Giovanni Ponti researcher (ORCID 0000-0002-1971-7306)
Ponti, Giovanni
VIAF ID: 79149842032702842390 ( Personal )
Permalink: http://viaf.org/viaf/79149842032702842390
Preferred Forms
4xx's: Alternate Name Forms (2)
Works
| Title | Sources |
|---|---|
| Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome. |
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| Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations |
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| Attitude of the Italian general population towards prevention and screening of the most common tumors, with special emphasis on colorectal malignancies |
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| BRAF mutations in multiple sebaceous hyperplasias of patients belonging to MYH-associated polyposis pedigrees. |
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| Brooke-Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor-suppressor genes. |
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| Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumor. |
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| Can noninvasive imaging tools potentially predict the risk of ulceration in invasive melanomas showing blue and black colors? |
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| Cancer-associated genodermatoses: skin neoplasms as clues to hereditary tumor syndromes. |
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| Clinical utility gene card for: Gorlin syndrome--update 2013 |
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| Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas. |
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| "Collision" metastasis from unknown primary squamous cell carcinoma and papillary microcarcinoma of thyroid presenting as lateral cervical cystic mass |
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| Complete pathological response in a patient with multiple liver metastases from colon cancer treated with Folfox-6 chemotherapy plus bevacizumab: a case report. |
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| Cytogenetic abnormalities and clinical features in a patient cohort affected by three or more synchronous or metachronous primitive malignancies |
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| Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome. |
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| Dugi put prema upotrebi mikroskopa u kliničkoj medicini in vivo : od prvih pionirskih prijedloga do modernih perspektiva optičke biopsije |
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| Fluorescence in-situ hybridization and dermoscopy in the assessment of controversial melanocytic tumors. |
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| Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC |
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| Giuseppe Moscati (1880-1927): a holistic approach to medicine. |
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| Giuseppe Moscati : a man, a physician and a scientist |
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| Giuseppe Moscati : čovjek, liječnik i znanstvenik |
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| Hereditary trichilemmal cysts: a proposal for the assessment of diagnostic clinical criteria |
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| High magnification digital dermoscopy of basal cell carcinoma: a single-centre study on 400 cases. |
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| Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis. |
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| Innovative use of magnesium oxide in the treatment of "neuralgia of the celiac plexus of rheumatic origin" by G. Moscati in 1923 |
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| Inovativna uporaba magnezijeva oksida u liječenju "neuralgije celijačnog pleksusa reumatoidnog podrijetla" G. Moscatija 1923. |
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| Is confocal microscopy a valuable tool in diagnosing nodular lesions? A study of 140 cases. |
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| Italian Euromelanoma Day Screening Campaign (2005-2007) and the planning of melanoma screening strategies. |
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| Leser-Trélat syndrome in patients affected by six multiple metachronous primitive cancers. |
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| The long road to the use of microscope in clinical medicine in vivo : from early pioneering proposals to the modern perspectives of optical biopsy |
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| Malignant and benign tumors associated with multiple primary melanomas: just the starting block for the involvement of MITF, PTEN and CDKN2A in multiple cancerogenesis? |
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| Malignant melanoma in patients with hereditary nonpolyposis colorectal cancer. |
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| Microsatellite instability and mismatch repair protein expression in sebaceous tumors, keratocanthoma, and basal cell carcinomas with sebaceous differentiation in Muir-Torre syndrome. |
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| Molecular genetic alterations and clinical features in early-onset colorectal carcinomas and their role for the recognition of hereditary cancer syndromes. |
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| Multiphoton laser tomography and fluorescence lifetime imaging of basal cell carcinoma: morphologic features for non-invasive diagnostics. |
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| Multiple primary melanomas versus single melanoma of the head and neck: a comparison of genetic, diagnostic, and therapeutic implications |
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| Overwhelming response to Dabrafenib in a patient with double BRAF mutation (V600E; V600M) metastatic malignant melanoma |
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| p16 immunohistochemistry of multiple primary melanomas as screening to identify Familial Melanoma Syndrome |
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| Prognostic significance of histological features and biological parameters in stage I (pT1 and pT2) colorectal adenocarcinoma |
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| Proteomic analysis of PTCH1+/- fibroblast lysate and conditioned culture media isolated from the skin of healthy subjects and nevoid basal cell carcinoma syndrome patients. |
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| Quantitative evaluation of healthy epidermis by means of multiphoton microscopy and fluorescence lifetime imaging microscopy. |
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| Relationship between MUC5AC and altered expression of MLH1 protein in mucinous and non-mucinous colorectal carcinomas. |
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| 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. |
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| The somatic affairs of BRAF: tailored therapies for advanced malignant melanoma and orphan non-V600E (V600R-M) mutations. |
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| Stem cell properties in cell cultures from different stage of melanoma progression. |
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| Trend of incidence, subsite distribution and staging of colorectal neoplasms in the 15-year experience of a specialised cancer registry |
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| Value and prognostic significance of mitotic rate in a retrospective series of pT1 cutaneous malignant melanoma patients. |
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| Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas |
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| Variegated dermoscopy of in situ melanoma. |
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