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Gene Therapy|February 4, 1999
Corrective gene transfer of keratinocytes from patients with junctional epidermolysis bullosa restores assembly of hemidesmosomes in reconstructed epitheliaJ Vailly, L Gagnoux-Palacios, E Dell'Ambra, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|December 11, 2013
Sensitivity of different assays for the serological diagnosis of epidermolysis bullosa acquisita: analysis of a cohort of 24 Italian patientsV Calabresi, A Sinistro, E Cozzani, et al.The British Journal of Dermatology|January 7, 2014
A truncating mutation in the laminin-332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migrationG Di Zenzo, M El Hachem, A Diociaiuti, et al.Immunology|May 1, 1995
In vitro infection of human epidermal Langerhans' cells with HIV-1E Ramazzotti, A Marconi, M C Re, et al.The Journal of Investigative Dermatology|May 12, 2001
Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21F Capon, S Semprini, S Chimenti, et al.Clinical Genetics|September 13, 2006
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterizationB Drera, D Castiglia, N Zoppi, et al.Clinical Genetics|August 27, 2014
FERMT1 promoter mutations in patients with Kindler syndromeC Has, N Chmel, L Levati, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|September 21, 2021
Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin DiseasesC Has, M El Hachem, H Bučková, et al.The British Journal of Dermatology|January 5, 2011
Expression of the soluble vascular endothelial growth factor receptor-1 in cutaneous melanoma: role in tumour progressionF Ruffini, C M Failla, A Orecchia, et al.Cell Death & Disease|October 26, 2012
Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosisA Terrinoni, V Serra, A Codispoti, et al.Pageof 12