Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Naomi De Luca"'
Autor:
Francesco Moro, Feliciana Mariotti, Anna Pira, Naomi De Luca, Biagio Didona, Gianluca Pagnanelli, Giovanni Di Zenzo
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
BackgroundBullous pemphigoid (BP) is the most common autoimmune-blistering disease, clinically characterized by erythematous urticarial plaques, blisters, and intense pruritus, induced by autoantibodies against two proteins of the dermo-epidermal jun
Externí odkaz:
https://doaj.org/article/980182f4f0434000995b73d0401b26bf
Autor:
Daniele Castiglia, Paola Fortugno, Angelo Giuseppe Condorelli, Sabina Barresi, Naomi De Luca, Simone Pizzi, Iria Neri, Claudio Graziano, Diletta Trojan, Diego Ponzin, Sabrina Rossi, Giovanna Zambruno, Marco Tartaglia
Publikováno v:
Genes, Vol 12, Iss 5, p 716 (2021)
Junctional epidermolysis bullosa (JEB) is a clinically and genetically heterogeneous skin fragility disorder frequently caused by mutations in genes encoding the epithelial laminin isoform, laminin-332. JEB patients also present mucosal involvement,
Externí odkaz:
https://doaj.org/article/c94d10ca86354e6da0c250182f6eb839
Autor:
Paola Fortugno, Angelo Giuseppe Condorelli, Elena Dellambra, Liliana Guerra, Francesca Cianfarani, Lavinia Tinaburri, Vittoria Proto, Naomi De Luca, Francesca Passarelli, Francesca Ricci, Giovanna Zambruno, Daniele Castiglia
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1426 (2020)
Variably reduced expression of the basement membrane component laminin-332 (α3aβ3γ2) causes junctional epidermolysis bullosa generalized intermediate (JEB-GI), a skin fragility disorder with an increased susceptibility to squamous cell carcinoma (
Externí odkaz:
https://doaj.org/article/af7854217c754981b6e555c33d79a2b4
Autor:
Paola Fortugno, Marco Tartaglia, Claudio Graziano, Daniele Castiglia, Diletta Trojan, Sabrina Rossi, Naomi De Luca, Iria Neri, Angelo Giuseppe Condorelli, Giovanna Zambruno, Sabina Barresi, Simone Pizzi, Diego Ponzin
Publikováno v:
Genes
Volume 12
Issue 5
Genes, Vol 12, Iss 716, p 716 (2021)
Volume 12
Issue 5
Genes, Vol 12, Iss 716, p 716 (2021)
Junctional epidermolysis bullosa (JEB) is a clinically and genetically heterogeneous skin fragility disorder frequently caused by mutations in genes encoding the epithelial laminin isoform, laminin-332. JEB patients also present mucosal involvement,
Autor:
Angelo Giuseppe Condorelli, Daniele Castiglia, Liliana Guerra, Paola Fortugno, Vittoria Proto, Giovanna Zambruno, Francesca Passarelli, Francesca Cianfarani, Lavinia Tinaburri, Naomi De Luca, Francesca Ricci, Elena Dellambra
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1426 (2020)
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1426 (2020)
Variably reduced expression of the basement membrane component laminin-332 (α3aβ3γ2) causes junctional epidermolysis bullosa generalized intermediate (JEB-GI), a skin fragility disorder with an increased susceptibility to squamous cell carcinoma (
Autor:
Valeria Pacifico, Dario Didona, Feliciana Mariotti, Biagio Didona, Naomi De Luca, Damiano Abeni, Cinzia Mazzanti, Luca Fania, Giovanni Di Zenzo
Publikováno v:
The Journal of Dermatology. 45:1135-1140
The clinical features of bullous pemphigoid are extremely polymorphous. Several atypical forms of bullous pemphigoid have been described, and the diagnosis critically relies on immunopathological findings. We describe three bullous pemphigoid patient
Autor:
Maria Letizia Zaccaria, Erwin Tschachler, Simona Avitabile, Naomi De Luca, Laura Tatangelo, Teresa Odorisio, Cristina Maria Failla, Emanuela De Domenico, Heidemarie Rossiter
Publikováno v:
Journal of Dermatological Science. 90:93-96
Autor:
Giovanna Zambruno, Andrea Cavani, Monica Pascucci, Andrea Diociaiuti, Naomi De Luca, Teresa Carbone, Daniele Castiglia, May El Hachem
Publikováno v:
Acta Dermato Venereologica. 94:307-311
Epidermolysis bullosa simplex with migratory circinate erythema (EBS-MCE) is a rare EBS subtype characterised by migratory blistering lesions that resolve with brownish pigmentation. It is caused by a recurrent readthrough mutation, c.1649delG, in th
Autor:
Valentina Calabresi, Naomi De Luca, Liliana Guerra, Cinzia Mazzanti, Giovanna Zambruno, Giovanni Di Zenzo
Publikováno v:
Acta dermato-venereologica. 96(5)
Autor:
Elena Pagani, Silvia Bernardini, Naomi De Luca, Enzo Bonmassar, Sabrina Falcinelli, Alberto Pacchiarotti, Giovanna Zambruno, Ester Alvino, Daniele Castiglia, Stefania D'Atri
Publikováno v:
Genes, Chromosomes and Cancer. 47:614-624
Constitutive activation of the Wnt pathway plays a key role in the development of colorectal cancer and has also been implicated in the pathogenesis of other malignancies. Deregulation of Wnt signaling mainly occurs through genetic alterations of APC