Lista de obras - L Bertario - Dominio Público Uruguay

A proposed staging system and stage-specific interventions for familial adenomatous polyposis

artículo científico publicado en 2016

A randomized placebo-controlled prevention trial of aspirin and/or resistant starch in young people with familial adenomatous polyposis

artículo científico publicado en 2011

APC Genotype Is Not a Prognostic Factor in Familial Adenomatous Polyposis Patients With Colorectal Cancer

artículo científico publicado en 2004

APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes.

artículo científico publicado en 2015

Aberrant DNA methylation profiles of inherited and sporadic colorectal cancer.

artículo científico publicado en 2015

Age of onset in familial adenomatous polyposis: heterogeneity within families and among APC mutations.

artículo científico publicado en 1994

BRAF mutation analysis is a valid tool to implement in Lynch syndrome diagnosis in patients classified according to the Bethesda guidelines.

artículo científico publicado en 2014

BRAF mutations in multiple sebaceous hyperplasias of patients belonging to MYH-associated polyposis pedigrees.

artículo científico publicado en 2007

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

artículo científico publicado en 2015

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

artículo científico publicado en 2017

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.

artículo científico publicado en 2013

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

artículo científico publicado en 1996

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

scientific article published on 24 July 2019

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

article by Juul T. Wijnen et al published 20 August 1998 in The New England Journal of Medicine

Colonoscopy in ostomy patients. Results at the first postoperative examination

scientific article published on 01 September 1987

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

artículo científico publicado en 2017

Colorectal carcinoma in children and adolescents: The experience of the Istituto Nazionale Tumori of Milan, Italy

article

Combined use of MLPA and nonfluorescent multiplex PCR analysis by high performance liquid chromatography for the detection of genomic rearrangements

artículo científico publicado en 2006

Comment on Koskenvuo et al.: Risk of cancer and secondary proctectomy after colectomy and ileorectal anastomosis in familial adenomatous polyposis.

artículo científico publicado en 2014

Comment on Ueno et al.: Prevalence of laparoscopic surgical treatment and its clinical outcomes in patients with familial adenomatous polyposis in Japan

artículo científico publicado en 2016

Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal Cancer.

artículo científico publicado en 2015

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

artículo científico publicado en 2020

Cyclooxygenase-2 and platelet-derived growth factor receptors as potential targets in treating aggressive fibromatosis

artículo científico publicado en 2007

Different genetic features associated with colon and rectal carcinogenesis.

artículo científico publicado en 2004

Double versus single stapling technique in rectal anastomosis

artículo científico publicado en 1992

Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome

artículo científico publicado en 2008

Effects of celecoxib on prostanoid biosynthesis and circulating angiogenesis proteins in familial adenomatous polyposis

artículo científico publicado en 2012

Family history, surgery, and APC mutation are risk factors for desmoid tumors in familial adenomatous polyposis: an international cohort study.

artículo científico publicado en 2011

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

artículo científico publicado en 2007

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

artículo científico publicado en 2008

Hepatoblastoma and familial adenomatous polyposis

artículo científico publicado en 1988

Homeodomain-interacting protein kinase-2 restrains cytosolic phospholipase A2-dependent prostaglandin E2 generation in human colorectal cancer cells.

artículo científico publicado en 2006

Human leukocyte antigen class II genes and Helicobacter pylori infection: does genotype overwhelm environmental exposure?

artículo científico publicado en 2003

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

artículo científico publicado en 2007

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

artículo científico publicado en 2016

Integrative analysis of hereditary nonpolyposis colorectal cancer: the contribution of allele-specific expression and other assays to diagnostic algorithms

artículo científico publicado en 2013

Involvement of MBD4 inactivation in mismatch repair-deficient tumorigenesis

artículo científico publicado en 2015

Is laparoscopic surgery an option to support prophylactic colectomy in adolescent patients with Familial Adenomatous Polyposis (FAP)?

artículo científico publicado en 2012

Laparoscopic colectomy and restorative proctocolectomy for familial adenomatous polyposis.

artículo científico publicado en 2010

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

artículo científico publicado en 2011

Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

article

Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis.

artículo científico publicado en 2003

Multiplex Tetra-Primer Amplification Refractory Mutation System PCR to Detect 6 Common Germline Mutations of the MUTYH Gene Associated with Polyposis and Colorectal Cancer

artículo científico publicado en 2006

Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

artículo científico publicado en 2015

PI3KCA/PTEN deregulation contributes to impaired responses to cetuximab in metastatic colorectal cancer patients

artículo científico publicado en 2008

Parity and breast cancer: confirmed evidence of an effect on age at diagnosis

artículo científico publicado en 1982

Pathological features of rectal cancer after preoperative radiochemotherapy

scientific article published on 01 January 1998

Peutz-Jeghers Syndrome After Oral Surgery

scientific article published on 01 August 2009

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

scientific article published on July 2010

Phosphatase Protein Homologue to Tensin Expression and Phosphatidylinositol-3 Phosphate Kinase Mutations in Colorectal Cancer

Predictors of metachronous colorectal neoplasms in sporadic adenoma patients.

artículo científico publicado en 2003

Preoperative radiotherapy for resectable cancer of the middle-distal rectum: its effect on the primary lesion as determined by endorectal ultrasound using flexible echo colonoscope

scientific article published on 01 January 1996

Prevalence of adenomas and hyperplastic polyps in mismatch repair mutation carriers among CAPP2 participants: report by the colorectal adenoma/carcinoma prevention programme 2.

artículo científico publicado en 2008

Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.

artículo científico publicado en 2004

Putative common origin of two MLH1 mutations in Italian-Quebec hereditary non-polyposis colorectal cancer families

article

Quantitative and qualitative characterization of plasma DNA identifies primary and recurrent colorectal cancer

artículo científico publicado en 2008

Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.

artículo científico publicado en 2009

Rectal Cancer Risk in Hereditary Nonpolyposis Colorectal Cancer After Abdominal Colectomy

artículo científico publicado en 1997

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

artículo científico publicado en 2013

Risk of desmoid tumours after open and laparoscopic colectomy in patients with familial adenomatous polyposis

artículo científico publicado en 2014

Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome Database

scientific article published on 18 July 2020

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

artículo científico publicado en 2020

Sensitivity of Hemoccult test for large bowel cancer in high-risk subjects

artículo científico publicado en 1988

Surveillance in hereditary nonpolyposis colorectal cancer

scientific article published on 01 January 1993

Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds

artículo científico publicado en 2009

The familial adenomatous polyposis region exhibits many different haplotypes

artículo científico publicado en 1998

The protocol for a european double-blind trial of aspirin and resistant starch in familial adenomatous polyposis: The capp study

artículo científico publicado en 1995

Tissue localization of TGFalpha and apoptosis are inversely related in colorectal tumors

scientific article published on 22 January 2002

Ultradeep sequencing of a human ultraconserved region reveals somatic and constitutional genomic instability

artículo científico publicado en 2010

Whole exome sequencing and single nucleotide polymorphism array analyses to identify germline alterations in genes associated with testosterone metabolism in a patient with androgen insensitivity syndrome and early-onset colorectal cancer

artículo científico publicado en 2016

Wireless capsule endoscopy in adolescents with familial adenomatous polyposis

artículo científico

Lista de obras de L Bertario

A proposed staging system and stage-specific interventions for familial adenomatous polyposis

A randomized placebo-controlled prevention trial of aspirin and/or resistant starch in young people with familial adenomatous polyposis

APC Genotype Is Not a Prognostic Factor in Familial Adenomatous Polyposis Patients With Colorectal Cancer

APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes.

Aberrant DNA methylation profiles of inherited and sporadic colorectal cancer.

Age of onset in familial adenomatous polyposis: heterogeneity within families and among APC mutations.

BRAF mutation analysis is a valid tool to implement in Lynch syndrome diagnosis in patients classified according to the Bethesda guidelines.

BRAF mutations in multiple sebaceous hyperplasias of patients belonging to MYH-associated polyposis pedigrees.

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

Colonoscopy in ostomy patients. Results at the first postoperative examination

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

Colorectal carcinoma in children and adolescents: The experience of the Istituto Nazionale Tumori of Milan, Italy

Combined use of MLPA and nonfluorescent multiplex PCR analysis by high performance liquid chromatography for the detection of genomic rearrangements

Comment on Koskenvuo et al.: Risk of cancer and secondary proctectomy after colectomy and ileorectal anastomosis in familial adenomatous polyposis.

Comment on Ueno et al.: Prevalence of laparoscopic surgical treatment and its clinical outcomes in patients with familial adenomatous polyposis in Japan

Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal Cancer.

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Cyclooxygenase-2 and platelet-derived growth factor receptors as potential targets in treating aggressive fibromatosis

Different genetic features associated with colon and rectal carcinogenesis.

Double versus single stapling technique in rectal anastomosis

Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome

Effects of celecoxib on prostanoid biosynthesis and circulating angiogenesis proteins in familial adenomatous polyposis

Family history, surgery, and APC mutation are risk factors for desmoid tumors in familial adenomatous polyposis: an international cohort study.

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

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

Hepatoblastoma and familial adenomatous polyposis

Homeodomain-interacting protein kinase-2 restrains cytosolic phospholipase A2-dependent prostaglandin E2 generation in human colorectal cancer cells.

Human leukocyte antigen class II genes and Helicobacter pylori infection: does genotype overwhelm environmental exposure?

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

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

Integrative analysis of hereditary nonpolyposis colorectal cancer: the contribution of allele-specific expression and other assays to diagnostic algorithms

Involvement of MBD4 inactivation in mismatch repair-deficient tumorigenesis

Is laparoscopic surgery an option to support prophylactic colectomy in adolescent patients with Familial Adenomatous Polyposis (FAP)?

Laparoscopic colectomy and restorative proctocolectomy for familial adenomatous polyposis.

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis.

Multiplex Tetra-Primer Amplification Refractory Mutation System PCR to Detect 6 Common Germline Mutations of the MUTYH Gene Associated with Polyposis and Colorectal Cancer

Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

PI3KCA/PTEN deregulation contributes to impaired responses to cetuximab in metastatic colorectal cancer patients

Parity and breast cancer: confirmed evidence of an effect on age at diagnosis

Pathological features of rectal cancer after preoperative radiochemotherapy

Peutz-Jeghers Syndrome After Oral Surgery

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

Phosphatase Protein Homologue to Tensin Expression and Phosphatidylinositol-3 Phosphate Kinase Mutations in Colorectal Cancer

Predictors of metachronous colorectal neoplasms in sporadic adenoma patients.

Preoperative radiotherapy for resectable cancer of the middle-distal rectum: its effect on the primary lesion as determined by endorectal ultrasound using flexible echo colonoscope

Prevalence of adenomas and hyperplastic polyps in mismatch repair mutation carriers among CAPP2 participants: report by the colorectal adenoma/carcinoma prevention programme 2.

Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.

Putative common origin of two MLH1 mutations in Italian-Quebec hereditary non-polyposis colorectal cancer families

Quantitative and qualitative characterization of plasma DNA identifies primary and recurrent colorectal cancer

Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.

Rectal Cancer Risk in Hereditary Nonpolyposis Colorectal Cancer After Abdominal Colectomy

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

Risk of desmoid tumours after open and laparoscopic colectomy in patients with familial adenomatous polyposis

Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome Database

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Sensitivity of Hemoccult test for large bowel cancer in high-risk subjects

Surveillance in hereditary nonpolyposis colorectal cancer

Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds

The familial adenomatous polyposis region exhibits many different haplotypes

The protocol for a european double-blind trial of aspirin and resistant starch in familial adenomatous polyposis: The capp study

Tissue localization of TGFalpha and apoptosis are inversely related in colorectal tumors

Ultradeep sequencing of a human ultraconserved region reveals somatic and constitutional genomic instability

Whole exome sequencing and single nucleotide polymorphism array analyses to identify germline alterations in genes associated with testosterone metabolism in a patient with androgen insensitivity syndrome and early-onset colorectal cancer

Wireless capsule endoscopy in adolescents with familial adenomatous polyposis