Pigmented nodular melanoma: the predictive value of dermoscopic features using multivariate analysis

Autor: Pizzichetta, Ma, Kittler, H, Stanganelli, I, Bono, R, Cavicchini, S, De Giorgi, V, Ghigliotti, G, Quaglino, P, Rubegni, P, Argenziano, G, Talamini, R, Italian Melanoma Intergroup, Guardoli, D, Alaibac, MAURO SALVATORE ALESSANDRO, Astorino, S, Ayala, F, Corradin, Mt, Gonzales, M, Zampieri, P, Magi, S, Mazzoni, L, Seidenari, S, Pellacani, G, Specchio, F, Serraino, D, Soyer, H. P.

Background Nodular melanoma (NM), representing 10-30% of all melanomas, plays a major role in global mortality related to melanoma. Nonetheless, the literature on dermoscopy of NM is scanty. Objectives To assess odds ratios (ORs) to quantify dermosco

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c8cd0e74bdb5678f73afabcd04c4f7e
http://hdl.handle.net/11368/2939317

Quantitative evaluation of healthy epidermis by means of multiphoton microscopy and fluorescence lifetime imaging microscopy

Autor: Benati, E., Bellini, V., Borsari, S., Dunsby, C., Ferrari, C., French, P., Guanti, M., Guardoli, D., Koenig, K., Pellacani, Giovanni, Ponti, Giovanni, Schianchi, S., Talbot, C., Seidenari, S.

Publikováno v: Skin Research and Technology; Vol 17
Skin research and technology 17 (2011): 295–303. doi:10.1111/j.1600-0846.2011.00496.x
info:cnr-pdr/source/autori:Benati, Elisa; Bellini, Valerio; Borsari, Stefania; Dunsby, Christopher; Ferrari, Chiara; French, Paul; Guanti, Mario; Guardoli, Davide; Koenig, Karsten; Pellacani, Giovanni; Ponti, Giovanni; Schianchi, Simona; Talbot, Clifford; Seidenari, Stefania/titolo:Quantitative evaluation of healthy epidermis by means of multiphoton microscopy and fluorescence lifetime imaging microscopy/doi:10.1111%2Fj.1600-0846.2011.00496.x/rivista:Skin research and technology/anno:2011/pagina_da:295/pagina_a:303/intervallo_pagine:295–303/volume:17

Multiphoton microscopy (MPM) enables the assessment of unstained living biological tissue with submicron resolution, whereas fluorescence lifetime imaging microscopy (FLIM) generates image contrast between different states of tissue characterized by

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::416f9bdd10dcf16843e26fc57bf86eb9
https://pubmed.ncbi.nlm.nih.gov/21518012

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