Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

CEFALU', Angelo Baldassare
 Distribuzione geografica
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Continente #
NA - Nord America 21.329
EU - Europa 10.753
AS - Asia 9.238
SA - Sud America 1.626
AF - Africa 276
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 10
Totale 43.256
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Nazione #
US - Stati Uniti d'America 20.947
SG - Singapore 3.335
RU - Federazione Russa 2.786
CN - Cina 2.319
IT - Italia 2.145
FI - Finlandia 1.294
BR - Brasile 1.281
HK - Hong Kong 920
UA - Ucraina 897
DE - Germania 892
VN - Vietnam 885
PL - Polonia 604
FR - Francia 503
GB - Regno Unito 484
IE - Irlanda 428
JP - Giappone 392
BD - Bangladesh 308
KR - Corea 229
CA - Canada 202
SE - Svezia 194
IN - India 188
TR - Turchia 125
AR - Argentina 117
IQ - Iraq 97
NL - Olanda 94
AT - Austria 85
MX - Messico 83
BE - Belgio 76
ZA - Sudafrica 61
RO - Romania 55
CI - Costa d'Avorio 52
PK - Pakistan 52
EC - Ecuador 48
ES - Italia 47
CL - Cile 44
UZ - Uzbekistan 41
VE - Venezuela 41
CO - Colombia 37
MA - Marocco 36
IR - Iran 34
CH - Svizzera 33
KE - Kenya 32
MY - Malesia 32
ID - Indonesia 31
SA - Arabia Saudita 31
JM - Giamaica 28
PY - Paraguay 26
PH - Filippine 25
AE - Emirati Arabi Uniti 24
NP - Nepal 23
JO - Giordania 22
AZ - Azerbaigian 21
EG - Egitto 21
AU - Australia 19
DZ - Algeria 19
GR - Grecia 18
IL - Israele 15
LT - Lituania 15
BG - Bulgaria 14
PE - Perù 13
TH - Thailandia 13
HN - Honduras 12
PT - Portogallo 12
UY - Uruguay 12
CZ - Repubblica Ceca 10
KZ - Kazakistan 10
SN - Senegal 10
TN - Tunisia 10
AL - Albania 9
CR - Costa Rica 9
HU - Ungheria 9
PA - Panama 9
RS - Serbia 8
TT - Trinidad e Tobago 8
BH - Bahrain 7
BO - Bolivia 7
GE - Georgia 7
LB - Libano 7
NI - Nicaragua 7
OM - Oman 7
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
MK - Macedonia 5
PR - Porto Rico 5
QA - Qatar 5
TW - Taiwan 5
BY - Bielorussia 4
DK - Danimarca 4
EU - Europa 4
GT - Guatemala 4
LV - Lettonia 4
MD - Moldavia 4
NZ - Nuova Zelanda 4
PS - Palestinian Territory 4
Totale 43.200
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Città #
Ashburn 2.674
Fairfield 2.291
Singapore 2.206
San Jose 1.257
Chandler 1.201
Woodbridge 1.189
Houston 1.066
Wilmington 986
Seattle 977
Hong Kong 886
Cambridge 743
Ann Arbor 598
Zgierz 528
Moscow 478
Jacksonville 454
Dublin 425
Medford 388
Tokyo 370
Beijing 362
Palermo 351
Santa Clara 335
Dallas 312
Los Angeles 286
Council Bluffs 285
Ho Chi Minh City 282
New York 270
Frankfurt am Main 268
Nanjing 253
Princeton 242
Lauterbourg 238
Des Moines 222
Altamura 218
Boardman 216
Hanoi 213
San Diego 187
Lawrence 156
Chicago 148
Dearborn 138
Hefei 133
Tulsa 131
Helsinki 129
Milan 115
São Paulo 114
Buffalo 111
Shenyang 98
The Dalles 95
London 94
Nanchang 87
Orem 86
Seongnam 77
Rome 76
Hebei 74
Jinan 74
Tianjin 72
Changsha 70
Munich 70
Brussels 69
Jiaxing 56
Ludwigshafen am Rhein 53
Phoenix 53
Abidjan 52
Guangzhou 52
Amsterdam 51
Izmir 51
Rio de Janeiro 50
Nuremberg 49
Atlanta 48
Venice 46
Da Nang 44
Haiphong 44
Chennai 43
Johannesburg 43
Warsaw 42
Columbus 41
Verona 41
Ningbo 40
Montreal 39
Saint Petersburg 39
Toronto 38
Düsseldorf 37
Brooklyn 35
Salt Lake City 34
Zhengzhou 34
Baghdad 32
Tashkent 32
Vienna 32
Bremen 31
Denver 31
Lappeenranta 31
Naples 31
Stockholm 31
Hangzhou 30
Shanghai 30
Boston 29
Manchester 28
Nairobi 28
Ottawa 28
Belo Horizonte 27
City of London 26
Turku 26
Totale 27.132
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Nome #
Multiple food hypersensitivity as a cause of refractory chronic constipation in adults 504
IgA anti-actin antibodies ELISA in coeliac disease: A multicentre study. 402
A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily 308
Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease 294
Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study 293
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 290
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA 286
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 274
ApoE polymorphism in a small Mediterranean island: Relationships with plasma lipids, lipoproteins and LDL particle size 273
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA 272
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA 266
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 264
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography 263
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. 262
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. 261
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE 257
BETA-2-GLYCOPROTEIN I IS GROWTH REGULATED AND PLAYS A ROLE AS SURVIVAL FACTOR FOR HEPATOCYTES 256
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred 256
FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease 254
Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population 252
The metabolic syndrome predicts cardiovascular events in subjects with normal fasting glucose: Results of a 15 years follow-up in a Mediterranean population. 251
Circulating Molecular Chaperones in Subjects with Amnestic Mild Cognitive Impairment and Alzheimer's Disease: Data from the Zabùt Aging Project 249
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. 249
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent 247
Effects of Steatosis on Hepatic Hemodynamics in Patients with Metabolic Syndrome 246
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 246
A Novel Mutation of the DHCR7 Gene in a Sicilian Compound Heterozygote with Smith-Lemli-Opitz Syndrome 244
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study 243
Association of estrogen receptor alpha gene with Alzheimer's disease: a case-control study 241
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 240
Heparin induces an accumulation of atherogenic lipoproteins during hemodialysis in normolipidemic end-stage renal disease patients. 237
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 234
Association between plasma lipid levels and migraine in subjects aged > or =50 years: preliminary data from the Zabùt Aging Project 232
INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY 231
A novel putative interactor for the low density lipoprotein receptor cytoplasmic domain 231
Clinical, pathologic, and genetic features of massive soft tissue neurofibromas in a Sicilian patient 228
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 227
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 226
Prediction of incident type 2 diabetes mellitus based on a twenty-year follow-up of the Ventimiglia heart study 221
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing 220
A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. 219
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 219
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). 218
Decreased plasma soluble RAGE in patients with hypercholesterolemia: Effects of statins 216
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. 215
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 214
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 212
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (LDL) receptor 212
The ANP Genetic Variant RS5068 is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population 212
Metabolomic analysis of plasma from Alzheimer disease patients 212
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 210
Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an “FCS score” 209
No association between the cystatin C gene polymorphism and Alzheimer's disease: a case-control study in an Italian population. 208
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. 206
FAMILIAL LIGAND-DEFECTIVE APOLIPOPROTEIN B: IDENTIFICATION OF A FAMILY HARBOURING THE ARG3531CYS (FDB3531) OF THE APOB GENE 206
Obesity and the metabolic syndrome in a student cohort from Southern Italy 206
Transient chylomicronemia preceding the onset of insulin-dependent diabetes in a young girl with no humoral markers of islet autoimmunity. 206
MISSENSE MUTATION ALA34VAL IN EXON 2 OF THE LIPOPROTEIN LIPASE GENE IN A YOUNG MAN WITH CHYLOMICRONEMIA. 205
Cystatin C levels are decreased in acute myocardial infarction: Effect of cystatin C G73A gene polymorphism on plasma levels 205
Molecular diagnosis of hypobetalipoproteinemia: An ENID review 204
Enhanced Lipid Peroxidation and Platelet Activation as Potential Contributors to Increased Cardiovascular Risk in the Low-HDL Phenotype 203
CLINICAL CHARACTERISTICS AND PLASMA LIPIDS IN SUBJECTS WITH FAMILIAL COMBINED HYPOLIPIDEMIA: A POOLED ANALYSIS 203
A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia 202
Novel mutations of CETP gene in Italian subjects with hyeralphalipoproteinemia 201
Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction 200
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene. 200
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 200
Role of Nutraceuticals in Hypolipidemic Therapy 199
PREVALENCE OF ANGPTL3 AND APOB GENE MUTATIONS IN SUBJECTS WITH COMBINED HYPOLIPIDEMIA 198
LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY 197
Determinants of enhanced thromboxane biosynthesis in renal transplantation 197
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia 197
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 196
DIFFERENCE IN THE PREVALENCE OF METABOLIC SYNDROME AND CARDIOVASCULAR RISK FACTORS AFTER 14 YEARS IN THE POPULATION OF VENTIMIGLIA DI SICILIA 196
Genetic epidemiology of ARH in Sicily 196
ENHANCED LIPID PEROXIDATION AND PLATELET ACTIVATION AS POTENTIAL CONTRIBUTORS TO INCREASED CARDIOVASCULAR RISK IN THE LOW-HDL PHENOTYPE. 195
The C(-260)>T gene polymorphism in the promoter of the CD14 monocyte receptor gene is not associated with acute myocardial infarction 194
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. 194
Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. 193
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 193
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. 192
Plasma calprotectin levels in patients suffering from acute pancreatitis. 191
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. 191
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia 190
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects 190
Food hypersensitivity as a cause of rectal bleeding in adults 190
Additive effect of mutations in LDLR and PCSK9 genes on the phenotyoe of familial hypercholesterolemia 190
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia 190
MUSCLE DAMAGE AND PAIN IN HYPERCHOLESTEROLEMIC OUT-PATIENTS POPULATION ON STATIN TREATMENT. 189
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia 188
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. 187
Plasma levels of lipoproteins and apolipoproteins in congenital hypothyroidism: effects of L-thyroxine substitution therapy 187
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS 186
IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING A MUTATION IN THE LDL-R GENE AND IN THE PCSK9 GENE 185
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography 185
Lipid and apoprotein composition of HDL in partial or complete CETP deficiency 184
FUNCTIONAL CHARACTERIZATION OF NOVEL AMINO ACID VARIANTS IN APOB IN FAMILIAL HYPOBETALIPOPROTEINEMIA 183
ENHANCED LIPID PEROXIDATION AND PLATELET ACTIVATION AS POTENTIAL CONTRIBUTORS TO INCREASED CARDIOVASCULAR RISK IN THE “LOW-HDL” PHENOTYPE. 182
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL 182
Anti-PCSK9 treatment: Is ultra-low LDL always good? 180
Totale 22.440
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Categoria #
all - tutte 152.320
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 152.320
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/202616.119 1.071 546 831 1.085 1.416 2.400 2.157 1.693 1.234 2.334 635 717
2026/2027502 502 0 0 0 0 0 0 0 0 0 0 0
Totale 44.481