IRIS UniCatt

Capoluongo, Ettore Domenico
 Distribuzione geografica
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Continente #
NA - Nord America 10.382
EU - Europa 7.676
AS - Asia 7.010
SA - Sud America 1.298
AF - Africa 175
Continente sconosciuto - Info sul continente non disponibili 19
OC - Oceania 17
AN - Antartide 1
Totale 26.578
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Nazione #
US - Stati Uniti d'America 10.132
SG - Singapore 3.266
DE - Germania 2.548
CN - Cina 1.718
SE - Svezia 1.319
BR - Brasile 1.058
IT - Italia 850
VN - Vietnam 703
FR - Francia 661
UA - Ucraina 652
GB - Regno Unito 350
IE - Irlanda 315
FI - Finlandia 284
IN - India 275
ID - Indonesia 200
RU - Federazione Russa 164
PL - Polonia 156
TR - Turchia 147
CA - Canada 132
HK - Hong Kong 123
BD - Bangladesh 107
JP - Giappone 101
AR - Argentina 90
NL - Olanda 90
BE - Belgio 73
MX - Messico 67
IQ - Iraq 58
IR - Iran 50
ES - Italia 48
EC - Ecuador 46
ZA - Sudafrica 39
PK - Pakistan 38
AT - Austria 36
CI - Costa d'Avorio 33
CO - Colombia 26
PH - Filippine 26
SA - Arabia Saudita 25
VE - Venezuela 25
EG - Egitto 23
CL - Cile 20
JO - Giordania 20
UZ - Uzbekistan 20
CH - Svizzera 18
KR - Corea 18
IL - Israele 16
KE - Kenya 16
PY - Paraguay 16
AE - Emirati Arabi Uniti 15
AU - Australia 14
DZ - Algeria 14
LT - Lituania 13
NP - Nepal 13
CZ - Repubblica Ceca 12
EU - Europa 12
JM - Giamaica 12
MA - Marocco 12
RO - Romania 9
HU - Ungheria 8
KZ - Kazakistan 8
MY - Malesia 8
TN - Tunisia 8
BG - Bulgaria 7
CR - Costa Rica 7
MD - Moldavia 7
NO - Norvegia 7
PE - Perù 7
DK - Danimarca 6
GR - Grecia 6
LK - Sri Lanka 6
PT - Portogallo 6
SN - Senegal 6
TH - Thailandia 6
AL - Albania 5
AZ - Azerbaigian 5
BO - Bolivia 5
DO - Repubblica Dominicana 5
GT - Guatemala 5
KG - Kirghizistan 5
LB - Libano 5
LY - Libia 5
PA - Panama 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
TT - Trinidad e Tobago 3
A1 - Anonimo 2
AM - Armenia 2
AO - Angola 2
BH - Bahrain 2
BS - Bahamas 2
BY - Bielorussia 2
Totale 26.532
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Città #
Singapore 1.861
Chandler 1.493
Ashburn 1.058
San Jose 852
Jacksonville 393
San Mateo 346
Dublin 309
Ann Arbor 286
Beijing 281
Nanjing 252
New York 249
Los Angeles 233
Ho Chi Minh City 222
Wilmington 208
Hanoi 191
Jakarta 184
Milan 172
Lauterbourg 167
Boston 157
Woodbridge 157
Dallas 156
Nürnberg 134
Frankfurt am Main 130
Dearborn 128
Cattolica 126
Cambridge 122
Munich 115
The Dalles 114
Fairfield 111
Helsinki 110
Hefei 108
Houston 107
Lawrence 106
Hong Kong 105
Chicago 103
Seattle 101
Izmir 97
Moscow 92
Rome 92
São Paulo 89
Warsaw 89
Nanchang 86
Redwood City 84
Bremen 81
Marseille 81
Santa Clara 78
Tokyo 78
Boardman 69
Princeton 68
Lancaster 65
Buffalo 64
Shanghai 55
Mountain View 54
Hangzhou 52
Brussels 51
Kraków 51
Hebei 47
Kunming 47
London 47
Shenyang 43
Guangzhou 40
Orem 40
Turku 40
University Park 40
Zhengzhou 40
Detroit 39
Da Nang 38
Leawood 38
Rio de Janeiro 36
Haiphong 34
Tianjin 34
Abidjan 33
Montreal 33
Nuremberg 33
Atlanta 32
Norwalk 31
Paris 31
Augusta 29
Fremont 29
Kent 29
Stockholm 29
Brooklyn 28
Toronto 28
Council Bluffs 27
Denver 27
Düsseldorf 27
Phoenix 27
San Francisco 27
Changsha 26
Pune 26
Baghdad 25
Jiaxing 25
Philadelphia 25
Belo Horizonte 23
Hyderabad 23
Johannesburg 23
Redmond 22
Ottawa 21
Waanrode 21
Brasília 20
Totale 13.806
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Nome #
Hypophysitis Outcome and Factors Predicting Responsiveness to Glucocorticoid Therapy: A Prospective and Double-Arm Study. 347
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. 270
Polymorphisms in base excision DNA repair genes and association with melanoma risk in a pilot study on Central-South Italian population 246
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 236
A new standardized absolute quantitative RT-PCR method for detection of tyrosinase mRNAs in melanoma patients: technical and operative instructions. 236
Comments to ``A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency{''} 235
Secretory phospholipase A2 and neoantal di stress: pilot study on broncho-alveolar lavage 227
Association of IL-8 and eNOS polymorphisms with clinical outcomes in bevacizumab-treated breast cancer patients: an exploratory analysis 227
Insight into a Novel p53 Single Point Mutation (G389E) by Molecular Dynamics Simulations 223
Small Amplicons High Resolution Melting Analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population 219
Serum levels of seven cytokines in premature ventilated newborns: correlations with old and new forms of bronchopulmonary dysplasia 218
Increased levels of IGF-1 and beta2-microglobulin in epithelial lining fluid of preterm newborns developing chronic lung disease effects of rhG-CSF 218
A novel MEN1 frameshift germline mutation in two Italian monozygotic twins 213
DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism 213
BRCA mutational status, initial disease presentation, and clinical outcome in high-grade serous advanced ovarian cancer: a multicenter study 212
Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation 210
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: The Italian multicentre study 208
Correspondence between clinical improvement and proteomic changes of the salivary peptide complex ina child with primary Sjogren syndrome 206
Disability, More than multimorbidity, was predictive of mortality among older persons aged 80 years and older. 200
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement 197
A vascular endothelial growth factor deficiency characterises scleroderma lung disease 196
Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia 195
Incidental Finding of a Homozygous p.M348K Asymptomatic Italian Patient Confirms the Many Faces of Cystic Fibrosis 195
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 194
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 192
Is quantitative real time polymerase chain reaction MCAM transcript assay really suitable for prognostic and predictive management of melanoma patients? 192
The Hemo One Autoanalyzer for Glycated Hemoglobin Assay 192
Comparison of serum levels of seven cytokines in premature newborns undergoing different ventilatory procedures: high frequency oscillatory ventilation or synchronized intermittent mandatory ventilation 191
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 190
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients 188
HFOV in premature neonates: effects on pulmonary mechanics and epithelial lining fluid cytokines. A randomized controlled trial 187
Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia 184
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 184
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants 183
Sarcopenia as a risk factor for falls in elderly individuals: Results from the ilSIRENTE study 180
Advanced tools for BRCA1/2 mutational screening: Comparison between two methods for large genomic rearrangements (LGRs) detection 178
Midarm muscle circumference, physical performance and mortality: results from the aging and longevity study in the Sirente geographic area (ilSIRENTE study). 177
Bronchoalveolar lavage fluid peptidomics suggests a possible matrix metalloproteinase-3 role in bronchopulmonary dysplasia 175
Saffron Supplementation Improves Retinal Flicker Sensitivity in Early Age-Related Macular Degeneration 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
A new founder BRCA1 haplotype identified in the Puglia region is associated with a specific age-related cancer onset in three unrelated families 174
Analytical assessment of bone serum markers in patients suffering from spina bifida 173
Reliability and correlation study of a new homocysteine assay. 173
Gene symbol: CYP21A2. Disease: Adrenal hyperplasia 171
Surfactant and Varespladib Co-Administration in Stimulated Rat Alveolar Macrophages Culture 171
Bronchoalveolar lavage fluid peptidomics suggests a possibile matrix metalloproteinase-3 role in bronchopulmonary dysplasia 169
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: Comparison of two methods and implications in molecular diagnostics 168
First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome 167
Role of distinct phospholipases A2 and their modulators in meconium aspiration syndrome in human neonates. 167
A longitudinal follow-up study of saffron supplementation in early age-related macular degeneration: sustained benefits to central retinal function 167
Nonsteroidal Anti-Inflammatory Drug (NSAID) Use and Sarcopenia in Older People: Results From the ilSIRENTE Study 166
Circulating endothelial cell levels in psoriatic patients and their modification after an anti-TNF-alpha (Etanercept) treatment 165
Association of anorexia with sarcopenia in a community-dwelling elderly population: results from the ilSIRENTE study 162
Sarcopenia and mortality risk in frail older persons aged 80 years and older: results from ilSIRENTE study 161
Circulating endothelial cells as marker of endothelial damage in male hypogonadism 160
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review 160
Lactose intolerance genetic testing: Is it useful as routine screening? Results on 1426 south-central Italy patients 160
Bile acids cause secretory phospholipase A2 activity enhancement, revertible by exogenous surfactant administration. 159
GSTM1-null polymorphism as possible risk marker for hypertension: results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study) 159
L' era del PCA3: risultati preliminari di uno studio pragmatico monocentrico 159
Influence of saffron supplementation on retinal flicker sensitivity in early age-related macular degeneration. 158
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100B, LDH, NSE biochemical markers. 158
Description of an Automated Method for Urea Nitrogen Determination in Bronchoalveolar Lavage Fluid (BALF) of Neonates and Infants 158
BRCA Mutation Status in Triple-Negative Breast Cancer Patients Treated with Neoadjuvant Chemotherapy: A Pivotal Role for Treatment Decision-Making 156
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 156
Prospective phase II trial of trabectedin in BRCA-mutated and/or BRCAness phenotype recurrent ovarian cancer patients: the MITO 15 trial 155
Human cardiac progenitor cells with regenerative potential can be isolated and characterized from 3D-electro-anatomic guided endomyocardial biopsies 155
IL-8 and eNOS polymorphisms predict bevacizumab-based first line treatment outcomes in RAS mutant metastatic colorectal cancer patients 155
Serum levels of C-terminal agrin fragment (CAF) are associated with sarcopenia in older multimorbid community-dwellers: Results from the ilSIRENTE study 154
High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism 153
Genes, pseudogenes and like genes: The case of 21-hydroxylase in Italian population 152
CYP21A2 p.E238 Deletion as Result of Multiple Microconversion Events: A Genetic Study on an Italian Congenital Adrenal Hyperplasia (CAH) Family 151
The Changing Clinical Spectrum of Hypophysitis 149
Let‐7a‐5p, mir‐100‐5p, mir‐101‐3p, and mir‐199a‐3p hyperexpression as potential predictive biomarkers in early breast cancer patients 149
Molecular and Genetic Immune Biomarkers of Primary and Immune-Therapy Induced Hypophysitis: From Laboratories to the Clinical Practice 149
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 148
Non-catalytic region of tyrosine kinase adaptor protein 2 (NCK2) pathways as factor promoting aggressiveness in ovarian cancer 148
Epithelial lining fluid Neutrophil-gelatinase-associated lipocalin levels in premature newborns with bronchopulmonary dysplasia and patency of ductus arteriosus 147
Evaluation of Endothelial Dysfunction in Psoriatic Patients by Different Techniques 147
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations 146
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms? 146
A rapid screening of a recurrent CYP24A1 pathogenic variant opens the way to molecular testing for Idiopathic Infantile Hypercalcemia (IIH) 146
Secretory phospholipase A₂ pathway during pediatric acute respiratory distress syndrome: a preliminary study. 145
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the "old" and update of the new mutations 145
p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients 145
Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report. 144
A novel CYP24A1 genotype associated to a clinical picture of hypercalcemia, nephrolithiasis and low bone mass 144
Gene symbol: CYP21A2. Disease: Non-classic 21-Hydroxylase deficiency. 143
CYP21A2 genetics: When genotype does not fit phenotype 142
Clinical and biological role of secretory phospholipase A2 in acute respiratory distress syndrome infants 141
ACE I allele is associated with more severe portal hypertension in patients with liver cirrhosis: A pilot study 141
Ex Vivo Effect of Varespladib on Secretory Phospholipase A2 Alveolar Activity in Infants with ARDS 140
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 140
FOXM1 expression is significantly associated with chemotherapy resistance and adverse prognosis in non-serous epithelial ovarian cancer patients 140
IGF-1 and microvascular complications of diabetes: alternative interpretation of recently published data 139
Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100, LDH, NSE, byochemical markers 139
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome 139
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 139
Rapid detection of CFH (p.Y402H) and ARMS2 (p.A69S) polymorphisms in age-related macular degeneration using high-resolution melting analysis 138
Effect of prenatal steroidal inhibition of sPLA2 in a rat model of preterm lung 138
Totale 17.471
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Categoria #
all - tutte 103.558
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 103.558
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20268.859 1.302 260 515 945 1.638 459 1.715 531 509 524 277 184
2026/2027196 196 0 0 0 0 0 0 0 0 0 0 0
Totale 26.865