PEDRONI, Monica
 Distribuzione geografica
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Continente #
NA - Nord America 17.347
AS - Asia 7.026
EU - Europa 6.208
SA - Sud America 1.010
AF - Africa 141
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 5
Totale 31.747
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Nazione #
US - Stati Uniti d'America 17.151
SG - Singapore 2.685
GB - Regno Unito 2.640
CN - Cina 1.745
HK - Hong Kong 819
BR - Brasile 785
VN - Vietnam 699
SE - Svezia 660
DE - Germania 628
IT - Italia 618
UA - Ucraina 355
FI - Finlandia 326
RU - Federazione Russa 293
TR - Turchia 235
FR - Francia 227
KR - Corea 154
IN - India 138
BG - Bulgaria 130
BD - Bangladesh 93
CA - Canada 83
AR - Argentina 79
IQ - Iraq 72
MX - Messico 70
ID - Indonesia 65
BE - Belgio 56
NL - Olanda 55
JP - Giappone 48
ZA - Sudafrica 45
IE - Irlanda 43
AE - Emirati Arabi Uniti 38
EC - Ecuador 38
CO - Colombia 31
MY - Malesia 29
ES - Italia 28
PK - Pakistan 27
UZ - Uzbekistan 27
PL - Polonia 25
VE - Venezuela 25
PH - Filippine 22
CL - Cile 21
AT - Austria 20
MA - Marocco 17
NP - Nepal 17
CZ - Repubblica Ceca 15
KE - Kenya 14
LT - Lituania 14
TN - Tunisia 14
DZ - Algeria 13
EG - Egitto 13
JO - Giordania 13
TH - Thailandia 11
SA - Arabia Saudita 10
KZ - Kazakistan 9
LV - Lettonia 9
PE - Perù 9
TW - Taiwan 9
UY - Uruguay 9
AZ - Azerbaigian 8
CH - Svizzera 8
IL - Israele 8
AU - Australia 7
BO - Bolivia 7
CR - Costa Rica 7
DO - Repubblica Dominicana 7
PA - Panama 7
PR - Porto Rico 7
PT - Portogallo 7
SY - Repubblica araba siriana 7
AL - Albania 6
ET - Etiopia 6
JM - Giamaica 6
KG - Kirghizistan 6
RO - Romania 6
IR - Iran 5
PS - Palestinian Territory 5
AO - Angola 4
GE - Georgia 4
HR - Croazia 4
HU - Ungheria 4
LK - Sri Lanka 4
NO - Norvegia 4
OM - Oman 4
PY - Paraguay 4
SK - Slovacchia (Repubblica Slovacca) 4
A2 - ???statistics.table.value.countryCode.A2??? 3
BY - Bielorussia 3
DK - Danimarca 3
GT - Guatemala 3
LB - Libano 3
NZ - Nuova Zelanda 3
QA - Qatar 3
RS - Serbia 3
SI - Slovenia 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
EU - Europa 2
GR - Grecia 2
ML - Mali 2
MT - Malta 2
NI - Nicaragua 2
Totale 31.721
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Città #
Southend 2.004
Singapore 1.812
Santa Clara 1.470
Fairfield 1.438
Ashburn 1.400
Woodbridge 1.005
Hong Kong 807
Chandler 768
Houston 768
Chicago 762
Jacksonville 678
Ann Arbor 594
Wilmington 565
Seattle 557
San Jose 520
Dearborn 502
Los Angeles 486
Cambridge 482
Hefei 456
Nyköping 413
Beijing 356
Salt Lake City 309
London 305
Ho Chi Minh City 214
Helsinki 190
Hanoi 185
The Dalles 174
Modena 167
Tampa 155
Elk Grove Village 143
Seoul 143
New York 138
San Diego 138
Council Bluffs 137
Princeton 137
Izmir 126
Sofia 126
Eugene 120
Bremen 104
Lauterbourg 101
Dallas 88
Shanghai 87
Lancaster 85
Munich 82
Buffalo 78
Moscow 74
Frankfurt am Main 73
Sterling 70
São Paulo 67
Columbus 59
Des Moines 54
Miami 54
Orem 54
Milan 50
Fremont 49
Da Nang 44
Brussels 42
Detroit 42
Dublin 42
Dulles 42
Tokyo 38
Jakarta 37
Phoenix 36
Falls Church 35
Atlanta 31
Rio de Janeiro 31
Haiphong 29
Boardman 28
Rome 27
Baghdad 26
Nanjing 26
Turku 26
Chennai 25
Tashkent 25
Guangzhou 24
Mexico City 24
Pittsburgh 23
Dhaka 22
Kunming 22
Brooklyn 21
Hounslow 21
Kansas City 20
Montreal 20
Ottawa 20
Belo Horizonte 19
Norwalk 19
Warsaw 19
Jersey City 18
Quito 18
Denver 17
Grafing 17
San Francisco 17
Toronto 17
Curitiba 16
Philadelphia 16
Changsha 15
Nuremberg 15
Amsterdam 14
Jinan 14
Kent 14
Totale 23.093
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Nome #
Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations. 443
Relationship between MUC5AC and altered expression of MLH1 protein in mucinous and non-mucinous colorectal carcinomas 436
Molecular genetic alterations and clinical features in early-onset colorectal carcinomas and their role for the recognition of hereditary cancer syndromes 434
BRAF mutations in multiple sebaceous hyperplasias of patients belonging to MYH-asociated polyposis pedigrees 423
Myeloperoxidase-positive cell infiltration in colorectal carcinogenesis as indicator of colorectal cancer risk. 419
K-ras and p53 mutations in hereditary non-polyposis colorectal cancers 406
Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or Keratoacanthomas 403
Attenuated polyposis of the large bowel: a morphologic and molecular approach 397
Different phenotypes in Muir-Torre Syndrome: clinical and biomolecular characterization in two italian families 383
Autophagy is upregulated during colorectal carcinogenesis, and in DNA microsatellite stable carcinomas 382
Microsatellite instability in multiple colorectal tumors 380
Molecular features and methylation status in early onset (< 40 years) colorectal cancer: a population based, case-control study 373
Aetiology of colorectal cancer and relevance of monogenic inheritance. 365
Incidence, clinical features and possible etiology of early onset (≤40 years) colorectal neoplasms. 363
Molecular screening for Hereditary Non Polyposis Colorectal Cancer (HNPCC): a prospective, population-based study 362
Analysis of telomere dynamics in peripheral blood cells from patients with Lynch syndrome 360
Aberrant crypt foci in colorectal carcinogenesis. Cell and crypt dynamics 359
Aberrant crypt foci in patients with colorectal cancer 358
Incidence and survival of patients with Dukes' A (stages T1 and T2) colorectal carcinoma: a 15-year population-based study. 357
Argyrophilic nucleolar organizer regions and bromodeoxyuridine and h3-thymidine labelling indices in colorectal cancer 354
Staging and survival of colorectal cancer: are we making progress? The 14-year experience of a Specialized cancer Registry 353
An unusual case of familial adenomatous polyposis with very early symptom occurrence 351
Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC. 349
Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors 341
A mononucleotide markers panel to identify hMLH1/hMSH2 germline mutations 336
Frequency and clinical features of multiple tumors of the large bowel in the general population and in patients with hereditary colorectal carcinoma 334
Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis 334
Histology of aberrant crypt foci in the human colon 329
Relative role of APC and MUTYH mutations in the pathogenesis of familial adenomatous polyposis. 327
Genomic instability and target gene mutations in colon cancers with different degrees of allelic shifts 326
Attenuated adenomatous polyposis of the large bowel: Present and future 318
Small bowel carcinoma in hereditary nonpolyposis colorectal cancer 318
Th Inducing POZ-Kruppel Factor (ThPOK) Is a Key Regulator of the Immune Response since the Early Steps of Colorectal Carcinogenesis 316
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database 313
Epidemiology of colorectal cancer: the 21-year experience of a specialised registry. 313
Problems in the identification of hereditary nonpolyposis colorectal cancer in two families with late development of full-blown clinical spectrum 311
Clinical outcome of low- and high-risk malignant colorectal polyps: results of a population-based study and meta-analysis of the available literature 307
Identification of Muir-Torre Syndrome among patients with sebaceous tumors and keratoacanthomas: role of clinical features, microsatellite instability and immunohistochemistry 305
Biologic characterization of Hereditary Non-Polyposis Colorectal Cancer. Nuclear ploidy, AgNOR count, microvessel distribution, oncogene expression, and grade-related parameters. 303
Aberrant DNA methylation profiles of inherited and sporadic colorectal cancer 298
Myeloperoxidase-positive cell infiltration of normal colorectal mucosa is related to body fatness and is predictive of adenoma occurrence 298
Methylation pattern of different regions of the MLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer. 296
Clinical features, frequency and prognosis of Dukes' a colorectal carcinoma: A population-based investigation 292
Microsatellite instability and colorectal cancer prognosis. 291
Lymph node evaluation in stage IIA colorectal cancer and its impact on patient prognosis: A population-based study 290
Investigation of APC mutations in a Turkish familial adenomatous polyposis family by heterodublex analysis 289
Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis 285
Prognostic significance of histological features and biological parameters in stage I (pT1 and pT2) colorectal adenocarcinoma 282
Prognostic relevance of microsatellite instability in pT3N0M0 colon cancer: a population-based study 280
Evaluation of the replication error phenotype in relation to molecular and clinicopathological features in hereditary and early onset colorectal cancer. 280
Clinical and molecular diagnosis of hereditary non-polyposis colorectal cancer: problems and pitfalls in an extended pedigree 279
Clinical and molecular features of attenuated adenomatous polyposis in northern Italy. 279
Characterization of MLH1 and MSH2 alternative splicing and its relevance to molecular testing of colorectal cancer susceptibility. 271
Risk of colorectal polyps and of malignancies in asymptomatic carriers of mutations in the main DNA mismatch repair genes 271
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. 269
Trend of incidence, subsite distribution and staging of colorectal neoplasms in the 15-year experience of a specialised cancer registry. 269
A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis 265
Colorectal carcinoma in different age groups: A population based investigation 264
I tumori in Italia. Rapporto 2011: La sopravvivenza dei pazienti oncologici in Italia 264
Risk of cancer revealed by follow-up of families with hereditary non-polyposis colorectal cancer: a population-based study 263
Analysis of mismatch repair gene mutations in Turkish HNPCC patients. 262
Diagnosis of hereditary non-polyposis colorectal cancer (HNPCC) [2] (multiple letters) 262
Alternative marker panel for microsatellite instability analysis in detection of constitutional MLH1 and MSH2 mutations. 261
O6-methylguanine-DNA methyltransferase promoter hypermethylation in colorectal carcinogenesis 259
L'immunoistochimica delle proteine del mismatch repair può essere un utile test per identificare i pazienti HNPCC? 255
Genetic testing among high-risk individuals in families with hereditary non polyposis colorectal cancer 253
Biological characterization of mucinous carcinoma of the colon and rectum 253
Incidence trend of malignant polyps through the data of a specialized colorectal cancer registry: clinical features and effect of screening. 253
Clinical and biologic heterogeneity of Hereditary NonPolyposis Colorectal Cancer. 249
MLH1 constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria 242
Overweight, inflammation of normal colorectal mucosa, and cancer risk 240
Alternative marker panel for Microsatellite Instability analysis in deection of contitutional MLH1 and MSH2 mutations. 236
Massive juvenile polyposis of the stomach in a family with SMAD4 gene mutation 235
Epidemiologic and genetic factor in colorectal cancer: development of cancer in dizygotic twins in a family with Lynch syndrome 234
Lack of PMS2 gene-truncating mutations in patients with hereditary colorectal cancer 233
Increased expression of autophagy-related proteins in human colorectal cancer development, and correlation with DNA Microsatellite Stable and Unstable 233
Prognostic relevance of MLH1 and MSH2 mutations in hereditary non-polyposis colorectal cancer patients. 230
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. 225
[Italian cancer figures, report 2010: Cancer prevalence in Italy. Patients living with cancer, long-term survivors and cured patients] 224
Duodenal carcinoma in a 37-year-old man with Cowden/Bannayan syndrome. 223
Clinical and molecular characterization of colorectal cancer in young Moroccan patients 223
Induction of altered cellular response to oxydative stress in HT29 colon cancer cells treated with metformin 220
Italian cancer figures, report 2013: Multiple tumours 219
Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework 215
Il registro dei tumori colorettali 210
Microsatellite instability and prognosis of colorectal cancer 205
Genotype-phenotype correlations in individuals with a founder mutation in the MLH1 gene and hereditary non-polyposis colorectal cancer 204
Cell kinetics evaluation of colorectal tumours after in vivo administration of bromodeoxyuridine 202
HMSH6 immunohistochemistry in patients with clinical suspicion of Hereditary Non-Polyposis Colorectal Cancer. 199
MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events 196
Epidemiology of cancer of the large bowel - The 12-year experience of a specialized registry in Northern Italy 195
Caratterizzazione immunoistochimica e biomolecolare del carcinoma colorettale giovanile 189
Expression of Autophagic and Inflammatory Markers in Normal Mucosa of Individuals with Colorectal Adenomas: A Cross Sectional Study among Italian Outpatients Undergoing Colonoscopy 189
MSH3 protein expression and nodal status in MLH1-deficient colorectal cancers. 187
Microsatellite instability and mismatch-repair protein expression in hereditary and sporadic colorectal carcinogenesis 185
Epidemiologia dei tumori del colon-retto. Incidenza, mortalità, familiarità e sopravvivenza nella ex USL di Modena, 1984-1998. 184
The role of hPMS1 and hPMS2 in predisposing to colorectal cancer 182
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristics 179
Identification and biomolecular characterization of Muir-Torre Syndrome 173
Scanning electron microscopy of aberrant crypt foci in human colorectal mucosa 169
Totale 28.603
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Categoria #
all - tutte 125.065
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 125.065
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021524 0 0 0 0 0 0 0 0 0 282 125 117
2021/20222.332 102 309 201 146 37 111 152 83 229 181 527 254
2022/20232.136 270 252 163 208 289 326 38 189 235 21 74 71
2023/20241.327 47 68 90 86 340 155 135 165 27 12 62 140
2024/20255.084 156 51 83 346 1.069 785 442 311 536 161 496 648
2025/202610.813 615 332 737 1.749 3.386 642 1.224 480 883 765 0 0
Totale 31.879