IRIS
RIGOLI, Luciana Concetta
 Distribuzione geografica
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Continente #
NA - Nord America 3.946
EU - Europa 3.426
AS - Asia 1.064
SA - Sud America 6
Continente sconosciuto - Info sul continente non disponibili 5
AF - Africa 1
OC - Oceania 1
Totale 8.449
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Nazione #
US - Stati Uniti d'America 3.941
IE - Irlanda 1.035
SE - Svezia 967
CN - Cina 566
SG - Singapore 427
IT - Italia 340
UA - Ucraina 306
DE - Germania 246
FI - Finlandia 172
GB - Regno Unito 117
PL - Polonia 56
BE - Belgio 52
FR - Francia 51
IN - India 30
AT - Austria 23
CZ - Repubblica Ceca 12
RU - Federazione Russa 12
VN - Vietnam 11
ID - Indonesia 10
NL - Olanda 10
PT - Portogallo 8
IR - Iran 7
CA - Canada 5
ES - Italia 5
EU - Europa 5
LV - Lettonia 4
DK - Danimarca 3
IQ - Iraq 3
KR - Corea 3
CH - Svizzera 2
EC - Ecuador 2
IL - Israele 2
AR - Argentina 1
AU - Australia 1
BD - Bangladesh 1
BG - Bulgaria 1
BR - Brasile 1
CY - Cipro 1
HU - Ungheria 1
LU - Lussemburgo 1
MA - Marocco 1
MD - Moldavia 1
NO - Norvegia 1
OM - Oman 1
PE - Perù 1
PH - Filippine 1
SA - Arabia Saudita 1
VE - Venezuela 1
Totale 8.449
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Città #
Dublin 1.035
Chandler 818
Jacksonville 670
Nyköping 465
Singapore 350
Ashburn 252
Beijing 246
Messina 177
Ann Arbor 171
Dearborn 163
Princeton 163
Medford 151
Cambridge 149
Des Moines 125
Boardman 110
New York 66
Warsaw 56
Brussels 50
Woodbridge 49
Wilmington 43
Shenyang 42
Jinan 41
Lancaster 41
San Mateo 36
Bremen 26
Los Angeles 24
Vienna 23
Haikou 21
Tianjin 21
Nanjing 20
Helsinki 19
Washington 18
Lancenigo-Villorba 17
Zhengzhou 17
Hebei 16
Houston 16
Pune 16
Strasbourg 15
Seattle 14
Taizhou 14
Munich 13
Brno 12
Hangzhou 12
Ningbo 12
Dong Ket 11
Guangzhou 10
Jakarta 10
Norwalk 9
Catania 8
Changsha 8
Rome 8
Ardabil 7
Augusta 7
Hyderabad 7
Rosolini 7
Barga 6
Fuzhou 6
Nanchang 6
Auburn Hills 5
Kunming 5
Taiyuan 5
Espoo 4
Falls Church 4
Kemerovo 4
Lanzhou 4
Lappeenranta 4
Tappahannock 4
Amsterdam 3
Clearwater 3
Jiaxing 3
Leawood 3
Milan 3
Phoenix 3
Riposto 3
Shanghai 3
Bronte 2
Butera 2
Caltanissetta 2
Casalecchio di Reno 2
Chengdu 2
Hefei 2
Jeffries 2
Langfang 2
Machachi 2
Madrid 2
Marseille 2
Monmouth Junction 2
Montréal 2
Riva 2
Saint Louis 2
Torre del Greco 2
Vanløse 2
Waanrode 2
Xiangfen 2
Zurich 2
Arbus 1
Atlanta 1
Bangalore 1
Belovo 1
Bitonto 1
Totale 6.033
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Nome #
Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject 99
Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease 91
Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and deafness in an Italian family 85
Identification of a new Beta globin variant (beta133 GTG>ATG) in a family from Messina (Sicily-Italy). 82
Phagocytosis (cannibalism) of apoptotic neutrophils by tumor cells in gastric micropapillary carcinomas 82
Molecular analysis of the CART gene in overweight and obese Italian children using family-based association methods. 81
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 80
Serum levels of interleukin-18 in splenectomized and nonsplenectomized thalassemic patients: preliminary considerations. 78
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 78
Apolipoprotein AI-CIII-AIV genetic polymorphisms and coronary heart disease in type 2 diabetes mellitus 77
Allelic association of gene markers on chromosome 11q in Italian families with atopy 77
Allergen immunotherapy, routes of administration and cytokine networks: an update 77
Allelic association of gene markers on chromosome 11q in Italian families with atopy 76
Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family 75
Anatomo-clinical considerations on early gastric cancer 75
Identification of alpha-thalassemia mutations in subjects from Eastern Sicily(Italy) with abnormal hematological indices and normal Hb A2. 74
A GENETIC-POLYMORPHISM OF THE APOLIPOPROTEIN AI-CIII GENE- CLUSTER IS ASSOCIATED WITH CORONARY HEART-DISEASE IN NON- INSULIN-DEPENDENT DIABETES-MELLITUS 74
Concomitant inheritance of globin defects: results of a survey family 74
Wolfram syndrome and WSF1 gene 73
Diagnostica molecolare della fibrosi cistica 73
Modifications of nuclear envelope in tumour cells of human gastric carcinomas: an ultrastructural study 72
TLR4 and NOD2/CARD15 genetic polymorphisms and their possible role in gastric carcinogenesis. 72
Tumor-Associated Neutrophils (TANs) in Gastric Carcinomas: Clinicopathological and Prognostic Implications 71
Allelic association of gene markers on chromosome 11q in Italian families with atopy 70
1ST-PHASE INSULIN-RESPONSE TO INTRAVENOUS GLUCOSE IN CYSTIC- FIBROSIS PATIENTS WITH DIFFERENT DEGREES OF GLUCOSE-TOLERANCE 70
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 70
Individuato il terzo caso di ipoacusia neurosensoriale bilaterale del gene GJB2 dovuto allamutazione M163V in una popolazione siciliana 69
Uteroglobin-related protein 1 gene -112G/a polymorphism and atopic asthma in Sicilian children. 69
Morphological evidence of neutrophil-tumor cell phagocytosis (cannibalism) in human gastric adenocarcinomas 67
Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies 66
Prevalence of deafness-associated connexin-26 (GJB2) and connexin-30 (GJB6) pathogenic alleles in a large patient cohort from Eastern Sicily 65
Immunohistochemical expression of autophagy-related proteins in advanced tubular gastric adenocarcinomas and its implications 65
Analisi molecolare di pazienti con beta-talassemia in un'area ad alta incidenza del Sud Italia 64
Mutational screening of Italian Wolfram Syndrome patients by DHPLC 64
Lysozyme and mucins in gastric adenomas. 64
Microsatellite instability in early gastric cancer 64
Correlation between serum ICAM-1 and oxidative stress in patients with β-thalassemia Major 64
Thalassaemia major and infectious risk: High Mobility Group Box-1 represents a novel diagnostic and prognostic biomarker 64
null 63
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 63
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 63
Genotoxicity biomarkers in thalassaemic patients 63
Molecular analysis of beta-thalassaemia patients in a high incidence area of southern Italy. 63
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 63
Allelic association of gene markers in the FC epsilon receptor I beta gene and IL-4 gene promoter in Italian atopic children 62
Gastric adenomas: relationship between clinicopathological findings, Helicobacter pylori infection, APC mutations and COX-2 expression 62
Mast cell interaction with tumor cells in small early gastric cancer: Ultrastructural observations 62
Genetic evidence of Helicobacter pylori infection and status of the APC gene in sporadic gastric adenomas 60
Prognostic value of intratumoral neutrophils in advanced gastric carcinoma in a high-risk area in northern Italy 60
Clinicopathological features of early gastric cancer in younger versus older patients in a high incidence area of northern Italy 60
Ultrastructural observations on the microvasculature in advanced gastric carcinoma. 60
Eosinophil-tumor cell interaction in advanced gastric carcinoma: An electron microscopic approach 60
Wolfram Syndrome. Clinical and Genetic Study in an Italian Family 60
TLR2 and TLR4 gene polymorphisms and atopic dermatitis in Italian children: a multicenter study 60
Neutrophil-rich gastric carcinomas: light and electron microscopic study of 9 cases with particular reference to neutrophil apoptosis. 60
HER2 status in premalignant, early, and advanced neoplastic lesions of the stomach 60
Livelli sierici di IL18 in soggetti talassemici splenectomizzati e non 59
APOLIPOPROTEIN-B AND APOLIPOPROTEIN-A-I/C-III GENETIC POLYMORPHISMS AND CORONARY HEART-DISEASE IN DIABETES-MELLITUS 59
Eosinophil-Specific Granules in Tumor Cell Cytoplasm: Unusual Ultrastructural Findings in a Case of Diffuse-Type Gastric Carcinoma 59
Somatic mitochondrial mutation in early gastric cancer 58
Focal parietal cell differentiation in a well-differentiated (intestinal-type) early gastric cancer 58
Wolfram syndrome. Clinical and genetic study in an Italian family 58
Individuato il terzo caso di ipoacusia bilaterale del gene GJB2 dovuto alla mutazione M163V in una popolazione siciliana. 58
Un caso di priapismo in paziente affetto da drepanocitosi 58
Molecular analysis of toll-like receptor gene in patients with β-thalassemia 58
Mastocitosi, bassa statura, microtia e ipoacusia conduttiva (OMIM 248910): descrizione del terzo caso 57
Molecular analysis of sequence variants in the Fcepsilon receptor I beta gene andIL-4 gene promoter in Italian atopic families. 57
Microsatellite instability in early gastric cancer 56
Foveolar cells phagocytose apoptotic neutrophils in chronic active Helicobacter pylori gastritis 56
An Atypical Case of Late-Onset Wolfram Syndrome 1 without Diabetes Insipidus 55
Infezione da Helicobacter Pylori e alterazioni genetiche del gene APC in adenoma gastrico sporadico 55
Allelic association of gene markers on chromosome 11q in Italian families with atopy 55
Genetic evidence of Helicobacter pylori infection and status of the APC gene in sporadic gastric adenomas 55
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. 55
LA SINDROME DI DIGEORGE: PECULIARITÀ CLINICHE E GENETICHE 55
Composite early carcinoma (ordinary adenocarcinoma, carcinoid, microglandular-goblet cell carcinoid, neuroendocrine mucinous carcinoma) of the stomach 55
Coereditarietà di più difetti molecolari dei geni globinici: risultati di una indagine familiare 55
Analisi del DNA mitocondriale in pazienti con diabete mellito ereditato per via materna associato o no a sordità neurosensoriale 54
Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus 54
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia (OMIM 248910) 54
Iron overload and malignancies in patients with haemoglobinopathies: A single center experience 54
A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting 53
CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome Related Disorders 53
The role of the incidence of genetic adnormalities on the onset and on the results of the surgical repair of varicocele 53
Chronic allergic-like inflammation in the tumor stroma of human gastriccarcinomas: an ultrastructural study. 53
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 53
Oncogeni e cancro gastrico. 52
Mitochondrial 3243 BP mutation: A case report 52
Correlazione fra valori sierici di Icam-1 e stress ossidativo in pazienti con β-talassemia 52
Morphological and cellular features of innate immune reaction in helicobacter pylori gastritis: A brief review 52
A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1 51
Considerazioni anatomo-cliniche sull'early gastric cancer 51
Focal parietal cell differentiation in a well-differentiated (intestinal-type) early gastric cancer 51
Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1 51
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders 50
La disfunzione multipla di organo nell'asfissia perinatale: aspetti clinico-metabolici, emoreologici e neurosonologici 49
Immunohistochemical studies on gastric adenomas 49
Hematologic and molecular characterization of a Sicilian cohort of alpha thalassernia carriers 49
Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus 48
Mutational screening of Italian Wolfram syndrome patients by DHPLC 48
Totale 6.272
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Categoria #
all - tutte 36.569
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 36.569
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020869 0 0 0 0 0 172 160 120 27 180 196 14
2020/20211.084 121 10 221 68 61 120 17 86 90 144 85 61
2021/20221.204 14 140 24 40 52 13 79 52 11 264 144 371
2022/20233.013 222 274 156 272 241 300 23 164 1.254 12 77 18
2023/2024735 54 112 44 112 66 183 21 31 5 17 16 74
2024/2025558 42 36 53 206 110 111 0 0 0 0 0 0
Totale 8.711