic alleviation in LAMB3‐mutated severe junctional epidermolysis bullosa

Journal of the European Academy of Dermatology and Venereology, 2022-08, Vol.36 (8), p.e631-e634

2022

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Aberrant heterodimerization of keratin 16 with keratin 6A in HaCaT keratinocytes results in diminished cellular migration

Mechanisms of ageing and development, 2010-05, Vol.131 (5), p.346-353

2010

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Epidermolysis bullosa naevi reveal a distinctive dermoscopic pattern

British journal of dermatology (1951), 2005-07, Vol.153 (1), p.97-102

2005

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Laryngo‐onycho‐cutaneous (‐like) syndrome due to mutated Plectin

Journal of the European Academy of Dermatology and Venereology, 2017-08, Vol.31 (8), p.e373-e374

2017

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CD4+ T cells, but not non-classical monocytes, are dispensable for the development of chronic lymphocytic leukemia in the TCL1-tg murine model

Leukemia, 2016-06, Vol.30 (6), p.1409-1413

2016

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Vismodegib for recurrent locally destructive basal cell carcinoma in a renal transplant patient

Journal of the European Academy of Dermatology and Venereology, 2018-01, Vol.32 (1), p.e7-e8

2018

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Increased levels of matrix metalloproteinase-9 and interleukin-8 in blister fluids of dystrophic and junctional epidermolysis bullosa patients

Journal of the European Academy of Dermatology and Venereology, 2015-02, Vol.29 (2), p.396-398

2015

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Development of spliceosome-mediated RNA trans-splicing (SMaRT™) for the correction of inherited skin diseases

Experimental dermatology, 2003-02, Vol.12 (1), p.37-46

2003

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Squamous cell carcinoma in junctional and dystrophic epidermolysis bullosa

Acta dermato-venereologica, 2001-06, Vol.81 (3), p.189-192

2001

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Longitudinal expression of type I interferon responsive genes in systemic lupus erythematosus

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

Matrix metalloproteinase-7 activates heparin-binding epidermal growth factor-like growth factor in cutaneous squamous cell carcinoma

Another twist of the allogenic haematopoietic cell transplantation story

Expanding the use of allogeneic haematopoietic cell transplantation in dermatology

Photodynamic therapy using topical methyl 5-aminolevulinate compared with cryotherapy for actinic keratosis: A prospective, randomized study

Cytokeratin 8 interacts with clumping factor B: a new possible virulence factor target

MicroRNAs: one for all, all for one

Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab

Successful allogeneic cord blood transplantation in a patient with Evans syndrome leads to correction of hereditary angioedema type I as secondary effect

Transformation-specific matrix metalloproteinases (MMP)-7 and MMP-13 are expressed by tumour cells in epidermolysis bullosa-associated squamous cell carcinomas

An ex vivo RNA trans‐splicing strategy to correct human generalized severe epidermolysis bullosa simplex

Construction and validation of an RNA trans-splicing molecule suitable to repair a large number of COL7A1 mutations

Type XVII collagen gene mutations in junctional epidermolysis bullosa and prospects for gene therapy

Increased tumour cell PD‐L1 expression, macrophage and dendritic cell infiltration characterise the tumour microenvironment of ulcerated primary melanomas

Metformin shows anti‐neoplastic properties by inhibition of oxidative phosphorylation and glycolysis in epidermolysis bullosa‐associated aggressive cutaneous squamous cell carcinoma

Phenotypic alleviation in LAMB3‐mutated severe junctional epidermolysis bullosa

Aberrant heterodimerization of keratin 16 with keratin 6A in HaCaT keratinocytes results in diminished cellular migration

Epidermolysis bullosa naevi reveal a distinctive dermoscopic pattern

Laryngo‐onycho‐cutaneous (‐like) syndrome due to mutated Plectin

CD4+ T cells, but not non-classical monocytes, are dispensable for the development of chronic lymphocytic leukemia in the TCL1-tg murine model

Vismodegib for recurrent locally destructive basal cell carcinoma in a renal transplant patient

Increased levels of matrix metalloproteinase-9 and interleukin-8 in blister fluids of dystrophic and junctional epidermolysis bullosa patients

Development of spliceosome-mediated RNA trans-splicing (SMaRT™) for the correction of inherited skin diseases

Squamous cell carcinoma in junctional and dystrophic epidermolysis bullosa

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