IRIS PubliCatt

Capoluongo, Ettore Domenico
 Distribuzione geografica
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Continente #
NA - Nord America 6.448
EU - Europa 6.198
AS - Asia 1.535
AF - Africa 34
SA - Sud America 20
Continente sconosciuto - Info sul continente non disponibili 17
OC - Oceania 7
Totale 14.259
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Nazione #
US - Stati Uniti d'America 6.413
DE - Germania 2.259
SE - Svezia 1.272
CN - Cina 965
UA - Ucraina 635
IT - Italia 600
FR - Francia 333
IE - Irlanda 300
GB - Regno Unito 212
SG - Singapore 182
FI - Finlandia 160
IN - India 144
RU - Federazione Russa 136
PL - Polonia 108
TR - Turchia 107
BE - Belgio 66
IR - Iran 46
NL - Olanda 45
CI - Costa d'Avorio 30
CA - Canada 29
JP - Giappone 21
HK - Hong Kong 20
BR - Brasile 12
EU - Europa 12
CH - Svizzera 11
PH - Filippine 11
VN - Vietnam 10
AT - Austria 9
CZ - Repubblica Ceca 9
ES - Italia 9
RO - Romania 8
AU - Australia 6
CL - Cile 5
MX - Messico 5
HU - Ungheria 4
KR - Corea 4
MD - Moldavia 4
A2 - ???statistics.table.value.countryCode.A2??? 3
DK - Danimarca 3
ID - Indonesia 3
IL - Israele 3
KZ - Kazakistan 3
LK - Sri Lanka 3
TH - Thailandia 3
A1 - Anonimo 2
AR - Argentina 2
BG - Bulgaria 2
EG - Egitto 2
GR - Grecia 2
HR - Croazia 2
LU - Lussemburgo 2
NO - Norvegia 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
TW - Taiwan 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BD - Bangladesh 1
CR - Costa Rica 1
ET - Etiopia 1
IQ - Iraq 1
KW - Kuwait 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PK - Pakistan 1
PT - Portogallo 1
SA - Arabia Saudita 1
TZ - Tanzania 1
Totale 14.259
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Città #
Chandler 1.493
Ashburn 520
Jacksonville 386
San Mateo 346
Dublin 296
Ann Arbor 286
Nanjing 252
Wilmington 204
Woodbridge 156
New York 155
Nürnberg 134
Boston 133
Dearborn 128
Milan 128
Cattolica 126
Fairfield 111
Lawrence 106
Singapore 101
Izmir 97
Seattle 91
Houston 89
Moscow 89
Nanchang 86
Redwood City 84
Bremen 81
Marseille 81
Beijing 68
Princeton 68
Chicago 64
Lancaster 63
Boardman 60
Rome 57
Mountain View 54
Warsaw 54
Hangzhou 52
Kraków 51
Hebei 47
Kunming 45
Los Angeles 45
Brussels 44
Shenyang 40
University Park 40
Cambridge 38
Leawood 38
Detroit 37
Zhengzhou 35
Shanghai 33
Helsinki 31
Norwalk 31
Abidjan 30
Fremont 29
Tianjin 29
Munich 28
Guangzhou 27
Augusta 26
Jiaxing 25
Changsha 24
Pune 24
Redmond 22
Waanrode 21
Hefei 17
Philadelphia 17
Falls Church 14
Washington 14
Andover 12
Hong Kong 12
Lanzhou 12
Jinan 11
Ardabil 10
Changchun 10
Ottawa 10
Hanoi 9
Kish 9
Simi Valley 9
Zurich 9
Chengdu 8
Clearwater 8
Edinburgh 8
Enterprise 8
Monmouth Junction 8
San Francisco 8
São Paulo 8
Berlin 7
Busto Arsizio 7
London 7
Taizhou 7
Vienna 7
Wuhan 7
Phoenix 6
Toronto 6
Brno 5
Centrale 5
Costa Mesa 5
Ningbo 5
Pasig 5
Sandston 5
Caserta 4
Chisinau 4
Chongqing 4
Frankfurt am Main 4
Totale 7.470
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Nome #
Hypophysitis Outcome and Factors Predicting Responsiveness to Glucocorticoid Therapy: A Prospective and Double-Arm Study. 228
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 163
A new standardized absolute quantitative RT-PCR method for detection of tyrosinase mRNAs in melanoma patients: technical and operative instructions. 163
A novel MEN1 frameshift germline mutation in two Italian monozygotic twins 155
Small Amplicons High Resolution Melting Analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population 148
Comments to ``A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency{''} 143
Association of IL-8 and eNOS polymorphisms with clinical outcomes in bevacizumab-treated breast cancer patients: an exploratory analysis 143
Increased levels of IGF-1 and beta2-microglobulin in epithelial lining fluid of preterm newborns developing chronic lung disease effects of rhG-CSF 140
Secretory phospholipase A2 and neoantal di stress: pilot study on broncho-alveolar lavage 134
Insight into a Novel p53 Single Point Mutation (G389E) by Molecular Dynamics Simulations 133
Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation 131
A preliminary Quality Control (QC) for next generation sequencing (NGS) library evaluation turns out to be a very useful tool for a rapid detection of BRCA1/2 deleterious mutations 131
Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia 130
DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism 129
Incidental Finding of a Homozygous p.M348K Asymptomatic Italian Patient Confirms the Many Faces of Cystic Fibrosis 129
Is quantitative real time polymerase chain reaction MCAM transcript assay really suitable for prognostic and predictive management of melanoma patients? 127
The Hemo One Autoanalyzer for Glycated Hemoglobin Assay 127
A vascular endothelial growth factor deficiency characterises scleroderma lung disease 127
Serum levels of seven cytokines in premature ventilated newborns: correlations with old and new forms of bronchopulmonary dysplasia 125
Analytical assessment of bone serum markers in patients suffering from spina bifida 125
Common genetic variants of MUTYH are not associated with cutaneous malignant melanoma: application of molecular screening by means of high-resolution melting technique in a pilot case-control study. 122
Correspondence between clinical improvement and proteomic changes of the salivary peptide complex ina child with primary Sjogren syndrome 119
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 119
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 119
BRCA mutational status, initial disease presentation, and clinical outcome in high-grade serous advanced ovarian cancer: a multicenter study 119
HFOV in premature neonates: effects on pulmonary mechanics and epithelial lining fluid cytokines. A randomized controlled trial 118
Polymorphisms in base excision DNA repair genes and association with melanoma risk in a pilot study on Central-South Italian population 116
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement 111
A longitudinal follow-up study of saffron supplementation in early age-related macular degeneration: sustained benefits to central retinal function 111
Nonsteroidal Anti-Inflammatory Drug (NSAID) Use and Sarcopenia in Older People: Results From the ilSIRENTE Study 111
Association of anorexia with sarcopenia in a community-dwelling elderly population: results from the ilSIRENTE study 109
Sarcopenia as a risk factor for falls in elderly individuals: Results from the ilSIRENTE study 108
Disability, More than multimorbidity, was predictive of mortality among older persons aged 80 years and older. 107
L' era del PCA3: risultati preliminari di uno studio pragmatico monocentrico 107
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 107
A new founder BRCA1 haplotype identified in the Puglia region is associated with a specific age-related cancer onset in three unrelated families 107
First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome 105
Saffron Supplementation Improves Retinal Flicker Sensitivity in Early Age-Related Macular Degeneration 104
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 103
Circulating endothelial cell levels in psoriatic patients and their modification after an anti-TNF-alpha (Etanercept) treatment 102
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants 101
Advanced tools for BRCA1/2 mutational screening: Comparison between two methods for large genomic rearrangements (LGRs) detection 101
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 101
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms? 101
Reliability and correlation study of a new homocysteine assay. 100
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: Comparison of two methods and implications in molecular diagnostics 99
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 98
Bile acids cause secretory phospholipase A2 activity enhancement, revertible by exogenous surfactant administration. 97
Bronchoalveolar lavage fluid peptidomics suggests a possibile matrix metalloproteinase-3 role in bronchopulmonary dysplasia 96
p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients 96
Comparison of serum levels of seven cytokines in premature newborns undergoing different ventilatory procedures: high frequency oscillatory ventilation or synchronized intermittent mandatory ventilation 95
Serum levels of C-terminal agrin fragment (CAF) are associated with sarcopenia in older multimorbid community-dwellers: Results from the ilSIRENTE study 94
Role of distinct phospholipases A2 and their modulators in meconium aspiration syndrome in human neonates. 93
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100B, LDH, NSE biochemical markers. 92
Multidisciplinary team for elucidation of any new mutation and how this approach can be useful to individualize any genetic result: the case of BRCA2 c.631G > A/c.7008-2A > T genotype 92
Influence of saffron supplementation on retinal flicker sensitivity in early age-related macular degeneration. 91
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome 90
IGF-1 and microvascular complications of diabetes: alternative interpretation of recently published data 89
A rare case of juvenile hypertension: coexistence of type 2 multiple endocrine neoplasia -related bilateral pheochromocytoma and reninoma in a young patient with ACE gene polymorphism 89
GSTM1-null polymorphism as possible risk marker for hypertension: results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study) 88
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the "old" and update of the new mutations 88
Sarcopenia and mortality risk in frail older persons aged 80 years and older: results from ilSIRENTE study 88
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 88
Description of an Automated Method for Urea Nitrogen Determination in Bronchoalveolar Lavage Fluid (BALF) of Neonates and Infants 87
Clinical and biological role of secretory phospholipase A2 in acute respiratory distress syndrome infants 86
The First Case of Association Between Postpartum Thyroiditis and Thyroid Hormone Resistance in an Italian Patient Showing a Novel p.V283A THRB Mutation 85
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review 85
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 84
Gene symbol: CYP21A2. Disease: Non-classic 21-Hydroxylase deficiency. 84
Insulin-like growth factor I (CA) repeats are associated with higher melanoma's Breslow index but not associated with the presence of the melanoma. A pilot study 84
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100, LDH, NSE, byochemical markers 83
A Prolonged Neonatal Jaundice Associated With a Rare G6PD Mutation 83
Midarm muscle circumference, physical performance and mortality: results from the aging and longevity study in the Sirente geographic area (ilSIRENTE study). 82
Prospective phase II trial of trabectedin in BRCA-mutated and/or BRCAness phenotype recurrent ovarian cancer patients: the MITO 15 trial 82
The Changing Clinical Spectrum of Hypophysitis 82
Interaction between GSTM1 genotype and IL-6 on mortality in older adults: results from the ilSIRENTE study. 81
Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report. 80
Evaluation of Endothelial Dysfunction in Psoriatic Patients by Different Techniques 80
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 80
Epithelial lining fluid Neutrophil-gelatinase-associated lipocalin levels in premature newborns with bronchopulmonary dysplasia and patency of ductus arteriosus 79
Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia 79
CYP21A2 genetics: When genotype does not fit phenotype 79
Identification of RFLP G6PD mutations by using microcapillary electrophoretic chips (Experion(TM)). 78
High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism 78
Bronchoalveolar lavage fluid peptidomics suggests a possible matrix metalloproteinase-3 role in bronchopulmonary dysplasia 78
Insulin-like growth factor-I and complications of prematurity: a focus on bronchopulmonary dysplasia. 78
Blood presence of circulating oncofetal fibronectin mRNA, by RT-PCR, does not represent a useful specific marker for the management and follow-up of thyroid cancer patients 78
PCA3 score of 20 could improve prostate cancer detection: Results obtained on 734 Italian individuals 78
Interaction between GSTM1 genotype and IL-6 on mortality in older adults: results from the ilSIRENTE study 77
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 77
Secretory phospholipase A₂ pathway during pediatric acute respiratory distress syndrome: a preliminary study. 76
ANGIOTENSIN-CONVERTING ENZYME I/D POLYMORPHISM IS ASSOCIATED WITH SIGNIFICANTLY DIFFERENT VALUES OF HEPATIC VENOUS PRESSURE GRADIENT IN PATIENTS WITH LIVER CIRRHOSIS 75
Differentiated Thyroid Cancer in Two Patients with Resistance to Thyroid Hormone 75
CYP21A2 p.E238 Deletion as Result of Multiple Microconversion Events: A Genetic Study on an Italian Congenital Adrenal Hyperplasia (CAH) Family 75
Rapid detection of CFH (p.Y402H) and ARMS2 (p.A69S) polymorphisms in age-related macular degeneration using high-resolution melting analysis 74
G6PD Murcia, G6PD Ube and G6PD Orissa: report of three G6PD mutations unusual for Italian population. 74
Homocysteinemia is inversely correlated with platelet count and inversely correlated with sE-and sP-selectin levels in females homozygous for C677T methylenetetrahydrofolate reductase 73
Surfactant and Varespladib Co-Administration in Stimulated Rat Alveolar Macrophages Culture 73
Multiple endocrine neoplasia type 1 (MEN1): An update of 208 new germline variants reported in the last nine years 73
XRCC1 Arg399Gln gene polymorphism and hepatocellular carcinoma risk in the Italian population 73
Totale 10.150
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Categoria #
all - tutte 52.656
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 52.656
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.876 389 87 113 102 167 144 202 88 125 94 225 140
2020/20211.556 120 159 52 139 165 59 228 57 177 82 269 49
2021/20221.729 120 190 33 107 117 73 33 318 92 99 203 344
2022/20234.098 490 677 334 583 252 533 159 383 429 63 117 78
2023/20241.600 73 454 37 75 82 265 74 81 22 57 174 206
2024/202574 74 0 0 0 0 0 0 0 0 0 0 0
Totale 14.442