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International Bullous Diseases Group: consensus on diagnostic criteria for epidermolysis bullosa acquisita

British journal of dermatology (1951), 2018-07, Vol.179 (1), p.30-41

2018

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Keratinocyte footprint assay discriminates antilaminin‐332 pemphigoid from all other forms of pemphigoid diseases

British journal of dermatology (1951), 2020-02, Vol.182 (2), p.373-381

2020

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Gene expression profiling of skin and blood in hidradenitis suppurativa

British journal of dermatology (1951), 2016-06, Vol.174 (6), p.1392-1394

2016

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IgE autoantibodies in serum and skin of non‐bullous and bullous pemphigoid patients

Journal of the European Academy of Dermatology and Venereology, 2021-04, Vol.35 (4), p.973-980

2021

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The n- vs. u-serration is a learnable criterion to differentiate pemphigoid from epidermolysis bullosa acquisita in direct immunofluorescence serration pattern analysis

British journal of dermatology (1951), 2013-07, Vol.169 (1), p.100-105

2013

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The many faces of epidermolysis bullosa acquisita after serration pattern analysis by direct immunofluorescence microscopy

British journal of dermatology (1951), 2011-07, Vol.165 (1), p.92-98

2011

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Direct and indirect immunofluorescence staining patterns in the diagnosis of paraneoplastic pemphigus

British journal of dermatology (1951), 2016-04, Vol.174 (4), p.912-915

2016

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Low sensitivity of type VII collagen enzyme-linked immunosorbent assay in epidermolysis bullosa acquisita: serration pattern analysis on skin biopsy is required for diagnosis

British journal of dermatology (1951), 2013-07, Vol.169 (1), p.164-167

2013

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Amelioration of junctional epidermolysis bullosa due to exon skipping

British journal of dermatology (1951), 2016-06, Vol.174 (6), p.1375-1379

2016

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Immunofluorescence serration pattern analysis as a diagnostic criterion in antilaminin-332 mucous membrane pemphigoid: immunopathological findings and clinical experience in 10 Dutch patients

British journal of dermatology (1951), 2011-10, Vol.165 (4), p.815-822

2011

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Ultrastructure of acantholysis in pemphigus foliaceus re-examined from the current perspective

British journal of dermatology (1951), 2012-12, Vol.167 (6), p.1265-1271

2012

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U-serrated immunodeposition pattern differentiates type VII collagen targeting bullous diseases from other subepidermal bullous autoimmune diseases

British journal of dermatology (1951), 2004-07, Vol.151 (1), p.112-118

2004

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Junctional epidermolysis bullosa of late onset explained by mutations in COL17A1

British journal of dermatology (1951), 2011-06, Vol.164 (6), p.1280-1284

2011

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The ultrastructure of acantholysis in pemphigus vulgaris

British journal of dermatology (1951), 2009-02, Vol.160 (2), p.460-461

2009

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A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome

Journal of dermatological science, 2012-01, Vol.65 (1), p.74-76

2012

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Ustekinumab in hidradenitis suppurativa: clinical results and a search for potential biomarkers in serum

British journal of dermatology (1951), 2016-04, Vol.174 (4), p.839-846

2016

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Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology

British journal of dermatology (1951), 2015-04, Vol.172 (4), p.867-877

2015

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Localized and generalized forms of blistering in junctional epidermolysis bullosa due to COL17A1 mutations in the Netherlands

British journal of dermatology (1951), 2007-05, Vol.156 (5), p.861-870

2007

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Coexistence of IgA antibodies to desmogleins 1 and 3 in pemphigus vulgaris, pemphigus foliaceus and paraneoplastic pemphigus

British journal of dermatology (1951), 2007-04, Vol.156 (4), p.635-641

2007

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Antiplectin autoantibodies in subepidermal blistering diseases

British journal of dermatology (1951), 2009-10, Vol.161 (4), p.762-771

2009

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Pemphigus. S2 Guideline for diagnosis and treatment - guided by the European Dermatology Forum (EDF) in cooperation with the European Academy of Dermatology and Venereology (EADV)

Journal of the European Academy of Dermatology and Venereology, 2015-03, Vol.29 (3), p.405-414

2015

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一种可帮助诊断特定类型类天疱疮的新实验室检查

British journal of dermatology (1951), 2020-02, Vol.182 (2)

2020

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Novel insights into the epidemiology of epidermolysis bullosa (EB) from the Dutch EB Registry: EB more common than previously assumed?

Journal of the European Academy of Dermatology and Venereology, 2021-04, Vol.35 (4), p.995-1006

2021

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Image Gallery: Paraneoplastic pemphigus and follicular dendritic cell sarcoma

British journal of dermatology (1951), 2018-02, Vol.178 (2), p.e146-e146

2018

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075 Keratinocyte footprint assay discriminates anti-laminin-332 mucous membrane pemphigoid from all other forms of pemphigoid

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S13-S13

2018

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International Bullous Diseases Group: consensus on diagnostic criteria for epidermolysis bullosa acquisita

Keratinocyte footprint assay discriminates antilaminin‐332 pemphigoid from all other forms of pemphigoid diseases

Gene expression profiling of skin and blood in hidradenitis suppurativa

IgE autoantibodies in serum and skin of non‐bullous and bullous pemphigoid patients

The n- vs. u-serration is a learnable criterion to differentiate pemphigoid from epidermolysis bullosa acquisita in direct immunofluorescence serration pattern analysis

The many faces of epidermolysis bullosa acquisita after serration pattern analysis by direct immunofluorescence microscopy

Direct and indirect immunofluorescence staining patterns in the diagnosis of paraneoplastic pemphigus

Low sensitivity of type VII collagen enzyme-linked immunosorbent assay in epidermolysis bullosa acquisita: serration pattern analysis on skin biopsy is required for diagnosis

Amelioration of junctional epidermolysis bullosa due to exon skipping

Immunofluorescence serration pattern analysis as a diagnostic criterion in antilaminin-332 mucous membrane pemphigoid: immunopathological findings and clinical experience in 10 Dutch patients

Ultrastructure of acantholysis in pemphigus foliaceus re-examined from the current perspective

U-serrated immunodeposition pattern differentiates type VII collagen targeting bullous diseases from other subepidermal bullous autoimmune diseases

Junctional epidermolysis bullosa of late onset explained by mutations in COL17A1

The ultrastructure of acantholysis in pemphigus vulgaris

A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome

Ustekinumab in hidradenitis suppurativa: clinical results and a search for potential biomarkers in serum

Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology

Localized and generalized forms of blistering in junctional epidermolysis bullosa due to COL17A1 mutations in the Netherlands

Coexistence of IgA antibodies to desmogleins 1 and 3 in pemphigus vulgaris, pemphigus foliaceus and paraneoplastic pemphigus

Antiplectin autoantibodies in subepidermal blistering diseases

Pemphigus. S2 Guideline for diagnosis and treatment - guided by the European Dermatology Forum (EDF) in cooperation with the European Academy of Dermatology and Venereology (EADV)

一种可帮助诊断特定类型类天疱疮的新实验室检查

Novel insights into the epidemiology of epidermolysis bullosa (EB) from the Dutch EB Registry: EB more common than previously assumed?

Image Gallery: Paraneoplastic pemphigus and follicular dendritic cell sarcoma

075 Keratinocyte footprint assay discriminates anti-laminin-332 mucous membrane pemphigoid from all other forms of pemphigoid

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