Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Tiziana Lepre"'
Autor:
Federico Ricci, Giovanni Staurenghi, Tiziana Lepre, Filippo Missiroli, Stefania Zampatti, Raffaella Cascella, Paola Borgiani, Luigi Tonino Marsella, Chiara Maria Eandi, Andrea Cusumano, Giuseppe Novelli, Emiliano Giardina
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e66978 (2013)
BACKGROUND:Age-related macular degeneration (AMD) is the main cause of blindness in the developed world. The etiology of AMD is multifactorial due to the interaction between genetic and environmental factors. IL-8 has a role in inflammation and angio
Externí odkaz:
https://doaj.org/article/be2a52db8bc145168592d3a5225663fb
Autor:
Federico Ricci, Giovanni Staurenghi, Tiziana Lepre, Filippo Missiroli, Stefania Zampatti, Raffaella Cascella, Paola Borgiani, Luigi Tonino Marsella, Chiara Maria Eandi, Andrea Cusumano, Giuseppe Novelli, Emiliano Giardina
Publikováno v:
PLoS ONE, Vol 8, Iss 7 (2013)
Externí odkaz:
https://doaj.org/article/1a83b077682f44f6a47547fa7886b0f5
Autor:
Livia Biancone, Giuseppe Novelli, Francesco Pallone, Emiliano Giardina, Giovanna Condino, Paola Borgiani, Sara Onali, Tiziana Lepre, Cinzia Ciccacci, Davide Di Fusco, Micaela Ranieri
Publikováno v:
Journal of Crohn's and Colitis. 7:44-52
Background and aims Genome-wide association (GWA) studies recently identified a novel gene, TRAF3IP2, involved in the susceptibility to psoriasis. Common immune-mediated mechanisms involving the skin or the gut have been suggested. We therefore aimed
Autor:
Tiziana Lepre, Michele Ragazzo, Emiliano Giardina, Raffaella Cascella, Giuseppe Novelli, Elena Galli
Publikováno v:
British Journal of Dermatology. 168:1106-1108
Background Atopic eczema (AE) (OMIM %603165) is the most common chronic inflammatory skin disease characterized by xerosis, pruritus, and erythematous lesions with increased transepidermal water loss. It’s a complex disease due to the interaction b
Autor:
Giuseppe Novelli, Viviana Moschese, Paola Fortugno, Valeria Foti Cuzzola, Emiliano Giardina, Elena Galli, Tiziana Lepre, Loredana Chini, Raffaella Cascella, Cinzia Mazzanti
Publikováno v:
Journal of Investigative Dermatology. 131(4):982-984
Autor:
Tiziana Lepre, Andrea Cusumano, Giovanni Staurenghi, Luigi Tonino Marsella, Federico Ricci, Stefania Zampatti, Giuseppe Novelli, Chiara M. Eandi, Emiliano Giardina, Raffaella Cascella, Paola Borgiani, Filippo Missiroli
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 7 (2013)
PLoS ONE, Vol 8, Iss 7 (2013)
Author Francesco Viola was omitted from the author byline. The full, correct list of authors and affiliations is as follows
Publikováno v:
eLS
Psoriasis (OMIM #177900) is a common chronic disease of the skin that affects approximately 2–3% of the population. Typical lesions of psoriasis are characterised by red and scaly skin patches, usually found on the scalp, elbows and knees and often
Autor:
Jaya Ravindran, Tiziana Lepre, Giuseppe Novelli, Frank Behrens, Ulrike Hüffmeier, André Reis, Harald Burkhardt, Eleanor Korendowych, Neil McHugh, Emiliano Giardina
Publikováno v:
Arthritis and rheumatism. 63(12)
Objective The strongest susceptibility locus of psoriatic arthritis (PsA) is within the major histocompatibility complex (MHC) region (psoriasis susceptibility region 1, or PSORS1), and HLA–Cw*06:02 has been reported as the PSORS1 susceptibility al
Autor:
Cecilia De Felici, Federico Ricci, Emiliano Giardina, Tiziana Lepre, Filippo Missiroli, Chiara M. Eandi, Stefania Zampatti, Raffaella Cascella, Andrea Cusumano, Giuseppe Novelli, Fabiana Taglia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c079bef5cd9baff113052f810a242f3
http://hdl.handle.net/2108/16575
http://hdl.handle.net/2108/16575
Autor:
Tiziana Lepre, Lucia Tanga, Marco Centofanti, Luciano Quaranta, Giuseppe Novelli, Cristina Peconi, Paolo Frezzotti, Francesco Oddone, Emiliano Giardina, Gianluca Manni
Publikováno v:
BMC Ophthalmology
Background Single nucleotide polymorphisms (SNPs) within the LOXL1 gene are associated with pseudoesfoliation syndrome and pseudoesfoliation glaucoma. The aim of our study is to investigate a potential involvement of LOXL1 gene in the pathogenesis of