IRIS UniCatt

Capoluongo, Ettore Domenico
 Distribuzione geografica
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Continente #
NA - Nord America 9.842
EU - Europa 7.570
AS - Asia 6.961
SA - Sud America 1.271
AF - Africa 175
Continente sconosciuto - Info sul continente non disponibili 18
OC - Oceania 17
AN - Antartide 1
Totale 25.855
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Nazione #
US - Stati Uniti d'America 9.614
SG - Singapore 3.259
DE - Germania 2.546
CN - Cina 1.706
SE - Svezia 1.319
BR - Brasile 1.046
IT - Italia 779
VN - Vietnam 703
FR - Francia 654
UA - Ucraina 652
GB - Regno Unito 348
IE - Irlanda 314
FI - Finlandia 284
IN - India 274
ID - Indonesia 200
RU - Federazione Russa 164
PL - Polonia 154
TR - Turchia 147
HK - Hong Kong 120
CA - Canada 117
JP - Giappone 100
AR - Argentina 86
NL - Olanda 86
BD - Bangladesh 83
BE - Belgio 73
MX - Messico 67
IQ - Iraq 58
IR - Iran 50
EC - Ecuador 43
ES - Italia 40
ZA - Sudafrica 39
PK - Pakistan 38
AT - Austria 36
CI - Costa d'Avorio 33
PH - Filippine 26
SA - Arabia Saudita 25
VE - Venezuela 25
CO - Colombia 23
EG - Egitto 23
JO - Giordania 20
UZ - Uzbekistan 20
KR - Corea 18
CL - Cile 16
IL - Israele 16
KE - Kenya 16
AE - Emirati Arabi Uniti 15
PY - Paraguay 15
AU - Australia 14
CH - Svizzera 14
DZ - Algeria 14
LT - Lituania 13
CZ - Repubblica Ceca 12
EU - Europa 12
MA - Marocco 12
NP - Nepal 12
JM - Giamaica 11
RO - Romania 9
HU - Ungheria 8
KZ - Kazakistan 8
MY - Malesia 8
TN - Tunisia 8
BG - Bulgaria 7
CR - Costa Rica 7
PE - Perù 7
DK - Danimarca 6
LK - Sri Lanka 6
MD - Moldavia 6
NO - Norvegia 6
SN - Senegal 6
TH - Thailandia 6
AL - Albania 5
AZ - Azerbaigian 5
BO - Bolivia 5
DO - Repubblica Dominicana 5
GR - Grecia 5
KG - Kirghizistan 5
LB - Libano 5
LY - Libia 5
PA - Panama 5
PT - Portogallo 5
BB - Barbados 4
EE - Estonia 4
ET - Etiopia 4
GE - Georgia 4
HN - Honduras 4
HR - Croazia 4
RS - Serbia 4
SK - Slovacchia (Repubblica Slovacca) 4
UY - Uruguay 4
A2 - ???statistics.table.value.countryCode.A2??? 3
OM - Oman 3
TJ - Tagikistan 3
A1 - Anonimo 2
AM - Armenia 2
AO - Angola 2
BH - Bahrain 2
BY - Bielorussia 2
CY - Cipro 2
GT - Guatemala 2
KW - Kuwait 2
Totale 25.813
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Città #
Singapore 1.859
Chandler 1.493
Ashburn 999
San Jose 764
Jacksonville 387
San Mateo 346
Dublin 308
Ann Arbor 286
Beijing 277
Nanjing 252
New York 230
Los Angeles 229
Ho Chi Minh City 222
Wilmington 207
Hanoi 191
Jakarta 184
Lauterbourg 167
Milan 161
Woodbridge 157
Boston 156
Dallas 149
Nürnberg 134
Frankfurt am Main 130
Dearborn 128
Cattolica 126
Cambridge 122
Munich 115
The Dalles 114
Fairfield 111
Helsinki 110
Hefei 108
Lawrence 106
Houston 103
Hong Kong 102
Seattle 100
Izmir 97
Chicago 95
Moscow 92
São Paulo 88
Warsaw 88
Nanchang 86
Redwood City 84
Bremen 81
Marseille 81
Rome 81
Tokyo 78
Princeton 68
Lancaster 65
Boardman 63
Buffalo 63
Santa Clara 61
Mountain View 54
Shanghai 53
Hangzhou 52
Brussels 51
Kraków 51
Hebei 47
Kunming 47
London 46
Shenyang 43
Guangzhou 40
Turku 40
University Park 40
Zhengzhou 40
Orem 39
Da Nang 38
Detroit 38
Leawood 38
Haiphong 34
Rio de Janeiro 34
Tianjin 34
Abidjan 33
Montreal 33
Nuremberg 33
Norwalk 31
Paris 31
Augusta 29
Fremont 29
Kent 29
Stockholm 29
Atlanta 27
Council Bluffs 27
Düsseldorf 27
San Francisco 27
Brooklyn 26
Changsha 26
Pune 26
Toronto 26
Baghdad 25
Denver 25
Jiaxing 25
Belo Horizonte 23
Hyderabad 23
Johannesburg 23
Phoenix 23
Redmond 22
Waanrode 21
Brasília 20
Ottawa 20
Philadelphia 20
Totale 13.522
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Nome #
Hypophysitis Outcome and Factors Predicting Responsiveness to Glucocorticoid Therapy: A Prospective and Double-Arm Study. 305
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. 266
Polymorphisms in base excision DNA repair genes and association with melanoma risk in a pilot study on Central-South Italian population 245
Comments to ``A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency{''} 234
A new standardized absolute quantitative RT-PCR method for detection of tyrosinase mRNAs in melanoma patients: technical and operative instructions. 233
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 232
Association of IL-8 and eNOS polymorphisms with clinical outcomes in bevacizumab-treated breast cancer patients: an exploratory analysis 226
Secretory phospholipase A2 and neoantal di stress: pilot study on broncho-alveolar lavage 220
Insight into a Novel p53 Single Point Mutation (G389E) by Molecular Dynamics Simulations 220
Small Amplicons High Resolution Melting Analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population 218
Serum levels of seven cytokines in premature ventilated newborns: correlations with old and new forms of bronchopulmonary dysplasia 214
Increased levels of IGF-1 and beta2-microglobulin in epithelial lining fluid of preterm newborns developing chronic lung disease effects of rhG-CSF 213
DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism 212
A novel MEN1 frameshift germline mutation in two Italian monozygotic twins 209
BRCA mutational status, initial disease presentation, and clinical outcome in high-grade serous advanced ovarian cancer: a multicenter study 209
Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation 205
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 204
Correspondence between clinical improvement and proteomic changes of the salivary peptide complex ina child with primary Sjogren syndrome 203
Disability, More than multimorbidity, was predictive of mortality among older persons aged 80 years and older. 197
Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia 194
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement 194
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 193
Incidental Finding of a Homozygous p.M348K Asymptomatic Italian Patient Confirms the Many Faces of Cystic Fibrosis 193
The Hemo One Autoanalyzer for Glycated Hemoglobin Assay 191
A vascular endothelial growth factor deficiency characterises scleroderma lung disease 190
Comparison of serum levels of seven cytokines in premature newborns undergoing different ventilatory procedures: high frequency oscillatory ventilation or synchronized intermittent mandatory ventilation 188
Is quantitative real time polymerase chain reaction MCAM transcript assay really suitable for prognostic and predictive management of melanoma patients? 187
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 187
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 186
HFOV in premature neonates: effects on pulmonary mechanics and epithelial lining fluid cytokines. A randomized controlled trial 185
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 184
Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia 183
Sarcopenia as a risk factor for falls in elderly individuals: Results from the ilSIRENTE study 180
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants 176
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 175
Advanced tools for BRCA1/2 mutational screening: Comparison between two methods for large genomic rearrangements (LGRs) detection 174
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 174
Analytical assessment of bone serum markers in patients suffering from spina bifida 172
Saffron Supplementation Improves Retinal Flicker Sensitivity in Early Age-Related Macular Degeneration 170
Bronchoalveolar lavage fluid peptidomics suggests a possibile matrix metalloproteinase-3 role in bronchopulmonary dysplasia 169
Reliability and correlation study of a new homocysteine assay. 168
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: Comparison of two methods and implications in molecular diagnostics 167
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 167
A new founder BRCA1 haplotype identified in the Puglia region is associated with a specific age-related cancer onset in three unrelated families 167
First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome 166
Midarm muscle circumference, physical performance and mortality: results from the aging and longevity study in the Sirente geographic area (ilSIRENTE study). 165
Surfactant and Varespladib Co-Administration in Stimulated Rat Alveolar Macrophages Culture 165
A longitudinal follow-up study of saffron supplementation in early age-related macular degeneration: sustained benefits to central retinal function 164
Nonsteroidal Anti-Inflammatory Drug (NSAID) Use and Sarcopenia in Older People: Results From the ilSIRENTE Study 164
Role of distinct phospholipases A2 and their modulators in meconium aspiration syndrome in human neonates. 163
Circulating endothelial cell levels in psoriatic patients and their modification after an anti-TNF-alpha (Etanercept) treatment 163
Association of anorexia with sarcopenia in a community-dwelling elderly population: results from the ilSIRENTE study 159
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 159
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 158
Sarcopenia and mortality risk in frail older persons aged 80 years and older: results from ilSIRENTE study 157
GSTM1-null polymorphism as possible risk marker for hypertension: results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study) 156
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100B, LDH, NSE biochemical markers. 156
L' era del PCA3: risultati preliminari di uno studio pragmatico monocentrico 155
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review 155
Bronchoalveolar lavage fluid peptidomics suggests a possible matrix metalloproteinase-3 role in bronchopulmonary dysplasia 154
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 154
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 154
Influence of saffron supplementation on retinal flicker sensitivity in early age-related macular degeneration. 153
Bile acids cause secretory phospholipase A2 activity enhancement, revertible by exogenous surfactant administration. 153
Description of an Automated Method for Urea Nitrogen Determination in Bronchoalveolar Lavage Fluid (BALF) of Neonates and Infants 153
BRCA Mutation Status in Triple-Negative Breast Cancer Patients Treated with Neoadjuvant Chemotherapy: A Pivotal Role for Treatment Decision-Making 152
Serum levels of C-terminal agrin fragment (CAF) are associated with sarcopenia in older multimorbid community-dwellers: Results from the ilSIRENTE study 152
Genes, pseudogenes and like genes: The case of 21-hydroxylase in Italian population 150
High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism 149
Prospective phase II trial of trabectedin in BRCA-mutated and/or BRCAness phenotype recurrent ovarian cancer patients: the MITO 15 trial 149
IL-8 and eNOS polymorphisms predict bevacizumab-based first line treatment outcomes in RAS mutant metastatic colorectal cancer patients 149
CYP21A2 p.E238 Deletion as Result of Multiple Microconversion Events: A Genetic Study on an Italian Congenital Adrenal Hyperplasia (CAH) Family 147
Non-catalytic region of tyrosine kinase adaptor protein 2 (NCK2) pathways as factor promoting aggressiveness in ovarian cancer 147
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 146
The Changing Clinical Spectrum of Hypophysitis 146
Let‐7a‐5p, mir‐100‐5p, mir‐101‐3p, and mir‐199a‐3p hyperexpression as potential predictive biomarkers in early breast cancer patients 145
Secretory phospholipase A₂ pathway during pediatric acute respiratory distress syndrome: a preliminary study. 144
p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients 144
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations 144
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms? 144
A rapid screening of a recurrent CYP24A1 pathogenic variant opens the way to molecular testing for Idiopathic Infantile Hypercalcemia (IIH) 144
Epithelial lining fluid Neutrophil-gelatinase-associated lipocalin levels in premature newborns with bronchopulmonary dysplasia and patency of ductus arteriosus 143
Evaluation of Endothelial Dysfunction in Psoriatic Patients by Different Techniques 143
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the "old" and update of the new mutations 142
A novel CYP24A1 genotype associated to a clinical picture of hypercalcemia, nephrolithiasis and low bone mass 142
CYP21A2 genetics: When genotype does not fit phenotype 141
Gene symbol: CYP21A2. Disease: Non-classic 21-Hydroxylase deficiency. 140
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome 139
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100, LDH, NSE, byochemical markers 138
FOXM1 expression is significantly associated with chemotherapy resistance and adverse prognosis in non-serous epithelial ovarian cancer patients 138
Clinical and biological role of secretory phospholipase A2 in acute respiratory distress syndrome infants 138
Recommendations for the implementation of BRCA testing in the care and treatment pathways of ovarian cancer patients 136
IGF-1 and microvascular complications of diabetes: alternative interpretation of recently published data 135
Ex Vivo Effect of Varespladib on Secretory Phospholipase A2 Alveolar Activity in Infants with ARDS 135
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 135
In silico investigation of the molecular effects caused by R123H variant in secretory phospholipase A2-IIA associated with ARDS 135
Feasibility of tumor testing for BRCA status in high-grade serous ovarian cancer using fresh-frozen tissue based approach 135
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 134
Effect of prenatal steroidal inhibition of sPLA2 in a rat model of preterm lung 134
Molecular and Genetic Immune Biomarkers of Primary and Immune-Therapy Induced Hypophysitis: From Laboratories to the Clinical Practice 134
Totale 17.074
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Categoria #
all - tutte 97.029
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 97.029
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021400 0 0 0 0 0 0 0 0 0 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
2025/20268.331 1.302 260 515 945 1.638 459 1.715 531 509 457 0 0
Totale 26.141