| Nome |
# |
|
Non-blood sources of cell-free DNA for cancer molecular profiling in clinical pathology and oncology, file e31e124d-bd00-987f-e053-3705fe0a095a
|
1.363
|
|
Microsatellite instability, immunohistochemistry and germline mismatch repair gene mutations for the diagnosis of Muir-Torre syndrome in immunosuppressed patients, file e31e124b-c072-987f-e053-3705fe0a095a
|
1.352
|
|
Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome, file e31e124b-bede-987f-e053-3705fe0a095a
|
861
|
|
Quick assessment of cell-free DNA in seminal fluid and fragment size for early non-invasive prostate cancer diagnosis, file e31e124d-b8fd-987f-e053-3705fe0a095a
|
679
|
|
Skeletal stigmata as keys to access to the composite and ancient Gorlin-Goltz syndrome history: The Egypt, Pompeii and Herculaneum lessons, file e31e124b-b417-987f-e053-3705fe0a095a
|
483
|
|
Wall paintings facies and their possible genetic correlates in the ancient Pompeii: A bio-anthropologic message from the past?, file e31e124b-b415-987f-e053-3705fe0a095a
|
441
|
|
Giuseppe Moscati: a man, a physician and a scientist, file e31e124e-166a-987f-e053-3705fe0a095a
|
342
|
|
Role of microsatellite instability, immunohistochemistry and Mismatch Repair germline aberrations in immunosuppressed transplant patients: a phenocopy dilemma in Muir-Torre Syndrome., file e31e124b-b9e5-987f-e053-3705fe0a095a
|
330
|
|
BRAFp.V600E, p.V600K, and p.V600R Mutations in Malignant Melanoma: Do They Also Differ in Immunohistochemical Assessment and Clinical Features?, file e31e124b-b9ea-987f-e053-3705fe0a095a
|
247
|
|
Novel PTCH1 Mutations in Patients with Keratocystic Odontogenic Tumors Screened for Nevoid Basal Cell Carcinoma (NBCC) Syndrome., file e31e124a-a342-987f-e053-3705fe0a095a
|
214
|
|
Grey-blue regression in melanoma in situ-evaluation on 111 cases., file e31e124a-abee-987f-e053-3705fe0a095a
|
190
|
|
Multiphoton laser tomography and fluorescence lifetime imaging of melanoma: morphologic features and quantitative data for sensitive and specific non-invasive diagnostics., file e31e124a-a5e5-987f-e053-3705fe0a095a
|
185
|
|
BRAF
,NRASandC-KITAdvanced Melanoma: Clinico-pathological Features, Targeted-Therapy Strategies and Survival, file e31e124e-b40e-987f-e053-3705fe0a095a
|
175
|
|
Hereditary trichilemmal cysts: a proposal for the assessment of diagnostic clinical criteria, file e31e124e-e095-987f-e053-3705fe0a095a
|
172
|
|
Clinical, pathological and dermoscopic phenotype of MITF p.E318K carrier cutaneous melanoma patients, file e31e124e-3bfe-987f-e053-3705fe0a095a
|
170
|
|
Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients, file e31e124e-e245-987f-e053-3705fe0a095a
|
168
|
|
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, file e31e124e-fa2e-987f-e053-3705fe0a095a
|
167
|
|
Overwhelming response to Dabrafenib in a patient with double BRAF mutation (V600E; V600M) metastatic malignant melanoma, file e31e124a-a4ae-987f-e053-3705fe0a095a
|
160
|
|
A mononucleotide markers panel to identify hMLH1/hMSH2 germline mutations., file e31e124a-ab7f-987f-e053-3705fe0a095a
|
156
|
|
Mutazioni somatiche di BRAF in pazienti affetti da melanoma maligno metastatico ed efficacia clinica degli approcci terapeutici a bersaglio molecolare con inibitori di BRAF, file e31e124e-6e34-987f-e053-3705fe0a095a
|
155
|
|
Innovative use of magnesium oxide in the treatment of "neuralgia of the celiac plexus of rheumatic origin" by G. Moscati in 1923, file e31e124e-14b4-987f-e053-3705fe0a095a
|
148
|
|
Non-blood sources of cell-free DNA for cancer molecular profiling in clinical pathology and oncology, file e31e1250-2783-987f-e053-3705fe0a095a
|
148
|
|
Congenital Glioblastoma multiforme and eruptive disseminated Spitz nevi, file e31e124e-a9b0-987f-e053-3705fe0a095a
|
141
|
|
NF1 truncating mutations associated to aggressive clinical phenotype with elephantiasis neuromatosa and solid malignancies, file e31e124e-e24a-987f-e053-3705fe0a095a
|
139
|
|
Desmoplastic melanoma: a challenge for the oncologist, file e31e124b-bae5-987f-e053-3705fe0a095a
|
132
|
|
High Magnification Digital Dermoscopy of Basal Cell Carcinoma: A Single-centre Study on 400 cases., file e31e124d-ee27-987f-e053-3705fe0a095a
|
130
|
|
PTCH1 germline mutations and the basaloid follicular hamartoma values in the tumor spectrum of basal cell carcinoma syndrome (NBCCS), file e31e124e-ac62-987f-e053-3705fe0a095a
|
128
|
|
Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I, file e31e1250-0a5e-987f-e053-3705fe0a095a
|
124
|
|
Insights into Genetic Susceptibility to Melanoma by Gene Panel Testing: Potential Pathogenic Variants in ACD, ATM, BAP1, and POT1, file e31e124e-70e9-987f-e053-3705fe0a095a
|
122
|
|
Immunohistochemical mismatch repair proteins expression as a tool to predict the melanoma immunotherapy response, file e31e124d-f529-987f-e053-3705fe0a095a
|
120
|
|
Giant elephantiasis neuromatosa in the setting of neurofibromatosis type 1: A case report, file e31e124e-a9ae-987f-e053-3705fe0a095a
|
118
|
|
Complete pathological response in a patient with multiple liver metastases from colon cancer treated with Folfox-6 chemotherapy plus bevacizumab: a case report, file e31e124a-a2d0-987f-e053-3705fe0a095a
|
117
|
|
Leser-Trélat syndrome in patients affected by six multiple metachronous primitive cancers., file e31e124a-aba0-987f-e053-3705fe0a095a
|
114
|
|
Proteomic Analysis of PTCH1+/- Fibroblast Lysate and Conditioned Culture Media Isolated from the Skin of Healthy Subjects and Nevoid Basal Cell Carcinoma Syndrome Patients., file e31e124b-21a3-987f-e053-3705fe0a095a
|
105
|
|
Molecular Targeted Approaches for Advanced BRAF V600, N-RAS, c-KIT, and GNAQ Melanomas, file e31e124e-0afb-987f-e053-3705fe0a095a
|
105
|
|
Fibroepithelioma of Pinkus: Solitary tumor or sign of a complex gastrointestinal syndrome, file e31e124e-e418-987f-e053-3705fe0a095a
|
103
|
|
Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report, file e31e124e-a7e6-987f-e053-3705fe0a095a
|
91
|
|
Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas., file e31e124a-ab7d-987f-e053-3705fe0a095a
|
82
|
|
Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome, file e31e124e-e241-987f-e053-3705fe0a095a
|
82
|
|
M09Quantification of circulating cell-free DNA by fluorimetry (Qubit) and spectrophotometry (NanoDrop) in patients with malignant melanoma and prostate cancer, file e31e124f-b75a-987f-e053-3705fe0a095a
|
77
|
|
Erratum: Molecular targeted approaches for advanced BRAF V600, N-RAS, c-KIT, and GNAQ melanoma (Disease Markers), file e31e124e-0d9f-987f-e053-3705fe0a095a
|
73
|
|
Caso di Neurofibromatosi diagnosticata a 71 anni, file e31e124e-6e30-987f-e053-3705fe0a095a
|
56
|
|
Sphenoid asymmetry associated to other skeletal anomalies in a clear cut case of PTCH1 mutated Gorlin-Goltz syndrome: a novel finding?, file e31e124e-6e3d-987f-e053-3705fe0a095a
|
26
|
|
The long road to the use of microscope in clinical medicine in vivo: From early pioneering proposals to the modern perspectives of optical biopsy, file 39f15393-d1f5-4bd7-875d-5f5dfd296843
|
18
|
|
Are the neck malignant melanomas different from the ones affecting the head? Clinicopathologic, dermoscopic and prognostic findings, file e31e124e-a7f3-987f-e053-3705fe0a095a
|
18
|
|
BRAFV600E mutated and wild type melanomas: dermoscopy and reflectance confocal microscopy characterization, file e31e124e-474b-987f-e053-3705fe0a095a
|
13
|
|
COVID-19 spreading across world correlates with C677T allele of the methylenetetrahydrofolate reductase (MTHFR) gene prevalence, file f43a2925-498f-4b0d-8642-367aebaa455e
|
7
|
|
Stem cell properties in cell cultures from different stage of melanoma progression., file 9ee7385b-6450-4fa3-8c6e-61b0c1a7d2e8
|
5
|
|
Quantitative evaluation of healthy epidermis by means of multiphoton microscopy and fluorescence lifetime imaging microscopy, file e31e124a-ad56-987f-e053-3705fe0a095a
|
5
|
|
Fluorescence in-situ hybridization and dermoscopy in the assessment of controversial melanocytic tumors., file 172a1cef-f9af-4a00-be21-85b6736dea66
|
4
|
|
Proteomic analysis of PTCH1+/- fibroblast lysate and conditioned culture media isolated from the skin of healthy subjects and Nevoid Basal Cell Carcinoma Syndrome (NBCCS) patients., file e31e124a-a8c6-987f-e053-3705fe0a095a
|
4
|
|
Variegated Dermoscopy of in situ Melanoma., file e31e124a-ab7c-987f-e053-3705fe0a095a
|
4
|
|
Seminal Cell-Free DNA Assessment as a Novel Prostate Cancer Biomarker, file e31e124d-5006-987f-e053-3705fe0a095a
|
4
|
|
Italian Euromelanoma Day Screening Campaign (2005-2007) and the planning of melanoma screening strategies., file d9c01f36-35e2-4c6a-a360-4f9b3779bc67
|
3
|
|
Genetic testing among high-risk individuals in families with hereditary non polyposis colorectal cancer, file e31e124a-abed-987f-e053-3705fe0a095a
|
3
|
|
Clinical application of lung ultrasound score on COVID-19 setting: A regional experience in Southern Italy, file d2efa992-56fc-4465-86c5-c3fa555df822
|
2
|
|
Muir-Torre syndrome, file e31e124a-95fc-987f-e053-3705fe0a095a
|
2
|
|
Wnt pathway, angiogenetic and hormonal markers in sporadic and familial adenomatous polyposis-associated juvenile nasopharyngeal angiofibromas (JNA), file e31e124a-9ab1-987f-e053-3705fe0a095a
|
2
|
|
Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or Keratoacanthomas, file e31e124a-9e8e-987f-e053-3705fe0a095a
|
2
|
|
BRAF mutations in multiple sebaceous hyperplasias of patients belonging to MYH-asociated polyposis pedigrees, file e31e124a-9f9e-987f-e053-3705fe0a095a
|
2
|
|
Different phenotypes in Muir-Torre Syndrome: clinical and biomolecular characterization in two italian families, file e31e124a-9fd6-987f-e053-3705fe0a095a
|
2
|
|
Malignant and benign tumors associated to multiple primary melanomas: just the starting block for the involvement of MITF, PTEN and CDKN2A in multiple cancerogenesis?, file e31e124a-a4b9-987f-e053-3705fe0a095a
|
2
|
|
Identification of Muir-Torre Syndrome among patients with sebaceous tumors and keratoacanthomas: role of clinical features, microsatellite instability and immunohistochemistry, file e31e124a-a9f4-987f-e053-3705fe0a095a
|
2
|
|
Italian Euromelanoma Day Screening Campaign (2005-2007) and the planning of melanoma screening strategies., file e31e124a-ab78-987f-e053-3705fe0a095a
|
2
|
|
The impact of histopathologic diagnosis on the proper management of testis neoplasms., file e31e124a-ab7e-987f-e053-3705fe0a095a
|
2
|
|
Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis, file e31e124a-ab82-987f-e053-3705fe0a095a
|
2
|
|
Cytogenetic abnormalities and clinical features in a patient cohort affected by three or more synchronous or metachronous primitive malignancies., file e31e124a-aba1-987f-e053-3705fe0a095a
|
2
|
|
Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumor, file e31e124b-d499-987f-e053-3705fe0a095a
|
2
|
|
Dabrafenib-trametinib combination in 'field-practice': An Italian experience, file e31e124e-9ab9-987f-e053-3705fe0a095a
|
2
|
|
Relationship between MUC5AC and altered expression of MLH1 protein in mucinous and non-mucinous colorectal carcinomas, file e31e124a-969b-987f-e053-3705fe0a095a
|
1
|
|
Aetiology of colorectal cancer and relevance of monogenic inheritance., file e31e124a-9d8a-987f-e053-3705fe0a095a
|
1
|
|
Attitude of the Italian general population towards prevention and screening of the most common tumors, with special emphasis on colorectal malignancies., file e31e124a-9ded-987f-e053-3705fe0a095a
|
1
|
|
Malignant melanoma in patients with hereditary nonpolyposis colorectal cancer, file e31e124a-9f20-987f-e053-3705fe0a095a
|
1
|
|
Gastrointestinal stromal tumor and other primary metachronous and synchronous neoplasms as a suspicious criterion for syndromic setting, file e31e124a-a2cf-987f-e053-3705fe0a095a
|
1
|
|
High resolution diagnosis of common nevi by multiphoton laser tomography and fluorescence lifetime imaging., file e31e124a-a3ec-987f-e053-3705fe0a095a
|
1
|
|
Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations., file e31e124a-a9f3-987f-e053-3705fe0a095a
|
1
|
|
Cancer-associated genodermatoses: Skin neoplasms as clues to hereditary tumor syndromes., file e31e124a-ab74-987f-e053-3705fe0a095a
|
1
|
|
Diagnosis of BCC by multiphoton laser tomography., file e31e124a-ab77-987f-e053-3705fe0a095a
|
1
|
|
Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basal cell carcinoma (Gorlin) syndrome., file e31e124a-ab7b-987f-e053-3705fe0a095a
|
1
|
|
Epidemiology of colorectal cancer: the 21-year experience of a specialised registry., file e31e124a-ab80-987f-e053-3705fe0a095a
|
1
|
|
Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC., file e31e124a-ab81-987f-e053-3705fe0a095a
|
1
|
|
Incidence and survival of patients with Dukes' A (stages T1 and T2) colorectal carcinoma: a 15-year population-based study., file e31e124a-abea-987f-e053-3705fe0a095a
|
1
|
|
Molecular genetic alterations and clinical features in early-onset colorectal carcinomas and their role for the recognition of hereditary cancer syndromes., file e31e124a-abeb-987f-e053-3705fe0a095a
|
1
|
|
Value and prognostic significance of mitotic rate in a retrospective series of pT1 cutaneous malignant melanoma patients, file e31e124a-ad55-987f-e053-3705fe0a095a
|
1
|
|
Microsatellite instability and colorectal cancer prognosis., file e31e124a-ad7b-987f-e053-3705fe0a095a
|
1
|
|
Reticular grey-blue areas of regression as a dermoscopic marker of melanoma in situ., file e31e124a-af09-987f-e053-3705fe0a095a
|
1
|
|
The value of fluorimetry (Qubit) and spectrophotometry (NanoDrop) in the quantification of cell-free DNA (cfDNA) in malignant melanoma and prostate cancer patients, file e31e124d-12d1-987f-e053-3705fe0a095a
|
1
|
|
Seminal cell-free DNA molecular profile as a novel diagnostic and prognostic prostate cancer biomarkers, file e31e124d-491c-987f-e053-3705fe0a095a
|
1
|
|
Quick assessment of cell-free DNA in seminal fluid and fragment size for early non-invasive prostate cancer diagnosis, file e31e124f-7d5f-987f-e053-3705fe0a095a
|
1
|
|
Fordyce granules and hyperplastic mucosal sebaceous glands as distinctive stigmata in Muir-Torre syndrome patients: characterization with reflectance confocal microscopy, file e31e124f-825e-987f-e053-3705fe0a095a
|
1
|
| Totale |
10.628 |
