Zobrazeno 1 - 10
of 159
pro vyhledávání: '"Daniele Castiglia"'
Autor:
Elena Dellambra, Sonia Cordisco, Francesca Delle Monache, Sergio Bondanza, Massimo Teson, Ezio Maria Nicodemi, Biagio Didona, Angelo Giuseppe Condorelli, Giovanna Camerino, Daniele Castiglia, Liliana Guerra
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-20 (2022)
Abstract Background Secreted R-spondin (RSPO) proteins play a key role in reproductive organ development, epithelial stem cell renewal and cancer induction by reinforcing canonical Wnt signaling. We have previously reported that palmoplantar keratode
Externí odkaz:
https://doaj.org/article/b8e473838ba44368bd41b054eff3bdac
Autor:
Damiano Abeni, Roberta Rotunno, Andrea Diociaiuti, Simona Giancristoforo, Domenico Bonamonte, Carmelo Schepis, Iria Neri, Daniele Castiglia, Giovanna Zambruno, May El Hachem
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Abstract Background Autosomal recessive congenital ichthyoses (ARCI) are a genetically heterogeneous group of rare and chronic disorders characterized by generalized skin scaling and hyperkeratosis, erythroderma, and palmoplantar keratoderma. Additio
Externí odkaz:
https://doaj.org/article/d79a0697e9b94a8baa22205810a3a020
Autor:
Giovanni Di Zenzo, Giovanna Floriddia, Sabrina Rossi, Feliciana Mariotti, Alessia Primerano, Angelo Giuseppe Condorelli, Biagio Didona, Daniele Castiglia
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Autoimmune response to cutaneous basement membrane components superimposed on a genetic skin fragility disease, hereditary epidermolysis bullosa (EB), has been described, but its effects on disease course remain unclear. We report a 69-year-old indiv
Externí odkaz:
https://doaj.org/article/3d4e38c3a6ce4243ab9e27c11bca0a40
Autor:
Angelo Giuseppe Condorelli, May El Hachem, Giovanna Zambruno, Alexander Nystrom, Eleonora Candi, Daniele Castiglia
Publikováno v:
Journal of Biomedical Science, Vol 28, Iss 1, Pp 1-17 (2021)
Abstract Fibrosis can be defined as an excessive and deregulated deposition of extracellular matrix proteins, causing loss of physiological architecture and dysfunction of different tissues and organs. In the skin, fibrosis represents the hallmark of
Externí odkaz:
https://doaj.org/article/edf4e354c14449f8876a72aac3b5aa23
Autor:
Enrico Scala, Stefania Madonna, Daniele Castiglia, Alessandro Scala, Elisabetta Caprini, Roberto Paganelli
Publikováno v:
Biomedicines, Vol 11, Iss 1, p 202 (2023)
(1) Background: Atopic dermatitis constitutes one of the most common inflammatory skin manifestations of the pediatric population. The onset of many inborn errors occurs early in life with an AD–like picture associated with a deregulated IgE respon
Externí odkaz:
https://doaj.org/article/d4f73b605f3e49e688b2a13825ab3a8e
Autor:
Damiano Abeni, Roberta Rotunno, Andrea Diociaiuti, Simona Giancristoforo, Domenico Bonamonte, Angela Filoni, Carmelo Schepis, Maddalena Siragusa, Iria Neri, Annalucia Virdi, Daniele Castiglia, Giovanna Zambruno, Christine Bodemer, May El Hachem
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 6, p adv00477 (2021)
Autosomal recessive congenital ichthyoses (ARCI) are characterized by generalized skin scaling, hyperkeratosis, erythroderma, and disabling features affecting the skin (palmoplantar keratoderma, fissures, pain, itch), eyes, ears, and joints. Disease
Externí odkaz:
https://doaj.org/article/f436a179d79c40c4aee9aec604ea082f
Autor:
Sara Guerrero-Aspizua, Claudio J. Conti, Maria Jose Escamez, Daniele Castiglia, Giovanna Zambruno, Leila Youssefian, Hassan Vahidnezhad, Luis Requena, Peter Itin, Gianluca Tadini, Ivelina Yordanova, Ludovic Martin, Jouni Uitto, Cristina Has, Marcela Del Rio
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-15 (2019)
Abstract Background Kindler Syndrome (KS) is a rare genodermatosis characterized by skin fragility, skin atrophy, premature aging and poikiloderma. It is caused by mutations in the FERMT1 gene, which encodes kindlin-1, a protein involved in integrin
Externí odkaz:
https://doaj.org/article/2039cab014194ad7a6c6aa5ac424b587
Autor:
Liliana Guerra, Angelo Giuseppe Condorelli, Paola Fortugno, Valentina Calabresi, Cristina Pedicelli, Giovanni Di Zenzo, Daniele Castiglia
Publikováno v:
Acta Dermato-Venereologica, Vol 98, Iss 4, Pp 411-415 (2018)
Circulating anti-type VII collagen autoantibodies are frequently detected in patients with recessive dystrophic epidermolysis bullosa (RDEB). However, evidence supporting their pathogenic role in inducing epidermolysis bullosa acquisita (EBA) has bee
Externí odkaz:
https://doaj.org/article/5d36889c2e6443a399d70a01fe69befe
Autor:
Liliana Guerra, Fabio Bergamo, Maria Rosaria D'Apice, Francesco Angelucci, Stefano di Girolamo, Letizia Camerota, Rosanna Monetta, Giorgio Annessi, Daniele Castiglia, Giuseppe Novelli, Mauro Paradisi, Francesco Brancati
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 12, Pp 1192-1194 (2019)
Abstract is missing (Short communication)
Externí odkaz:
https://doaj.org/article/5d19b1bd99194a1c91b73384cc4ca428
Autor:
Claudia Carnevale, Daniele Castiglia, Andrea Diociaiuti, Vittoria Proto, Simona Giancristoforo, Renata Boldrini, Giovanna Zambruno, Maya El Hachem
Publikováno v:
Acta Dermato-Venereologica, Vol 97, Iss 10, Pp 1249-1251 (2017)
Externí odkaz:
https://doaj.org/article/e8335c5b678e471bafbc8113e34c5f00