Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Giovanna Floriddia"'
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:
M. El Hachem, R Mariani, Alessandra Stracuzzi, Giovanna Floriddia, Claudia Cesario, Rita Alaggio, Andrea Diociaiuti, Renata Boldrini, Giovanna Zambruno, Daniele Castiglia, Antonio Novelli, Sabrina Rossi, Elisa Pisaneschi, Damiano Abeni
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADVReferences. 35(4)
BACKGROUND Epidermolysis bullosa (EB) comprises a heterogeneous group of skin fragility disorders, classified in four major types based on skin cleavage level, i.e. EB simplex (EBS), junctional EB (JEB), dystrophic EB (DEB), Kindler EB, and in more t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97a513d0e22182736f2ab3be729eaf3c
https://pubmed.ncbi.nlm.nih.gov/33274474
https://pubmed.ncbi.nlm.nih.gov/33274474
Autor:
Sami Abdennader, T. Schneiter, Jie Zheng, H. Coignard, Martin Leverkus, Marie-Dominique Vignon-Pennamen, Werner Kempf, B. Cribier, Pascal Reygagne, Bungo Ohyama, Ying-Wei Chen, Druck Reinhardt Druck Basel, K.D. Mertz, Georg Stingl, Christine Bangert, Brigitte Peters, Hirohiko Sueki, K. Kerl, A. Fourtanier, Thomas Bieber, Olivier Join-Lambert, Peter Itin, Hayriye Sarıcaoğlu, Daniele Castiglia, C. Mainetti, A.C. Green, P. Giovanoli, Achim Guettner, P. McBride, Yoko Nagashima, G. Palmedo, I. Kolm, Erwin Kump, Han Tian, W. Kempf, Sara Pruneddu, Stephen K. Tyring, Anne-Sophie Le Guern, M. Schmid, Alexander Rufle, Hélène Guet-Revillet, Masumi Akita, Xavier Nassif, Alessandro Giunta, P. Itin, T. Hunziker, Anne Leflèche, Adam Ferguson, Hakan Turan, Wie Huang, Jean-Paul Ortonne, Sylvain Poirée, Sergio Chimenti, Tetsuya Tsuchida, Michael J. Cork, Florence Ribadeau-Dumas, M. Pfaltz, Sylvie Behillil, M. Pithon, Jens Ulrich, Sophia Weise-Riccardi, R.P. Braun, Zhen-Min Niu, L. Schärer, Francesca Cottoni, Peter Häusermann, Andreas W. Arnold, Harald Gollnick, Anna Pokrywka, M.T. Fernández Figueras, Paul Henri Consigny, Jean-Philippe Jais, J. Kamarashev, Daniela Göppner, Jing Zhang, Tamara Kopp, Patrick Berche, Alessandro Di Stefani, Sylvie Fraitag, Koji Iida, B. Burger, Wen-Tao Yuan, Jacques Thèze, Vincent Jullien, Jean Hatchuel, Thomas A. Luger, Giovanna Floriddia, A. Andrade, Rupert C. Ecker, Giovanna Zambruno, Xiao-Ying Chen, Bettina Burger, M.C.B. Hughes, Bruce Strober, Li-Wei Jin, Arife Oz, Olivier Lortholary, Aude Nassif, Takashi Hashimoto, Satz Mengensatzproduktion, L.E. French, Norito Ishii, H. Kutzner
Publikováno v:
Dermatology. 222:93-96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::436b7c813c925bab17032cbcf22dd579
https://doi.org/10.1159/000324363
https://doi.org/10.1159/000324363
Publikováno v:
Dermatology. 222:10-14
Dystrophic epidermolysis bullosa (DEB) is a rare, clinically heterogeneous, blistering genodermatosis inherited as either autosomal dominant or recessive trait. All DEB forms are caused by mutations in the COL7A1 gene, which encodes for type VII coll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11199d7f86663fa58f07a4c536c6991c
https://doi.org/10.1159/000322619
https://doi.org/10.1159/000322619
Autor:
Giovanna Floriddia, S. Heath, Marco Castori, S. Madonna, Daniele Castiglia, Francesco Brancati, M Foglio, Giovanna Zambruno, J Fischer
Publikováno v:
Clinical Genetics. 79:92-95
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd1396e0c8621d3ea98e691f08409cc5
https://doi.org/10.1111/j.1399-0004.2010.01513.x
https://doi.org/10.1111/j.1399-0004.2010.01513.x
Autor:
Monica Pascucci, W. Daoud, Daniele Castiglia, F. Cherif, Giovanna Floriddia, Selma Kassar, Amel Ben Osman-Dhahri, Houyem Ouragini, Sonia Abdelhak, Samir Boubaker
Publikováno v:
Journal of Dermatological Science. 54:114-120
Background Dystrophic epidermolysis bullosa (DEB) is a clinically heterogeneous blistering disorder of the skin and mucous membranes. DEB is caused by mutations in the COL7A1 gene encoding type VII collagen, the major component of anchoring fibrils.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d458e92b8e27a910f902ee300a812fc5
https://doi.org/10.1016/j.jdermsci.2009.01.006
https://doi.org/10.1016/j.jdermsci.2009.01.006
Autor:
Isabella Torrente, Claudia Covaciu, Giovanna Floriddia, Daniele Castiglia, Mauro Paradisi, Elisa Pisaneschi, Marco Castori
Publikováno v:
Journal of Dermatological Science. 51:58-61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1a3858ad92902a2ce164d2cae79137e
https://doi.org/10.1016/j.jdermsci.2008.02.006
https://doi.org/10.1016/j.jdermsci.2008.02.006
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bd00a9bbf6ce6f0242cc994309ed3e1
https://doi.org/10.1111/j.1399-0004.2006.00679.x
https://doi.org/10.1111/j.1399-0004.2006.00679.x
Autor:
Sara, Pruneddu, Daniele, Castiglia, Giovanna, Floriddia, Francesca, Cottoni, Giovanna, Zambruno
Publikováno v:
Dermatology (Basel, Switzerland). 222(1)
Dystrophic epidermolysis bullosa (DEB) is a rare, clinically heterogeneous, blistering genodermatosis inherited as either autosomal dominant or recessive trait. All DEB forms are caused by mutations in the COL7A1 gene, which encodes for type VII coll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::63db7d46ba3bbb2c37fb3b64049e585f
https://pubmed.ncbi.nlm.nih.gov/21196708
https://pubmed.ncbi.nlm.nih.gov/21196708
Autor:
Daniele Castiglia, Marina Colombi, F. Forzano, Sergio Barlati, Giovanna Floriddia, Giovanna Zambruno, Bruno Drera
Publikováno v:
The British journal of dermatology. 161(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1f5b50ba1f3fc36333922345f611a40
https://pubmed.ncbi.nlm.nih.gov/19416260
https://pubmed.ncbi.nlm.nih.gov/19416260