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pro vyhledávání: '"Alessandro Stella"'
Autor:
Alessandro Stella, Martina Lepore Signorile, Ivan Lolli, Valentina Grossi, Candida Fasano, Claudio Lotesoriere, Filomena Cariola, Nicoletta Resta, Vittoria Disciglio, Cristiano Simone, Giovanna Forte, Paola Sanese
Publikováno v:
Journal of Medical Genetics
Germline mutations of the APC gene, which encodes a multidomain protein of 2843 amino acid residues, cause familial adenomatous polyposis (FAP). Three FAP clinical variants are correlated with the location of APC mutations: (1) classic FAP with profu
Autor:
Cristina Mareni, Viviana Gismondi, Cristiana Marchese, Mariapina Montera, Alessandro Stella, Liliana Varesco, Francesca Piaggio, Nicoletta Resta, Ginevra Guanti
Publikováno v:
Journal of Medical Genetics. 38:863-867
Editor—Familial adenomatous polyposis (FAP) is an autosomal dominantly inherited disorder characterised by the development of hundreds to thousands of adenomatous polyps in the colon and rectum. If left untreated, there is a very high risk of color
Autor:
Alessandro Stella, I. Miccolis, A Quagliarella, Patrizia Lastella, Ginevra Guanti, Nicoletta Resta
Publikováno v:
Scopus-Elsevier
Hereditary non-polyposis colorectal cancer (MIM 114500) is the most common inherited colorectal cancer syndrome, affecting 1 in 1000 people. Patients with hereditary non-polyposis colorectal cancer show predisposition to an early onset of synchronous