L Roncucci
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Explore the profile of L Roncucci including associated specialties, affiliations and a list of published articles.
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84
Citations
900
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Recent Articles
1.
Mariani F, Boarino V, Bertani A, Merighi A, Pedroni M, Rossi G, et al.
Int J Obes (Lond)
. 2017 Mar;
41(6):982-985.
PMID: 28356561
Body fatness is a risk factor for colorectal cancer, and promotes an inflammatory environment. Indeed, inflammation in normal colorectal mucosa may be a factor linking body fatness to colorectal carcinogenesis....
2.
Ponz de Leon M, Urso E, Pucciarelli S, Agostini M, Nitti D, Roncucci L, et al.
Tech Coloproctol
. 2012 Sep;
17(1):79-87.
PMID: 22976915
Background: Attenuated familial adenomatous polyposis (AFAP) is characterized by the presence of 10-99 colorectal adenomas. The disease may be associated with mutations in either APC or MUTYH genes. We purposed...
3.
Zirilli L, Benatti P, Romano S, Roncucci L, Rossi G, Diazzi C, et al.
Exp Clin Endocrinol Diabetes
. 2009 Feb;
117(5):234-9.
PMID: 19235129
Aims: Peutz-Jeghers Syndrome (PJS) is a rare dominantly inherited disease characterized by hamartomatous small bowel polyposis, mucocutaneous hyperpigmentation, and increased risk of cancer. Differentiated thyroid cancers (DTCs) present mainly as...
4.
Ponz de Leon M, Rossi G, Di Gregorio C, De Gaetani C, Rossi F, Ponti G, et al.
Intern Emerg Med
. 2007 Dec;
2(4):269-79.
PMID: 18060471
Unlabelled: Cancer registries can be viewed as one of the main strategies for improving our understanding of cancer, as they may reveal the importance of specific trends in cancer incidence...
5.
Roncari B, Pedroni M, Maffei S, Di Gregorio C, Ponti G, Scarselli A, et al.
Clin Genet
. 2007 Aug;
72(3):230-7.
PMID: 17718861
A large majority of constitutional mutations in hereditary non-polyposis colorectal cancer (HNPCC) are because of the MHL 1 or MSH 2 genes. In a lower fraction of cases, another gene...
6.
Ponz de Leon M, Roncucci L
Intern Emerg Med
. 2007 Jul;
2(2):156.
PMID: 17634827
No abstract available.
7.
Pedroni M, Roncari B, Maffei S, Losi L, Scarselli A, Di Gregorio C, et al.
Dis Markers
. 2007 May;
23(3):179-87.
PMID: 17473388
Hereditary NonPolyposis Colorectal Cancer (Lynch syndrome) is an autosomal dominant disease caused by germline mutations in a class of genes deputed to maintain genomic integrity during cell replication, mutations result...
8.
Ponti G, Ponz de Leon M, Maffei S, Pedroni M, Losi L, Di Gregorio C, et al.
Clin Genet
. 2005 Oct;
68(5):442-7.
PMID: 16207212
Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations.Peculiar dermatologic manifestations are present in several heritable gastrointestinal disorders. Muir-Torre syndrome (MTS) is a genodermatosis...
9.
Roncucci L
Minerva Chir
. 2005 Jun;
60(3):167-78.
PMID: 15985992
Data from cancer registries show that incidence of rectal cancer is still high in Italy, while mortality rates are slightly decreasing in most recent years. Surgery is the treatment of...
10.
Ponti G, Ponz de Leon M, Losi L, Di Gregorio C, Benatti P, Pedroni M, et al.
Br J Dermatol
. 2005 Jun;
152(6):1335-8.
PMID: 15949004
The Muir-Torre syndrome (MTS) is an autosomal dominant genodermatosis characterized by the presence of sebaceous gland tumours, with or without keratoacanthomas, associated with visceral malignancies. We describe and characterize two...