Lista de obras - Giovanni Ponti - Dominio Público Uruguay

"Collision" metastasis from unknown primary squamous cell carcinoma and papillary microcarcinoma of thyroid presenting as lateral cervical cystic mass

scientific article published on 10 July 2008

Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome.

artículo científico publicado en 2012

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

article

Attitude of the Italian general population towards prevention and screening of the most common tumors, with special emphasis on colorectal malignancies

article

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

artículo científico publicado en 2007

Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumor.

artículo científico publicado en 2014

Brooke-Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor-suppressor genes.

artículo científico publicado en 2011

Can noninvasive imaging tools potentially predict the risk of ulceration in invasive melanomas showing blue and black colors?

artículo científico publicado en 2013

Cancer-associated genodermatoses: skin neoplasms as clues to hereditary tumor syndromes.

artículo científico

Clinical utility gene card for: Gorlin syndrome--update 2013

artículo científico publicado en 2013

Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas.

artículo científico publicado en 2011

Complete pathological response in a patient with multiple liver metastases from colon cancer treated with Folfox-6 chemotherapy plus bevacizumab: a case report.

artículo científico publicado en 2009

Cytogenetic abnormalities and clinical features in a patient cohort affected by three or more synchronous or metachronous primitive malignancies

artículo científico publicado en 2010

Diagnosis of BCC by multiphoton laser tomography.

artículo científico publicado en 2012

Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome.

artículo científico publicado en 2012

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

artículo científico publicado en 2007

Fluorescence in-situ hybridization and dermoscopy in the assessment of controversial melanocytic tumors

artículo científico

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

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

article

Giuseppe Moscati (1880-1927): a holistic approach to medicine

artículo científico publicado en 2013

Hereditary trichilemmal cysts: a proposal for the assessment of diagnostic clinical criteria

artículo científico publicado en 2012

High magnification digital dermoscopy of basal cell carcinoma: a single-centre study on 400 cases.

artículo científico publicado en 2014

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

Is confocal microscopy a valuable tool in diagnosing nodular lesions? A study of 140 cases.

artículo científico publicado en 2013

Italian Euromelanoma Day Screening Campaign (2005-2007) and the planning of melanoma screening strategies

artículo científico publicado en 2012

Leser-Trélat syndrome in patients affected by six multiple metachronous primitive cancers.

artículo científico publicado en 2010

Malignant and benign tumors associated with multiple primary melanomas: just the starting block for the involvement of MITF, PTEN and CDKN2A in multiple cancerogenesis?

artículo científico publicado en 2013

Malignant melanoma in patients with hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2008

Microsatellite instability and colorectal cancer prognosis.

artículo científico publicado en 2005

Microsatellite instability and mismatch repair protein expression in sebaceous tumors, keratocanthoma, and basal cell carcinomas with sebaceous differentiation in Muir-Torre syndrome.

artículo científico publicado en 2013

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

Muir-Torre syndrome.

artículo científico publicado en 2005

Multiphoton laser tomography and fluorescence lifetime imaging of basal cell carcinoma: morphologic features for non-invasive diagnostics.

artículo científico publicado en 2012

Multiphoton laser tomography and fluorescence lifetime imaging of melanoma: morphologic features and quantitative data for sensitive and specific non-invasive diagnostics

artículo científico publicado en 2013

Multiple primary melanomas versus single melanoma of the head and neck: a comparison of genetic, diagnostic, and therapeutic implications

artículo científico publicado en 2014

Overwhelming response to Dabrafenib in a patient with double BRAF mutation (V600E; V600M) metastatic malignant melanoma

artículo científico publicado en 2012

Patched homolog 1 gene mutation (p.G1093R) induces nevoid basal cell carcinoma syndrome and non-syndromic keratocystic odontogenic tumors: A case report ⬇️

artículo científico publicado el 8 de mayo de 2012

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

artículo científico publicado en 2006

Proteomic analysis of PTCH1+/- fibroblast lysate and conditioned culture media isolated from the skin of healthy subjects and nevoid basal cell carcinoma syndrome patients.

artículo científico publicado en 2013

Quantitative evaluation of healthy epidermis by means of multiphoton microscopy and fluorescence lifetime imaging microscopy

artículo científico publicado en 2011

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

artículo científico publicado en 2004

Reticular grey-blue areas of regression as a dermoscopic marker of melanoma in situ.

artículo científico publicado en 2010

Skeletal and cranio-facial signs in Gorlin syndrome from ancient Egypt to the modern age: sphenoid asymmetry in a patient with a novel PTCH1 mutation

artículo científico publicado en 2014

Stem cell properties in cell cultures from different stage of melanoma progression.

artículo científico publicado en 2014

The dermoscopic variability of pigment network in melanoma in situ

artículo científico publicado en 2012

The somatic affairs of BRAF: tailored therapies for advanced malignant melanoma and orphan non-V600E (V600R-M) mutations.

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

Value and prognostic significance of mitotic rate in a retrospective series of pT1 cutaneous malignant melanoma patients.

artículo científico publicado en 2011

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

Variegated dermoscopy of in situ melanoma

artículo científico publicado en 2012

p16 immunohistochemistry of multiple primary melanomas as screening to identify Familial Melanoma Syndrome

artículo científico publicado en 2011

Lista de obras de Giovanni Ponti

"Collision" metastasis from unknown primary squamous cell carcinoma and papillary microcarcinoma of thyroid presenting as lateral cervical cystic mass

Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome.

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

Attitude of the Italian general population towards prevention and screening of the most common tumors, with special emphasis on colorectal malignancies

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

Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumor.

Brooke-Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor-suppressor genes.

Can noninvasive imaging tools potentially predict the risk of ulceration in invasive melanomas showing blue and black colors?

Cancer-associated genodermatoses: skin neoplasms as clues to hereditary tumor syndromes.

Clinical utility gene card for: Gorlin syndrome--update 2013

Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas.

Complete pathological response in a patient with multiple liver metastases from colon cancer treated with Folfox-6 chemotherapy plus bevacizumab: a case report.

Cytogenetic abnormalities and clinical features in a patient cohort affected by three or more synchronous or metachronous primitive malignancies

Diagnosis of BCC by multiphoton laser tomography.

Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome.

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

Fluorescence in-situ hybridization and dermoscopy in the assessment of controversial melanocytic tumors

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.

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

Giuseppe Moscati (1880-1927): a holistic approach to medicine

Hereditary trichilemmal cysts: a proposal for the assessment of diagnostic clinical criteria

High magnification digital dermoscopy of basal cell carcinoma: a single-centre study on 400 cases.

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.

Is confocal microscopy a valuable tool in diagnosing nodular lesions? A study of 140 cases.

Italian Euromelanoma Day Screening Campaign (2005-2007) and the planning of melanoma screening strategies

Leser-Trélat syndrome in patients affected by six multiple metachronous primitive cancers.

Malignant and benign tumors associated with multiple primary melanomas: just the starting block for the involvement of MITF, PTEN and CDKN2A in multiple cancerogenesis?

Malignant melanoma in patients with hereditary nonpolyposis colorectal cancer

Microsatellite instability and colorectal cancer prognosis.

Microsatellite instability and mismatch repair protein expression in sebaceous tumors, keratocanthoma, and basal cell carcinomas with sebaceous differentiation in Muir-Torre syndrome.

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

Muir-Torre syndrome.

Multiphoton laser tomography and fluorescence lifetime imaging of basal cell carcinoma: morphologic features for non-invasive diagnostics.

Multiphoton laser tomography and fluorescence lifetime imaging of melanoma: morphologic features and quantitative data for sensitive and specific non-invasive diagnostics

Multiple primary melanomas versus single melanoma of the head and neck: a comparison of genetic, diagnostic, and therapeutic implications

Overwhelming response to Dabrafenib in a patient with double BRAF mutation (V600E; V600M) metastatic malignant melanoma

Patched homolog 1 gene mutation (p.G1093R) induces nevoid basal cell carcinoma syndrome and non-syndromic keratocystic odontogenic tumors: A case report ⬇️

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

Proteomic analysis of PTCH1+/- fibroblast lysate and conditioned culture media isolated from the skin of healthy subjects and nevoid basal cell carcinoma syndrome patients.

Quantitative evaluation of healthy epidermis by means of multiphoton microscopy and fluorescence lifetime imaging microscopy

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

Reticular grey-blue areas of regression as a dermoscopic marker of melanoma in situ.

Skeletal and cranio-facial signs in Gorlin syndrome from ancient Egypt to the modern age: sphenoid asymmetry in a patient with a novel PTCH1 mutation

Stem cell properties in cell cultures from different stage of melanoma progression.

The dermoscopic variability of pigment network in melanoma in situ

The somatic affairs of BRAF: tailored therapies for advanced malignant melanoma and orphan non-V600E (V600R-M) mutations.

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

Value and prognostic significance of mitotic rate in a retrospective series of pT1 cutaneous malignant melanoma patients.

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

Variegated dermoscopy of in situ melanoma

p16 immunohistochemistry of multiple primary melanomas as screening to identify Familial Melanoma Syndrome