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Guidelines for the clinical management of familial adenomatous polyposis (FAP)

Gut, 2008-05, Vol.57 (5), p.704-713

2008

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Lymphatic vessel density and its prognostic value in stage I colorectal carcinoma

Journal of clinical pathology, 2011-01, Vol.64 (1), p.6-12

2011

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Peutz–Jeghers syndrome: a systematic review and recommendations for management

Gut, 2010-07, Vol.59 (7), p.975-986

2010

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Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors

Techniques in coloproctology, 2014-03, Vol.18 (3), p.285-289

2014

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Understanding variations in survival for colorectal cancer in Europe: a EUROCARE high resolution study

Gut, 2000-10, Vol.47 (4), p.533-538

2000

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Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations

Clinical genetics, 2005-11, Vol.68 (5), p.442-447

2005

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Clinical and molecular features of attenuated adenomatous polyposis in northern Italy

Techniques in coloproctology, 2013-02, Vol.17 (1), p.79-87

2013

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Trend of incidence, subsite distribution and staging of colorectal neoplasms in the 15-year experience of a specialised cancer registry

Annals of oncology, 2004-06, Vol.15 (6), p.940-946

2004

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Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer

British journal of cancer, 2004-02, Vol.90 (4), p.882-887

2004

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Epidemiology of colorectal cancer: the 21-year experience of a specialised registry

Internal and emergency medicine, 2007-12, Vol.2 (4), p.269-279

2007

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Survival differences between European and US patients with colorectal cancer: role of stage at diagnosis and surgery

Gut, 2005-02, Vol.54 (2), p.268-273

2005

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Impact of Surgery on the Development of Duodenal Cancer in Patients with Familial Adenomatous Polyposis

Diseases of the colon & rectum, 2006-12, Vol.49 (12), p.1860-1866

2006

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Differentiated thyroid carcinoma (DTC) in a young woman with Peutz-Jeghers syndrome: are these two conditions associated?

Experimental and clinical endocrinology & diabetes, 2009-05, Vol.117 (5), p.234-239

2009

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Management of rectal cancers in relation to treatment guidelines: a population-based study comparing Italian and French patients

Digestive and liver disease, 2014-07, Vol.46 (7), p.645-651

2014

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Cancer survival in Europe 1999–2007 by country and age: results of EUROCARE-5—a population-based study

The lancet oncology, 2014, Vol.15 (1), p.23-34

2014

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Molecular Screening for Hereditary Nonpolyposis Colorectal Cancer: A Prospective, Population-Based Study

Journal of clinical oncology, 2001-10, Vol.19 (19), p.3944-3950

2001

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Histology of aberrant crypt foci in the human colon

Histopathology, 1997-04, Vol.30 (4), p.328-334

1997

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Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC

Clinical genetics, 2007-09, Vol.72 (3), p.230-237

2007

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A 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

Journal of medical genetics, 2004-03, Vol.41 (3), p.e34-34

2004

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Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis

Gut, 1999-07, Vol.45 (1), p.32-38

1999

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Aetiology of colorectal cancer and relevance of monogenic inheritance

Gut, 2004-01, Vol.53 (1), p.115-122

2004

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A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability

Clinical genetics, 2006-03, Vol.69 (3), p.254-262

2006

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EUROCARE-3: survival of cancer patients diagnosed 1990–94—results and commentary

Annals of oncology, 2003-12, Vol.14, p.v61-v118

2003

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Pathogenesis of colorectal cancer

Digestive and Liver Disease, 2000-12, Vol.32 (9), p.807-821

2000

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EUROCARE-3 summary: cancer survival in Europe at the end of the 20th century

Annals of oncology, 2003-12, Vol.14, p.v128-v149

2003

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Guidelines for the clinical management of familial adenomatous polyposis (FAP)

Lymphatic vessel density and its prognostic value in stage I colorectal carcinoma

Peutz–Jeghers syndrome: a systematic review and recommendations for management

Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors

Understanding variations in survival for colorectal cancer in Europe: a EUROCARE high resolution study

Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations

Clinical and molecular features of attenuated adenomatous polyposis in northern Italy

Trend of incidence, subsite distribution and staging of colorectal neoplasms in the 15-year experience of a specialised cancer registry

Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer

Epidemiology of colorectal cancer: the 21-year experience of a specialised registry

Survival differences between European and US patients with colorectal cancer: role of stage at diagnosis and surgery

Impact of Surgery on the Development of Duodenal Cancer in Patients with Familial Adenomatous Polyposis

Differentiated thyroid carcinoma (DTC) in a young woman with Peutz-Jeghers syndrome: are these two conditions associated?

Management of rectal cancers in relation to treatment guidelines: a population-based study comparing Italian and French patients

Cancer survival in Europe 1999–2007 by country and age: results of EUROCARE-5—a population-based study

Molecular Screening for Hereditary Nonpolyposis Colorectal Cancer: A Prospective, Population-Based Study

Histology of aberrant crypt foci in the human colon

Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC

A 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

Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis

Aetiology of colorectal cancer and relevance of monogenic inheritance

A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability

EUROCARE-3: survival of cancer patients diagnosed 1990–94—results and commentary

Pathogenesis of colorectal cancer

EUROCARE-3 summary: cancer survival in Europe at the end of the 20th century

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