Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Cristian Fidanzi"'
Autor:
Flavia Manzo Margiotta, Alessandra Michelucci, Salvatore Panduri, Laura Angeloni, Cristian Fidanzi, Giammarco Granieri, Riccardo Morganti, Marco Romanelli, Valentina Dini
Publikováno v:
JEADV Clinical Practice, Vol 3, Iss 1, Pp 65-75 (2024)
Abstract Background Monoclonal antibodies (mAbs) directed against tumour necrosis factor alpha (TNF‐α) and interleukin (IL)‐17 and ‐23 represent the ultimate therapeutic strategy in treating psoriasis patients, but scientific literature still
Externí odkaz:
https://doaj.org/article/176c0e5f08a049e89e6abc9d3b151a82
Publikováno v:
Travel Medicine and Infectious Disease, Vol 59, Iss , Pp 102716- (2024)
Externí odkaz:
https://doaj.org/article/2fe41ac4d0d944978dd917f7b8a30d23
Autor:
Cristian Fidanzi, Flavia Manzo Margiotta, Matteo Bevilacqua, Angelo Massimiliano D'Erme, Giovanni Bagnoni, Valentina Dini, Agata Janowska
Publikováno v:
Travel Medicine and Infectious Disease, Vol 56, Iss , Pp 102652- (2023)
Externí odkaz:
https://doaj.org/article/07ba23c596f249d599dad1baafe64efb
Autor:
Angelo Massimiliano D'Erme, Cristian Fidanzi, Marco Romanelli, Valentina Dini, Giovanni Bagnoni, Agata Janowska
Publikováno v:
Dermatology Reports (2023)
Not available
Externí odkaz:
https://doaj.org/article/ff113267ddab49ccb2cdc857f6e3eb31
Autor:
Giorgia Salvia, Nicola Zerbinati, Flavia Manzo Margiotta, Alessandra Michelucci, Giammarco Granieri, Cristian Fidanzi, Riccardo Morganti, Marco Romanelli, Valentina Dini
Publikováno v:
Diagnostics, Vol 13, Iss 17, p 2761 (2023)
Dermal hyaluronic acid (HA) fillers are used for nasolabial fold correction, but no study is still available on the use of ultra-high-frequency ultrasound (UHFUS) with 70 MHz probes for the evaluation of HA distribution and wrinkle amelioration. We s
Externí odkaz:
https://doaj.org/article/bdc50c025eb84f89b39cf75bd2f47832
Autor:
Cristian Fidanzi, Flavia Manzo Margiotta, Matteo Bevilacqua, Valerio Ortenzi, Valerio Rocchi, Giammarco Granieri, Marco Romanelli, Elisabetta Manni
Publikováno v:
Indian Journal of Dermatology, Vol 68, Iss 4, Pp 490-490 (2023)
Externí odkaz:
https://doaj.org/article/4e494afa4fd340a6835b16e98621cee7
Autor:
Angelo Massimiliano D'Erme, Roberta Iozzo, Paolo Viacava, Agata Janowska, Valentina Dini, Marco Romanelli, Cristian Fidanzi, Giovanni Bagnoni
Publikováno v:
Dermatology Reports (2021)
A very rare variant of MPD is the Pigmented Mammary Paget Disease (PMPD), first described by Culberson et al. in 1956. It is very difficult to distinguish this variant from melanoma both clinically and dermoscopically. The diagnosis is confirmed by h
Externí odkaz:
https://doaj.org/article/c80ffc5214204816bd2747cf2388f937
Autor:
Michela Iannone, Giorgia Salvia, Cristian Fidanzi, Matteo Bevilacqua, Agata Janowska, Riccardo Morganti, Marco Romanelli, Valentina Dini
Publikováno v:
Skin Appendage Disorders. :1-4
Introduction: Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease with systemic inflammation and high impact on quality of life. Treatment strategies are still inadequate with a lack of inflammation biomarkers. We conducted a prospec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85c13b7457987f2b69d98a3ad8221425
https://doi.org/10.1159/000528658
https://doi.org/10.1159/000528658
Autor:
Cristian Fidanzi, Silviu Flavius Troaca, Giuseppe Nicolò Fanelli, Marco Romanelli, Valentina Dini, Paolo Viacava, Riccardo Marconcini, Riccardo Morganti, Angelo Massimiliano D’Erme, Giovanni Bagnoni, Agata Janowska
Publikováno v:
European Journal of Cancer Prevention. 32:298-300
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f83945045c38b9fd8a199a9da26de3f
https://doi.org/10.1097/cej.0000000000000774
https://doi.org/10.1097/cej.0000000000000774
Autor:
Matteo Bevilacqua, Giammarco Granieri, Cristian Fidanzi, Giorgia Salvia, Flavia Margiotta, Alessandra Michelucci, Marco Romanelli, Valentina Dini
Publikováno v:
Wounds: a compendium of clinical research and practice. 35:e123-e125
Introduction. Dubowitz syndrome is a rare genetic disease with only a few cases reported in the literature. It is characterized by growth retardation, microcephaly, facial dysmorphism and higher risk of developing cancer and cardiomyopathies. PG is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a5f0ed3b915c2d1f2955ed528fbf051
https://doi.org/10.25270/wnds/22051
https://doi.org/10.25270/wnds/22051