Lista de obras - Pedro Lage - Dominio Público Uruguay

APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.

artículo científico publicado en 2009

Aggressive phenotype of MYH-associated polyposis with jejunal cancer and intra-abdominal desmoid tumor: report of a case.

artículo científico publicado en 2009

Association of colonic and endometrial carcinomas in Portuguese families with hereditary nonpolyposis colorectal carcinoma significantly increases the probability of detecting a pathogenic mutation in mismatch repair genes, primarily the MSH2 gene.

artículo científico publicado en 2004

Bethesda criteria for microsatellite instability testing: impact on the detection of new cases of Lynch syndrome

artículo científico publicado en 2012

Colonic cancer in a 34-yr-old woman: should it prompt microsatellite instability studies and mismatch repair gene testing?

article

Colorectal adenomas in young patients: microsatellite instability is not a useful marker to detect new cases of Lynch syndrome

scientific article published on 29 February 2008

Colorectal cancers show distinct mutation spectra in members of the canonical WNT signaling pathway according to their anatomical location and type of genetic instability

artículo científico publicado en 2010

Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status

artículo científico publicado en 2004

Effect of folate supplementation on DNA methylation of rectal mucosa in patients with colonic adenomas: correlation with nutrient intake

artículo científico publicado en 1998

Esophageal stenosis with sloughing esophagitis: A curious manifestation of graft-vs-host disease

artículo científico publicado en 2015

Familial colorectal cancer type X syndrome: two distinct molecular entities?

artículo científico publicado en 2011

Gastric malt lymphoma: Analysis of a series of consecutive patients over 20 years.

artículo científico publicado en 2015

High Rate of Percutaneous Endoscopic Gastrostomy Site Infections Due to Oropharyngeal Colonization

artículo científico publicado en 2006

Management of Portuguese patients with hyperplastic polyposis and screening of at-risk first-degree relatives: a contribution for future guidelines based on a clinical study.

artículo científico publicado en 2004

Pemphigus vulgaris with exclusive involvement of the esophagus: case report and review.

artículo científico publicado en 2004

Serrated polyposis associated with a family history of colorectal cancer and/or polyps: The preferential location of polyps in the colon and rectum defines two molecular entities

artículo científico publicado en 2016

Stents in patients with esophageal cancer before chemoradiotherapy: high risk of complications and no impact on the nutritional status.

artículo científico publicado en 2015

Treatment of gastric MALT lymphoma by Helicobacter pylori eradication: a study controlled by endoscopic ultrasonography

scientific article published on 01 May 1998

Lista de obras de Pedro Lage

APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.

Aggressive phenotype of MYH-associated polyposis with jejunal cancer and intra-abdominal desmoid tumor: report of a case.

Association of colonic and endometrial carcinomas in Portuguese families with hereditary nonpolyposis colorectal carcinoma significantly increases the probability of detecting a pathogenic mutation in mismatch repair genes, primarily the MSH2 gene.

Bethesda criteria for microsatellite instability testing: impact on the detection of new cases of Lynch syndrome

Colonic cancer in a 34-yr-old woman: should it prompt microsatellite instability studies and mismatch repair gene testing?

Colorectal adenomas in young patients: microsatellite instability is not a useful marker to detect new cases of Lynch syndrome

Colorectal cancers show distinct mutation spectra in members of the canonical WNT signaling pathway according to their anatomical location and type of genetic instability

Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status

Effect of folate supplementation on DNA methylation of rectal mucosa in patients with colonic adenomas: correlation with nutrient intake

Esophageal stenosis with sloughing esophagitis: A curious manifestation of graft-vs-host disease

Familial colorectal cancer type X syndrome: two distinct molecular entities?

Gastric malt lymphoma: Analysis of a series of consecutive patients over 20 years.

High Rate of Percutaneous Endoscopic Gastrostomy Site Infections Due to Oropharyngeal Colonization

Management of Portuguese patients with hyperplastic polyposis and screening of at-risk first-degree relatives: a contribution for future guidelines based on a clinical study.

Pemphigus vulgaris with exclusive involvement of the esophagus: case report and review.

Serrated polyposis associated with a family history of colorectal cancer and/or polyps: The preferential location of polyps in the colon and rectum defines two molecular entities

Stents in patients with esophageal cancer before chemoradiotherapy: high risk of complications and no impact on the nutritional status.

Treatment of gastric MALT lymphoma by Helicobacter pylori eradication: a study controlled by endoscopic ultrasonography