QUATTRUCCI, Serena
 Distribuzione geografica
Continente #
NA - Nord America 5.702
EU - Europa 2.399
AS - Asia 978
SA - Sud America 53
AF - Africa 28
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 9.164
Nazione #
US - Stati Uniti d'America 5.636
RO - Romania 642
IT - Italia 587
SG - Singapore 405
UA - Ucraina 386
IN - India 335
SE - Svezia 249
CN - Cina 210
FI - Finlandia 180
DE - Germania 76
GB - Regno Unito 70
CA - Canada 62
AR - Argentina 46
AT - Austria 35
RU - Federazione Russa 32
IE - Irlanda 30
BG - Bulgaria 29
BE - Belgio 26
TG - Togo 23
NL - Olanda 14
GR - Grecia 9
ID - Indonesia 9
PT - Portogallo 9
FR - Francia 8
CL - Cile 4
MX - Messico 4
IR - Iran 3
LT - Lituania 3
MY - Malesia 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
BR - Brasile 2
CH - Svizzera 2
CZ - Repubblica Ceca 2
ES - Italia 2
EU - Europa 2
IQ - Iraq 2
KZ - Kazakistan 2
LV - Lettonia 2
SC - Seychelles 2
SI - Slovenia 2
AM - Armenia 1
BJ - Benin 1
BY - Bielorussia 1
DK - Danimarca 1
EC - Ecuador 1
HK - Hong Kong 1
HU - Ungheria 1
IL - Israele 1
JP - Giappone 1
MA - Marocco 1
MN - Mongolia 1
RS - Serbia 1
SA - Arabia Saudita 1
VN - Vietnam 1
ZA - Sudafrica 1
Totale 9.164
Città #
Fairfield 838
Horia 628
Chandler 497
Woodbridge 473
Ashburn 379
Seattle 343
Singapore 294
Houston 293
Ann Arbor 272
Cambridge 263
Wilmington 262
Princeton 175
Jacksonville 154
Plano 153
Rome 144
Santa Clara 130
Beijing 126
Dearborn 92
Boston 84
San Paolo di Civitate 79
Lawrence 73
San Diego 72
Boardman 59
Millbury 55
Federal 46
Des Moines 40
Andover 37
Helsinki 33
Norwalk 33
Toronto 31
Vienna 31
Dublin 30
Sofia 29
Ottawa 24
Lomé 23
Brussels 21
Falls Church 21
Moscow 19
Southend 18
Milan 16
New York 16
San Mateo 14
Falkenstein 13
Bühl 12
Shanghai 12
Auburn Hills 11
Bremen 11
Fremont 11
Mannheim 10
Jakarta 9
Lisbon 9
Florence 8
Hefei 8
Naples 8
Los Angeles 7
Nanjing 7
Sora 7
Torino 7
London 6
Siena 6
Venice 6
Bologna 5
Brescia 5
Buffalo 5
Casarano 5
Frankfurt am Main 5
Kunming 5
Nanchang 5
Redmond 5
Bari 4
Cogollo Del Cengio 4
Dallas 4
Guangzhou 4
Jinan 4
Mexico City 4
Morlupo 4
San Jose 4
Washington 4
Baltimore 3
Colleferro 3
Forlì 3
Genova 3
Grafing 3
Guidonia Montecelio 3
Jönköping 3
Las Vegas 3
Mestre 3
Morcone 3
Phoenix 3
Turin 3
Villanova 3
Yellow Springs 3
Ad Diwaniyah 2
Bengaluru 2
Bergamo 2
Braine-le-Comte 2
Capannori 2
Castrolibero 2
Cava de' Tirreni 2
Cereda 2
Totale 6.722
Nome #
Achromobacter xylosoxidans Genomic Characterization and Correlation of Randomly Amplified Polymorphic DNA Profiles of Cystic Fibrosis Patients 176
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Allelic Variants Relate to Shifts in Faecal Microbiota of Cystic Fibrosis Patients 175
Bdellovibrio bacteriovorus directly attacks Pseudomonas aeruginosa and Staphylococcus aureus Cystic fibrosis isolates 175
Cystic fibrosis transmembrane conductance regulator (CFTR) allelic variants relate to shifts in faecal microbiota of cystic fibrosis patients 174
Cystic fibrosis transmembrane conductance regulator (CFTR) allelic variants relate to shifts in fecal microbiota of cystic fibrosis patients. 134
Strategie terapeutiche innovative basate sulla duplice attività, antibatterica e probiotica, del predatore batterico Bdellovibrio bacteriovorus 134
Impact of clonally-related Burkholderia contaminans strains in two patients attending an Italian cystic fibrosis centre. A case report 118
Il pattern mutazionale del gene CFTR in diverse forme di fibrosi cistica influenza le caratteriastiche operative del test genetico. 107
Dysfunctional CFTR Alters the Bactericidal Activity of Human Macrophages against Pseudomonas aeruginosa 106
La conversione da ciclosporina A (CyA) a Tacrolimus nel trapianto polmonare per fibrosi cistica 103
Scedosporium apiospermum atrial mycetomas after lung transplantation for cystic fibrosis 99
Assessment of CF lung disease using motion corrected PROPELLER MRI: a comparison with CT 98
Deregulation of the growth hormone/insulin-like growth factor-1 axis in adults with cystic fibrosis 98
Is daily physical activity affected by dynamic hyperinflation in adults with cystic fibrosis? 96
Automation of CFTR re-sequencing: time and costs analysis 92
Molecular Characterization of Stenotrophomonas maltophilia Isolates from Cystic Fibrosis Patients and the Hospital Environment 91
Effects of inhaled hypertonic (7%) saline on lung function test in preschool children with cystic fibrosis: Results of a crossover, randomized clinical trial 90
3-Min step test and treadmill exercise for evaluating exercise-induced asthma 88
Reactive-Oxygen-Species-Mediated P. aeruginosa Killing Is Functional in Human Cystic Fibrosis Macrophages 86
Relationship between daily physical activity and aerobic fitness in adults with cystic fibrosis 86
A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis 85
A new complex allele of the CFTR gene partially explains the variable phenotype of the L997F mutation 83
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients 83
The Impact on Genetic Testing of Mutational Patterns of CFTR Gene in Different Clinical Macrocategories of Cystic Fibrosis. 82
Lung transplantation for cystic fibrosis: Ten years of experience 81
Treatment of Complex Airway Lesions After Lung Transplantation With Self-Expandable Nitinol Stents: Early Experience 79
Clostridium difficile-related pancolitis in lung-transplanted patients with cystic fibrosis 79
Relationship between pulmonary exacerbations and daily physical activity in adults with cystic fibrosis 79
Increased plasma levels of adrenomedullin, a vasoactive peptide, in patients with end-stage pulmonary disease 78
Improved results with lung transplantation for cystic fibrosis: a 6-year experience 78
Association of cholesterol oxidation and abnormalities in fatty acid metabolism in cystic fibrosis 77
La caratterizzazione genotipica dei microrganismi come buona pratica per valutarne la trasmissibilità ed il potenziale di diffusione nei pazienti con fibrosi cistica: il caso di Stenotrophomonas maltophilia. 76
Lung transplantation for cystic fibrosis in Italy 76
Cystic fibrosis transmembrane conductance regulator (CFTR) expression in human platelets: impact on mediators and mechanisms of the inflammatory response 75
Proteomics investigation of human platelets in healthy donors and cystic fibrosis patients by shotgun nUPLC-MSE and 2DE: a comparative study 75
Evaluation of a home telemonitoring service for adult patients with cystic fibrosis: a pilot study 75
Recovery of chronic renal impairment with sirolimus after lung transplantation. 74
High frequency of (TG)m Tn variant tracts in the Cystic Fibrosis Transmembrane Conductance Regulator Gene in men with high semen viscosity 74
Six-minute walk test vs cardiopulmonary exercise test in the assessment of exercise tolerance in adults with cystic fibrosis 74
The role of ceramide in the host defense against pseudomonas aeruginosa infection 73
Genotype-phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles 73
IL VIRUS RESPIRATORIO SINCIZIALE: LA PATOGENESI DEL DANNO 72
Microaspiration in infants with laryngomalacia 71
Does male fertility impairment due to idiopathic semen hyperviscosity depend on CFTR gene mutations? 71
Elevated levels of miR-145 correlate with SMAD3 down-regulation in Cystic Fibrosis patients 71
Improved results with lung transplantation for cystic fibrosis 70
A 96-well formatted method for exon and exon/intron boundary full sequencing of the CFTR gene 70
Pulmonary hypertension is associated with higher mortality in cystic fibrosis patients awaiting lung transplantation. 70
Plasma adrenomedullin and endothelin-1 concentration during low-dose dobutamine infusion: Relationship between pulmonary uptake and pulmonary vascular pressure/flow characteristics 70
Isolated lung transplantation for end-stage pulmonary disease 69
Usefulness of 2D echo Doppler in the preoperative assessment of cystic fibrosis patients who are candidates for lung transplantation 69
Lung Transplantation for Cystic Fibrosis After Thoracic Surgical Procedures 69
Synergistic Post-Transcriptional Regulation of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) by miR-101 and miR-494 Specific Binding 68
null 68
Timing and priorities for cystic fibrosis patients candidates to lung transplantation 67
Lung macrophages from CF patients show a severely compromised bactericidal activity against Pseudomonas aeruginosa that is independent from intracellular ROS production 67
Chronic expectoration of staples after reductive pneumoplasty in a lung transplantation patient 67
Neutrophil glutamine deficiency in relation to genotype in children with cystic fibrosis 67
Burkholderia pyrrocinia in Cystic Fibrosis Lung Transplantation: A Case Report. 67
Malignancies and lung transplant 65
An automated methodology for high-throughput mutational analysis of CFTR 65
Analisi retrospettiva su 67 pazienti sottoposti a fibrobroncoscopia per sospetta inalazione di corpo estraneo afferenti a 4 Centri di Pneumologia Pediatrica del Gruppo di Studio di Endoscopia della Società Italiana per le Malattie Respiratorie Infantili 64
Neutrophil generation of inflammatory precursors is not modulated by docosahexaenoic acid 64
Clinical expression of patients with the D1152H CFTR mutation 64
Extensive CFTR mutational analysis in patients with CBAVD 64
Assenza congenita dei vasi deferenti: fenotipo della fibrosi cistica? 62
Hemorrhagic bowel necrosis associated with acute digitalis in an infant. 61
Spondylodiscitis after bilateral sequential lung transplantation in a patient with cystic fibrosis 61
Il pattern mutazionale del gene CFTR in diverse forme di fibrosi cistica influenza le caratteristiche operative del test genetico 61
Does cystic fibrosis neonatal screening detect atypical CF forms? Extended genetic characterization and 4-year clinical follow-up 59
Comparison of two different protocols of neonatal screening for cystic fibrosis 59
Survival after lung transplant for cystic fibrosis in italy. A single center experience with 20 years of follow-up 59
Selezione di varianti genomiche in forme atipiche di Fibrosi Cistica 58
Indagine mutazionale su neonati eterozigoti per la fibrosi cistica con ipertripsinenia alla nascita e test del sudore negativo 58
Clinical expression of cystic fibrosis in a large cohort of Italian siblings 58
Transferrin subtypes in Cystic Fibrosis 58
Bronchial adenoma: An unusual cause of recurrent pneumonia in childhood 58
The development of an octavalent conjugate P. aeruginosa (PA) vaccine for Cystic Fibrosis (CF) patients: results from two Phase II studies 57
A Genotypic-oriented View of CFTR Genetics Highlights Specific Mutational Patterns Underlying Clinical Macro-categories of Cystic Fibrosis. 57
Influenza del pattern mutazionale del gene CFTR sul test genetico e sulla relazione genotipo-fenotipo in diverse forme di fibrosi cistica. 57
Acute pulmonary vascular response to inhaled nitric oxide,dobutamine and their association in patients with secondary pulmonary hypertension. 56
Effect of a medium dose of Ursodeoxycholic acid with or without Taurine supplementation on the nutritional status of patients with Cystic fibrosis:A randomized, placebo-controlled,crossover trial 55
Caratterizzazione di mutazioni rare del gene CFTR 55
Is there a relationship between sex of cystic fibrosis carriers and sex ratio of their offspring? 55
miR‑125b/NRF2/HO‑1 axis is involved in protection against oxidative stress of cystic fibrosis: a pilot study 55
A multitask biosensor for micro-volumetric detection of N-3-oxo-dodecanoyl-homoserine lactone quorum sensing signal 55
Automation of CFTR re-sequencing: time and cost analysis 54
Isolated lung transplantation for end-stage lung disease 54
Measuring habitual physical activity in adults with cystic fibrosis 54
Trans-heterozygosity for mutations enhances the risk of recurrent/chronic pancreatitis in patients with Cystic Fibrosis 53
WS14.6 Gender differences and exercise performance in adults with cystic fibrosis 52
Neutrophil unsaturated fatty acid release by GM-CSF is impaired in cystic fibrosis 52
null 52
Usefullness of lung function tests in detetcting rejection and respiratory infection after lung transplantation in cystic fibrosis 51
Quali sono i parametri di funzionalità respiratoria più utili nel valutare la "fitness" e l'effetto dell'attività fisica nel bambino asmatico? 50
Detection, by a high sensitivity protocol for mutational analysis, of two novel CFTR mutations. 50
Precipitating Pseudomonas aeruginosa antibodies and antimicrobial therapy in cystic fibrosis patients. 50
Double lung transplantation for septic lung disease. 48
Lung transplantation for cystic fibrosis: 6-year follow-up 48
Hepatobiliary involvement in adolescents and adults with Cystic Fibrosis 46
Totale 7.512
Categoria #
all - tutte 26.305
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 26.305


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.054 0 0 0 0 0 0 251 239 203 210 94 57
2020/20211.301 102 99 28 662 14 44 19 61 62 106 40 64
2021/20221.639 19 100 137 57 223 32 35 142 134 142 270 348
2022/20231.629 315 279 79 226 217 174 15 94 136 28 57 9
2023/2024678 47 124 30 55 58 70 26 50 6 92 54 66
2024/2025631 102 35 113 76 140 164 1 0 0 0 0 0
Totale 9.452