IRIS
RIGOLI, Luciana Concetta
 Distribuzione geografica
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Continente #
NA - Nord America 6.079
EU - Europa 4.060
AS - Asia 3.094
SA - Sud America 1.232
AF - Africa 77
Continente sconosciuto - Info sul continente non disponibili 7
OC - Oceania 4
Totale 14.553
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Nazione #
US - Stati Uniti d'America 5.989
SG - Singapore 1.337
BR - Brasile 1.095
IE - Irlanda 1.044
SE - Svezia 990
CN - Cina 880
HK - Hong Kong 400
DE - Germania 396
IT - Italia 388
UA - Ucraina 316
FI - Finlandia 202
VN - Vietnam 179
GB - Regno Unito 163
RU - Federazione Russa 142
FR - Francia 116
PL - Polonia 91
AR - Argentina 63
IN - India 60
BE - Belgio 52
AT - Austria 41
CA - Canada 36
ZA - Sudafrica 32
IQ - Iraq 31
MX - Messico 31
EC - Ecuador 29
TR - Turchia 27
BD - Bangladesh 24
ES - Italia 22
JP - Giappone 20
MA - Marocco 20
CZ - Repubblica Ceca 18
ID - Indonesia 18
NL - Olanda 17
KZ - Kazakistan 12
IR - Iran 10
LV - Lettonia 10
PK - Pakistan 10
VE - Venezuela 10
AE - Emirati Arabi Uniti 9
CO - Colombia 9
LT - Lituania 9
PE - Perù 9
PT - Portogallo 9
AZ - Azerbaigian 8
JO - Giordania 8
NP - Nepal 8
UZ - Uzbekistan 8
EG - Egitto 7
OM - Oman 7
CL - Cile 6
IL - Israele 6
TN - Tunisia 6
DO - Repubblica Dominicana 5
EU - Europa 5
MD - Moldavia 5
PY - Paraguay 5
AM - Armenia 4
CI - Costa d'Avorio 4
JM - Giamaica 4
TT - Trinidad e Tobago 4
AL - Albania 3
BH - Bahrain 3
BY - Bielorussia 3
CH - Svizzera 3
DK - Danimarca 3
DZ - Algeria 3
HN - Honduras 3
KE - Kenya 3
KG - Kirghizistan 3
KR - Corea 3
LU - Lussemburgo 3
SA - Arabia Saudita 3
UY - Uruguay 3
AU - Australia 2
BG - Bulgaria 2
BO - Bolivia 2
CR - Costa Rica 2
GR - Grecia 2
HU - Ungheria 2
LB - Libano 2
MY - Malesia 2
NI - Nicaragua 2
NO - Norvegia 2
PA - Panama 2
PH - Filippine 2
RO - Romania 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
BS - Bahamas 1
CY - Cipro 1
EE - Estonia 1
GE - Georgia 1
GY - Guiana 1
KW - Kuwait 1
LK - Sri Lanka 1
MN - Mongolia 1
NZ - Nuova Zelanda 1
PF - Polinesia Francese 1
Totale 14.547
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Città #
Dublin 1.043
Chandler 818
Dallas 757
Jacksonville 671
Ashburn 654
Singapore 647
Nyköping 467
Beijing 403
Hong Kong 400
Messina 181
Ann Arbor 171
Princeton 164
Dearborn 163
Medford 152
Cambridge 151
Los Angeles 137
The Dalles 133
Des Moines 126
Boardman 110
New York 109
Munich 99
Warsaw 87
Buffalo 84
São Paulo 74
Ho Chi Minh City 59
Redondo Beach 52
Brussels 50
Woodbridge 49
Tianjin 48
Shenyang 44
Wilmington 43
Jinan 41
Lancaster 41
Moscow 40
San Mateo 37
Vienna 32
Belo Horizonte 31
Frankfurt am Main 31
Rio de Janeiro 30
Hanoi 29
Turku 27
Bremen 26
Houston 25
Stockholm 22
Haikou 21
Nanjing 21
Rome 20
Tokyo 20
Düsseldorf 19
Helsinki 19
Seattle 19
Brasília 18
Porto Alegre 18
Washington 18
Johannesburg 17
Lancenigo-Villorba 17
Santa Clara 17
Zhengzhou 17
Hebei 16
Phoenix 16
Pune 16
Boston 15
Nuremberg 15
San Francisco 15
Strasbourg 15
Atlanta 14
Denver 14
Montreal 14
Taizhou 14
Council Bluffs 13
Hangzhou 13
Brno 12
Curitiba 12
Guangzhou 12
Ningbo 12
Salvador 12
Chicago 11
Dong Ket 11
Guayaquil 11
Orem 11
Brooklyn 10
Changsha 10
Chennai 10
Guarulhos 10
Haiphong 10
Jakarta 10
Juiz de Fora 10
Lauterbourg 10
Manaus 10
Ribeirão Preto 10
Baghdad 9
Campinas 9
Catania 9
Goiânia 9
London 9
Norwalk 9
Poplar 9
Roubaix 9
São José dos Campos 9
Amman 8
Totale 9.302
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Nome #
1ST-PHASE INSULIN-RESPONSE TO INTRAVENOUS GLUCOSE IN CYSTIC- FIBROSIS PATIENTS WITH DIFFERENT DEGREES OF GLUCOSE-TOLERANCE 172
A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1 155
Apolipoprotein AI-CIII-AIV genetic polymorphisms and coronary heart disease in type 2 diabetes mellitus 153
Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject 153
Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease 151
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 142
Allelic association of gene markers on chromosome 11q in Italian families with atopy 141
Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family 136
Allelic association of gene markers in the FC epsilon receptor I beta gene and IL-4 gene promoter in Italian atopic children 136
Anatomo-clinical considerations on early gastric cancer 136
A GENETIC-POLYMORPHISM OF THE APOLIPOPROTEIN AI-CIII GENE- CLUSTER IS ASSOCIATED WITH CORONARY HEART-DISEASE IN NON- INSULIN-DEPENDENT DIABETES-MELLITUS 136
Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and deafness in an Italian family 135
Allelic association of gene markers on chromosome 11q in Italian families with atopy 135
Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies 134
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders 130
Affective Control and Life Satisfaction in Thalassemics 129
Allergen immunotherapy, routes of administration and cytokine networks: an update 127
Molecular analysis of the CART gene in overweight and obese Italian children using family-based association methods. 126
A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting 124
An Atypical Case of Late-Onset Wolfram Syndrome 1 without Diabetes Insipidus 123
Allelic association of gene markers on chromosome 11q in Italian families with atopy 120
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 120
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 119
TLR4 and NOD2/CARD15 genetic polymorphisms and their possible role in gastric carcinogenesis. 118
Molecular analysis of beta-thalassaemia patients in a high incidence area of southern Italy. 117
Identification of a new Beta globin variant (beta133 GTG>ATG) in a family from Messina (Sicily-Italy). 116
Diagnostica molecolare della fibrosi cistica 113
Uteroglobin-related protein 1 gene -112G/a polymorphism and atopic asthma in Sicilian children. 113
Endocrinopathies, metabolic disorders, and iron overload in major and intermedia thalassemia: Serum ferritin as diagnostic and predictive marker associated with liver and cardiac T2* MRI assessment 113
Phagocytosis (cannibalism) of apoptotic neutrophils by tumor cells in gastric micropapillary carcinomas 112
Allelic association of gene markers on chromosome 11q in Italian families with atopy 111
Serum levels of interleukin-18 in splenectomized and nonsplenectomized thalassemic patients: preliminary considerations. 111
Wolfram syndrome and WSF1 gene 111
Concomitant inheritance of globin defects: results of a survey family 111
Modifications of nuclear envelope in tumour cells of human gastric carcinomas: an ultrastructural study 109
Genotoxicity biomarkers in thalassaemic patients 107
Individuato il terzo caso di ipoacusia neurosensoriale bilaterale del gene GJB2 dovuto allamutazione M163V in una popolazione siciliana 105
Neutrophil-rich gastric carcinomas: light and electron microscopic study of 9 cases with particular reference to neutrophil apoptosis. 105
Considerazioni anatomo-cliniche sull'early gastric cancer 105
Apoptotic -like tumor cells and apoptotic neutrophils in mitochondrion-rich gastric adenocarcinomas: a comparative study with light and electron microscopy between these two forms of cell death 105
Morphological evidence of neutrophil-tumor cell phagocytosis (cannibalism) in human gastric adenocarcinomas 104
Microsatellite instability in early gastric cancer 104
Chronic allergic-like inflammation in the tumor stroma of human gastriccarcinomas: an ultrastructural study. 104
Foveolar cells phagocytose apoptotic neutrophils in chronic active Helicobacter pylori gastritis 104
LA SINDROME DI DIGEORGE: PECULIARITÀ CLINICHE E GENETICHE 103
HER2 status in premalignant, early, and advanced neoplastic lesions of the stomach 103
Focal parietal cell differentiation in a well-differentiated (intestinal-type) early gastric cancer 103
Eosinophil-Specific Granules in Tumor Cell Cytoplasm: Unusual Ultrastructural Findings in a Case of Diffuse-Type Gastric Carcinoma 103
Focal parietal cell differentiation in a well-differentiated (intestinal-type) early gastric cancer 101
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 101
Analisi molecolare di pazienti con beta-talassemia in un'area ad alta incidenza del Sud Italia 100
Mutational screening of Italian Wolfram Syndrome patients by DHPLC 100
Coereditarietà di più difetti molecolari dei geni globinici: risultati di una indagine familiare 100
Identification of alpha-thalassemia mutations in subjects from Eastern Sicily(Italy) with abnormal hematological indices and normal Hb A2. 99
A novel mutation of the δ-Globin Gene in an Asymptomatic 30-Year-Old Female 99
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1 99
Eosinophil-tumor cell interaction in advanced gastric carcinoma: An electron microscopic approach 98
Correlation between serum ICAM-1 and oxidative stress in patients with β-thalassemia Major 98
Iron overload and malignancies in patients with haemoglobinopathies: A single center experience 98
Mast cell interaction with tumor cells in small early gastric cancer: Ultrastructural observations 97
Thalassaemia major and infectious risk: High Mobility Group Box-1 represents a novel diagnostic and prognostic biomarker 97
Correlazione fra valori sierici di Icam-1 e stress ossidativo in pazienti con β-talassemia 96
Lysozyme and mucins in gastric adenomas. 95
Molecular analysis of toll-like receptor gene in patients with β-thalassemia 95
Tumor-Associated Neutrophils (TANs) in Gastric Carcinomas: Clinicopathological and Prognostic Implications 95
Analisi del DNA mitocondriale in pazienti con diabete mellito ereditato per via materna associato o no a sordità neurosensoriale 94
Individuato il terzo caso di ipoacusia bilaterale del gene GJB2 dovuto alla mutazione M163V in una popolazione siciliana. 93
Immunohistochemical expression of autophagy-related proteins in advanced tubular gastric adenocarcinomas and its implications 93
Microsatellite instability in early gastric cancer 92
Wolfram syndrome and WFS1 gene 92
Investigation of the eotaxin gene -426C-->T, -384A-->G and 67G-->a single-nucleotide polymorphisms and atopic dermatitis in Italian children using family-based association methods. 91
Wolfram syndrome. Clinical and genetic study in an Italian family 91
APOLIPOPROTEIN-B AND APOLIPOPROTEIN-A-I/C-III GENETIC POLYMORPHISMS AND CORONARY HEART-DISEASE IN DIABETES-MELLITUS 90
Ultrastructural observations on the microvasculature in advanced gastric carcinoma. 90
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 90
Livelli sierici di IL18 in soggetti talassemici splenectomizzati e non 89
Composite early carcinoma (ordinary adenocarcinoma, carcinoid, microglandular-goblet cell carcinoid, neuroendocrine mucinous carcinoma) of the stomach 89
CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome Related Disorders 88
Clinicopathological features of early gastric cancer in younger versus older patients in a high incidence area of northern Italy 87
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia (OMIM 248910) 86
Prevalence of deafness-associated connexin-26 (GJB2) and connexin-30 (GJB6) pathogenic alleles in a large patient cohort from Eastern Sicily 86
Genetic evidence of Helicobacter pylori infection and status of the APC gene in sporadic gastric adenomas 85
Wolfram Syndrome. Clinical and Genetic Study in an Italian Family 85
Morphological and cellular features of innate immune reaction in helicobacter pylori gastritis: A brief review 85
Early identification of cardiovascular involvement in patients with β-thalassemia major 85
Genetic basis of non syndromic hypodontia: a DNA investigation performed on three couples of monozygotic twins about PAX9 mutation 84
Un caso di priapismo in paziente affetto da drepanocitosi 84
Prognostic value of intratumoral neutrophils in advanced gastric carcinoma in a high-risk area in northern Italy 83
Molecular analysis of sequence variants in the Fcepsilon receptor I beta gene andIL-4 gene promoter in Italian atopic families. 83
Microvascular changes in human gastric carcinomas with coagulative necrosis: anultrastructural study. 82
Wolfram syndrome 1 and Wolfram syndrome 2. 82
Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus 81
Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus 81
Early identification of vascular involvement in patients with Beta Thalassaemia: the role of e-tracking 81
TLR2 and TLR4 gene polymorphisms and atopic dermatitis in Italian children: a multicenter study 81
Wolfram syndrome epidemiology: a hot-spot area in north-eastern Sicily 81
RILIEVI MORFOEPIDEMIOLOGICI SUL CARCINOMA GASTRICO CARDIALE 81
Gene-environment interaction in childhood asthma 80
M1 Polarized Tumor-Associated Macrophages (TAMs) as Promising Prognostic Signature in Stage I–II Gastric Adenocarcinomas 80
Mastocitosi, bassa statura, microtia e ipoacusia conduttiva (OMIM 248910): descrizione del terzo caso 79
Totale 10.515
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Categoria #
all - tutte 55.978
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 55.978
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021603 0 0 0 0 0 120 17 86 90 144 85 61
2021/20221.209 14 140 24 41 52 13 80 52 11 264 145 373
2022/20233.022 223 274 157 272 241 300 23 164 1.261 12 77 18
2023/2024736 54 112 44 113 66 183 21 31 5 17 16 74
2024/20253.159 43 36 53 206 111 114 57 636 798 233 327 545
2025/20263.499 488 694 720 705 786 106 0 0 0 0 0 0
Totale 14.835