Lista de obras - Gabriela Möslein - Dominio Público Uruguay

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

artículo científico publicado en 2011

Age-dependent performance of BRAF mutation testing in Lynch syndrome diagnostics

artículo científico publicado en 2020

Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome

scientific article published on 08 January 2020

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 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

Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study

scientific article published on 24 May 2020

Chromosomal instability in MYH- and APC-mutant adenomatous polyps

artículo científico publicado en 2006

Clinical implications of molecular diagnosis in hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2003

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

artículo científico publicado en 2017

Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2.

artículo científico publicado en 2010

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

Cross-species comparison of human and mouse intestinal polyps reveals conserved mechanisms in adenomatous polyposis coli (APC)-driven tumorigenesis

artículo científico publicado en 2008

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

artículo científico publicado en 2008

Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2009

Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue

artículo científico publicado en 2004

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

artículo científico publicado en 2016

Frequency and spectrum of cancers in the Peutz-Jeghers syndrome

artículo científico publicado en 2006

GENETICS. The Human Variome Project

artículo científico publicado en 2008

Gender-Specific Aspects of Lynch Syndrome and Familial Adenomatous Polyposis

artículo científico publicado en 2014

Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH

artículo científico publicado en 2004

How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.

artículo científico publicado en 2010

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

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

scientific article published on 28 February 2019

Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients

artículo científico publicado en 2015

Lynch syndrome: clinical, pathological, and genetic insights ⬇️

artículo científico publicado el 24 de febrero de 2012

Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies

artículo científico publicado en 2011

No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies

artículo científico publicado en 2018

Nuclear Pedigree Criteria of Suspected HNPCC.

artículo científico publicado en 2003

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

scientific article published on July 2008

Preventive surgery for colon cancer in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer syndrome

artículo científico publicado en 2003

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

artículo científico publicado en 2013

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

Surgical considerations in FAP-related pouch surgery: Could we do better?

artículo científico publicado en 2016

The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance

artículo científico publicado en 2020

The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype

artículo científico publicado en 2003

[Current recommendations for surveillance, risk reduction and therapy in Lynch syndrome patients]

scientific article published on 18 November 2019

Lista de obras de Gabriela Möslein

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

Age-dependent performance of BRAF mutation testing in Lynch syndrome diagnostics

Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome

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

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

Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study

Chromosomal instability in MYH- and APC-mutant adenomatous polyps

Clinical implications of molecular diagnosis in hereditary nonpolyposis colorectal cancer

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

Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2.

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

Cross-species comparison of human and mouse intestinal polyps reveals conserved mechanisms in adenomatous polyposis coli (APC)-driven tumorigenesis

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

Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer

Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

Frequency and spectrum of cancers in the Peutz-Jeghers syndrome

GENETICS. The Human Variome Project

Gender-Specific Aspects of Lynch Syndrome and Familial Adenomatous Polyposis

Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH

How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.

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

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients

Lynch syndrome: clinical, pathological, and genetic insights ⬇️

Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies

No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies

Nuclear Pedigree Criteria of Suspected HNPCC.

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

Preventive surgery for colon cancer in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer syndrome

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

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

Surgical considerations in FAP-related pouch surgery: Could we do better?

The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance

The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype

[Current recommendations for surveillance, risk reduction and therapy in Lynch syndrome patients]