B. Didona

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Connexin 26 (GJB2) mutations, causing KID Syndrome, are associated with cell death due to calcium gating deregulation.

G. Melino, A. Terrinoni, R. Nisticò, 2010, Biochemical and biophysical research communications.

Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss.

G. Melino, A. Terrinoni, M. Paradisi, 2010, Biochemical and biophysical research communications.

A homozygous nonsense mutation in type XVII collagen gene (COL17A1) uncovers an alternatively spliced mRNA accounting for an unusually mild form of non-Herlitz junctional epidermolysis bullosa.

G. Zambruno, P. Posteraro, D. Castiglia, 2001, The Journal of investigative dermatology.

Vitiligo: Pathogenesis, clinical variants and treatment approaches.

D. Didona, A. Greco, G. Iannella, 2016, Autoimmunity reviews.

Association of segmental neurofibromatosis 1 and oculo-auriculo-vertebral spectrum in a 24-year-old female.

M. Castori, P. Grammatico, G. Zambruno, 2008, EJD. European journal of dermatology.

Oral liarozole in the treatment of patients with moderate/severe lamellar ichthyosis: results of a randomized, double-blind, multinational, placebo-controlled phase II/III trial

A. Vahlquist, H. Traupe, B. Didona, 2014, The British journal of dermatology.

Reduced frequency of non-melanoma skin cancer in 72,739 patients with psoriasis: a retrospective study

D. Abeni, A. Paradisi, B. Didona, 2017, European Journal of Dermatology.

Reduced frequency of melanoma in 72,739 patients with psoriasis: A retrospective study

D. Abeni, A. Paradisi, B. Didona, 2015, European Journal of Dermatology.

Cornification Diseases (Skin Cell Death)

G. Melino, E. Candi, A. Terrinoni, 2009 .

Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis

G. Melino, E. Candi, M. Annicchiarico-Petruzzelli, 2012, Cell Death and Disease.

UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients

R. Corona, I. Vořechovský, E. Dogliotti, 2000, Oncogene.

Multiple skin tumors in long‐term treatment with hydroxyurea

G. Papa, R. Stasi, B. Didona, 1992, European journal of haematology.

Multiple skin tumors on light-exposed areas during long-term treatment with hydroxyurea.

G. Papa, R. Stasi, B. Didona, 1993, Journal of the American Academy of Dermatology.

Cutaneous mosaicism, in KRT1 pI479T patient, caused by the somatic loss of the wild‐type allele, leads to the increase in local severity of the disease

G. Melino, M. Annicchiarico-Petruzzelli, A. Terrinoni, 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development

E. Dellambra, S. Bondanza, G. Camerino, 2022, Orphanet Journal of Rare Diseases.

Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita.

G. Melino, A. Verloes, D. Hohl, 2001, The Journal of investigative dermatology.

Keratin 13 point mutation underlies the hereditary mucosal epithelia disorder white sponge nevus

S. Bale, V. Laurenzi, J. Compton, 1995, Nature Genetics.

Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene

G. Melino, A. Terrinoni, A. Irvine, 2004, The British journal of dermatology.

Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.

J. McGrath, I. Leigh, R. Eady, 2004, The Journal of investigative dermatology.

Pemphigus Vulgaris: Present and Future Therapeutic Strategies

R. Pampena, G. Paolino, D. Didona, 2022, Dermatology practical & conceptual.

Eosin treatment for psoriasis reduces skin leukocyte infiltration and secretion of inflammatory chemokines and angiogenic factors

F. Facchiano, S. Madonna, A. Cavani, 2018, European Journal of Dermatology.

Paraneoplastic Dermatoses: A Brief General Review and an Extensive Analysis of Paraneoplastic Pemphigus and Paraneoplastic Dermatomyositis

R. Eming, M. Hertl, D. Didona, 2020, International journal of molecular sciences.

Case report: bullous pemphigoid development underlies dystrophic epidermolysis bullosa disease worsening

D. Castiglia, F. Mariotti, B. Didona, 2022, Frontiers in Immunology.

Interferon-γ promotes exaggerated cytokine production in keratinocytes cultured from patients with atopic dermatitis☆☆☆★★★

G. Girolomoni, S. Pastore, B. Didona, 1998 .

Chronic hepatitis C virus infection, mixed cryoglobulinaemia, leukocytoclastic vasculitis and antineutrophil cytoplasmic antibodies

O. De Pità, B. Didona, L. Chinni, 1997, Lupus.

Pemphigus autoantibodies generated through somatic mutations target the desmoglein-3 cis-interface.

F. Sallusto, A. Lanzavecchia, R. Eming, 2012, The Journal of clinical investigation.

Cutaneous Rosai‐Dorfman disease after Covid 19 vaccination treated with thalidomide

F. Perino, D. Abeni, A. Paradisi, 2022, Dermatologic therapy.

Etanercept therapy for toxic epidermal necrolysis.

D. Didona, D. Abeni, A. Paradisi, 2014, Journal of the American Academy of Dermatology.

Persistent subcutaneous Scedosporium apiospermum infection.

G. Fadda, B. Posteraro, P. Posteraro, 2003, EJD. European journal of dermatology.

Koebner Phenomenon in an ANCA‐Positive Patient with Pyoderma Gangrenosum

O. De Pità, B. Didona, L. Chinni, 1997, The Journal of dermatology.

Treatment of severe pemphigus with rituximab: report of 12 cases and a review of the literature.

R. Corona, P. Puddu, G. Cianchini, 2007, Archives of dermatology.

Pemphigus foliaceus treated with etanercept.

G. Annessi, F. Atzori, E. Gubinelli, 2006, Journal of the American Academy of Dermatology.

Paraneoplastic Pemphigus: Insight into the Autoimmune Pathogenesis, Clinical Features and Therapy

S. Calvieri, G. Paolino, M. Donati, 2017, International journal of molecular sciences.

Quality of life in patients with pemphigus receiving adjuvant therapy

C. Di Pietro, F. Sampogna, D. Abeni, 2012, Clinical and experimental dermatology.

Sensitivity of different assays for the serological diagnosis of epidermolysis bullosa acquisita: analysis of a cohort of 24 Italian patients

G. Zambruno, A. Parodi, A. Sinistro, 2014, Journal of the European Academy of Dermatology and Venereology : JEADV.

A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus.

G. Melino, E. Candi, V. de Laurenzi, 2000, The Journal of investigative dermatology.

Paraneoplastic pemphigus: A trait d’union between dermatology and oncology

A. Richetta, S. Calvieri, G. Paolino, 2015 .

Unusual clinical presentations of vasculitis: what some clinical aspects can tell us about the pathogenesis.

B. Didona, M. Papi, 1999, Clinics in dermatology.

Vasculitis: Some Clinical Aspects Can Tell Us About the

B. Didona, M. Papi, 1999 .

Bullous pemphigoid with hyperkeratosis and palmoplantar keratoderma: Three cases

D. Didona, D. Abeni, F. Mariotti, 2018, The Journal of dermatology.

Painful Facial Ulceration

D. Didona, B. Didona, 2019, Pediatric Autoimmunity and Transplantation.

Increased prevalence of diabetes mellitus in bullous pemphigoid patients during the last decade

D. Abeni, B. Didona, L. Fania, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

An SRY‐negative XX male with Huriez syndrome

G. Melino, V. de Laurenzi, A. Terrinoni, 2000, Clinical Genetics.

RSPO1-mutated fibroblasts from non-tumoural areas of palmoplantar keratoderma display a cancer-associated phenotype

E. Dellambra, M. Teson, L. Guerra, 2021, European Journal of Dermatology.

Quality-of-life assessment in patients with pemphigus using a minimum set of evaluation tools.

C. Di Pietro, F. Sampogna, D. Abeni, 2009, Journal of the American Academy of Dermatology.

Supportive care in the acute phase of Stevens–Johnson syndrome and toxic epidermal necrolysis: an international, multidisciplinary Delphi‐based consensus

R. Stern, C. Bodemer, L. French, 2021, The British journal of dermatology.

The Hidradenitis Suppurativa (HS) “Multidisciplinary Unit”: a rationale and practical proposal for an organised clinical approach

G. Fabbrocini, M. Romanelli, G. Micali, 2018, European Journal of Dermatology.

Primary cutaneous CD30+ T‐cell lymphoma responsive to topical imiquimod (Aldara®)

P. Amerio, B. Didona, F. Canzona, 2004, The British journal of dermatology.

Markedly reduced incidence of melanoma and nonmelanoma skin cancer in a nonconcurrent cohort of 10,040 patients with vitiligo.

D. Abeni, A. Paradisi, B. Didona, 2014, Journal of the American Academy of Dermatology.

Case report: Bullous pemphigoid arising in a patient with scleroderma and multiple sclerosis

F. Mariotti, B. Didona, F. Moro, 2022, Frontiers in Medicine.

Etanercept in the Treatment of Psoriasis: The Emerging Evidence of its Therapeutic Value

A. Migliore, A. Galluccio, G. Caldarola, 2011 .

Biologics for pityriasis rubra pilaris treatment: A review of the literature

M. Napolitano, D. Abeni, B. Didona, 2018, Journal of the American Academy of Dermatology.

Ustekinumab treatment of pityriasis rubra pilaris: A report of five cases

M. Napolitano, D. Didona, D. Abeni, 2018, The Journal of dermatology.

Eosinophilic ulcer of the tongue - Case report*

S. Calvieri, G. Paolino, M. Donati, 2015, Anais brasileiros de dermatologia.

PURPLE (atrophie blanche): clinical, histological and immunological study of twelve patients

B. Didona, L. Silvestri, O. Pitá, 1997 .

IgE Sensitization Profile in Patients with Netherton Syndrome

R. Paganelli, D. Castiglia, B. Didona, 2022, International Archives of Allergy and Immunology.

Betapapillomavirus in multiple non‐melanoma skin cancers of Netherton syndrome: Case report and published work review

G. Zambruno, A. Sinistro, L. Guerra, 2015, The Journal of dermatology.

Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.

J. McGrath, C. Has, G. Zambruno, 2006, The Journal of investigative dermatology.

Livedo vasculopathy vs small vessel cutaneous vasculitis: cytokine and platelet P-selectin studies.

S. Giulio, O. De Pità, B. Didona, 1998, Archives of dermatology.

Bullous pemphigoid in elderly woman affected by non-small cell lung cancer treated with pembrolizumab: A case report and review of literature

D. Didona, L. Rossi, B. Didona, 2020, Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners.

Characterization of the ultraviolet B and X‐ray response of primary cultured epidermal cells from patients with disseminated superficial actinic porokeratosis

R. Corona, E. Dogliotti, M. D'errico, 2004, The British journal of dermatology.

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

G. Zambruno, F. Cianfarani, D. Castiglia, 2018, The British journal of dermatology.

Acne fulminans following isotretinoin therapy.

G. Paolino, D. Didona, C. Cantisani, 2019, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia.

Bullous Pemphigoid Associated With COVID-19 Vaccines: An Italian Multicentre Study

L. Atzori, C. Moltrasio, A. Parodi, 2022, Frontiers in Medicine.

Case Report: Complete and Fast Recovery From Severe COVID-19 in a Pemphigus Patient Treated With Rituximab

J. Sinagra, A. Salemme, B. Didona, 2021, Frontiers in Immunology.

Toxic epidermal necrolysis successfully treated with etanercept

E. Gubinelli, D. Raskovic, B. Didona, 2009, The Journal of dermatology.

A new case series on etanercept treatment for toxic epidermal necrolysis

D. Didona, D. Abeni, A. Paradisi, 2020, European Journal of Dermatology.

Toxic epidermal necrolysis-like acute cutaneous lupus erythematosus successfully treated with a single dose of etanercept: report of three cases.

M. Napolitano, D. Didona, B. Didona, 2013, Journal of American Academy of Dermatology.

Assessment of Treatment Approaches and Outcomes in Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: Insights From a Pan-European Multicenter Study.

E. Oppel, L. French, K. Kridin, 2021, JAMA dermatology.

Spiny keratoderma of the palms in a patient with diabetes mellitus type 1: what came first, the chicken or the egg?

G. Paolino, D. Didona, C. Cantisani, 2018, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia.

Post Zygotic, Somatic, Deletion in KERATIN 1 V1 Domain Generates Structural Alteration of the K1/K10 Dimer, Producing a Monolateral Palmar Epidermolytic Nevus

F. Iacovelli, M. Falconi, A. Terrinoni, 2021, International Journal of Molecular Sciences.

Role of the keratin 1 and keratin 10 tails in the pathogenesis of ichthyosis hystrix of Curth Macklin

G. Melino, G. Chillemi, E. Candi, 2018, PloS one.

Interferon-gamma promotes exaggerated cytokine production in keratinocytes cultured from patients with atopic dermatitis.

G. Girolomoni, S. Pastore, B. Didona, 1998, Journal of Allergy and Clinical Immunology.

X-linked dominant chondrodysplasia punctata (Happle syndrome) with uncommon symmetrical shortening of the tubular bones.

F. Atzori, B. Didona, T. Gobello, 1995, Dermatology.

Resolution of a case of pediatric pemphigus vulgaris treated with rituximab.

S. Calvieri, G. Paolino, M. Donati, 2014, Acta dermatovenerologica Croatica : ADC.

A randomized controlled trial to evaluate short‐term treatment with eosin vs. topical steroids in psoriasis

P. Gisondi, C. Di Pietro, F. Sampogna, 2009, Clinical and experimental dermatology.

Dermatomyositis: a comprehensive review of clinical manifestations, serological features, and therapeutic approaches.

M. Hertl, D. Didona, B. Didona, 2023, Italian journal of dermatology and venereology.

Pleomorphicskin eruptions in a COVID‐19 affected patient: Case report and review of the literature

A. Trové, F. Passarelli, S. Chiloiro, 2021, Immunity, inflammation and disease.

Erythromycin‐induced pemphigus foliaceus successfully treated with etanercept

D. Didona, B. Didona, L. Fania, 2020, Dermatologic therapy.

The Broad-Spectrum Impact of Hidradenitis Suppurativa on Quality of Life: A Comparison with Psoriasis

F. Sampogna, D. Abeni, S. Mastroeni, 2019, Dermatology.

The impact of hidradenitis suppurativa on general health is higher than that of hypertension, congestive heart failure, type 2 diabetes, myocardial infarction and depression

F. Sampogna, D. Abeni, S. Mastroeni, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Prevalence and incidence of hidradenitis suppurativa: an exercise on indirect estimation from psoriasis data

F. Sampogna, D. Abeni, B. Didona, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

Bleomycin-induced chromosome aberrations in lymphocytes derived from patients with lamellar ichthyosis.

G. Melino, D. Caporossi, B. Didona, 1999, Cancer genetics and cytogenetics.

Novel and recurrent ALDH3A2 mutations in Italian patients with Sjögren-Larsson syndrome

E. Bertini, G. Melino, A. Terrinoni, 2007, Journal of Human Genetics.

Generalized acquired cutis laxa and urticarial dermatosis associated with k-chain IgA micromolecular myeloma

B. Didona, L. Fania, G. Moretta, 2021, Dermatology reports.

Association of Dermoscopic Profiles of Telangiectases with Nailfold Videocapillaroscopic Patterns in Patients with Systemic Sclerosis

A. Facchiano, C. Mondino, M. Cutolo, 2013, The Journal of Rheumatology.

Detection and characterization of IgG, IgE, and IgA autoantibodies in patients with bullous pemphigoid associated with dipeptidyl peptidase‐4 inhibitors

D. Abeni, A. Salemme, B. Didona, 2017, Journal of the American Academy of Dermatology.

Hereditary palmoplantar keratodermas. Part II: syndromic palmoplantar keratodermas – Diagnostic algorithm and principles of therapy

M. Castori, G. Zambruno, L. Guerra, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Amelanotic melanoma mimicking cutaneous epitheliomas.

G. Annessi, M. Napolitano, R. Bono, 2014, Journal of American Academy of Dermatology.

Gliptin-associated bullous pemphigoid shows peculiar features of anti-BP180 and -BP230 humoral response: results from a multicenter study.

C. De Simone, F. Passarelli, A. Parodi, 2022, Journal of the American Academy of Dermatology.

Environmental factors in autoimmune bullous diseases with a focus on seasonality: new insights

L. Quintarelli, M. Caproni, E. Cozzani, 2023, Dermatology reports.

Etanercept therapy for toxic epidermal necrolysis.

D. Didona, D. Abeni, A. Paradisi, 2014, Journal of the American Academy of Dermatology.

Management of Adult Patients With Drug Reaction With Eosinophilia and Systemic Symptoms: A Delphi-Based International Consensus.

E. Oppel, B. Kaffenberger, M. Rosenbach, 2023, JAMA dermatology.

Pemphigus: trigger and predisposing factors

A. Salemme, F. Mariotti, B. Didona, 2023, Frontiers in medicine.

RIPK4 regulates cell-cell adhesion in epidermal development and homeostasis.

F. Brancati, A. Costanzo, M. Salvatore, 2022, Human Molecular Genetics.

Association of Dermoscopic Profiles of Telangiectases with Nailfold Videocapillaroscopic Patterns in Patients with Systemic Sclerosis

A. Facchiano, C. Mondino, M. Cutolo, 2013, Journal of Rheumatology.