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Laboratory diagnosis of pemphigus: direct immunofluorescence remains the gold standard

British journal of dermatology (1951), 2016-07, Vol.175 (1), p.185-186

2016

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Laboratory diagnosis of paraneoplastic pemphigus

British journal of dermatology (1951), 2013-11, Vol.169 (5), p.1016-1024

2013

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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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IgG-induced clustering of desmogleins 1 and 3 in skin of patients with pemphigus fits with the desmoglein nonassembly depletion hypothesis

British journal of dermatology (1951), 2011-09, Vol.165 (3), p.552-562

2011

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Microalbuminuria is common, also in a nondiabetic, nonhypertensive population, and an independent indicator of cardiovascular risk factors and cardiovascular morbidity

Journal of internal medicine, 2001-06, Vol.249 (6), p.519-526

2001

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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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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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Lethal acantholytic epidermolysis bullosa due to a novel homozygous deletion in DSP: expanding the phenotype and implications for desmoplakin function in skin and heart

British journal of dermatology (1951), 2010-06, Vol.162 (6), p.1388-1394

2010

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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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Eosinophilic dermatoses

Dermatologie (Heidelberg, Germany), 2022-12, Vol.73 (12), p.965-972

2022

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Keratolysis exfoliativa (dyshidrosis lamellosa sicca): a distinct peeling entity

British journal of dermatology (1951), 2012-11, Vol.167 (5), p.1076-1084

2012

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Complement in bullous pemphigoid: results from a large observational study

British journal of dermatology (1951), 2017-02, Vol.176 (2), p.517-519

2017

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Eligibility criteria for programmed death receptor 1 inhibitors vs. real‐world advice: a retrospective analysis of 69 patients with advanced cutaneous squamous cell carcinoma of the head and neck

British journal of dermatology (1951), 2022-02, Vol.186 (2), p.371-372

2022

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Infiltration analysis of eosinophils and basophils and co‐expression of CD69, CD63, IL‐31 and IgE in patients with bullous and non‐bullous pemphigoid

Journal of the European Academy of Dermatology and Venereology, 2024-03, Vol.38 (3), p.e278-e281

2024

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Cardiomyopathy in patients with epidermolysis bullosa simplex with mutations in KLHL24

British journal of dermatology (1951), 2018-11, Vol.179 (5), p.1181-1183

2018

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Orf-induced pemphigoid with antilaminin-332 antibodies

British journal of dermatology (1951), 2012-10, Vol.167 (4), p.956-958

2012

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Response to Letter to the editor of Borradori et al. How to diagnose bullous pemphigoid and its variants: the question is still open

Journal of the European Academy of Dermatology and Venereology, 2021-07, Vol.35 (7), p.e435-e436

2021

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Subepidermal type VII collagen speckles as an additional clue for diagnosing epidermolysis bullosa acquisita by salt‐split skin serum analysis

Journal of the European Academy of Dermatology and Venereology, 2022-05, Vol.36 (5), p.e384-e386

2022

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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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Foreign body reaction triggered by cytotoxic T lymphocyte‐associated protein 4 blockade 25 years after dermal filler injection

British journal of dermatology (1951), 2016-12, Vol.175 (6), p.1351-1353

2016

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Single glycine deletion in COL7A1 acting as glycine substitution in dystrophic epidermolysis bullosa

Journal of the European Academy of Dermatology and Venereology, 2021-09, Vol.35 (9), p.e597-e600

2021

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Response to ‘Serological diagnostics in the detection of IgG autoantibodies against human collagen VII in epidermolysis bullosa acquisita: a multicentre analysis’

British journal of dermatology (1951), 2018-02, Vol.178 (2), p.573-573

2018

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Patients suffering from dystrophic epidermolysis bullosa are prone to developing autoantibodies against skin proteins: A longitudinal confirmational study

Experimental dermatology, 2024-02, Vol.33 (2), p.e15035-n/a

2024

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Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing

Journal of the European Academy of Dermatology and Venereology, 2024-03

2024

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Laboratory diagnosis of pemphigus: direct immunofluorescence remains the gold standard

Laboratory diagnosis of paraneoplastic pemphigus

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

IgG-induced clustering of desmogleins 1 and 3 in skin of patients with pemphigus fits with the desmoglein nonassembly depletion hypothesis

Microalbuminuria is common, also in a nondiabetic, nonhypertensive population, and an independent indicator of cardiovascular risk factors and cardiovascular morbidity

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

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

Lethal acantholytic epidermolysis bullosa due to a novel homozygous deletion in DSP: expanding the phenotype and implications for desmoplakin function in skin and heart

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

Eosinophilic dermatoses

Keratolysis exfoliativa (dyshidrosis lamellosa sicca): a distinct peeling entity

Complement in bullous pemphigoid: results from a large observational study

Eligibility criteria for programmed death receptor 1 inhibitors vs. real‐world advice: a retrospective analysis of 69 patients with advanced cutaneous squamous cell carcinoma of the head and neck

Infiltration analysis of eosinophils and basophils and co‐expression of CD69, CD63, IL‐31 and IgE in patients with bullous and non‐bullous pemphigoid

Cardiomyopathy in patients with epidermolysis bullosa simplex with mutations in KLHL24

Orf-induced pemphigoid with antilaminin-332 antibodies

Response to Letter to the editor of Borradori et al. How to diagnose bullous pemphigoid and its variants: the question is still open

Subepidermal type VII collagen speckles as an additional clue for diagnosing epidermolysis bullosa acquisita by salt‐split skin serum analysis

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

Foreign body reaction triggered by cytotoxic T lymphocyte‐associated protein 4 blockade 25 years after dermal filler injection

Single glycine deletion in COL7A1 acting as glycine substitution in dystrophic epidermolysis bullosa

Response to ‘Serological diagnostics in the detection of IgG autoantibodies against human collagen VII in epidermolysis bullosa acquisita: a multicentre analysis’

Patients suffering from dystrophic epidermolysis bullosa are prone to developing autoantibodies against skin proteins: A longitudinal confirmational study

Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing

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