about
Incidence trend of malignant polyps through the data of a specialized colorectal cancer registry: clinical features and effect of screening.Aberrant crypt foci in patients with colorectal cancer.MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events.Muir-Torre syndrome.Th inducing POZ-Kruppel Factor (ThPOK) is a key regulator of the immune response since the early steps of colorectal carcinogenesis.Understanding variations in survival for colorectal cancer in Europe: a EUROCARE high resolution studyA founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instability.The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer.Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European expertsHistology of aberrant crypt foci in the human colon.Identification and classification of hereditary nonpolyposis colorectal cancer (Lynch syndrome): adapting old concepts to recent advancements. Report from the Italian Association for the study of Hereditary Colorectal Tumors Consensus Group.Effects of acute changes of bile acid pool composition on biliary lipid secretion.Identification of Lynch syndrome among patients with colorectal cancer.Infliximab-related hepatitis: discussion of a case and review of the literature.Clinical outcome of low- and high-risk malignant colorectal polyps: results of a population-based study and meta-analysis of the available literature.Epidemiology of colorectal cancer: the 21-year experience of a specialised registry.Inheritance and susceptibility to tumours of the large bowel: a new classification of colorectal malignancies.Lymph node evaluation in stage IIA colorectal cancer and its impact on patient prognosis: a population-based study.Neutrophil gelatinase-associated lipocalin: a new prognostic marker in stage I colorectal carcinoma?A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis.Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.Microsatellite instability and colorectal cancer prognosis.Relationship between MUC5AC and altered expression of MLH1 protein in mucinous and non-mucinous colorectal carcinomas.Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors.Matrix metalloproteinases 15 and 19 are stromal regulators of colorectal cancer development from the early stages.Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instability.Different molecular mechanisms underlie genomic deletions in the MLH1 Gene.Long-term survey of patients with curable colorectal cancer with specific reference to the quality of life.Survival analysis in families affected by hereditary non-polyposis colorectal cancer.Regional inequalities in cancer care persist in Italy and can influence survival.Decrease in plasma tryptophan after a tryptophan-free amino acid solution. A comparison between cirrhotic and control subjects.Duodenal carcinoma in a 37-year-old man with Cowden/Bannayan syndrome.Role of clinical criteria in the diagnosis of hereditary non-polyposis colorectal cancer (HNPCC): results of a multivariate analysis.Tumour spectrum in hereditary non-polyposis colorectal cancer (HNPCC) and in families with "suspected HNPCC". A population-based study in northern Italy. Colorectal Cancer Study Group.Suspected HNPCC and Amsterdam criteria II: evaluation of mutation detection rate, an international collaborative study.First observation of microadenomas in the ileal mucosa of patients with familial adenomatous polyposis and colectomies.An unusual case of familial adenomatous polyposis with very early symptom occurrence.Relative role of APC and MUTYH mutations in the pathogenesis of familial adenomatous polyposis.
P50
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P50
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հետազոտող
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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M Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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Maurizio Ponz de Leon
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P1053
A-9356-2015
P106
P1153
14918864300
P21
P31
P3829
P496
0000-0003-4465-1043