Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

CEFALU', Angelo Baldassare
 Distribuzione geografica
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Continente #
NA - Nord America 20.381
EU - Europa 10.585
AS - Asia 9.069
SA - Sud America 1.593
AF - Africa 275
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 9
Totale 41.936
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Nazione #
US - Stati Uniti d'America 20.107
SG - Singapore 3.328
RU - Federazione Russa 2.786
CN - Cina 2.310
IT - Italia 2.002
FI - Finlandia 1.292
BR - Brasile 1.267
HK - Hong Kong 917
UA - Ucraina 895
DE - Germania 891
VN - Vietnam 883
PL - Polonia 603
FR - Francia 499
GB - Regno Unito 483
IE - Irlanda 428
JP - Giappone 392
KR - Corea 223
SE - Svezia 194
IN - India 187
BD - Bangladesh 171
CA - Canada 143
TR - Turchia 125
AR - Argentina 115
IQ - Iraq 97
NL - Olanda 94
AT - Austria 85
MX - Messico 81
BE - Belgio 76
ZA - Sudafrica 61
RO - Romania 55
CI - Costa d'Avorio 52
PK - Pakistan 52
EC - Ecuador 44
ES - Italia 44
CL - Cile 41
UZ - Uzbekistan 40
VE - Venezuela 40
MA - Marocco 36
IR - Iran 34
KE - Kenya 32
CO - Colombia 31
ID - Indonesia 31
SA - Arabia Saudita 31
CH - Svizzera 30
MY - Malesia 30
PH - Filippine 25
PY - Paraguay 25
AE - Emirati Arabi Uniti 24
JO - Giordania 22
NP - Nepal 22
AZ - Azerbaigian 21
EG - Egitto 21
AU - Australia 19
DZ - Algeria 19
GR - Grecia 16
IL - Israele 15
JM - Giamaica 15
LT - Lituania 15
BG - Bulgaria 13
TH - Thailandia 13
UY - Uruguay 12
PE - Perù 11
KZ - Kazakistan 10
PT - Portogallo 10
SN - Senegal 10
TN - Tunisia 10
CZ - Repubblica Ceca 9
HU - Ungheria 9
AL - Albania 8
PA - Panama 8
RS - Serbia 8
BH - Bahrain 7
BO - Bolivia 7
GE - Georgia 7
LB - Libano 7
OM - Oman 7
CR - Costa Rica 6
DO - Repubblica Dominicana 6
HR - Croazia 6
KG - Kirghizistan 6
LK - Sri Lanka 6
NG - Nigeria 6
AO - Angola 5
ET - Etiopia 5
GA - Gabon 5
HN - Honduras 5
MK - Macedonia 5
QA - Qatar 5
TW - Taiwan 5
BY - Bielorussia 4
EU - Europa 4
LV - Lettonia 4
MD - Moldavia 4
NZ - Nuova Zelanda 4
PS - Palestinian Territory 4
SK - Slovacchia (Repubblica Slovacca) 4
TT - Trinidad e Tobago 4
XK - ???statistics.table.value.countryCode.XK??? 4
BA - Bosnia-Erzegovina 3
DK - Danimarca 3
Totale 41.896
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Città #
Ashburn 2.606
Fairfield 2.291
Singapore 2.202
Chandler 1.201
Woodbridge 1.189
Houston 1.062
San Jose 1.035
Wilmington 985
Seattle 975
Hong Kong 883
Cambridge 742
Ann Arbor 598
Zgierz 528
Moscow 478
Jacksonville 452
Dublin 425
Medford 388
Tokyo 370
Beijing 360
Palermo 340
Santa Clara 312
Dallas 300
Council Bluffs 285
Ho Chi Minh City 281
Los Angeles 276
Frankfurt am Main 268
New York 255
Nanjing 253
Princeton 242
Lauterbourg 238
Des Moines 222
Altamura 218
Hanoi 213
San Diego 184
Lawrence 156
Boardman 153
Dearborn 138
Chicago 137
Hefei 133
Tulsa 131
Helsinki 128
São Paulo 112
Buffalo 102
Shenyang 98
Milan 96
The Dalles 95
London 94
Nanchang 87
Orem 85
Seongnam 77
Hebei 74
Jinan 74
Tianjin 72
Changsha 70
Munich 70
Brussels 69
Rome 63
Jiaxing 56
Ludwigshafen am Rhein 53
Abidjan 52
Guangzhou 52
Amsterdam 51
Izmir 51
Phoenix 50
Nuremberg 49
Rio de Janeiro 49
Venice 46
Da Nang 44
Haiphong 44
Chennai 43
Johannesburg 43
Warsaw 42
Verona 41
Ningbo 40
Saint Petersburg 39
Columbus 37
Düsseldorf 37
Atlanta 35
Montreal 35
Salt Lake City 34
Zhengzhou 34
Baghdad 32
Tashkent 32
Vienna 32
Bremen 31
Denver 31
Lappeenranta 31
Stockholm 31
Toronto 31
Brooklyn 30
Hangzhou 30
Shanghai 30
Boston 28
Nairobi 28
Belo Horizonte 27
Manchester 27
City of London 26
Turku 26
Ottawa 24
Redwood City 24
Totale 26.579
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Nome #
Multiple food hypersensitivity as a cause of refractory chronic constipation in adults 480
IgA anti-actin antibodies ELISA in coeliac disease: A multicentre study. 390
A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily 293
Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease 290
Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study 289
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 288
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA 272
ApoE polymorphism in a small Mediterranean island: Relationships with plasma lipids, lipoproteins and LDL particle size 265
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA 263
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA 262
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 260
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. 259
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography 257
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. 254
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE 253
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred 251
FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease 249
BETA-2-GLYCOPROTEIN I IS GROWTH REGULATED AND PLAYS A ROLE AS SURVIVAL FACTOR FOR HEPATOCYTES 248
Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population 248
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 247
The metabolic syndrome predicts cardiovascular events in subjects with normal fasting glucose: Results of a 15 years follow-up in a Mediterranean population. 246
Circulating Molecular Chaperones in Subjects with Amnestic Mild Cognitive Impairment and Alzheimer's Disease: Data from the Zabùt Aging Project 246
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 245
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent 242
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. 242
A Novel Mutation of the DHCR7 Gene in a Sicilian Compound Heterozygote with Smith-Lemli-Opitz Syndrome 240
Association of estrogen receptor alpha gene with Alzheimer's disease: a case-control study 238
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 236
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study 236
Effects of Steatosis on Hepatic Hemodynamics in Patients with Metabolic Syndrome 233
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 231
Heparin induces an accumulation of atherogenic lipoproteins during hemodialysis in normolipidemic end-stage renal disease patients. 231
Association between plasma lipid levels and migraine in subjects aged > or =50 years: preliminary data from the Zabùt Aging Project 228
A novel putative interactor for the low density lipoprotein receptor cytoplasmic domain 226
INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY 224
Clinical, pathologic, and genetic features of massive soft tissue neurofibromas in a Sicilian patient 224
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 222
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 219
Prediction of incident type 2 diabetes mellitus based on a twenty-year follow-up of the Ventimiglia heart study 216
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing 215
A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. 214
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. 213
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 212
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). 211
Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins 210
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 208
The ANP Genetic Variant RS5068 is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population 208
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (LDL) receptor 207
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 207
Metabolomic analysis of plasma from Alzheimer disease patients 206
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. 204
FAMILIAL LIGAND-DEFECTIVE APOLIPOPROTEIN B: IDENTIFICATION OF A FAMILY HARBOURING THE ARG3531CYS (FDB3531) OF THE APOB GENE 204
No association between the cystatin C gene polymorphism and Alzheimer's disease: a case-control study in an Italian population. 204
Transient chylomicronemia preceding the onset of insulin-dependent diabetes in a young girl with no humoral markers of islet autoimmunity. 204
Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an “FCS score” 204
LA LIPIDOMICA DELLA NON ALCOHOLIC FATTY LIVER DISEASE: ANALISI DELLA CINETICA DELL’ACIDO PALMITICO MEDIANTE L’USO DI UN ISOTOPO STABILE IN UN MODELLO IN VITRO 203
MISSENSE MUTATION ALA34VAL IN EXON 2 OF THE LIPOPROTEIN LIPASE GENE IN A YOUNG MAN WITH CHYLOMICRONEMIA. 202
Obesity and the metabolic syndrome in a student cohort from Southern Italy 201
Enhanced Lipid Peroxidation and Platelet Activation as Potential Contributors to Increased Cardiovascular Risk in the Low-HDL Phenotype 200
Cystatin C levels are decreased in acute myocardial infarction: Effect of cystatin C G73A gene polymorphism on plasma levels 200
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene. 199
Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction 198
A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia 197
Novel mutations of CETP gene in Italian subjects with hyeralphalipoproteinemia 196
PREVALENCE OF ANGPTL3 AND APOB GENE MUTATIONS IN SUBJECTS WITH COMBINED HYPOLIPIDEMIA 195
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 195
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia 195
UNA NUOVA MUTAZIONE DELL’INTRONE 16 (G>A a 2390 -1) DEL RECETTORE DELLE LDL RESPONSABILE DI IPERCOLESTEROLEMIA FAMILIARE. EFFETTI SULLA ESPRESSIONE DELL’mRNA DEL RECETTORE DELLE LDL 193
Genetic epidemiology of ARH in Sicily 193
ENHANCED LIPID PEROXIDATION AND PLATELET ACTIVATION AS POTENTIAL CONTRIBUTORS TO INCREASED CARDIOVASCULAR RISK IN THE LOW-HDL PHENOTYPE. 192
CLINICAL CHARACTERISTICS AND PLASMA LIPIDS IN SUBJECTS WITH FAMILIAL COMBINED HYPOLIPIDEMIA: A POOLED ANALYSIS 192
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. 192
DIFFERENCE IN THE PREVALENCE OF METABOLIC SYNDROME AND CARDIOVASCULAR RISK FACTORS AFTER 14 YEARS IN THE POPULATION OF VENTIMIGLIA DI SICILIA 190
LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY 190
Role of Nutraceuticals in Hypolipidemic Therapy 190
Determinants of enhanced thromboxane biosynthesis in renal transplantation 190
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. 189
Plasma calprotectin levels in patients suffering from acute pancreatitis. 189
The C(-260)>T gene polymorphism in the promoter of the CD14 monocyte receptor gene is not associated with acute myocardial infarction 189
Molecular diagnosis of hypobetalipoproteinemia: An ENID review 188
Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. 188
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 188
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. 186
Additive effect of mutations in LDLR and PCSK9 genes on the phenotyoe of familial hypercholesterolemia 186
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia 186
Plasma levels of lipoproteins and apolipoproteins in congenital hypothyroidism: effects of L-thyroxine substitution therapy 186
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia 186
ASSOCIAZIONE DEL POLIMORFISMO Q192R DEL GENE DELLA PARAOXONASI I (PON1) CON LA MALATTIA CORONARICA IN UN CAMPIONE DI PZ CON INFARTO MIOCARDICO, MALATTIA CORONARICA NON INFARTUALE E SOGGETTI NORMALI. 184
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects 184
MUSCLE DAMAGE AND PAIN IN HYPERCHOLESTEROLEMIC OUT-PATIENTS POPULATION ON STATIN TREATMENT. 183
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography 182
Lipid and apoprotein composition of HDL in partial or complete CETP deficiency 180
IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING A MUTATION IN THE LDL-R GENE AND IN THE PCSK9 GENE 179
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS 179
ENHANCED LIPID PEROXIDATION AND PLATELET ACTIVATION AS POTENTIAL CONTRIBUTORS TO INCREASED CARDIOVASCULAR RISK IN THE “LOW-HDL” PHENOTYPE. 178
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia 178
Food hypersensitivity as a cause of rectal bleeding in adults 178
FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION. 176
CETP levels rather than polymorphisms as markers of coronary risk: healthy athlete with high HDL-C and coronary disease--effectiveness of probucol. 176
Association between familial hypobetalipoproteinemia and the risk of diabetes. Is this the other side of the cholesterol–diabetes connection? A systematic review of literature 176
Totale 21.871
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Categoria #
all - tutte 145.876
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 145.876
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021587 0 0 0 0 0 0 0 0 0 0 263 324
2021/20222.725 81 575 110 86 66 100 110 144 379 387 147 540
2022/20233.485 368 628 75 385 418 534 170 257 382 33 149 86
2023/20241.761 80 266 127 205 104 412 161 73 27 47 47 212
2024/20254.894 97 281 308 371 190 187 363 355 455 489 685 1.113
2025/202615.286 1.071 546 831 1.085 1.416 2.400 2.157 1.693 1.234 2.334 519 0
Totale 43.146