Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

NOTO, Davide
 Distribuzione geografica
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Continente #
NA - Nord America 12.939
EU - Europa 4.033
AS - Asia 1.613
AF - Africa 47
SA - Sud America 27
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 5
Totale 18.684
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Nazione #
US - Stati Uniti d'America 12.886
IT - Italia 1.334
CN - Cina 839
FI - Finlandia 761
UA - Ucraina 527
SG - Singapore 520
DE - Germania 315
IE - Irlanda 305
GB - Regno Unito 256
RU - Federazione Russa 104
FR - Francia 93
SE - Svezia 90
BE - Belgio 59
KR - Corea 57
TR - Turchia 55
RO - Romania 51
CA - Canada 41
IN - India 37
CI - Costa d'Avorio 36
NL - Olanda 26
HK - Hong Kong 25
IR - Iran 24
JP - Giappone 21
PL - Polonia 21
CH - Svizzera 17
AU - Australia 15
AT - Austria 14
BR - Brasile 12
BG - Bulgaria 11
MX - Messico 11
GR - Grecia 10
ES - Italia 9
BA - Bosnia-Erzegovina 6
NZ - Nuova Zelanda 5
PT - Portogallo 5
VN - Vietnam 5
CO - Colombia 4
EC - Ecuador 4
EU - Europa 4
ZA - Sudafrica 4
CL - Cile 3
CY - Cipro 3
HR - Croazia 3
HU - Ungheria 3
IQ - Iraq 3
MY - Malesia 3
UZ - Uzbekistan 3
CZ - Repubblica Ceca 2
IL - Israele 2
KG - Kirghizistan 2
LK - Sri Lanka 2
MN - Mongolia 2
NG - Nigeria 2
NO - Norvegia 2
PE - Perù 2
PH - Filippine 2
PK - Pakistan 2
PS - Palestinian Territory 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 1
BD - Bangladesh 1
BF - Burkina Faso 1
BY - Bielorussia 1
DK - Danimarca 1
EG - Egitto 1
GE - Georgia 1
KE - Kenya 1
KZ - Kazakistan 1
LV - Lettonia 1
MA - Marocco 1
MD - Moldavia 1
ME - Montenegro 1
MK - Macedonia 1
PA - Panama 1
RS - Serbia 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
TG - Togo 1
TH - Thailandia 1
UY - Uruguay 1
Totale 18.684
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Città #
Fairfield 2.105
Ashburn 1.251
Woodbridge 1.043
Chandler 998
Houston 941
Seattle 879
Wilmington 843
Cambridge 669
Ann Arbor 522
Singapore 414
Dublin 303
Medford 292
Jacksonville 281
Palermo 281
Altamura 212
Des Moines 201
Princeton 183
Nanjing 160
Lawrence 149
San Diego 144
Dearborn 130
New York 117
Boardman 94
Santa Clara 94
Tulsa 86
Shenyang 76
Beijing 69
Nanchang 61
London 59
Brussels 58
Ludwigshafen am Rhein 57
Changsha 56
Jinan 51
Hebei 50
Izmir 50
Milan 48
Jiaxing 42
Seongnam 42
Tianjin 39
Venice 37
Abidjan 36
Bremen 35
Munich 34
Helsinki 33
Falls Church 28
Ningbo 27
Phoenix 26
Norwalk 25
Saint Petersburg 25
Zhengzhou 24
San Paolo di Civitate 22
Washington 22
Ottawa 20
Guangzhou 17
Hangzhou 17
Redwood City 17
Rome 17
Columbus 15
Los Angeles 15
Shanghai 15
Taizhou 15
Düsseldorf 14
Taiyuan 14
Haikou 13
Naples 13
Chicago 12
Hong Kong 12
Kraków 12
Redmond 12
Verona 12
Kilburn 11
Kumar 11
Kunming 11
Lanzhou 11
Minamiyukigaya 11
Paris 11
San Mateo 11
Tehran 11
Council Bluffs 10
Lappeenranta 10
Orange 10
Sofia 10
Moscow 9
Amsterdam 8
Auburn Hills 8
Frankfurt am Main 8
Hefei 8
Montréal 8
Pune 8
Alcamo 7
Catania 7
Central 7
Dallas 7
Napoli 7
San Francisco 7
Berlin 6
Detroit 6
Favara 6
Reggio Emilia 6
Sarajevo 6
Totale 14.043
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Nome #
Multiple food hypersensitivity as a cause of refractory chronic constipation in adults 271
Resting energy expenditure and substrate oxidation in malnourished patients with type 1 glycogenosis 203
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 194
The production of 85 kDa N-terminal fragment of apolipoprotein B in mutant HepG2 cells generated by targeted modification of apoB gene occurs by ALLN-inhibitable protease cleavage during translocation. 179
Heparin induces an accumulation of atherogenic lipoproteins during hemodialysis in normolipidemic end-stage renal disease patients. 163
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred 163
Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population 162
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography 161
Lipoprotein-associated phospholipase A2 activity is increased in patients with definite familial hypercholesterolemia compared with other forms of hypercholesterolemia 161
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent 160
C-reactive protein but not soluble CD40 ligand and homocysteine is associated to common atherosclerotic risk factors in a cohort of coronary artery disease patients. 158
The ANP Genetic Variant RS5068 is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population 157
Novel mutations of CETP gene in Italian subjects with hyeralphalipoproteinemia 157
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. 154
A Novel Mutation of the DHCR7 Gene in a Sicilian Compound Heterozygote with Smith-Lemli-Opitz Syndrome 153
Enhanced Lipid Peroxidation and Platelet Activation as Potential Contributors to Increased Cardiovascular Risk in the Low-HDL Phenotype 153
FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease 153
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 152
BETA-2-GLYCOPROTEIN I IS GROWTH REGULATED AND PLAYS A ROLE AS SURVIVAL FACTOR FOR HEPATOCYTES 151
Chronic constipation and food intolerance: a model of proctitis causing constipation 151
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 151
A novel component of the metabolic syndrome : The oxidative stress 150
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 150
Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an “FCS score” 150
Low-density lipoproteins generated during an oral fat load in mild hypertriglyceridemic and healthy subjects are smaller, denser, and have an increased low-density lipoprotein receptor binding affinity. 149
Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease 149
Bovine seminal ribonuclease is cytotoxic for both malignant and normal telomerase-positive cells 149
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA 148
Role of Nutraceuticals in Hypolipidemic Therapy 148
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study 148
The metabolic syndrome predicts cardiovascular events in subjects with normal fasting glucose: Results of a 15 years follow-up in a Mediterranean population. 147
Clinical symptoms in celiac patients on a gluten-free diet. 146
Association of estrogen receptor alpha gene with Alzheimer's disease: a case-control study 145
Hypertension and diabetes mellitus are associated with cardiovascular events in the elderly without cardiovascular disease. Results of a 15-year follow-up in a Mediterranean population 144
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 143
Analysis of sterols by high-performance liquid chromatography/mass spectrometry combined with chemometrics 141
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. 141
INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY 140
No association between the cystatin C gene polymorphism and Alzheimer's disease: a case-control study in an Italian population. 140
Effects of diabetes definition on global surveillance of diabetes prevalence and diagnosis: A pooled analysis of 96 population-based studies with 331 288 participants 140
PREVALENCE OF ANGPTL3 AND APOB GENE MUTATIONS IN SUBJECTS WITH COMBINED HYPOLIPIDEMIA 139
LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY 138
Obesity and the metabolic syndrome in a student cohort from Southern Italy 137
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 137
Myristic acid is associated to low plasma HDL cholesterol levels in a Mediterranean population and increases HDL catabolism by enhancing HDL particles trapping to cell surface proteoglycans in a liver hepatoma cell model 137
Apolipoprotein AI and HDL are reduced in stable cirrhotic patients with adrenal insufficiency: A possible role in glucocorticoid deficiency 136
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing 136
A century of trends in adult human height 136
CLINICAL CHARACTERISTICS AND PLASMA LIPIDS IN SUBJECTS WITH FAMILIAL COMBINED HYPOLIPIDEMIA: A POOLED ANALYSIS 136
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia 135
Prediction of incident type 2 diabetes mellitus based on a twenty-year follow-up of the Ventimiglia heart study 134
Evaluation of nitric oxide metabolites in a group of subjects with metabolic syndrome. 134
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia 134
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 133
REPOSITIONING OF THE GLOBAL EPICENTRE OF NON-OPTIMAL CHOLESTEROL 133
Molecular diagnosis of hypobetalipoproteinemia: An ENID review 132
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE 131
Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene 129
Worldwide trends in blood pressure from 1975 to 2015: a pooled analysis of 1479 population-based measurement studies with 19.1 million participants 129
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 129
A novel putative interactor for the low density lipoprotein receptor cytoplasmic domain 126
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy 126
Effects of Steatosis on Hepatic Hemodynamics in Patients with Metabolic Syndrome 126
Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins 125
Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. 125
Nutritional characteristics of a rural Southern Italy population: the Ventimiglia di Sicilia Project 125
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene. 125
Prevalence of overweight and obesity in a rural southern Italy population and relationships with total and cardiovascular mortality: The Ventimiglia di Sicilia project 124
Lipid Peroxidation, Nitric Oxide Metabolites, and Their Ratio in a Group of Subjects with Metabolic Syndrome 123
The C(-260)>T gene polymorphism in the promoter of the CD14 monocyte receptor gene is not associated with acute myocardial infarction 123
Lack of association between angiotensin converting enzyme polymorphism and sporadic Alzheimer's disease 123
Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults 122
RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues 121
Beyond Statins: New Lipid Lowering Strategies to Reduce Cardiovascular Risk 121
Relationship of a Body Shape Index and Body Roundness Index with carotid atherosclerosis in arterial hypertension 121
Effects of PCSK9 variants on common carotid artery intima media thickness and relation to ApoE alleles. 120
Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction 120
Differential apolipoprotein(a) isoform expression in heterozygosity is an independent contributor to lipoprotein(a) levels variability 120
Contributions of mean and shape of blood pressure distribution to worldwide trends and variations in raised blood pressure: a pooled analysis of 1018 population-based measurement studies with 88.6 million participants 120
Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score 120
The Atrial Natriuretic Peptide Genetic Variant Rs5068 Is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population 119
Cystatin C levels are decreased in acute myocardial infarction: Effect of cystatin C G73A gene polymorphism on plasma levels 119
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients 119
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia 117
Leukocyte count, diabetes mellitus and age are strong predictors of stroke in a rural population in southern Italy: An 8-year follow-up 116
HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY 115
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia 115
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS 114
Genetic epidemiology of ARH in Sicily 114
Protein oxidation in a group of subjects with metabolic syndrome. 113
Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature 113
Statin therapy in patients with aortic stenosis after the ASTRONOMER trial: is there still any space? 111
A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. 111
Nonalcoholic fatty liver and metabolic syndrome in Italy: Results from a multicentric study of the Italian Arteriosclerosis society 110
Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis 109
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia 108
Efficacy of Lomitapide in the Treatment of Familial Homozygous Hypercholesterolemia: Results of a Real-World Clinical Experience in Italy 108
Down regulation of CD11b and CD18 expression in children with hypercholesterolemia: A preliminary report. 105
Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolaemia: a single-arm, open-label, phase 3 study 105
ApoE polymorphism in a small Mediterranean island: Relationships with plasma lipids, lipoproteins and LDL particle size 105
Totale 13.662
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Categoria #
all - tutte 74.981
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 74.981
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.647 0 0 0 0 579 711 576 375 564 229 423 190
2020/20212.635 120 330 162 236 183 223 291 176 209 267 202 236
2021/20222.267 92 432 110 52 60 86 94 129 364 321 123 404
2022/20232.957 316 612 61 329 340 440 172 188 304 28 112 55
2023/20241.366 66 184 99 171 92 320 116 42 22 37 41 176
2024/2025891 72 244 239 252 84 0 0 0 0 0 0 0
Totale 19.732