Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

CEFALU', Angelo Baldassare
 Distribuzione geografica
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Continente #
NA - Nord America 15.168
EU - Europa 5.693
AS - Asia 2.316
AF - Africa 58
SA - Sud America 39
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 5
Totale 23.295
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Nazione #
US - Stati Uniti d'America 15.111
IT - Italia 1.748
CN - Cina 1.189
FI - Finlandia 1.160
UA - Ucraina 870
SG - Singapore 807
DE - Germania 425
IE - Irlanda 405
GB - Regno Unito 319
SE - Svezia 169
RU - Federazione Russa 156
FR - Francia 135
KR - Corea 98
BE - Belgio 68
IN - India 54
RO - Romania 54
TR - Turchia 54
CI - Costa d'Avorio 48
CA - Canada 41
NL - Olanda 35
BR - Brasile 27
CH - Svizzera 27
IR - Iran 26
PL - Polonia 26
HK - Hong Kong 24
JP - Giappone 22
AT - Austria 17
AU - Australia 14
ES - Italia 14
GR - Grecia 13
MX - Messico 13
BG - Bulgaria 12
CZ - Repubblica Ceca 6
PT - Portogallo 6
VN - Vietnam 6
HR - Croazia 5
CL - Cile 4
CO - Colombia 4
DK - Danimarca 4
EU - Europa 4
IL - Israele 4
LK - Sri Lanka 4
PK - Pakistan 4
UZ - Uzbekistan 4
BD - Bangladesh 3
HU - Ungheria 3
IQ - Iraq 3
MK - Macedonia 3
PH - Filippine 3
SA - Arabia Saudita 3
SK - Slovacchia (Repubblica Slovacca) 3
EG - Egitto 2
LV - Lettonia 2
MD - Moldavia 2
NG - Nigeria 2
NZ - Nuova Zelanda 2
PA - Panama 2
RS - Serbia 2
ZA - Sudafrica 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AO - Angola 1
AR - Argentina 1
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
CR - Costa Rica 1
DZ - Algeria 1
EC - Ecuador 1
GE - Georgia 1
KE - Kenya 1
KG - Kirghizistan 1
LB - Libano 1
ME - Montenegro 1
MN - Mongolia 1
MY - Malesia 1
NO - Norvegia 1
OM - Oman 1
PY - Paraguay 1
SC - Seychelles 1
SI - Slovenia 1
TH - Thailandia 1
TW - Taiwan 1
Totale 23.295
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Città #
Fairfield 2.291
Ashburn 1.483
Chandler 1.214
Woodbridge 1.186
Houston 1.040
Wilmington 981
Seattle 957
Cambridge 742
Singapore 650
Ann Arbor 598
Jacksonville 448
Dublin 402
Medford 389
Palermo 301
Nanjing 252
Princeton 243
Altamura 220
Des Moines 203
San Diego 183
Lawrence 157
New York 154
Boardman 149
Dearborn 137
Tulsa 131
Santa Clara 108
Shenyang 97
Beijing 88
Nanchang 86
Milan 77
Seongnam 77
Hebei 74
Jinan 70
Changsha 67
London 66
Brussels 64
Tianjin 59
Ludwigshafen am Rhein 53
Jiaxing 52
Helsinki 50
Izmir 49
Abidjan 48
Munich 46
Venice 45
Rome 43
Ningbo 39
Saint Petersburg 39
Verona 38
Düsseldorf 33
Guangzhou 33
Zhengzhou 32
Bremen 31
Columbus 29
Los Angeles 24
Phoenix 24
Redwood City 24
San Paolo di Civitate 24
Hangzhou 23
Norwalk 23
San Mateo 23
Kumar 22
Auburn Hills 21
Falls Church 21
Ottawa 21
Haikou 20
Lanzhou 20
Taizhou 20
Washington 19
Kunming 18
Naples 18
Taiyuan 17
Tehran 17
Pune 16
Shanghai 16
Chicago 13
Hefei 13
Redmond 13
Kraków 12
Seoul 12
Minamiyukigaya 11
Moscow 11
Orange 11
Candelo 10
Hong Kong 10
Sofia 10
Frankfurt am Main 9
Groningen 9
Montréal 9
Turin 8
Alcamo 7
Amsterdam 7
Bologna 7
Edinburgh 7
Kiev 7
Napoli 7
Stockholm 7
São Paulo 7
Toronto 7
Central 6
Detroit 6
Deutschnofen 6
Totale 16.777
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Nome #
Multiple food hypersensitivity as a cause of refractory chronic constipation in adults 276
IgA anti-actin antibodies ELISA in coeliac disease: A multicentre study. 207
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 195
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. 181
A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily 167
Heparin induces an accumulation of atherogenic lipoproteins during hemodialysis in normolipidemic end-stage renal disease patients. 164
Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population 163
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred 163
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent 161
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography 161
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. 157
A Novel Mutation of the DHCR7 Gene in a Sicilian Compound Heterozygote with Smith-Lemli-Opitz Syndrome 156
FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease 156
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 154
Enhanced Lipid Peroxidation and Platelet Activation as Potential Contributors to Increased Cardiovascular Risk in the Low-HDL Phenotype 153
BETA-2-GLYCOPROTEIN I IS GROWTH REGULATED AND PLAYS A ROLE AS SURVIVAL FACTOR FOR HEPATOCYTES 152
Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an “FCS score” 152
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 151
Clinical, pathologic, and genetic features of massive soft tissue neurofibromas in a Sicilian patient 151
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 151
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study 151
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
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA 149
Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease 149
The metabolic syndrome predicts cardiovascular events in subjects with normal fasting glucose: Results of a 15 years follow-up in a Mediterranean population. 149
Role of Nutraceuticals in Hypolipidemic Therapy 148
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 145
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA 144
Circulating Molecular Chaperones in Subjects with Amnestic Mild Cognitive Impairment and Alzheimer's Disease: Data from the Zabùt Aging Project 144
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 143
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. 142
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
PREVALENCE OF ANGPTL3 AND APOB GENE MUTATIONS IN SUBJECTS WITH COMBINED HYPOLIPIDEMIA 139
Obesity and the metabolic syndrome in a student cohort from Southern Italy 138
LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY 138
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 138
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 138
Albumin versus solvent/detergent-treated pooled plasma as replacement fluid for long-term plasma exchange therapy in a patient with primary hypertriglyceridemia and recurrent hyperlipidemic pancreatitis 138
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 137
Plasma calprotectin levels in patients suffering from acute pancreatitis. 137
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing 137
Transient chylomicronemia preceding the onset of insulin-dependent diabetes in a young girl with no humoral markers of islet autoimmunity. 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 135
Plasma levels of lipoproteins and apolipoproteins in congenital hypothyroidism: effects of L-thyroxine substitution therapy 135
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia 134
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA 133
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 133
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE 132
Molecular diagnosis of hypobetalipoproteinemia: An ENID review 132
Determinants of enhanced thromboxane biosynthesis in renal transplantation 132
ENHANCED LIPID PEROXIDATION AND PLATELET ACTIVATION AS POTENTIAL CONTRIBUTORS TO INCREASED CARDIOVASCULAR RISK IN THE LOW-HDL PHENOTYPE. 131
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 130
Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene 129
Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. 129
Lipid and apoprotein composition of HDL in partial or complete CETP deficiency 128
Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins 126
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
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene. 126
Effects of Steatosis on Hepatic Hemodynamics in Patients with Metabolic Syndrome 126
Nutritional characteristics of a rural Southern Italy population: the Ventimiglia di Sicilia Project 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
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
SEVERE MALABSORPTION AND DECREASED TRIGLYCERIDE RICH LIPOPROTEINS PRODUCTION IN A PROBAND CARRYING A MUTATION ENCODING FOR A TRUNCATED APOLIPOPROTEIN B100 VARIANT (APO B 34.8). 121
RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues 121
Association between plasma lipid levels and migraine in subjects aged > or =50 years: preliminary data from the Zabùt Aging Project 121
Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction 121
Beyond Statins: New Lipid Lowering Strategies to Reduce Cardiovascular Risk 121
eNOS activation by HDL is impaired in genetic CETP deficiency 121
Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients 121
Effects of PCSK9 variants on common carotid artery intima media thickness and relation to ApoE alleles. 120
Differential apolipoprotein(a) isoform expression in heterozygosity is an independent contributor to lipoprotein(a) levels variability 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
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia 118
Leukocyte count, diabetes mellitus and age are strong predictors of stroke in a rural population in southern Italy: An 8-year follow-up 117
Genetic epidemiology of ARH in Sicily 116
Lack of Correlation of Plasma HDL With Fecal Cholesterol and Plasma Cholesterol Efflux Capacity Suggests Importance of HDL Functionality in Attenuation of Atherosclerosis 116
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia. 116
HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY 115
CETP levels rather than polymorphisms as markers of coronary risk: healthy athlete with high HDL-C and coronary disease--effectiveness of probucol. 115
Food hypersensitivity as a cause of rectal bleeding in adults 115
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia 115
A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. 114
Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature 114
An unexplained congenital disorder of glycosylation-II in a child with neurohepatic involvement, hypercholesterolemia and hypoceruloplasminemia 113
Lomitapide: a novel drug for homozygous familial hypercholesterolemia 112
MISSENSE MUTATION ALA34VAL IN EXON 2 OF THE LIPOPROTEIN LIPASE GENE IN A YOUNG MAN WITH CHYLOMICRONEMIA. 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 109
Totale 13.746
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Categoria #
all - tutte 96.171
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 96.171
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203.520 0 0 0 0 0 797 682 415 654 252 496 224
2020/20213.013 139 294 187 276 227 184 381 186 303 249 263 324
2021/20222.742 81 575 110 86 66 100 110 144 390 387 151 542
2022/20233.509 369 635 75 387 420 539 170 259 387 33 149 86
2023/20241.769 80 267 128 206 105 414 161 73 28 47 47 213
2024/20251.414 97 283 308 372 190 164 0 0 0 0 0 0
Totale 24.429