G. Zambruno

发表

New functions of XPC in the protection of human skin cells from oxidative damage

E. Parlanti, P. Degan, M. Crescenzi, 2006, The EMBO journal.

Adenovirus-mediated VEGF165 gene transfer enhances wound healing by promoting angiogenesis in CD1 diabetic mice

G Zambruno, M. Capogrossi, A. Mangoni, 2002, Gene Therapy.

Placenta growth factor in diabetic wound healing: altered expression and therapeutic potential.

F. Sera, M. Pesce, M. Capogrossi, 2006, The American journal of pathology.

Hereditary palmoplantar keratodermas. Part I. Non‐syndromic palmoplantar keratodermas: classification, clinical and genetic features

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

Characterization and expression analysis of the Spink5 gene, the mouse ortholog of the defective gene in Netherton syndrome.

Alain Hovnanian, A. Hovnanian, R. Roccasecca, 2005, Genomics.

Kindlin-1 Regulates Integrin Dynamics and Adhesion Turnover

A. Sonnenberg, M. Kreft, G. Zambruno, 2013, PloS one.

Placenta growth factor is induced in human keratinocytes during wound healing.

G. Zambruno, P. Puddu, F. Cianfarani, 2000, The Journal of investigative dermatology.

Free radical production during metabolism of organic hydroperoxides by normal human keratinocytes.

A. Iannone, A. Giannetti, G. Zambruno, 1993, The Journal of investigative dermatology.

Distinct vascular endothelial growth factor signals for lymphatic vessel enlargement and sprouting

M. Shibuya, K. Alitalo, H. Dvorak, 2007, The Journal of experimental medicine.

The intracellular and extracellular domains of BP180 antigen comprise novel epitopes targeted by pemphigoid gestationis autoantibodies.

G. Zambruno, M. Caproni, G. di Zenzo, 2007, The Journal of investigative dermatology.

A founder synonymous COL7A1 mutation in three Danish families with dominant dystrophic epidermolysis bullosa pruriginosa identifies exonic regulatory sequences required for exon 87 splicing

G. Zambruno, J. Hertz, D. Castiglia, 2011, The British journal of dermatology.

Denaturing HPLC-based approach for detection of COL7A1 gene mutations causing dystrophic epidermolysis bullosa.

A. Giannetti, M. Colombi, G. Zambruno, 2005, Biochemical and biophysical research communications.

Endemic pemphigus foliaceus: towards understanding autoimmune mechanisms of disease development.

L. Borradori, G. Zambruno, G. di Zenzo, 2012, The Journal of investigative dermatology.

Inhibition of endothelial cell migration and angiogenesis by a vascular endothelial growth factor receptor-1 derived peptide.

A. Tramontano, L. Tentori, P. Lacal, 2008, European journal of cancer.

Ichthyosis with confetti: clinics, molecular genetics and management

G. Zambruno, L. Guerra, D. Castiglia, 2015, Orphanet Journal of Rare Diseases.

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.

The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.

E. Bauer, H. Shimizu, J. Uitto, 2008, Journal of the American Academy of Dermatology.

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.

VLA protein expression on epidermal cells (keratinocytes, Langerhans cells, melanocytes): a light and electron microscopic immunohistochemical study

A. Giannetti, G. Zambruno, D. Soligo, 1991, The British journal of dermatology.

Pathomechanisms of Altered Wound Healing in Recessive Dystrophic Epidermolysis Bullosa.

G. Zambruno, F. Cianfarani, T. Odorisio, 2017, The American journal of pathology.

Corneodesmosomal cadherins are preferential targets of stratum corneum trypsin- and chymotrypsin-like hyperactivity in Netherton syndrome.

C. Bodemer, A. Ishida-Yamamoto, A. Hovnanian, 2006, The Journal of investigative dermatology.

Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity

A. Sonnenberg, M. Kreft, Y. Barrandon, 2005, Nature Genetics.

The 420K LEKTI variant alters LEKTI proteolytic activation and results in protease deregulation: implications for atopic dermatitis.

A. Hovnanian, M. Teson, G. Zambruno, 2012, Human molecular genetics.

Proteolytic activation cascade of the Netherton syndrome-defective protein, LEKTI, in the epidermis: implications for skin homeostasis.

G. Zambruno, C. Paolini, M. D’Alessio, 2011, The Journal of investigative dermatology.

Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases

C. Bodemer, C. Sălăvăstru, N. Bellon, 2020, Orphanet Journal of Rare Diseases.

Expansion of the clinical and molecular spectrum of an XPD‐related disorder linked to biallelic mutations in ERCC2 gene

M. Digilio, B. Dallapiccola, S. Rossi, 2021, Clinical genetics.

Family burden in epidermolysis bullosa is high independent of disease type/subtype.

C. Di Pietro, F. Sampogna, G. Zambruno, 2010, Acta dermato-venereologica.

Kindlin-1 mutant zebrafish as an in vivo model system to study adhesion mechanisms in the epidermis.

A. Sonnenberg, M. Kreft, H. Janssen, 2013, The Journal of investigative dermatology.

A truncating mutation in the laminin‐332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration

R. Boldrini, G. Zambruno, F. Cianfarani, 2014, The British journal of dermatology.

Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis

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

TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin

A. Lehmann, D. Orioli, J. Egly, 2015, Proceedings of the National Academy of Sciences.

Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients

J. Fischer, R. Betz, A. Irvine, 2021, Genes.

Sirtinol Treatment Reduces Inflammation in Human Dermal Microvascular Endothelial Cells

E. Cesarini, A. Mai, V. Sirri, 2011, PloS one.

Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibility

B. Dallapiccola, A. Pizzuti, G. Novelli, 1999, Human Genetics.

Bullous Pemphigoid: Clinical Features, Diagnostic Markers, and Immunopathogenic Mechanisms

E. Laffitte, L. Borradori, G. Zambruno, 2011 .

COL7A1 Recessive Mutations in Two Siblings with Distinct Subtypes of Dystrophic Epidermolysis Bullosa: Pruriginosa versus Nails Only

G. Zambruno, S. Pruneddu, D. Castiglia, 2010, Dermatology.

Clinical Practice Guidelines for Epidermolysis Bullosa Laboratory Diagnosis

C. Has, G. Zambruno, M. Escámez, 2019 .

Systematized organoid epidermal nevus with eccrine differentiation, multiple facial and oral congenital scars, gingival synechiae, and blepharophimosis: A novel epidermal nevus syndrome

G. Annessi, P. Cascone, M. Castori, 2010, American journal of medical genetics. Part A.

A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevus.

G. Melino, E. Candi, A. Terrinoni, 2000, The Journal of investigative 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.

Trichothiodystrophy and Chiari malformation type I in a child: more than a coincidence?

G. Zambruno, S. Giancristoforo, B. Spacca, 2019, European Journal of Dermatology.

Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype–phenotype relationships

A. Sarasin, A. Lehmann, J. Offman, 2007, Human mutation.

Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in the type VII collagen gene

N. Zoppi, M. Colombi, G. Zambruno, 2002, The British journal of dermatology.

Melanocytes lie on the epidermal basement membrane where they closely interact with surrounding basal ker- atinocytes to form a functional structure defined as the epi- dermal-melanin unit (Weiss and Greep, 1977). Melanocytes protect keratinocytes against ultraviolet damage (such as photocarcinogene

R. Cancedda, S. Bondanza, P. Marchisio, 1999 .

Local anesthesia in pediatric dermatologic surgery: Evaluation of a patient‐centered approach

M. L. Ciofi Degli Atti, G. Zambruno, S. Giancristoforo, 2018, Pediatric dermatology.

Bullous pemphigoid: from the clinic to the bench.

L. Borradori, G. Zambruno, G. di Zenzo, 2012, Clinics in dermatology.

Trisomic rescue causing reduction to homozygosity for a novel ABCA12 mutation in harlequin ichthyosis

J. Fischer, M. Castori, G. Zambruno, 2009, Clinical genetics.

Clonal analysis of B-cell response in pemphigus course: toward more effective therapies.

G. Zambruno, G. di Zenzo, G. Di Zenzo, 2015, The Journal of investigative dermatology.

Nambour Skin Cancer Study , the Rotterdam Study , Nurses ’ Health Study , the Health Professionals Follow-up Study , and the PUVA Follow-up Study have a tremendous scientific return on investment in many diseases , including skin cancer

G. Zambruno, G. Zenzo, G. D. Zenzo, 2015 .

In vitro antitumour activity of resveratrol in human melanoma cells sensitive or resistant to temozolomide

G. Zambruno, M. Fuggetta, G. Ravagnan, 2004, Melanoma research.

Ichthyosis Linearis Circumflexa as the Only Clinical Manifestation of Netherton Syndrome.

G. Zambruno, C. Pedicelli, L. Guerra, 2015, Acta dermato-venereologica.

Expression of the soluble vascular endothelial growth factor receptor‐1 in cutaneous melanoma: role in tumour progression

P. Lacal, R. Giavazzi, G. Zambruno, 2011, The British journal of dermatology.

A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome

T. Hashimoto, G. Zambruno, T. Hamada, 2016, Experimental dermatology.

Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families.

C. Bodemer, A. Hovnanian, A. Irvine, 2002, The Journal of investigative dermatology.

Discontinuous distribution of HIV-1 quasispecies in epidermal Langerhans cells of an AIDS patient and evidence for double infection.

S. Wain-Hobson, J. Vartanian, A. Giannetti, 1995, Advances in experimental medicine and biology.

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

D. Zillikens, L. Borradori, G. Zambruno, 2015, The British journal of dermatology.

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

C. Bodemer, J. Uitto, J. McGrath, 2020, The British journal of dermatology.

Palmoplantar Keratoderma and Woolly Hair Revealing Asymptomatic Arrhythmogenic Cardiomyopathy.

A. Novelli, G. Zambruno, L. Guerra, 2019, Acta dermato-venereologica.

Molecular testing in epidermolysis bullosa.

G. Zambruno, D. Castiglia, 2010, Dermatologic clinics.

Immunofluorescence analysis of villous trophoblasts: a tool for prenatal diagnosis of inherited epidermolysis bullosa with pyloric atresia.

G. Zambruno, M. D’Alessio, J. Lacour, 2008, The Journal of investigative dermatology.

First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses

S. Rossi, G. Zambruno, D. Castiglia, 2020, International journal of molecular sciences.

Hoarse cry in a newborn with epidermolysis bullosa simplex, generalized severe

R. Boldrini, G. Zambruno, S. Giancristoforo, 2020, Pediatric dermatology.

Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice‐site mutation in KRT10

M. Castori, G. Zambruno, P. Ghirri, 2010, The British journal of dermatology.

New Type of Epidermal Nevus Syndrome

R. Happle, G. Zambruno, T. Gobello, 2000, Dermatology.

Autosomal recessive epidermolysis bullosa simplex due to KRT14 mutation: two large Palestinian families and literature review

G. Zambruno, D. Castiglia, M. Naim, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Whole-exome sequencing in patients with ichthyosis reveals modifiers associated with increased IgE levels and allergic sensitizations To the

T. Jakob, J. Fischer, C. Has, 2014 .

Immunohistochemistry of Cutaneous Graft‐versus‐Host Disease after Allogeneic Bone Marrow Transplantation

A. Giannetti, G. Girolomoni, M. Andreani, 1991, The Journal of dermatology.

Spleen dendritic cells exhibit altered morphology and increased allostimulatory capacity after short‐term culture *

A. Giannetti, G. Girolomoni, G. Zambruno, 1992, Experimental dermatology.

Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients

M. del Río, P. Itin, J. Uitto, 2019, Orphanet journal of rare diseases.

Expression of B7 costimulatory molecule in cultured human epidermal Langerhans cells is regulated at the mRNA level.

S. Ferrari, V. Zacchi, A. Giannetti, 1994, The Journal of investigative dermatology.

Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees

G. Novelli, R. Mingarelli, S. Semprini, 2002, Human Genetics.

FERMT1 promoter mutations in patients with Kindler syndrome

L. Levati, C. Has, G. Zambruno, 2015, Clinical genetics.

Skin Equivalents: A Tool for the Discovery and Validation of Pharmacodynamic Biomarkers

G. Zambruno, P. Gallinari, C. Steinkühler, 2013, Cancer investigation.

Interleukin-22 Promotes Wound Repair in Diabetes by Improving Keratinocyte Pro-Healing Functions.

S. Madonna, G. Zambruno, A. Cavani, 2015, The Journal of investigative dermatology.

Gene Correction of Integrin β4-dependent Pyloric Atresia-Junctional Epidermolysis Bullosa Keratinocytes Establishes a Role for β4 Tyrosines 1422 and 1440 in Hemidesmosome Assembly*

E. Dellambra, O. Golisano, S. Bondanza, 2001, The Journal of Biological Chemistry.

A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia.

G. Zambruno, M. D’Alessio, G. Meneguzzi, 1997, The Journal of clinical investigation.

A proangiogenic peptide derived from vascular endothelial growth factor receptor-1 acts through alpha5beta1 integrin.

A. Tramontano, P. Lacal, L. Morbidelli, 2008, Blood.

A proangiogenic peptide derived from vascular endothelial growth factor receptor-1 acts through α5β1 integrin

A. Tramontano, P. Lacal, L. Morbidelli, 2008 .

MicroRNA‐145‐5p regulates fibrotic features of recessive dystrophic epidermolysis bullosa skin fibroblasts

M. Teson, G. Zambruno, F. Cianfarani, 2019, The British journal of dermatology.

Rituximab immunotherapy in pemphigus: therapeutic effects beyond B-cell depletion.

L. Borradori, G. Zambruno, 2008, The Journal of investigative dermatology.

Development of a novel ELISA system for detection of anti‐BP180 IgG and characterization of autoantibody profile in bullous pemphigoid patients

F. Sera, G. Zambruno, F. Mariotti, 2004, The British journal of dermatology.

Functional intercellular adhesion molecule-3 is expressed by freshly isolated epidermal Langerhans cells and is not regulated during culture.

V. Zacchi, A. Giannetti, G. Girolomoni, 1995, The Journal of investigative dermatology.

Early immunopathological diagnosis of ichthyosis with confetti in two sporadic cases with new mutations in keratin 10.

R. Boldrini, D. Martinelli, G. Zambruno, 2014, Acta dermato-venereologica.

Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study

A. Novelli, G. Zambruno, C. Quintarelli, 2022, Biomedicines.

X‐linked ichthyosis: Clinical and molecular findings in 35 Italian patients

A. Novelli, G. Zambruno, V. Alesi, 2018, Experimental dermatology.

Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa

C. Bodemer, S. Hadj-Rabia, Guglielmo Salvatori, 2014, Orphanet Journal of Rare Diseases.

Identification of a Novel Non-desmoglein Autoantigen in Pemphigus Vulgaris

A. Lanzavecchia, G. Zambruno, G. Di Lullo, 2019, Front. Immunol..

Direct detection of HIV-1 RNA in epidermal Langerhans cells of HIV-infected patients.

M. Negroni, A. Giannetti, G. Girolomoni, 1993, Journal of acquired immune deficiency syndromes.

MINI-REVIEW Pathomechanisms of Altered Wound Healing in Recessive Dystrophic Epidermolysis Bullosa

G. Zambruno, F. Cianfarani, T. Odorisio, 2022 .

Decorin counteracts disease progression in mice with recessive dystrophic epidermolysis bullosa.

P. Uva, G. Zambruno, D. Abeni, 2019, Matrix biology : journal of the International Society for Matrix Biology.

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)

D. Zillikens, L. Borradori, G. Zambruno, 2015, Journal of the European Academy of Dermatology and Venereology : JEADV.

Demonstration of epitope-spreading phenomena in bullous pemphigoid: results of a prospective multicenter study.

F. Sera, L. Borradori, G. Zambruno, 2011, The Journal of investigative dermatology.

Very late activation-3 integrin is the dominant beta 1-integrin on the glomerular capillary wall: an immunofluorescence study in nephrotic syndrome.

G. Annessi, G. Zambruno, L. Furci, 1992, Nephron.

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

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

β1 and β3 integrin upregulation in rapidly progressive glomerulonephritis

G. Zambruno, L. Lucchi, L. Furci, 1995 .

Beta 1 and beta 3 integrin upregulation in rapidly progressive glomerulonephritis.

G. Zambruno, L. Lucchi, L. Furci, 1995, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Activation of immature dendritic cells via membrane sialophorin (CD43).

G. Girolomoni, G. Zambruno, A. Cavani, 1997, Advances in experimental medicine and biology.

Langerhans cells and HIV infection.

A. Giannetti, G. Girolomoni, G. Zambruno, 1995, Immunology today.

Delayed diagnosis of dyskeratosis congenita in a 40‐year‐old woman with multiple head and neck squamous cell carcinomas

B. Dallapiccola, M. Castori, G. Zambruno, 2007, The British journal of dermatology.

A single cycle of treatment with temozolomide, alone or combined with O(6)-benzylguanine, induces strong chemoresistance in melanoma cell clones in vitro: role of O(6)-methylguanine-DNA methyltransferase and the mismatch repair system.

J. Jiricny, P. Lacal, E. Bonmassar, 2006, International journal of oncology.

Detection of HIV-1 in epidermal Langerhans cells of HIV-infected patients using the polymerase chain reaction.

A. Giannetti, G. Zambruno, A. Marconi, 1990, The Journal of investigative dermatology.

Linear IgA bullous dermatosis with autoantibodies to a 290 kd antigen of anchoring fibrils.

A. Giannetti, Jean Kanitakis, G. Zambruno, 1994, Journal of the American Academy of Dermatology.

Fibroblastic rheumatism: a case without rheumatological symptoms.

G. Annessi, G. Zambruno, P. Puddu, 2002, Acta dermato-venereologica.

A clinical, histopathological and laboratory study of 19 consecutive Italian paediatric patients with chilblain‐like lesions: lights and shadows on the relationship with COVID‐19 infection

M. L. Ciofi Degli Atti, S. Rossi, S. Zaffina, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Cutaneous phaeohyphomycosis due to Cladosporium cladosporioides

G. Annessi, G. Zambruno, A. Silverio, 1992, Mycoses.

Paraneoplastic Epidermolysis Bullosa Acquisita Associated with Thyroid Carcinoma.

G. Zambruno, L. Guerra, G. di Zenzo, 2016, Acta dermato-venereologica.

Epidermolysis bullosa acquisita ( EBA ) is a rare acquired subepithelial blistering disease of the skin and mucous membranes associated with autoantibodies against type

G. Zambruno, L. Guerra, A. Monopoli, 2016 .

Oral pemphigoid autoantibodies preferentially target BP180 ectodomain.

M. Carrozzo, G. Zambruno, A. Parodi, 2007, Clinical immunology.

Large International Validation of ABSIS and PDAI Pemphigus Severity Scores.

L. Misery, A. Dupuy, O. Dereure, 2019, The Journal of investigative dermatology.

Multicenter prospective study of the humoral autoimmune response in bullous pemphigoid.

F. Sera, L. Borradori, G. Zambruno, 2008, Clinical immunology.

European Guidelines (S3) on diagnosis and management of mucous membrane pemphigoid, initiated by the European Academy of Dermatology and Venereology – Part II

D. Zillikens, S. Rauz, D. Murrell, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.

European guidelines (S3) on diagnosis and management of mucous membrane pemphigoid, initiated by the European Academy of Dermatology and Venereology – Part I

D. Zillikens, S. Rauz, D. Murrell, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.

Sequential intramolecular epitope spreading of humoral responses to human BPAG2 in a transgenic model.

E. Olasz, K. Yancey, G. Zambruno, 2010, The Journal of investigative dermatology.

Characterization of the anti-BP180 autoantibody reactivity profile and epitope mapping in bullous pemphigoid patients.

F. Sera, L. Borradori, G. Zambruno, 2004, The Journal of investigative dermatology.

Calculation of cut‐off values based on the Autoimmune Bullous Skin Disorder Intensity Score (ABSIS) and Pemphigus Disease Area Index (PDAI) pemphigus scoring systems for defining moderate, significant and extensive types of pemphigus

M. Richard, D. Murrell, V. Werth, 2016, The British journal of dermatology.

Pemphigus vulgaris following cobalt therapy for bronchial carcinoma.

G. Girolomoni, G. Zambruno, E. Mazzone, 1989, Dermatologica.

Treatment of leg ulcers with cryopreserved allogeneic cultured epithelium. A multicenter study.

G Zambruno, R Cancedda, R. Cancedda, 1992, Archives of dermatology.

Isolated acral Darier's disease with haemorrhagic lesions in a kindred

G. Zambruno, C. Defilippi, R. Rosso, 1996, The British journal of dermatology.

Definitions and outcome measures for mucous membrane pemphigoid: recommendations of an international panel of experts.

E. Sprecher, D. Zillikens, D. Fivenson, 2015, Journal of the American Academy of Dermatology.

Updated S2 K guidelines for the management of bullous pemphigoid initiated by the European Academy of Dermatology and Venereology (EADV)

R. Bergman, E. Sprecher, D. Zillikens, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

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.

Prevalence of collagen VII-specific autoantibodies in patients with autoimmune and inflammatory diseases

Takashi Hashimoto, Markus F Neurath, Jonas Mudter, 2012, BMC Immunology.

Induction of senescence pathways in Kindler syndrome primary keratinocytes

E. Dellambra, C. Has, M. Teson, 2013, The British journal of dermatology.

Kindler syndrome: Extension of FERMT1 mutational spectrum and natural history

M. del Río, P. Itin, J. Fischer, 2011, Human mutation.

Clinical and genetic heterogeneity in keratosis follicularis spinulosa decalvans.

M. Castori, G. Zambruno, M. Paradisi, 2009, European journal of medical genetics.

[A case of anetoderma associated with discoid type lupus erythematosus. Clinico-histologic and pathogenetic observations].

G. Zambruno, G. Lembo, P. Candio, 1986, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia.

Definitions and outcome measures for bullous pemphigoid: recommendations by an international panel of experts.

H. Shimizu, M. Meurer, D. Zillikens, 2012, Journal of the American Academy of Dermatology.

Persistent unilateral orbital and eyelid oedema as a manifestation of Melkersson–Rosenthal syndrome

G. Annessi, G. Girolomoni, G. Zambruno, 2005, Journal of the European Academy of Dermatology and Venereology : JEADV.

Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification.

E. Bauer, H. Shimizu, J. Uitto, 2014, Journal of the American Academy of Dermatology.

Diabetes impairs adipose tissue–derived stem cell function and efficiency in promoting wound healing

G. Zambruno, F. Cianfarani, T. Odorisio, 2013, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

Mutation mechanisms.

G. Zambruno, D. Castiglia, 2010, Dermatologic clinics.

Compound heterozygosity for a recessive glycine substitution and a splice site mutation in the COL7A1 gene causes an unusually mild form of localized recessive dystrophic epidermolysis bullosa.

F. Atzori, G. Zambruno, L. Bruckner-Tuderman, 1998, The Journal of investigative dermatology.

A Novel Phenotype of Junctional Epidermolysis Bullosa with Transient Skin Fragility and Predominant Ocular Involvement Responsive to Human Amniotic Membrane Eyedrops

D. Ponzin, M. Tartaglia, S. Rossi, 2021, Genes.

Epidermal Langerhans cells after allogeneic bone marrow transplantation: depletion by chemotherapy conditioning regimen alone

A. Giannetti, G. Girolomoni, M. Andreani, 1992, Journal of cutaneous pathology.

The placenta growth factor in skin angiogenesis.

G. Zambruno, F. Cianfarani, C. Failla, 2006, Journal of dermatological science.

Mice overexpressing placenta growth factor exhibit increased vascularization and vessel permeability.

G. Zambruno, F. Cianfarani, C. Failla, 2002, Journal of cell science.

The control of epidermal stem cells (holoclones) in the treatment of massive full-thickness burns with autologous keratinocytes cultured on fibrin.

G. Pellegrini, S. Bondanza, G. Micali, 1999, Transplantation.

Clinical trial of ABCB5+ mesenchymal stem cells for recessive dystrophic epidermolysis bullosa

J. Tolar, J. McGrath, C. Ebens, 2021, JCI insight.

Non-Herlitz Junctional Epidermolysis bullosa without Hair Involvement Associated with BP180 Deficiency

C. De Simone, G. Zambruno, P. Posteraro, 2001, Dermatology.

Frequent Occurrence of Aplasia Cutis Congenita in Bullous Dermolysis of the Newborn.

R. Boldrini, A. Dotta, G. Zambruno, 2016, Acta dermato-venereologica.

Recessive Bullous Dermolysis of the Newborn in Preterm Siblings with a Missense Mutation in Type VII Collagen

G. Zambruno, G. Fabrizi, C. Pagliarello, 2015, Pediatric dermatology.

Long-term follow-up of a spontaneously improving patient with junctional epidermolysis bullosa associated with ITGB4 c.3977-19T>A splicing mutation.

R. Boldrini, G. Zambruno, D. Castiglia, 2013, Acta dermato-venereologica.

Long-term Follow-up of a Spontaneously Improving Patient with Junctional Epidermolysis Bullosa Associated with ITGB 4 c . 3977-19 T > A Splicing Mutation

R. Boldrini, G. Zambruno, D. Castiglia, 2012 .

Intracellular degradation of β4 integrin in lethal junctional epidermolysis bullosa with pyloric atresia

G. Zambruno, A. Micheloni, M. D’Alessio, 2004, The British journal of dermatology.

Novel and recurrent mutations in the integrin beta 4 subunit gene causing lethal junctional epidermolysis bullosa with pyloric atresia

H. Kayserili, G. Zambruno, E. Silvestri, 2003, Experimental dermatology.

Immunofluorescence mapping, electron microscopy and genetics in the diagnosis and sub‐classification of inherited epidermolysis bullosa: a single‐centre retrospective comparative study of 87 cases with long‐term follow‐up

R. Boldrini, S. Rossi, A. Novelli, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Proteasome-mediated degradation of keratins 7, 8, 17 and 18 by mutant KLHL24 in a foetal keratinocyte model: Novel insight in congenital skin defects and fragility of epidermolysis bullosa simplex with cardiomyopathy

E. Dellambra, E. Candi, V. Cianfanelli, 2021, Human molecular genetics.

Association of Piebaldism and Neurofibromatosis Type 1 in a Girl

G. Zambruno, M. Paradisi, C. Angelo, 2001, Pediatric dermatology.

TSH receptor and thyroid-specific gene expression in human skin.

E. Marchioni, A. Cavalli, M. Teson, 2010, The Journal of investigative dermatology.

Autologous in vitro reconstituted epidermis in the treatment of a large nevus depigmentosus.

S. Bondanza, R. Happle, G. Zambruno, 2006, Journal of the American Academy of Dermatology.

Corrective transduction of human epidermal stem cells in laminin-5-dependent junctional epidermolysis bullosa.

G. Pellegrini, E. Dellambra, O. Golisano, 1998, Human gene therapy.

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.

PR4 QUALITY OF LIFE IN PATIENTS WITH EPIDERMOLYSIS BULLOSA

F. Sampogna, G. Zambruno, D. Abeni, 2009 .

Quality of life in patients with epidermolysis bullosa

C. Di Pietro, F. Sampogna, G. Zambruno, 2009, The British journal of dermatology.

SPINK5, the defective gene in netherton syndrome, encodes multiple LEKTI isoforms derived from alternative pre-mRNA processing.

A. Hovnanian, G. Zambruno, F. Cianfarani, 2006, The Journal of investigative dermatology.

Notch-ing up knowledge on molecular mechanisms of skin fibrosis: focus on the multifaceted Notch signalling pathway

E. Candi, G. Zambruno, D. Castiglia, 2021, Journal of Biomedical Science.

Molecular characterization of 11 Italian patients with Darier disease.

F. Benedicenti, M. Castori, P. Grammatico, 2011, EJD. European journal of dermatology.

Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus

S. Chimenti, R. Mango, G. Novelli, 2004, Annals of human genetics.

AXIN2 germline mutations are rare in familial melanoma

M. Castori, P. Grammatico, G. Zambruno, 2011, Genes, chromosomes & cancer.

Concomitant activation of Wnt pathway and loss of mismatch repair function in human melanoma

E. Bonmassar, E. Pagani, G. Zambruno, 2008, Genes, chromosomes & cancer.

Involvement of the mismatch repair system in temozolomide-induced apoptosis.

J. Jiricny, L. Tentori, P. Lacal, 1998, Molecular pharmacology.

Monozygotic twins discordant for recessive dystrophic epidermolysis bullosa phenotype highlight the role of TGF-β signalling in modifying disease severity.

P. Uva, G. Zambruno, M. Di Salvio, 2014, Human molecular genetics.

Efficiency of translation termination in humans is highly dependent upon nucleotides in the neighbourhood of a (premature) termination codon

H. Schneider, G. Zambruno, D. Kiritsi, 2011, Journal of Medical Genetics.

Novel mutations in the LAMC2 gene in non-Herlitz junctional epidermolysis bullosa: effects on laminin-5 assembly, secretion, and deposition.

G. Zambruno, C. Angelo, P. Puddu, 2001, The Journal of investigative dermatology.

Corrective gene transfer of keratinocytes from patients with junctional epidermolysis bullosa restores assembly of hemidesmosomes in reconstructed epithelia

J. Ortonne, G. Zambruno, M. Luca, 1998, Gene Therapy.

Role of Integrins in Cell Adhesion and Polarity in Normal Keratinocytes and Human Skin Pathologies

G. Pellegrini, P. Marchisio, G. Zambruno, 1994, The Journal of dermatology.

Inactivation of p16INK4a (inhibitor of cyclin‐dependent kinase 4A) immortalizes primary human keratinocytes by maintaining cells in the stem cell compartment

E. Dellambra, S. Bondanza, Goberdhan P Dimri, 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Mutations in PYCR1 cause cutis laxa with progeroid features

Peter Nürnberg, Stefan Mundlos, Barry Merriman, 2009, Nature Genetics.

Severe osteoarticular involvement in isotretinoin‐triggered acne fulminans: two cases successfully treated with anakinra

T. Oranges, G. Zambruno, P. Tomà, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

Apoptosis and efficient repair of DNA damage protect human keratinocytes against UVB

E. Dogliotti, M. D'errico, A. Calcagnile, 2003, Cell Death and Differentiation.

Cockayne Syndrome Type A Protein Protects Primary Human Keratinocytes from Senescence.

E. Dellambra, P. Degan, D. Orioli, 2019, The Journal of investigative dermatology.

Granulocyte/macrophage colony‐stimulating factor treatment of human chronic ulcers promotes angiogenesis associated with de novo vascular endothelial growth factor transcription in the ulcer bed

G. Annessi, G. Zambruno, F. Cianfarani, 2006, The British journal of dermatology.

Epidermal growth factor and transferrin receptor expression in human embryonic and fetal epidermal cells

A. Giannetti, G. Girolomoni, G. Zambruno, 2004, Archives of Dermatological Research.

Biallelic somatic inactivation of the mismatch repair gene MLH1 in a primary skin melanoma

J. Jiricny, E. Pagani, G. Marra, 2003, Genes, chromosomes & cancer.

High-frequency microsatellite instability is associated with defective DNA mismatch repair in human melanoma.

J. Jiricny, E. Bonmassar, E. Pagani, 2002, The Journal of investigative dermatology.

Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formation.

F. Brancati, B. Dallapiccola, G. Cestra, 2014, The Journal of investigative dermatology.

Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin Diseases

C. Bodemer, C. Sălăvăstru, C. Has, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.

Vascular endothelial growth factor receptor-1 is deposited in the extracellular matrix by endothelial cells and is a ligand for theα 5β1 integrin

P. Lacal, V. Morea, G. Zambruno, 2003, Journal of Cell Science.

Teledermatology diagnosis of the first Italian patient affected with restrictive dermopathy due to ZMPSTE24 homozygous mutation

G. Zambruno, S. Giancristoforo, M. El Hachem, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes.

Barbara N. Pusey, Janice S. Lee, A. V. Vulto-van Silfhout, 2015, American journal of human genetics.

Genotype–phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD gene

S. Bondanza, D. Orioli, F. Benedicenti, 2009, Human mutation.

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.

Lethal Netherton Syndrome Due to Homozygous p.Arg371X Mutation in SPINK5

G. Zambruno, D. Castiglia, P. Fortugno, 2013, Pediatric dermatology.

A synonymous mutation in SPINK5 exon 11 causes Netherton syndrome by altering exonic splicing regulatory elements

G. Zambruno, D. Castiglia, P. Fortugno, 2012, Journal of Human Genetics.

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.

Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome.

S. Mundlos, F. Brancati, B. Dallapiccola, 2010, American journal of human genetics.

Spatial discontinuities in human immunodeficiency virus type 1 quasispecies derived from epidermal Langerhans cells of a patient with AIDS and evidence for double infection

S. Wain-Hobson, J. Vartanian, G. Zambruno, 1994, Journal of virology.

Transforming growth factor-beta 1 modulates beta 1 and beta 5 integrin receptors and induces the de novo expression of the alpha v beta 6 heterodimer in normal human keratinocytes: implications for wound healing

A. Giannetti, P. Marchisio, M. De Luca, 1995, The Journal of cell biology.

Transforming Growth-Factor-Beta-1 Modulates Beta-1 And Beta-5 Integrin Receptors And Induces The De-Novo Expression Of The Alpha-V-Beta-6 Heterodimer In Normal Human Keratinocytes - Implications For Wound-Healing. [5YIF: 10.77; Citations: 268]

A. Giannetti, P. Marchisio, G. Zambruno, 1995 .

Are SARS‐CoV‐2 IgA antibodies in paediatric patients with chilblain‐like lesions indicative of COVID‐19 asymptomatic or paucisymptomatic infection?

M. L. Ciofi Degli Atti, G. Zambruno, R. Carsetti, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Long-term engraftment of single genetically modified human epidermal holoclones enables safety pre-assessment of cutaneous gene therapy.

M. del Río, F. Larcher, J. Jorcano, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

Transforming Growth Factor-/ l Modulates # 1 and / 5 Integrin Receptors and Induces the de novo Expression of the ctv / 36 Heterodimer in Normal Human Keratinocytes : Implications for Wound Healing

A. Giannetti, P. Marchisio, M. De Luca, 2002 .

Increased melanoma growth and metastasis spreading in mice overexpressing placenta growth factor.

A. Ciucci, M. Pesce, P. Lacal, 2006, The American journal of pathology.

Updated S2K guidelines on the management of pemphigus vulgaris and foliaceus initiated by the european academy of dermatology and venereology (EADV)

R. Bergman, E. Sprecher, D. Zillikens, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Vascular endothelial growth factor‐C expression correlates with lymph node localization of human melanoma metastases

Jean Kanitakis, P. Lacal, G. Zambruno, 2003, Cancer.

The role of CSA in the response to oxidative DNA damage in human cells

I Iavarone, G Zambruno, E. Parlanti, 2007, Oncogene.

SARS-CoV-2 infection of thymus induces loss of function that correlates with disease severity

C. Agrati, V. Bordoni, S. Petrini, 2023, Journal of Allergy and Clinical Immunology.

Human melanoma cells secrete and respond to placenta growth factor and vascular endothelial growth factor.

P. Lacal, E. Pagani, G. Zambruno, 2000, The Journal of investigative dermatology.

In vitro infection of human epidermal Langerhans' cells with HIV-1.

A. Giannetti, G. Girolomoni, M. Re, 1995, Immunology.

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.

Quantitation by competitive PCR of HIV-1 proviral DNA in epidermal Langerhans cells of HIV-infected patients.

A. Giannetti, G. Girolomoni, A. Cimarelli, 1994, Journal of acquired immune deficiency syndromes.

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.

Epidermolysis Bullosa-Associated Squamous Cell Carcinoma: From Pathogenesis to Therapeutic Perspectives

E. Dellambra, G. Zambruno, D. Castiglia, 2019, International journal of molecular sciences.

Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa†

C. Has, G. Zambruno, P. Akker, 2019, The British journal of dermatology.

Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations.

G. Annessi, M. Castori, G. Zambruno, 2008, Acta dermato-venereologica.

Endothelial cell adhesion to soluble vascular endothelial growth factor receptor‐1 triggers a cell dynamic and angiogenic phenotype

Glenn C. Simon, P. Uva, G. Zambruno, 2014, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Genomic organization of the human integrin β4 gene

G. Zambruno, S. Iacovacci, M. D’Alessio, 1997, Mammalian Genome.

Genomic organization of the human integrin beta4 gene.

G. Zambruno, S. Iacovacci, M. D’Alessio, 1997, Mammalian genome : official journal of the International Mammalian Genome Society.

Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin Fragility.

M. Boerries, H. Busch, K. Tasanen, 2016, American journal of human genetics.

Binding properties, cell delivery, and gene transfer of adenoviral penton base displaying bacteriophage.

E. Cundari, G. Zambruno, C. Failla, 2001, Virology.

Phacomatosis cesioflammea with unilateral lipohypoplasia

R. Happle, M. Castori, P. Grammatico, 2008, American journal of medical genetics. Part A.

Epidermolysis Bullosa Simplex with KLHL24 Mutations Is Associated with Dilated Cardiomyopathy.

B. Rebolledo-Jaramillo, A. Paller, S. Duchatelet, 2019, The Journal of investigative dermatology.

Bmi-1 reduction plays a key role in physiological and premature aging of primary human keratinocytes.

E. Dellambra, S. Bondanza, G. Zambruno, 2010, The Journal of investigative dermatology.

A missense mutation (G1506E) in the adhesion G domain of laminin-5 causes mild junctional epidermolysis bullosa.

M. Scaturro, G. Zambruno, P. Posteraro, 2003, Biochemical and biophysical research communications.

Distinctive integrin expression in the newly forming epidermis during wound healing in humans.

A. Giannetti, G. Zambruno, A. Cavani, 1993, The Journal of investigative dermatology.

Toward epidermal stem cell-mediated ex vivo gene therapy of junctional epidermolysis bullosa.

G Zambruno, G. Pellegrini, E. Dellambra, 2000, Human gene therapy.

Compound heterozygosity for an out-of-frame deletion and a splice site mutation in the LAMB3 gene causes nonlethal junctional epidermolysis bullosa.

G. Zambruno, M. Paradisi, C. Angelo, 1998, Biochemical and biophysical research communications.

Glycated fibroblast growth factor-2 is quickly produced in vitro upon low-millimolar glucose treatment and detected in vivo in diabetic mice.

Antonio Facchiano, Vincenzo Fogliano, Francesco Facchiano, 2006, Molecular endocrinology.

Glycated-FGF-2 is quickly produced in vitro upon low-millimolar glucose treatment and detected in vivo in diabetic mice.

C. Peschle, D. Ribatti, F. Facchiano, 2006 .

factor receptor-1 acts through A proangiogenic peptide derived from vascular endothelial growth

P. Lacal, L. Morbidelli, M. Ziche, 2013 .

Two families confirm Schöpf‐Schulz‐Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum

S. Heath, F. Brancati, S. Madonna, 2011, Clinical genetics.

Prominent Follicular Keratosis in Multiple Intestinal Atresia with Combined Immune Deficiency Caused by a TTC7A Homozygous Mutation

G. Zambruno, D. Castiglia, R. de Vito, 2022, Genes.

Herlitz junctional epidermolysis bullosa: laminin‐5 mutational profile and carrier frequency in the Italian population

M. Castori, G. Zambruno, P. Ghirri, 2007, The British journal of dermatology.

Stromal microenvironment in type VII collagen-deficient skin: The ground for squamous cell carcinoma development.

G. Zambruno, T. Odorisio, L. Guerra, 2017, Matrix biology : journal of the International Society for Matrix Biology.

Differential role of transcription-coupled repair in UVB-induced response of human fibroblasts and keratinocytes.

E. Dogliotti, S. Soddu, M. D'errico, 2005, Cancer research.

Impaired keratinocyte proliferative and clonogenic potential in transgenic mice overexpressing 14-3-3σ in the epidermis.

E. Dellambra, G. Zambruno, C. Niessen, 2011, The Journal of investigative dermatology.

Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21.

C. Carcassi, S. Chimenti, B. Dallapiccola, 2001, The Journal of investigative dermatology.

The E3 ligase Itch knockout mice show hyperproliferation and wound healing alteration

G. Melino, E. Candi, A. Terrinoni, 2015, The FEBS journal.

Netherton syndrome and its multifaceted defective protein LEKTI.

A. Hovnanian, G. Zambruno, M. D’Alessio, 2013, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia.

A new SPINK5 donor splice site mutation in siblings with Netherton syndrome.

B. Tüysüz, G. Zambruno, D. Castiglia, 2010, Acta dermato-venereologica.

Identification of two novel RECQL4 exonic SNPs and genomic characterization of the IVS12 minisatellite

G. Zambruno, M. Paradisi, L. Larizza, 2003, Journal of Human Genetics.

Epidermolysis bullosa in Greece: the patients’ journey so far

D. Rigopoulos, G. Zambruno, A. Stratigos, 2018, International Journal of Research in Dermatology.

The international dystrophic epidermolysis bullosa patient registry: An online database of dystrophic epidermolysis bullosa patients and their COL7A1 mutations

Morris A Swertz, Cristina Has, Trebor Rengaw, 2011, Human mutation.

Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex

S. Llames, M. del Río, D. Mechan, 2011, The British journal of dermatology.

A Recurrent Nonsense Mutation Occurring as a de novo Event in a Patient with Recessive Dystrophic Epidermolysis Bullosa

M. del Río, C. Conti, G. Zambruno, 2011, Dermatology.

The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation

S. Llames, M. del Río, F. Larcher, 2010, The British journal of dermatology.

Acral skin atrophy in an infant: an early clue to Kindler syndrome diagnosis

R. Boldrini, G. Zambruno, S. Giancristoforo, 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

Kindler syndrome with severe mucosal involvement in a large Palestinian pedigree

G. Zambruno, D. Castiglia, P. Fortugno, 2015, European Journal of Dermatology.

A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome

G. Zambruno, N. Kaçar, D. Castiglia, 2008, The British journal of dermatology.

Genotype-phenotype correlation in italian patients with dystrophic epidermolysis bullosa.

J. McGrath, N. Zoppi, M. Colombi, 2002, The Journal of investigative dermatology.

Laminin-5 mutational analysis in an Italian cohort of patients with junctional epidermolysis bullosa.

G. Zambruno, C. Angelo, P. Posteraro, 2004, The Journal of investigative dermatology.

T-lymphocytes are directly involved in the clinical expression of migratory circinate erythema in epidermolysis bullosa simplex patients.

G. Zambruno, A. Cavani, D. Castiglia, 2014, Acta dermato-venereologica.

A case of neonatal linear IgA bullous dermatosis with severe eye involvement.

R. Boldrini, G. Zambruno, L. Romani, 2015, Acta dermato-venereologica.

Novel PNPLA1 mutations in two Italian siblings with autosomal recessive congenital ichthyosis

R. Boldrini, A. Novelli, G. Zambruno, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Corrective gene transfer of keratinocytes obtained from patients with junctional epidermolysis bullosa

E. Dellambra, J. Ortonne, G. Zambruno, 1998 .

Functional expression of ICAM-3 on human epidermal Langerhans cells.

V. Zacchi, A. Giannetti, G. Girolomoni, 1995, Advances in Experimental Medicine and Biology.

Kaposi's sarcoma with primary bone lesions in an HIV‐seronegative man

A. Giannetti, G. Girolomoni, G. Zambruno, 1996, The British journal of dermatology.

Ectodermal Dysplasia-Syndactyly Syndrome with Toe-Only Minimal Syndactyly Due to a Novel Mutation in NECTIN4: A Case Report and Literature Review

M. Rinelli, E. Bellacchio, G. Zambruno, 2021, Genes.

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

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

Antibodies against sialophorin (CD43) enhance the capacity of dendritic cells to cluster and activate T lymphocytes.

G. Girolomoni, G. Zambruno, A. Cavani, 1997, Journal of immunology.

Multiple Skin Squamous Cell Carcinomas in Junctional Epidermolysis Bullosa Due to Altered Laminin-332 Function

E. Dellambra, F. Ricci, F. Passarelli, 2020, International journal of molecular sciences.

ITGB4-mutated Junctional Epidermolysis Bullosa without Pyloric Atresia Presenting with Severe Urinary Involvement and Late-onset Minimal Skin Fragility: Diagnostic and Therapeutic Challenges

G. Zambruno, G. Mattioli, M. Carlucci, 2022, Acta dermato-venereologica.

Self-improving dominant dystrophic epidermolysis bullosa: phenotypic variability associated with COL7A1 mutation p.Gly2037Glu

S. Rossi, G. Zambruno, C. Guerriero, 2020, European Journal of Dermatology.

Autosomal recessive epidermolysis bullosa simplex due to EXPH5 mutation: neonatal diagnosis of the first Italian case and literature review

S. Rossi, G. Zambruno, M. El Hachem, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

Identification of the keratin K9 R162W mutation in patients of Italian origin with epidermolytic palmoplantar keratoderma.

G. Melino, E. Candi, A. Terrinoni, 2004, European journal of dermatology : EJD.

Childhood epidermolysis bullosa acquisita during squaric acid dibutyl ester immunotherapy for alopecia areata

G. Zambruno, C. Angelo, L. Guerra, 2017, The British journal of dermatology.

Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization

N. Zoppi, M. Colombi, G. Zambruno, 2006, Clinical genetics.

A. Giannetti, P. Marchisio, M. De Luca, 1995, The Journal of cell biology.

Epidermolysis bullosa care in Italy.

G. Zambruno, D. Castiglia, 2010, Dermatologia clinica.

The evaluation of family impact of recessive dystrophic epidermolysis bullosa using the Italian version of the Family Dermatology Life Quality Index

C. Di Pietro, F. Sampogna, G. Zambruno, 2013, Journal of the European Academy of Dermatology and Venereology : JEADV.

The atypical retinoid E-3-(3'-Adamantan-1-yl-4'-methoxybiphenyl-4-yl)-2-propenoic acid (ST1898) displays comedolytic activity in the rhino mouse model.

P. Luisi, C. Pisano, G. Zambruno, 2012, European journal of dermatology : EJD.

Two Italian Patients with ELOVL4-Related Neuro-Ichthyosis: Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization

S. Rossi, D. Martinelli, G. Zambruno, 2021, Genes.

Whole-exome sequencing in patients with ichthyosis reveals modifiers associated with increased IgE levels and allergic sensitizations.

T. Jakob, J. Fischer, C. Has, 2015, The Journal of allergy and clinical immunology.

Expression of integrin receptors and their role in adhesion, spreading and migration of normal human melanocytes.

R. Cancedda, S. Bondanza, P. Marchisio, 1993, Journal of cell science.

Circumscribed palmo‐plantar hypokeratosis: a disease of desquamation? Immunohistological study of five cases and literature review

Jean Kanitakis, G. Zambruno, M. Haftek, 2011, Journal of the European Academy of Dermatology and Venereology : JEADV.

Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes

D. Orioli, M. Teson, G. Zambruno, 2015, Experimental dermatology.

Biallelic mutations in RNF220 cause laminopathies featuring leukodystrophy, ataxia and deafness.

E. Bertini, C. Compagnucci, M. Tartaglia, 2021, Brain : a journal of neurology.

Immunity to Extracellular Matrix Antigens is Associated with Ultrastructural Alterations of the Stroma and Stratified Epithelium Basement Membrane in the Skin of Hashimoto's Thyroiditis Patients

C. Palumbo, R. Bei, L. Masuelli, 2006, International journal of immunopathology and pharmacology.

The Burden of Autosomal Recessive Congenital Ichthyoses on Patients and their Families: An Italian Multicentre Study

C. Bodemer, D. Bonamonte, A. Filoni, 2021, Acta dermato-venereologica.

S2k guidelines on the management of paraneoplastic pemphigus/paraneoplastic autoimmune multiorgan syndrome initiated by the European Academy of Dermatology and Venereology (EADV)

F. d'Amore, E. Sprecher, K. Tasanen, 2023, Journal of the European Academy of Dermatology and Venereology : JEADV.

Corrigendum to “The placenta growth factor in skin angiogenesis” [J. Dermatol. Sci. 41(2006) 11–19]

G. Zambruno, F. Cianfarani, C. Failla, 2006 .

Expression of placenta growth factor in mouse hair follicle cycle

G. Zambruno, F. Cianfarani, T. Odorisio, 2005 .

Immunofluorescence analysis of villous trophoblasts: a tool for prenatal diagnosis of inherited epidermolysis bullosa with pyloric atresia.

G. Zambruno, M. D’Alessio, J. Lacour, 2008, The Journal of investigative dermatology.

TSH receptor and thyroid-specific gene expression in human skin.

E. Marchioni, A. Cavalli, M. Teson, 2010, The Journal of investigative dermatology.

180‐kDa bullous pemphigoid antigen defective generalized atrophic benign epidermolysis bullosa: report of four cases with an unusually mild phenotype

G. Zambruno, M. Paradisi, P. Posteraro, 1998, The British journal of dermatology.

In vitro infection of human epidermal Langerhans cells with human immunodeficiency virus type 1.

A. Giannetti, G. Girolomoni, M. Re, 1995, Advances in Experimental Medicine and Biology.

Sensitivity of immunofluorescence studies vs enzyme-linked immunosorbent assay for diagnosis of bullous pemphigoid.

L. Borradori, G. Zambruno, P. Joly, 2011, Archives of dermatology.

A truncating mutation in the laminin‐332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration

R. Boldrini, G. Zambruno, F. Cianfarani, 2014, The British journal of dermatology.

Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations.

G. Annessi, M. Castori, G. Zambruno, 2008, Acta Dermato-Venereologica.

Lipoid Proteinosis: A Previously Unrecognized Mutation and Therapeutic Response to Acitretin.

R. Boldrini, G. Zambruno, S. Giancristoforo, 2017, Acta dermato-venereologica.

Sequential intramolecular epitope spreading of humoral responses to human BPAG2 in a transgenic model.

E. Olasz, K. Yancey, G. Zambruno, 2010, The Journal of investigative dermatology.