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Autor:
G. Fraternali Orcioni, Paolo Sena, D. Saraggi, Dario Piazzalunga, Barbara Valeri, G. Forte, A. Indini, Rebecca Senetta, Francesca Galli, Simone Ribero, Mara Cossa, Barbara Merelli, Alice Labianca, M. Tanaka, Roberto Patuzzo, Marcella Occelli, M. Fukayama, Andrea Maurichi, Jacopo Pigozzo, R. Salvatori, Giuseppe Palmieri, Daniela Massi, Laura Cattaneo, V. De Giorgi, Pietro Quaglino, Andrea Gianatti, Francesca Portelli, Mario Mandalà, Maria Cristina Montesco
Publikováno v:
The British journal of dermatologyReferences. 184(2)
The presence of ulceration has been recognized as an adverse prognostic factor in primary cutaneous melanoma (PCM).To investigate whether the extent of ulceration (EoU) predicts relapse-free survival (RFS) and overall survival (OS) in PCM.We retrieve
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 1:A364
Introduction La maladie xanthogranulomateuse de l’adulte est une rare hystiocytose a cellule non-Langerhans et mal diagnostiquee qui affecte la region orbitale et les annexes cutanees. Elle est classee en quatre types [le xanthogranulome de l’adu
Publikováno v:
Lymphology. 49(4)
Here we report the clinical, pathological, and immunological features of a rare case of Waldenström macroglobulinemia (WM) with pleural infiltrations. An atypical chylothorax, successfully treated by videothoracoscopy, represented the main clinical
Autor:
Emilio Berti, Aldo Maffi, Pier Luigi Zinzani, Elena Dallera, G. Fraternali-Orcioni, Sara Rattotti, Marco Lucioni, Silvia Franceschetti, Maria Giuseppina Cabras, Francesco Onida, Roberta Riboni, Serena Rupoli, Marco Paulli, Pietro Quaglino, Mariarosa Arra, Marco Santucci, Marcello Gambacorta, Maria Teresa Fierro, Nicola Zerbinati, Giorgio Alberto Croci, Nicola Pimpinelli, Antonio Ramponi, Mauro Alaibac, Luca Arcaini, Carlo Tomasini, Catherine Klersy, Stefano Ascani, Vieri Grandi, Gaia Goteri
Publikováno v:
Cancer Medicine
Categorization of primary cutaneous B‐cell lymphomas (PCBCL) other than marginal zone (MZL) represents a diagnostic challenge with relevant prognostic implications. The 2008 WHO lymphoma classification recognizes only primary cutaneous follicular c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e8b11c7755f4671ae8e07007116158f
http://hdl.handle.net/2158/1123092
http://hdl.handle.net/2158/1123092
Autor:
Ilaria Baldelli, Rodolfo Quarto, Morris E. Hartstein, Pier Luigi Santi, Francesco P. Bernardini, Alessandro Gennai, G. Fraternali-Orcioni, Erica Repaci, Alessandra Zambelli, Luigi Izzo
Publikováno v:
Aesthetic surgery journal. 35(5)
Background Although recent research on micro fat has shown the potential advantages of superficial implantation and high stem cell content, clinical applications thus far have been limited. Objectives The authors report their experience with superfic
Autor:
Vittorio Stefoni, Pier Luigi Zinzani, Sante Tura, Franco Gherlinzoni, Claudia Cellini, G. Fraternali Orcioni, Maurizio Bendandi, Stefano Pileri, Massimo Magagnoli
Publikováno v:
Annals of Oncology. 11:363-366
Summary Purpose In the last years, fludarabine (FLU) alone or in combination with other drugs has been reported to be effective in the treatment of previously treated low-grade non-Hodgkin's lymphomas (LG-NHL). The aim of this study was to define the
Autor:
Roberto Latagliata, Bruno Monarca, Franco Mandelli, Massimo Breccia, Maria Concetta Petti, Gianna Maria D'Elia, Stefano Pileri, G. Fraternali-Orcioni
Publikováno v:
Acta Haematologica. 104:34-37
Granulocytic sarcoma (GS) is a rare extramedullary tumor composed of immature myeloid cells. It is usually associated with leukemia or other myeloproliferative disorders, but can also occur without overt hematologic disease, i.e. in patients with a n
Autor:
Stefano Ascani, Milena Piccioli, P. Leoni, S. A. Pileri, G. Fraternali Orcioni, Brunangelo Falini, Franco Gherlinzoni, Pier Luigi Zinzani, I. Bearzi, M. Materazzi
Publikováno v:
Annals of Oncology. 10:649-653
T-cell chronic lymphocytic leukaemia (T-CLL) has recently been reclassified under the heading of T-cell prolymphocytic leukaemia (T-PLL) because of its unfavourable clinical course, independently of the morphologic features. This rare neoplasm usuall