Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Cristina Pedicelli"'
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, Cristina Pedicelli, Vittoria Proto, Angelo Giuseppe Condorelli, Cinzia Mazzanti, Daniele Castiglia
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 1, Pp 115-116 (2018)
Externí odkaz:
https://doaj.org/article/f2cada1cfe214cef89c6e319ccc31c36
Autor:
Ilaria Lazzareschi, Antonio Gatto, Antonietta Curatola, Cristina Pedicelli, Daniele Castiglia, Danilo Buonsenso, Giorgio Attinà, Piero Valentini
Publikováno v:
European Journal of Haematology. 103:523-526
Hereditary spherocytosis is the most common inherited hemolytic anemia characterized by the presence of spherical-shaped erythrocytes on peripheral blood smear. The clinical manifestations of HS are highly variable, from severe forms to asymptomatic
Autor:
Paola Fortugno, Cristina Pedicelli, Liliana Guerra, Valentina Calabresi, Angelo Giuseppe Condorelli, 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
Autor:
Vittoria Proto, Cristina Pedicelli, Daniele Castiglia, Cinzia Mazzanti, Liliana Guerra, Angelo Giuseppe Condorelli
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 1, Pp 115-116 (2018)
Autor:
Cristina Pedicelli, Stefania Alfani, Elisabetta Andreoli, Mauro Paradisi, Enzo D. Finore, Giuliana Palermi
Publikováno v:
Pediatric Dermatology. 24:E51-E56
The high visibility of dermatologic diseases and their easy accessibility make the skin a primary and direct target for dysfunctional behaviors. Self-harm tendencies can frequently be expressed through dermatologic lesions, and dermatitis artefacta f
Autor:
Vittoria Proto, Giovanna Zambruno, Paola Fortugno, Cristina Pedicelli, Daniele Castiglia, Liliana Guerra, Cinzia Mazzanti
Publikováno v:
Acta dermato-venereologica. 95(6)
Ichthyosis linearis circumflexa (ILC) presents as serpiginous and migratory erythematous patches with double-edged scales. ILC is rarely an isolated skin manifestation, but most commonly a part of Netherton syndrome (NS). NS is caused by SPINK5 mutat
Autor:
Giovanna Floriddia, Daniele Castiglia, Giovanna Zambruno, Cristina Pedicelli, Marina Colombi, Sergio Barlati, Nicoletta Zoppi, N. De Luca, Gianluca Tadini, Bruno Drera, Rita Gardella
Publikováno v:
Clinical Genetics. 70:339-347
Dystrophic epidermolysis bullosa (DEB) pruriginosa (DEB-Pr) is a rare variant of DEB due to COL7A1 dominant and recessive mutations, which is characterized by severe itching and lichenoid or nodular prurigo-like lesions, mainly involving the extremit
Autor:
Christian Wilhelm, John A. McGrath, Cristina Has, Vesarat Wessagowit, Leena Bruckner-Tuderman, Corinna Baer, Biagio Didona, Daniele Castiglia, Giovanna Zambruno, Andrea Locatelli, Monica Pascucci, G. H. S. Ashton, Gianluca Tadini, Jürgen Kohlhase, Cristina Pedicelli
Publikováno v:
Journal of Investigative Dermatology. 126:1776-1783
Kindler syndrome (KS) is a rare autosomal recessive disorder characterized by skin blistering in childhood followed by photosensitivity and progressive poikiloderma. Most cases of KS result from mutations in the KIND1 gene encoding kindlin-1, a compo
Autor:
Angela M. Christiano, Cristina Pedicelli, Mauro Paradisi, C. Angelo, Amalia Martinez-Mir, G. S. Chuang
Publikováno v:
Clinical and Experimental Dermatology. 28:535-538
Atrichia with papular lesions (APL) is a rare autosomal recessive disorder resulting in complete and irreversible hair loss shortly after birth. Affected individuals also develop papular lesions of keratin-filled follicular cysts over extensive areas