Capoluongo, Ettore Domenico
 Distribuzione geografica
Continente #
NA - Nord America 8.315
EU - Europa 7.234
AS - Asia 5.689
SA - Sud America 1.216
AF - Africa 145
Continente sconosciuto - Info sul continente non disponibili 18
OC - Oceania 15
AN - Antartide 1
Totale 22.633
Nazione #
US - Stati Uniti d'America 8.110
SG - Singapore 2.727
DE - Germania 2.515
CN - Cina 1.615
SE - Svezia 1.319
BR - Brasile 1.026
IT - Italia 714
UA - Ucraina 647
FR - Francia 484
GB - Regno Unito 332
IE - Irlanda 308
FI - Finlandia 274
VN - Vietnam 263
IN - India 250
ID - Indonesia 198
RU - Federazione Russa 164
PL - Polonia 150
TR - Turchia 140
CA - Canada 106
AR - Argentina 79
NL - Olanda 74
BE - Belgio 73
BD - Bangladesh 71
MX - Messico 61
HK - Hong Kong 60
JP - Giappone 55
IR - Iran 50
IQ - Iraq 45
EC - Ecuador 38
AT - Austria 36
ES - Italia 33
CI - Costa d'Avorio 32
PK - Pakistan 32
ZA - Sudafrica 32
SA - Arabia Saudita 20
EG - Egitto 19
VE - Venezuela 19
KR - Corea 18
PH - Filippine 18
CO - Colombia 17
JO - Giordania 17
KE - Kenya 16
CH - Svizzera 14
UZ - Uzbekistan 14
AE - Emirati Arabi Uniti 13
LT - Lituania 13
AU - Australia 12
CZ - Repubblica Ceca 12
EU - Europa 12
PY - Paraguay 12
IL - Israele 11
MA - Marocco 11
NP - Nepal 11
CL - Cile 10
DZ - Algeria 10
HU - Ungheria 8
JM - Giamaica 8
KZ - Kazakistan 8
RO - Romania 8
TN - Tunisia 7
BG - Bulgaria 6
DK - Danimarca 6
MD - Moldavia 6
MY - Malesia 6
NO - Norvegia 6
PE - Perù 6
CR - Costa Rica 5
DO - Repubblica Dominicana 5
KG - Kirghizistan 5
LB - Libano 5
LK - Sri Lanka 5
PT - Portogallo 5
TH - Thailandia 5
AZ - Azerbaigian 4
BB - Barbados 4
BO - Bolivia 4
EE - Estonia 4
ET - Etiopia 4
GR - Grecia 4
HN - Honduras 4
PA - Panama 4
RS - Serbia 4
SK - Slovacchia (Repubblica Slovacca) 4
SN - Senegal 4
UY - Uruguay 4
A2 - ???statistics.table.value.countryCode.A2??? 3
HR - Croazia 3
OM - Oman 3
TJ - Tagikistan 3
A1 - Anonimo 2
AO - Angola 2
BH - Bahrain 2
BY - Bielorussia 2
CY - Cipro 2
GT - Guatemala 2
KW - Kuwait 2
LU - Lussemburgo 2
LV - Lettonia 2
MN - Mongolia 2
NI - Nicaragua 2
Totale 22.604
Città #
Chandler 1.493
Singapore 1.346
Ashburn 779
Jacksonville 387
San Mateo 346
Dublin 303
Ann Arbor 286
Beijing 269
Nanjing 252
New York 218
Wilmington 207
Los Angeles 206
Jakarta 183
Woodbridge 157
Boston 156
Milan 150
Dallas 149
Nürnberg 134
Dearborn 128
Cattolica 126
Munich 115
Fairfield 111
Hefei 107
Frankfurt am Main 106
Lawrence 106
Houston 103
Helsinki 100
Seattle 100
Izmir 97
Moscow 92
Chicago 90
São Paulo 87
Nanchang 86
Warsaw 85
Redwood City 84
Ho Chi Minh City 83
Bremen 81
Marseille 81
Hanoi 78
Rome 72
Princeton 68
Lancaster 65
Boardman 63
Buffalo 59
Mountain View 54
Hangzhou 52
Hong Kong 52
Brussels 51
Kraków 51
Hebei 47
Kunming 47
The Dalles 47
Shanghai 45
Shenyang 43
London 41
Turku 40
University Park 40
Zhengzhou 40
Cambridge 38
Detroit 38
Leawood 38
Santa Clara 36
Guangzhou 35
Tokyo 35
Rio de Janeiro 33
Abidjan 32
Tianjin 32
Norwalk 31
Montreal 30
Nuremberg 30
Augusta 29
Fremont 29
Kent 29
Stockholm 29
Düsseldorf 27
San Francisco 27
Brooklyn 26
Changsha 26
Pune 26
Jiaxing 25
Denver 24
Hyderabad 23
Toronto 23
Belo Horizonte 22
Lauterbourg 22
Orem 22
Redmond 22
Atlanta 21
Phoenix 21
Waanrode 21
Brasília 20
Johannesburg 20
Philadelphia 20
Ottawa 19
Vienna 18
Baghdad 17
Amman 16
Curitiba 16
Dhaka 15
Salvador 15
Totale 11.122
Nome #
Hypophysitis Outcome and Factors Predicting Responsiveness to Glucocorticoid Therapy: A Prospective and Double-Arm Study. 277
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. 249
A new standardized absolute quantitative RT-PCR method for detection of tyrosinase mRNAs in melanoma patients: technical and operative instructions. 217
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 214
Association of IL-8 and eNOS polymorphisms with clinical outcomes in bevacizumab-treated breast cancer patients: an exploratory analysis 205
Comments to ``A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency{''} 203
Secretory phospholipase A2 and neoantal di stress: pilot study on broncho-alveolar lavage 197
Small Amplicons High Resolution Melting Analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population 195
A novel MEN1 frameshift germline mutation in two Italian monozygotic twins 193
Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation 191
Insight into a Novel p53 Single Point Mutation (G389E) by Molecular Dynamics Simulations 191
DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism 191
Increased levels of IGF-1 and beta2-microglobulin in epithelial lining fluid of preterm newborns developing chronic lung disease effects of rhG-CSF 191
Serum levels of seven cytokines in premature ventilated newborns: correlations with old and new forms of bronchopulmonary dysplasia 190
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 189
Disability, More than multimorbidity, was predictive of mortality among older persons aged 80 years and older. 182
Polymorphisms in base excision DNA repair genes and association with melanoma risk in a pilot study on Central-South Italian population 182
Correspondence between clinical improvement and proteomic changes of the salivary peptide complex ina child with primary Sjogren syndrome 178
Comparison of serum levels of seven cytokines in premature newborns undergoing different ventilatory procedures: high frequency oscillatory ventilation or synchronized intermittent mandatory ventilation 175
Incidental Finding of a Homozygous p.M348K Asymptomatic Italian Patient Confirms the Many Faces of Cystic Fibrosis 175
BRCA mutational status, initial disease presentation, and clinical outcome in high-grade serous advanced ovarian cancer: a multicenter study 175
Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia 174
The Hemo One Autoanalyzer for Glycated Hemoglobin Assay 173
Is quantitative real time polymerase chain reaction MCAM transcript assay really suitable for prognostic and predictive management of melanoma patients? 172
A vascular endothelial growth factor deficiency characterises scleroderma lung disease 171
HFOV in premature neonates: effects on pulmonary mechanics and epithelial lining fluid cytokines. A randomized controlled trial 168
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 168
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 164
Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia 160
Analytical assessment of bone serum markers in patients suffering from spina bifida 158
Sarcopenia as a risk factor for falls in elderly individuals: Results from the ilSIRENTE study 157
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 156
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement 155
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants 155
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 155
Advanced tools for BRCA1/2 mutational screening: Comparison between two methods for large genomic rearrangements (LGRs) detection 155
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 155
Saffron Supplementation Improves Retinal Flicker Sensitivity in Early Age-Related Macular Degeneration 154
First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome 152
Bronchoalveolar lavage fluid peptidomics suggests a possibile matrix metalloproteinase-3 role in bronchopulmonary dysplasia 152
A new founder BRCA1 haplotype identified in the Puglia region is associated with a specific age-related cancer onset in three unrelated families 152
Midarm muscle circumference, physical performance and mortality: results from the aging and longevity study in the Sirente geographic area (ilSIRENTE study). 151
Nonsteroidal Anti-Inflammatory Drug (NSAID) Use and Sarcopenia in Older People: Results From the ilSIRENTE Study 150
A longitudinal follow-up study of saffron supplementation in early age-related macular degeneration: sustained benefits to central retinal function 149
Association of anorexia with sarcopenia in a community-dwelling elderly population: results from the ilSIRENTE study 146
Reliability and correlation study of a new homocysteine assay. 146
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 144
L' era del PCA3: risultati preliminari di uno studio pragmatico monocentrico 143
Influence of saffron supplementation on retinal flicker sensitivity in early age-related macular degeneration. 142
Role of distinct phospholipases A2 and their modulators in meconium aspiration syndrome in human neonates. 142
Bronchoalveolar lavage fluid peptidomics suggests a possible matrix metalloproteinase-3 role in bronchopulmonary dysplasia 142
Circulating endothelial cell levels in psoriatic patients and their modification after an anti-TNF-alpha (Etanercept) treatment 142
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: Comparison of two methods and implications in molecular diagnostics 141
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 141
Bile acids cause secretory phospholipase A2 activity enhancement, revertible by exogenous surfactant administration. 140
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 140
GSTM1-null polymorphism as possible risk marker for hypertension: results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study) 138
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100B, LDH, NSE biochemical markers. 137
Description of an Automated Method for Urea Nitrogen Determination in Bronchoalveolar Lavage Fluid (BALF) of Neonates and Infants 136
Serum levels of C-terminal agrin fragment (CAF) are associated with sarcopenia in older multimorbid community-dwellers: Results from the ilSIRENTE study 136
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 136
Evaluation of Endothelial Dysfunction in Psoriatic Patients by Different Techniques 135
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review 135
The Changing Clinical Spectrum of Hypophysitis 135
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 134
CYP21A2 p.E238 Deletion as Result of Multiple Microconversion Events: A Genetic Study on an Italian Congenital Adrenal Hyperplasia (CAH) Family 132
Genes, pseudogenes and like genes: The case of 21-hydroxylase in Italian population 131
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 131
Non-catalytic region of tyrosine kinase adaptor protein 2 (NCK2) pathways as factor promoting aggressiveness in ovarian cancer 131
Prospective phase II trial of trabectedin in BRCA-mutated and/or BRCAness phenotype recurrent ovarian cancer patients: the MITO 15 trial 130
Surfactant and Varespladib Co-Administration in Stimulated Rat Alveolar Macrophages Culture 129
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms? 129
IL-8 and eNOS polymorphisms predict bevacizumab-based first line treatment outcomes in RAS mutant metastatic colorectal cancer patients 128
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100, LDH, NSE, byochemical markers 127
Epithelial lining fluid Neutrophil-gelatinase-associated lipocalin levels in premature newborns with bronchopulmonary dysplasia and patency of ductus arteriosus 127
p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients 127
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the "old" and update of the new mutations 126
Sarcopenia and mortality risk in frail older persons aged 80 years and older: results from ilSIRENTE study 126
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 125
In silico investigation of the molecular effects caused by R123H variant in secretory phospholipase A2-IIA associated with ARDS 125
A rapid screening of a recurrent CYP24A1 pathogenic variant opens the way to molecular testing for Idiopathic Infantile Hypercalcemia (IIH) 125
Clinical and biological role of secretory phospholipase A2 in acute respiratory distress syndrome infants 125
Differentiated Thyroid Cancer in Two Patients with Resistance to Thyroid Hormone 124
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome 124
BRCA Mutation Status in Triple-Negative Breast Cancer Patients Treated with Neoadjuvant Chemotherapy: A Pivotal Role for Treatment Decision-Making 123
High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism 123
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations 123
Gene symbol: CYP21A2. Disease: Non-classic 21-Hydroxylase deficiency. 122
FOXM1 expression is significantly associated with chemotherapy resistance and adverse prognosis in non-serous epithelial ovarian cancer patients 122
IGF-1 and microvascular complications of diabetes: alternative interpretation of recently published data 121
Secretory phospholipase A₂ pathway during pediatric acute respiratory distress syndrome: a preliminary study. 121
Interaction between GSTM1 genotype and IL-6 on mortality in older adults: results from the ilSIRENTE study 121
Ex Vivo Effect of Varespladib on Secretory Phospholipase A2 Alveolar Activity in Infants with ARDS 121
Absolute quantitative PCR for detection of molecular biomarkers in melanoma patients: a preliminary report 121
CYP21A2 genetics: When genotype does not fit phenotype 121
A novel CYP24A1 genotype associated to a clinical picture of hypercalcemia, nephrolithiasis and low bone mass 121
Feasibility of tumor testing for BRCA status in high-grade serous ovarian cancer using fresh-frozen tissue based approach 121
Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report. 119
The First Case of Association Between Postpartum Thyroiditis and Thyroid Hormone Resistance in an Italian Patient Showing a Novel p.V283A THRB Mutation 119
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 119
Totale 15.107
Categoria #
all - tutte 90.734
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 90.734


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021921 0 0 0 0 0 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
2024/20253.442 74 111 283 136 319 138 87 150 508 339 716 581
2025/20265.020 1.302 260 515 945 1.638 360 0 0 0 0 0 0
Totale 22.830