Lista de obras - Monica Pedroni - Dominio Público Uruguay

A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis.

artículo científico publicado en 2013

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.

artículo científico publicado en 2004

Aberrant crypt foci in colorectal carcinogenesis. Cell and crypt dynamics.

artículo científico publicado en 2000

Aberrant crypt foci in patients with colorectal cancer.

artículo científico publicado en 1998

Aetiology of colorectal cancer and relevance of monogenic inheritance

artículo científico publicado en 2004

An unusual case of familial adenomatous polyposis with very early symptom occurrence.

artículo científico publicado en 2014

Analysis of mismatch repair gene mutations in Turkish HNPCC patients.

artículo científico publicado en 2010

Analysis of telomere dynamics in peripheral blood cells from patients with Lynch syndrome

scientific article published on 08 March 2011

Argyrophilic nucleolar organizer regions and bromodeoxyuridine and3[H]-thymidine labelling indices in colorectal cancer

scientific article published on 01 September 1995

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

article

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

artículo científico publicado en 2007

Cell kinetics evaluation of colorectal tumors afterin vivo administration of bromodeoxyuridine

artículo científico publicado en 1992

Characterization of MLH1 and MSH2 alternative splicing and its relevance to molecular testing of colorectal cancer susceptibility

artículo científico publicado en 1998

Clinical and biologic heterogeneity of hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2001

Clinical and molecular characterization of colorectal cancer in young Moroccan patients.

artículo científico publicado en 2012

Clinical and molecular features of attenuated adenomatous polyposis in northern Italy.

artículo científico publicado en 2012

Clinical features, frequency and prognosis of Dukes' A colorectal carcinoma: A population-based investigation

artículo científico publicado en 1996

Clinical outcome of low- and high-risk malignant colorectal polyps: results of a population-based study and meta-analysis of the available literature.

artículo científico publicado en 2012

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

artículo científico publicado en 2013

Duodenal carcinoma in a 37-year-old man with Cowden/Bannayan syndrome.

artículo científico publicado en 2012

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

artículo científico publicado en 2007

Evaluation of the replication error phenotype in relation to molecular and clinicopathological features in hereditary and early onset colorectal cancer

artículo científico publicado en 1999

Frequency and clinical features of multiple tumors of the large bowel in the general population and in patients with hereditary colorectal carcinoma

artículo científico publicado en 1996

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

scientific article published on 01 September 2007

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

artículo científico publicado en 2004

Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts

article

Genotype-phenotype correlations in individuals with a founder mutation in the MLH1 gene and hereditary non-polyposis colorectal cancer

article

Histology of aberrant crypt foci in the human colon.

artículo científico publicado en 1997

Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas

artículo científico publicado en 2005

Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis.

artículo científico publicado en 2006

Incidence and survival of patients with Dukes' A (stages T1 and T2) colorectal carcinoma: a 15-year population-based study

artículo científico publicado en 2004

Incidence trend of malignant polyps through the data of a specialized colorectal cancer registry: clinical features and effect of screening

artículo científico publicado en 2013

Incidence, clinical features and possible etiology of early onset (≤40 years) colorectal neoplasms

artículo científico publicado en 2013

Investigation of APC mutations in a Turkish familial adenomatous polyposis family by heterodublex analysis.

artículo científico publicado en 2005

K-ras andp53 mutations in hereditary non-polyposis colorectal cancers

artículo científico publicado en 1997

Lanthanide doped upconverting colloidal CaF2 nanoparticles prepared by a single-step hydrothermal method: toward efficient materials with near infrared-to-near infrared upconversion emission

scientific article published on 18 February 2011

Lymph node evaluation in stage IIA colorectal cancer and its impact on patient prognosis: a population-based study.

artículo científico publicado en 2013

MLH1 constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria

artículo científico publicado en 2014

MSH3 protein expression and nodal status in MLH1-deficient colorectal cancers.

artículo científico publicado en 2012

MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events ⬇️

artículo científico publicado en 2013

Methylation pattern of different regions of theMLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer

article

Microsatellite instability and colorectal cancer prognosis.

artículo científico publicado en 2005

Microsatellite instability in multiple colorectal tumors

artículo científico publicado en 1999

Molecular genetic alterations and clinical features in early-onset colorectal carcinomas and their role for the recognition of hereditary cancer syndromes.

artículo científico publicado en 2005

Myeloperoxidase-positive cell infiltration in colorectal carcinogenesis as indicator of colorectal cancer risk

artículo científico publicado en 2008

Problems in the identification of hereditary nonpolyposis colorectal cancer in two families with late development of full-blown clinical spectrum

article

Prognostic significance of histological features and biological parameters in stage I (pT1 and pT2) colorectal adenocarcinoma

artículo científico publicado en 2006

Relationship between MUC5AC and altered expression of MLH1 protein in mucinous and non-mucinous colorectal carcinomas

artículo científico publicado en 2004

Relative role of APC and MUTYH mutations in the pathogenesis of familial adenomatous polyposis.

artículo científico publicado en 2009

Risk of cancer revealed by follow-up of families with hereditary non-polyposis colorectal cancer: A population-based study

artículo científico publicado en 1993

Risk of cancer revealed by follow-up of families with hereditary non-polyposis colorectal cancer: Reply to Dr. Eluf-Neto

scientific article published on 01 May 1995

Th inducing POZ-Kruppel Factor (ThPOK) is a key regulator of the immune response since the early steps of colorectal carcinogenesis

artículo científico publicado en 2013

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

scientific article published on 01 June 2004

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.

artículo científico publicado en 1993

Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas

artículo científico publicado en 2006

Lista de obras de Monica Pedroni

A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis.

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.

Aberrant crypt foci in colorectal carcinogenesis. Cell and crypt dynamics.

Aberrant crypt foci in patients with colorectal cancer.

Aetiology of colorectal cancer and relevance of monogenic inheritance

An unusual case of familial adenomatous polyposis with very early symptom occurrence.

Analysis of mismatch repair gene mutations in Turkish HNPCC patients.

Analysis of telomere dynamics in peripheral blood cells from patients with Lynch syndrome

Argyrophilic nucleolar organizer regions and bromodeoxyuridine and3[H]-thymidine labelling indices in colorectal cancer

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

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

Cell kinetics evaluation of colorectal tumors afterin vivo administration of bromodeoxyuridine

Characterization of MLH1 and MSH2 alternative splicing and its relevance to molecular testing of colorectal cancer susceptibility

Clinical and biologic heterogeneity of hereditary nonpolyposis colorectal cancer

Clinical and molecular characterization of colorectal cancer in young Moroccan patients.

Clinical and molecular features of attenuated adenomatous polyposis in northern Italy.

Clinical features, frequency and prognosis of Dukes' A colorectal carcinoma: A population-based investigation

Clinical outcome of low- and high-risk malignant colorectal polyps: results of a population-based study and meta-analysis of the available literature.

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

Duodenal carcinoma in a 37-year-old man with Cowden/Bannayan syndrome.

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

Evaluation of the replication error phenotype in relation to molecular and clinicopathological features in hereditary and early onset colorectal cancer

Frequency and clinical features of multiple tumors of the large bowel in the general population and in patients with hereditary colorectal carcinoma

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

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

Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts

Genotype-phenotype correlations in individuals with a founder mutation in the MLH1 gene and hereditary non-polyposis colorectal cancer

Histology of aberrant crypt foci in the human colon.

Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas

Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis.

Incidence and survival of patients with Dukes' A (stages T1 and T2) colorectal carcinoma: a 15-year population-based study

Incidence trend of malignant polyps through the data of a specialized colorectal cancer registry: clinical features and effect of screening

Incidence, clinical features and possible etiology of early onset (≤40 years) colorectal neoplasms

Investigation of APC mutations in a Turkish familial adenomatous polyposis family by heterodublex analysis.

K-ras andp53 mutations in hereditary non-polyposis colorectal cancers

Lanthanide doped upconverting colloidal CaF2 nanoparticles prepared by a single-step hydrothermal method: toward efficient materials with near infrared-to-near infrared upconversion emission

Lymph node evaluation in stage IIA colorectal cancer and its impact on patient prognosis: a population-based study.

MLH1 constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria

MSH3 protein expression and nodal status in MLH1-deficient colorectal cancers.

MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events ⬇️

Methylation pattern of different regions of theMLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer

Microsatellite instability and colorectal cancer prognosis.

Microsatellite instability in multiple colorectal tumors

Molecular genetic alterations and clinical features in early-onset colorectal carcinomas and their role for the recognition of hereditary cancer syndromes.

Myeloperoxidase-positive cell infiltration in colorectal carcinogenesis as indicator of colorectal cancer risk

Problems in the identification of hereditary nonpolyposis colorectal cancer in two families with late development of full-blown clinical spectrum

Prognostic significance of histological features and biological parameters in stage I (pT1 and pT2) colorectal adenocarcinoma

Relationship between MUC5AC and altered expression of MLH1 protein in mucinous and non-mucinous colorectal carcinomas

Relative role of APC and MUTYH mutations in the pathogenesis of familial adenomatous polyposis.

Risk of cancer revealed by follow-up of families with hereditary non-polyposis colorectal cancer: A population-based study

Risk of cancer revealed by follow-up of families with hereditary non-polyposis colorectal cancer: Reply to Dr. Eluf-Neto

Th inducing POZ-Kruppel Factor (ThPOK) is a key regulator of the immune response since the early steps of colorectal carcinogenesis

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

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.

Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas