Capoluongo, Ettore Domenico
 Distribuzione geografica
Continente #
NA - Nord America 6.938
EU - Europa 6.763
AS - Asia 2.748
SA - Sud America 506
AF - Africa 54
Continente sconosciuto - Info sul continente non disponibili 17
OC - Oceania 10
Totale 17.036
Nazione #
US - Stati Uniti d'America 6.859
DE - Germania 2.395
SE - Svezia 1.291
CN - Cina 1.131
SG - Singapore 912
IT - Italia 665
UA - Ucraina 639
BR - Brasile 469
FR - Francia 437
IE - Irlanda 303
GB - Regno Unito 254
FI - Finlandia 237
ID - Indonesia 186
IN - India 169
RU - Federazione Russa 148
PL - Polonia 120
TR - Turchia 112
BE - Belgio 73
NL - Olanda 65
CA - Canada 58
IR - Iran 46
VN - Vietnam 36
AT - Austria 31
CI - Costa d'Avorio 30
HK - Hong Kong 30
JP - Giappone 26
KR - Corea 18
ES - Italia 15
CH - Svizzera 14
AR - Argentina 12
CZ - Repubblica Ceca 12
EU - Europa 12
PH - Filippine 12
MX - Messico 9
AU - Australia 8
EC - Ecuador 8
RO - Romania 8
AE - Emirati Arabi Uniti 7
BD - Bangladesh 7
HU - Ungheria 7
CL - Cile 6
DK - Danimarca 6
IQ - Iraq 6
EG - Egitto 5
IL - Israele 5
KZ - Kazakistan 5
LK - Sri Lanka 5
LT - Lituania 5
BG - Bulgaria 4
CO - Colombia 4
DZ - Algeria 4
EE - Estonia 4
GR - Grecia 4
KG - Kirghizistan 4
MD - Moldavia 4
PK - Pakistan 4
PT - Portogallo 4
RS - Serbia 4
TH - Thailandia 4
UZ - Uzbekistan 4
A2 - ???statistics.table.value.countryCode.A2??? 3
DO - Repubblica Dominicana 3
KE - Kenya 3
MA - Marocco 3
NO - Norvegia 3
NP - Nepal 3
PA - Panama 3
PE - Perù 3
SA - Arabia Saudita 3
SK - Slovacchia (Repubblica Slovacca) 3
TN - Tunisia 3
ZA - Sudafrica 3
A1 - Anonimo 2
AZ - Azerbaigian 2
CR - Costa Rica 2
HR - Croazia 2
JM - Giamaica 2
JO - Giordania 2
LU - Lussemburgo 2
LV - Lettonia 2
NZ - Nuova Zelanda 2
PY - Paraguay 2
TW - Taiwan 2
AM - Armenia 1
BO - Bolivia 1
BW - Botswana 1
BY - Bielorussia 1
CY - Cipro 1
ET - Etiopia 1
HN - Honduras 1
IM - Isola di Man 1
KW - Kuwait 1
LC - Santa Lucia 1
MN - Mongolia 1
MY - Malesia 1
QA - Qatar 1
TM - Turkmenistan 1
TZ - Tanzania 1
VE - Venezuela 1
Totale 17.036
Città #
Chandler 1.493
Ashburn 544
Singapore 535
Jacksonville 386
San Mateo 346
Dublin 299
Ann Arbor 286
Nanjing 252
Wilmington 205
Jakarta 183
New York 161
Woodbridge 156
Boston 144
Milan 139
Nürnberg 134
Dearborn 128
Cattolica 126
Fairfield 111
Lawrence 106
Izmir 97
Helsinki 96
Seattle 95
Houston 89
Moscow 89
Los Angeles 87
Nanchang 86
Redwood City 84
Bremen 81
Marseille 81
Chicago 72
Beijing 70
Princeton 68
Rome 65
Lancaster 63
Warsaw 61
Boardman 60
Mountain View 54
Frankfurt am Main 53
Munich 53
Hangzhou 52
Brussels 51
Kraków 51
Hebei 47
Kunming 46
Shanghai 43
Shenyang 43
The Dalles 40
University Park 40
Zhengzhou 40
Cambridge 38
Leawood 38
Detroit 37
São Paulo 36
Guangzhou 34
Hefei 34
Norwalk 31
Abidjan 30
Tianjin 30
Fremont 29
Augusta 27
Düsseldorf 27
Changsha 26
Nuremberg 26
Jiaxing 25
Pune 24
Hyderabad 23
London 23
Hong Kong 22
Lauterbourg 22
Redmond 22
Waanrode 21
Hanoi 20
Ottawa 18
Philadelphia 17
San Francisco 17
Santa Clara 17
Vienna 17
Toronto 15
Falls Church 14
Seoul 14
Washington 14
Portsmouth 13
Andover 12
Belo Horizonte 12
Falkenstein 12
Lanzhou 12
Jinan 11
Turku 11
Zurich 11
Ardabil 10
Changchun 10
Paris 10
Brasília 9
Curitiba 9
Kish 9
Phoenix 9
Simi Valley 9
Sorocaba 9
Taizhou 9
Bologna 8
Totale 8.674
Nome #
Hypophysitis Outcome and Factors Predicting Responsiveness to Glucocorticoid Therapy: A Prospective and Double-Arm Study. 244
A new standardized absolute quantitative RT-PCR method for detection of tyrosinase mRNAs in melanoma patients: technical and operative instructions. 185
A novel MEN1 frameshift germline mutation in two Italian monozygotic twins 169
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 168
Comments to ``A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency{''} 167
Association of IL-8 and eNOS polymorphisms with clinical outcomes in bevacizumab-treated breast cancer patients: an exploratory analysis 161
Small Amplicons High Resolution Melting Analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population 160
Increased levels of IGF-1 and beta2-microglobulin in epithelial lining fluid of preterm newborns developing chronic lung disease effects of rhG-CSF 158
Insight into a Novel p53 Single Point Mutation (G389E) by Molecular Dynamics Simulations 153
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. 149
Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation 149
Secretory phospholipase A2 and neoantal di stress: pilot study on broncho-alveolar lavage 149
DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism 146
Incidental Finding of a Homozygous p.M348K Asymptomatic Italian Patient Confirms the Many Faces of Cystic Fibrosis 146
The Hemo One Autoanalyzer for Glycated Hemoglobin Assay 145
BRCA mutational status, initial disease presentation, and clinical outcome in high-grade serous advanced ovarian cancer: a multicenter study 144
A vascular endothelial growth factor deficiency characterises scleroderma lung disease 144
Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia 143
Is quantitative real time polymerase chain reaction MCAM transcript assay really suitable for prognostic and predictive management of melanoma patients? 143
Correspondence between clinical improvement and proteomic changes of the salivary peptide complex ina child with primary Sjogren syndrome 142
Serum levels of seven cytokines in premature ventilated newborns: correlations with old and new forms of bronchopulmonary dysplasia 142
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 142
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 141
Analytical assessment of bone serum markers in patients suffering from spina bifida 138
HFOV in premature neonates: effects on pulmonary mechanics and epithelial lining fluid cytokines. A randomized controlled trial 134
Polymorphisms in base excision DNA repair genes and association with melanoma risk in a pilot study on Central-South Italian population 134
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 129
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 128
Disability, More than multimorbidity, was predictive of mortality among older persons aged 80 years and older. 127
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 127
Sarcopenia as a risk factor for falls in elderly individuals: Results from the ilSIRENTE study 126
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement 125
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants 123
A new founder BRCA1 haplotype identified in the Puglia region is associated with a specific age-related cancer onset in three unrelated families 123
Association of anorexia with sarcopenia in a community-dwelling elderly population: results from the ilSIRENTE study 122
Nonsteroidal Anti-Inflammatory Drug (NSAID) Use and Sarcopenia in Older People: Results From the ilSIRENTE Study 122
Saffron Supplementation Improves Retinal Flicker Sensitivity in Early Age-Related Macular Degeneration 121
A longitudinal follow-up study of saffron supplementation in early age-related macular degeneration: sustained benefits to central retinal function 121
Advanced tools for BRCA1/2 mutational screening: Comparison between two methods for large genomic rearrangements (LGRs) detection 121
First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome 120
L' era del PCA3: risultati preliminari di uno studio pragmatico monocentrico 119
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 119
Role of distinct phospholipases A2 and their modulators in meconium aspiration syndrome in human neonates. 117
Bronchoalveolar lavage fluid peptidomics suggests a possibile matrix metalloproteinase-3 role in bronchopulmonary dysplasia 115
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 115
Reliability and correlation study of a new homocysteine assay. 114
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: Comparison of two methods and implications in molecular diagnostics 113
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 112
Influence of saffron supplementation on retinal flicker sensitivity in early age-related macular degeneration. 111
p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients 111
Circulating endothelial cell levels in psoriatic patients and their modification after an anti-TNF-alpha (Etanercept) treatment 111
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms? 110
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 109
GSTM1-null polymorphism as possible risk marker for hypertension: results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study) 108
Comparison of serum levels of seven cytokines in premature newborns undergoing different ventilatory procedures: high frequency oscillatory ventilation or synchronized intermittent mandatory ventilation 107
Midarm muscle circumference, physical performance and mortality: results from the aging and longevity study in the Sirente geographic area (ilSIRENTE study). 107
Bile acids cause secretory phospholipase A2 activity enhancement, revertible by exogenous surfactant administration. 106
Serum levels of C-terminal agrin fragment (CAF) are associated with sarcopenia in older multimorbid community-dwellers: Results from the ilSIRENTE study 106
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100B, LDH, NSE biochemical markers. 105
CYP21A2 p.E238 Deletion as Result of Multiple Microconversion Events: A Genetic Study on an Italian Congenital Adrenal Hyperplasia (CAH) Family 104
The Changing Clinical Spectrum of Hypophysitis 104
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the "old" and update of the new mutations 102
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 102
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review 102
Description of an Automated Method for Urea Nitrogen Determination in Bronchoalveolar Lavage Fluid (BALF) of Neonates and Infants 102
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome 102
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 101
Differentiated Thyroid Cancer in Two Patients with Resistance to Thyroid Hormone 100
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 100
Sarcopenia and mortality risk in frail older persons aged 80 years and older: results from ilSIRENTE study 100
The First Case of Association Between Postpartum Thyroiditis and Thyroid Hormone Resistance in an Italian Patient Showing a Novel p.V283A THRB Mutation 99
Clinical and biological role of secretory phospholipase A2 in acute respiratory distress syndrome infants 99
High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism 98
Secretory phospholipase A₂ pathway during pediatric acute respiratory distress syndrome: a preliminary study. 98
Bronchoalveolar lavage fluid peptidomics suggests a possible matrix metalloproteinase-3 role in bronchopulmonary dysplasia 98
IGF-1 and microvascular complications of diabetes: alternative interpretation of recently published data 97
Gene symbol: CYP21A2. Disease: Non-classic 21-Hydroxylase deficiency. 97
Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia 97
Evaluation of Endothelial Dysfunction in Psoriatic Patients by Different Techniques 97
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 96
Epithelial lining fluid Neutrophil-gelatinase-associated lipocalin levels in premature newborns with bronchopulmonary dysplasia and patency of ductus arteriosus 95
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 94
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100, LDH, NSE, byochemical markers 93
Interaction between GSTM1 genotype and IL-6 on mortality in older adults: results from the ilSIRENTE study 93
Genes, pseudogenes and like genes: The case of 21-hydroxylase in Italian population 93
Prospective phase II trial of trabectedin in BRCA-mutated and/or BRCAness phenotype recurrent ovarian cancer patients: the MITO 15 trial 93
CYP21A2 genetics: When genotype does not fit phenotype 93
A Prolonged Neonatal Jaundice Associated With a Rare G6PD Mutation 92
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations 91
Competitive PCR-High Resolution Melting Analysis (C-PCR-HRMA) for large genomic rearrangements (LGRs) detection: A new approach to assess quantitative status of BRCA1 gene in a reference laboratory 91
Rapid detection of CFH (p.Y402H) and ARMS2 (p.A69S) polymorphisms in age-related macular degeneration using high-resolution melting analysis 90
Ex Vivo Effect of Varespladib on Secretory Phospholipase A2 Alveolar Activity in Infants with ARDS 90
PCA3 score of 20 could improve prostate cancer detection: Results obtained on 734 Italian individuals 90
IL-8 and eNOS polymorphisms predict bevacizumab-based first line treatment outcomes in RAS mutant metastatic colorectal cancer patients 90
Identification of RFLP G6PD mutations by using microcapillary electrophoretic chips (Experion(TM)). 89
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 89
Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report. 88
Red blood cell PK deficiency: An update of PK-LR gene mutation database 88
A novel CYP24A1 genotype associated to a clinical picture of hypercalcemia, nephrolithiasis and low bone mass 88
Interaction between GSTM1 genotype and IL-6 on mortality in older adults: results from the ilSIRENTE study. 87
Totale 11.758
Categoria #
all - tutte 72.602
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 72.602


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020365 0 0 0 0 0 0 0 0 0 0 225 140
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
2024/20252.861 74 111 283 136 319 138 87 150 508 339 716 0
Totale 17.229