about
Contribution of the different modules in the utrophin carboxy-terminal region to the formation and regulation of the DAP complexOral pemphigoid autoantibodies preferentially target BP180 ectodomain.Prevalence of collagen VII-specific autoantibodies in patients with autoimmune and inflammatory diseasesPemphigus autoantibodies generated through somatic mutations target the desmoglein-3 cis-interface.Bullous pemphigoid: from the clinic to the bench.Urban legend series: mucous membrane pemphigoid.Oral lichenoid tissue reactions: diagnosis and classification.Immune response in pemphigus and beyond: progresses and emerging concepts.Meeting Report of the Pathogenesis of Pemphigus and Pemphigoid Meeting in Munich, September 2016.Sensitivity of different assays for the serological diagnosis of epidermolysis bullosa acquisita: analysis of a cohort of 24 Italian patients.Determining the Incidence of Pneumocystis Pneumonia in Patients With Autoimmune Blistering Diseases Not Receiving Routine Prophylaxis.The pathogenic activity of anti-desmoglein autoantibodies parallels disease severity in rituximab-treated patients with pemphigus vulgaris.Paraneoplastic pemphigus presenting as mild cutaneous features of pemphigus foliaceus and lichenoid stomatitis with antidesmoglein 1 antibodies.Monozygotic twins discordant for recessive dystrophic epidermolysis bullosa phenotype highlight the role of TGF-β signalling in modifying disease severity.Epidermolysis Bullosa Acquisita in an Adult Patient with Previously Unrecognized Mild Dystrophic EB and Biallelic COL7A1 Mutations.A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome.IgA tracheobronchial deposits underlie respiratory compromise in neonatal linear IgA bullous dermatosis.Prospective studies on the routine use of a novel multivariant enzyme-linked immunosorbent assay for the diagnosis of autoimmune bullous diseases.Serological diagnostics in the detection of IgG autoantibodies against human collagen VII in epidermolysis bullosa acquisita: a multicentre analysis.Detection And Characterization Of Igg, Ige And Iga Autoantibodies In Patients With Bullous Pemphigoid Associated With Dipeptidyl Peptidase-Iv Inhibitors.Increased prevalence of diabetes mellitus in bullous pemphigoid patients during the last decade.Autoantibody Profile of a Cohort of 78 Italian Patients with Mucous Membrane Pemphigoid: Correlation Between Reactivity Profile and Clinical Involvement.Lack of K140 immunoreactivity in junctional epidermolysis bullosa skin and keratinocytes associates with misfolded laminin epidermal growth factor-like motif 2 of the β3 short arm.A truncating mutation in the laminin-332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration.Childhood epidermolysis bullosa acquisita during squaric acid dibutyl ester immunotherapy for alopecia areata.The pathogenesis of pemphigus: Controversy vs complexity.Induction of senescence pathways in Kindler syndrome primary keratinocytes.Paraneoplastic Epidermolysis Bullosa Acquisita Associated with Thyroid Carcinoma.Humoral Epitope Spreading in Autoimmune Bullous Diseases.Sequential intramolecular epitope spreading of humoral responses to human BPAG2 in a transgenic modelDemonstration of Epitope-Spreading Phenomena in Bullous Pemphigoid: Results of a Prospective Multicenter StudyMulticenter prospective study of the humoral autoimmune response in bullous pemphigoidDevelopment of a novel ELISA system for detection of anti-BP180 IgG and characterization of autoantibody profile in bullous pemphigoid patientsThe intracellular and extracellular domains of BP180 antigen comprise novel epitopes targeted by pemphigoid gestationis autoantibodiesSensitivity of immunofluorescence studies vs enzyme-linked immunosorbent assay for diagnosis of bullous pemphigoidAnti-desmoplakin antibodies in erythema multiforme and Stevens-Johnson syndrome sera: pathogenic or epiphenomenon?Endemic pemphigus foliaceus: towards understanding autoimmune mechanisms of disease developmentParaneoplastic Autoimmune Multi-organ Syndrome: Association with Retroperitoneal Kaposi's SarcomaNew versatile monoclonal antibodies against type XVII collagen endodomain for diagnosis and subtyping COL17A1-associated junctional epidermolysis bullosaAre clinical phenotype and autoantibody profile always concordant in pemphigus? A study in a cohort of pemphigus patients
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Giovanni Di Zenzo
@ast
Giovanni Di Zenzo
@en
Giovanni Di Zenzo
@es
Giovanni Di Zenzo
@nl
Giovanni Di Zenzo
@sl
type
label
Giovanni Di Zenzo
@ast
Giovanni Di Zenzo
@en
Giovanni Di Zenzo
@es
Giovanni Di Zenzo
@nl
Giovanni Di Zenzo
@sl
prefLabel
Giovanni Di Zenzo
@ast
Giovanni Di Zenzo
@en
Giovanni Di Zenzo
@es
Giovanni Di Zenzo
@nl
Giovanni Di Zenzo
@sl
P106
P1153
15759309300
P21
P31
P496
0000-0001-6106-599X