Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Annalisa Vascellaro"'
Autor:
Bonamonte, Domenico, Hansel, Katharina, Romita, Paolo, Fortina, Anna Belloni, Girolomoni, Giampiero, Fabbrocini, Gabriella, Patruno, Cataldo, Napolitano, Maddalena, Patrizi, Annalisa, Argenziano, Giuseppe, Micali, Giuseppe, Calzavara Pinton, Piergiacomo, Foti, Caterina, Stingeni, Luca, Italian Society of Dermatology and Venereology, Pediatric Dermatology Group: Chiara Barlusconi, Francesco Bellinato, Stefano Caccavale, Giulia Calabrese, Francesca Caroppo, Aurora De Marco, Angela Filoni, Rossella Marietti, Maria Rita Nasca, Iria Neri, Donatella Schena, Marta Tramontana, Annalisa Vascellaro
Background: Contact allergy and atopic dermatitis (AD) are both common inflammatory T cell-mediated diseases and many factors may influence the prevalence of contact allergy in AD patients. In children, their possible correlation was debated with con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90df793226c10adbcace433773643edb
http://hdl.handle.net/11577/3450856
http://hdl.handle.net/11577/3450856
Autor:
Luisa Lorenzi, Marta Fusano, Marina Venturini, Annalisa Vascellaro, Piergiacomo Calzavara-Pinton, Mariachiara Arisi, Alessandra Gelmetti, Giorgio Pasolini, Giulia Petrilli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8a1c47ab0d1b8fe0e2eef94271fe73d
http://hdl.handle.net/11379/520214
http://hdl.handle.net/11379/520214
Autor:
Livia Garavelli, Piergiacomo Calzavara-Pinton, Anita Wischmeijer, Marina Venturini, Nicola Chiarelli, Stefano Quinzani, Michele Traversa, Emanuela Manfredini, Nicoletta Zoppi, Chiara Dordoni, Marco Ritelli, Annalisa Vascellaro, Marina Colombi
Publikováno v:
Orphanet Journal of Rare Diseases
Background Classic Ehlers–Danlos syndrome (cEDS) is a rare autosomal dominant connective tissue disorder that is primarily characterized by skin hyperextensibility, abnormal wound healing/atrophic scars, and joint hypermobility. A recent study demo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88923e0b05e3b0ce6a5eb860d2424182
https://doi.org/10.1186/1750-1172-8-58
https://doi.org/10.1186/1750-1172-8-58
Autor:
Annalisa Vascellaro, Piergiacomo Calzavara-Pinton, Marina Venturini, Marina Colombi, Chiara Dordoni, Lidia Pezzani, Nicola Chiarelli, Marco Ritelli
Publikováno v:
American journal of medical genetics. Part A. (5)
Visceroptosis is described in several heritable connective tissue disorders, including the hypermobility type of Ehlers-Danlos syndrome (hEDS), a.k.a. joint hypermobility syndrome (JHS). Clinical features of hEDS comprise joint hypermobility, mild sk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::559a4e867423288bb5fa7a9bf29ec799
https://pubmed.ncbi.nlm.nih.gov/23533212
https://pubmed.ncbi.nlm.nih.gov/23533212