IRIS PubliCatt

Capoluongo, Ettore Domenico
 Distribuzione geografica
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Continente #
NA - Nord America 6.557
EU - Europa 6.380
AS - Asia 2.217
AF - Africa 34
SA - Sud America 26
Continente sconosciuto - Info sul continente non disponibili 17
OC - Oceania 8
Totale 15.239
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Nazione #
US - Stati Uniti d'America 6.509
DE - Germania 2.298
SE - Svezia 1.272
CN - Cina 1.077
IT - Italia 640
UA - Ucraina 635
SG - Singapore 561
FR - Francia 341
IE - Irlanda 301
GB - Regno Unito 224
FI - Finlandia 221
ID - Indonesia 185
IN - India 144
RU - Federazione Russa 138
PL - Polonia 109
TR - Turchia 107
BE - Belgio 72
NL - Olanda 49
IR - Iran 46
CA - Canada 42
CI - Costa d'Avorio 30
HK - Hong Kong 24
JP - Giappone 21
BR - Brasile 16
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
HU - Ungheria 5
KR - Corea 5
MX - Messico 5
DK - Danimarca 4
KZ - Kazakistan 4
LK - Sri Lanka 4
LT - Lituania 4
MD - Moldavia 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AR - Argentina 3
GR - Grecia 3
IL - Israele 3
RS - Serbia 3
TH - Thailandia 3
A1 - Anonimo 2
AE - Emirati Arabi Uniti 2
BG - Bulgaria 2
EG - Egitto 2
HR - Croazia 2
LU - Lussemburgo 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
TW - Taiwan 2
AM - Armenia 1
BD - Bangladesh 1
CO - Colombia 1
CR - Costa Rica 1
ET - Etiopia 1
IQ - Iraq 1
KW - Kuwait 1
MY - Malesia 1
PE - Perù 1
PK - Pakistan 1
PT - Portogallo 1
TZ - Tanzania 1
Totale 15.239
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Città #
Chandler 1.493
Ashburn 524
Singapore 436
Jacksonville 386
San Mateo 346
Dublin 297
Ann Arbor 286
Nanjing 252
Wilmington 204
Jakarta 183
Woodbridge 156
New York 155
Nürnberg 134
Boston 133
Milan 130
Dearborn 128
Cattolica 126
Fairfield 111
Lawrence 106
Izmir 97
Helsinki 92
Seattle 91
Houston 89
Moscow 89
Nanchang 86
Redwood City 84
Bremen 81
Marseille 81
Beijing 69
Princeton 68
Chicago 64
Rome 64
Lancaster 63
Boardman 60
Los Angeles 57
Mountain View 54
Warsaw 54
Hangzhou 52
Kraków 51
Brussels 50
Munich 48
Hebei 47
Kunming 46
Shenyang 43
University Park 40
Zhengzhou 40
Shanghai 39
Cambridge 38
Leawood 38
Detroit 37
Norwalk 31
Abidjan 30
Guangzhou 30
Tianjin 30
Fremont 29
Augusta 26
Changsha 26
Jiaxing 25
Pune 24
Redmond 22
Waanrode 21
Hefei 17
Philadelphia 17
Hong Kong 16
London 16
Ottawa 15
Falls Church 14
Washington 14
Andover 12
Falkenstein 12
Lanzhou 12
Toronto 12
Jinan 11
Ardabil 10
Changchun 10
Frankfurt am Main 10
Paris 10
Hanoi 9
Kish 9
Simi Valley 9
São Paulo 9
Taizhou 9
Zurich 9
Chengdu 8
Clearwater 8
Edinburgh 8
Enterprise 8
Monmouth Junction 8
San Francisco 8
Santa Clara 8
Wuhan 8
Berlin 7
Bologna 7
Busto Arsizio 7
Vienna 7
Phoenix 6
Bari 5
Brno 5
Centrale 5
Chongqing 5
Totale 8.172
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Nome #
Hypophysitis Outcome and Factors Predicting Responsiveness to Glucocorticoid Therapy: A Prospective and Double-Arm Study. 236
A new standardized absolute quantitative RT-PCR method for detection of tyrosinase mRNAs in melanoma patients: technical and operative instructions. 171
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 165
A novel MEN1 frameshift germline mutation in two Italian monozygotic twins 163
Small Amplicons High Resolution Melting Analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population 153
Comments to ``A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency{''} 151
Association of IL-8 and eNOS polymorphisms with clinical outcomes in bevacizumab-treated breast cancer patients: an exploratory analysis 150
Increased levels of IGF-1 and beta2-microglobulin in epithelial lining fluid of preterm newborns developing chronic lung disease effects of rhG-CSF 146
Secretory phospholipase A2 and neoantal di stress: pilot study on broncho-alveolar lavage 141
Insight into a Novel p53 Single Point Mutation (G389E) by Molecular Dynamics Simulations 140
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 137
Incidental Finding of a Homozygous p.M348K Asymptomatic Italian Patient Confirms the Many Faces of Cystic Fibrosis 137
Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia 136
DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism 136
A vascular endothelial growth factor deficiency characterises scleroderma lung disease 136
Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation 135
Is quantitative real time polymerase chain reaction MCAM transcript assay really suitable for prognostic and predictive management of melanoma patients? 133
The Hemo One Autoanalyzer for Glycated Hemoglobin Assay 132
Serum levels of seven cytokines in premature ventilated newborns: correlations with old and new forms of bronchopulmonary dysplasia 131
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. 130
Analytical assessment of bone serum markers in patients suffering from spina bifida 129
BRCA mutational status, initial disease presentation, and clinical outcome in high-grade serous advanced ovarian cancer: a multicenter study 129
HFOV in premature neonates: effects on pulmonary mechanics and epithelial lining fluid cytokines. A randomized controlled trial 126
Correspondence between clinical improvement and proteomic changes of the salivary peptide complex ina child with primary Sjogren syndrome 125
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 123
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 121
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement 119
Polymorphisms in base excision DNA repair genes and association with melanoma risk in a pilot study on Central-South Italian population 119
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 119
Disability, More than multimorbidity, was predictive of mortality among older persons aged 80 years and older. 116
A longitudinal follow-up study of saffron supplementation in early age-related macular degeneration: sustained benefits to central retinal function 116
Sarcopenia as a risk factor for falls in elderly individuals: Results from the ilSIRENTE study 115
Nonsteroidal Anti-Inflammatory Drug (NSAID) Use and Sarcopenia in Older People: Results From the ilSIRENTE Study 114
L' era del PCA3: risultati preliminari di uno studio pragmatico monocentrico 112
Association of anorexia with sarcopenia in a community-dwelling elderly population: results from the ilSIRENTE study 112
A new founder BRCA1 haplotype identified in the Puglia region is associated with a specific age-related cancer onset in three unrelated families 112
First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome 110
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 110
Saffron Supplementation Improves Retinal Flicker Sensitivity in Early Age-Related Macular Degeneration 109
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants 107
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 107
Reliability and correlation study of a new homocysteine assay. 107
Advanced tools for BRCA1/2 mutational screening: Comparison between two methods for large genomic rearrangements (LGRs) detection 106
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: Comparison of two methods and implications in molecular diagnostics 105
Circulating endothelial cell levels in psoriatic patients and their modification after an anti-TNF-alpha (Etanercept) treatment 105
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms? 105
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 105
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 104
Role of distinct phospholipases A2 and their modulators in meconium aspiration syndrome in human neonates. 103
Bile acids cause secretory phospholipase A2 activity enhancement, revertible by exogenous surfactant administration. 102
Comparison of serum levels of seven cytokines in premature newborns undergoing different ventilatory procedures: high frequency oscillatory ventilation or synchronized intermittent mandatory ventilation 102
Bronchoalveolar lavage fluid peptidomics suggests a possibile matrix metalloproteinase-3 role in bronchopulmonary dysplasia 102
p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients 102
Influence of saffron supplementation on retinal flicker sensitivity in early age-related macular degeneration. 101
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 99
Serum levels of C-terminal agrin fragment (CAF) are associated with sarcopenia in older multimorbid community-dwellers: Results from the ilSIRENTE study 98
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100B, LDH, NSE biochemical markers. 97
Sarcopenia and mortality risk in frail older persons aged 80 years and older: results from ilSIRENTE study 94
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 94
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome 94
Description of an Automated Method for Urea Nitrogen Determination in Bronchoalveolar Lavage Fluid (BALF) of Neonates and Infants 93
GSTM1-null polymorphism as possible risk marker for hypertension: results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study) 92
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review 92
IGF-1 and microvascular complications of diabetes: alternative interpretation of recently published data 91
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the "old" and update of the new mutations 91
The Changing Clinical Spectrum of Hypophysitis 91
Clinical and biological role of secretory phospholipase A2 in acute respiratory distress syndrome infants 90
The First Case of Association Between Postpartum Thyroiditis and Thyroid Hormone Resistance in an Italian Patient Showing a Novel p.V283A THRB Mutation 89
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100, LDH, NSE, byochemical markers 88
Gene symbol: CYP21A2. Disease: Non-classic 21-Hydroxylase deficiency. 88
Midarm muscle circumference, physical performance and mortality: results from the aging and longevity study in the Sirente geographic area (ilSIRENTE study). 88
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 88
High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism 87
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 87
Epithelial lining fluid Neutrophil-gelatinase-associated lipocalin levels in premature newborns with bronchopulmonary dysplasia and patency of ductus arteriosus 87
Evaluation of Endothelial Dysfunction in Psoriatic Patients by Different Techniques 87
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 87
Prospective phase II trial of trabectedin in BRCA-mutated and/or BRCAness phenotype recurrent ovarian cancer patients: the MITO 15 trial 86
CYP21A2 genetics: When genotype does not fit phenotype 86
Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia 85
A Prolonged Neonatal Jaundice Associated With a Rare G6PD Mutation 85
Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report. 84
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 84
PCA3 score of 20 could improve prostate cancer detection: Results obtained on 734 Italian individuals 84
Identification of RFLP G6PD mutations by using microcapillary electrophoretic chips (Experion(TM)). 83
Differentiated Thyroid Cancer in Two Patients with Resistance to Thyroid Hormone 83
Interaction between GSTM1 genotype and IL-6 on mortality in older adults: results from the ilSIRENTE study 83
Interaction between GSTM1 genotype and IL-6 on mortality in older adults: results from the ilSIRENTE study. 83
CYP21A2 p.E238 Deletion as Result of Multiple Microconversion Events: A Genetic Study on an Italian Congenital Adrenal Hyperplasia (CAH) Family 83
Secretory phospholipase A₂ pathway during pediatric acute respiratory distress syndrome: a preliminary study. 82
Bronchoalveolar lavage fluid peptidomics suggests a possible matrix metalloproteinase-3 role in bronchopulmonary dysplasia 82
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 80
Rapid detection of CFH (p.Y402H) and ARMS2 (p.A69S) polymorphisms in age-related macular degeneration using high-resolution melting analysis 80
IL-8 and eNOS polymorphisms predict bevacizumab-based first line treatment outcomes in RAS mutant metastatic colorectal cancer patients 80
A rapid screening of a recurrent CYP24A1 pathogenic variant opens the way to molecular testing for Idiopathic Infantile Hypercalcemia (IIH) 80
Insulin-like growth factor-I and complications of prematurity: a focus on bronchopulmonary dysplasia. 79
Recommendations for the implementation of BRCA testing in the care and treatment pathways of ovarian cancer patients 79
XRCC1 Arg399Gln gene polymorphism and hepatocellular carcinoma risk in the Italian population 79
Effects of early dexamethasone therapy on pulmonary fibrogenic mediators and respiratory mechanics in preterm infants 78
G6PD Murcia, G6PD Ube and G6PD Orissa: report of three G6PD mutations unusual for Italian population. 78
Totale 10.736
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Categoria #
all - tutte 62.684
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 62.684
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.018 0 0 0 0 0 144 202 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
2024/20251.056 74 111 283 136 319 133 0 0 0 0 0 0
Totale 15.424