Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

VALENTI, Vincenza
 Distribuzione geografica
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Continente #
NA - Nord America 5.154
EU - Europa 3.236
AS - Asia 2.494
SA - Sud America 447
AF - Africa 77
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 4
Totale 11.419
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Nazione #
US - Stati Uniti d'America 5.051
SG - Singapore 860
RU - Federazione Russa 828
CN - Cina 747
FI - Finlandia 547
IT - Italia 525
BR - Brasile 352
UA - Ucraina 307
DE - Germania 246
VN - Vietnam 225
HK - Hong Kong 222
PL - Polonia 148
FR - Francia 143
IE - Irlanda 137
GB - Regno Unito 123
JP - Giappone 94
SE - Svezia 63
KR - Corea 54
IN - India 53
CA - Canada 52
BD - Bangladesh 47
BE - Belgio 43
TR - Turchia 33
AR - Argentina 29
MX - Messico 29
NL - Olanda 27
RO - Romania 22
ZA - Sudafrica 22
AT - Austria 21
IQ - Iraq 18
PK - Pakistan 17
CL - Cile 15
EC - Ecuador 15
MA - Marocco 15
VE - Venezuela 15
ES - Italia 14
CI - Costa d'Avorio 13
MY - Malesia 13
IR - Iran 12
UZ - Uzbekistan 12
NP - Nepal 11
JO - Giordania 9
AE - Emirati Arabi Uniti 8
CO - Colombia 8
PY - Paraguay 8
SA - Arabia Saudita 8
AZ - Azerbaigian 7
ID - Indonesia 7
CH - Svizzera 6
LT - Lituania 6
PH - Filippine 6
AU - Australia 5
CR - Costa Rica 5
DZ - Algeria 5
EG - Egitto 5
BH - Bahrain 4
HN - Honduras 4
IL - Israele 4
JM - Giamaica 4
LK - Sri Lanka 4
PA - Panama 4
TH - Thailandia 4
BO - Bolivia 3
BY - Bielorussia 3
ET - Etiopia 3
GR - Grecia 3
KE - Kenya 3
KW - Kuwait 3
MK - Macedonia 3
PR - Porto Rico 3
PT - Portogallo 3
SI - Slovenia 3
TN - Tunisia 3
AL - Albania 2
AO - Angola 2
BG - Bulgaria 2
HU - Ungheria 2
KZ - Kazakistan 2
LV - Lettonia 2
MM - Myanmar 2
NZ - Nuova Zelanda 2
QA - Qatar 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
XK - ???statistics.table.value.countryCode.XK??? 2
BA - Bosnia-Erzegovina 1
CZ - Repubblica Ceca 1
EU - Europa 1
GE - Georgia 1
GM - Gambi 1
HR - Croazia 1
KG - Kirghizistan 1
KY - Cayman, isole 1
LB - Libano 1
MD - Moldavia 1
MU - Mauritius 1
NG - Nigeria 1
NI - Nicaragua 1
OM - Oman 1
PE - Perù 1
Totale 11.413
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Città #
Ashburn 773
Singapore 560
Fairfield 367
San Jose 312
Chandler 275
Woodbridge 240
Houston 228
Hong Kong 218
Wilmington 208
Ann Arbor 191
Seattle 166
Jacksonville 162
Dublin 137
Cambridge 128
Beijing 126
Moscow 123
Zgierz 111
Medford 96
New York 93
Tokyo 93
Council Bluffs 91
Santa Clara 91
Nanjing 87
Des Moines 85
Palermo 81
Ho Chi Minh City 77
Los Angeles 77
Boardman 73
Frankfurt am Main 73
Dallas 68
Princeton 57
Lauterbourg 50
Tulsa 45
Hanoi 43
Hefei 42
Brussels 40
Helsinki 40
The Dalles 32
Buffalo 31
Tianjin 30
Orem 28
Altamura 27
Milan 27
Nanchang 27
Jinan 25
São Paulo 25
Changsha 24
Venice 24
San Diego 23
Düsseldorf 21
Rome 21
Shenyang 21
Dearborn 20
Hebei 20
Chicago 19
Warsaw 19
Munich 18
Johannesburg 17
Lawrence 17
Jiaxing 16
Atlanta 15
Haiphong 15
San Mateo 15
London 14
Ningbo 14
Seongnam 14
Abidjan 13
Ludwigshafen am Rhein 13
Amsterdam 12
Brooklyn 12
Da Nang 12
Guangzhou 12
Izmir 12
Kraków 12
Montreal 12
Stockholm 12
Verona 11
Zhengzhou 11
Auburn Hills 10
Kumar 10
Manchester 10
Phoenix 10
Shanghai 10
Tashkent 10
Brasília 9
Hangzhou 9
Toronto 9
Turku 9
Ankara 8
Boston 8
Chennai 8
City of London 8
Columbus 8
Rio de Janeiro 8
Saint Petersburg 8
Taiyuan 8
Taizhou 8
Tehran 8
Vienna 8
Washington 8
Totale 6.682
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Nome #
A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily 308
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 290
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 273
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA 271
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 263
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE 257
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred 256
Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population 252
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
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 240
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 234
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS 227
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 226
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 225
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing 220
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
A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. 218
LE IPERCOLESTEROLEMIE PRIMITIVE 215
Metabolomic analysis of plasma from Alzheimer disease patients 212
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 211
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
Obesity and the metabolic syndrome in a student cohort from Southern Italy 206
MISSENSE MUTATION ALA34VAL IN EXON 2 OF THE LIPOPROTEIN LIPASE GENE IN A YOUNG MAN WITH CHYLOMICRONEMIA. 205
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
PREVALENCE OF ANGPTL3 AND APOB GENE MUTATIONS IN SUBJECTS WITH 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
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. 193
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. 192
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. 190
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia 190
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects 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
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
FUNCTIONAL CHARACTERIZATION OF NOVEL AMINO ACID VARIANTS IN APOB IN FAMILIAL HYPOBETALIPOPROTEINEMIA 183
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL 182
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 178
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH 178
ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS. 176
Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore 175
MUTAZIONI DEL GENE DELL’APOB RESPONSABILI DI IPOBETALIPOPROTEINEMIA FAMILIARE IN SICILIA 172
A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL 172
HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY 171
FUNCTIONAL EFFECT OF NOVEL AMINO ACID VARIANTS OF APOLIPOPROTEIN B IN FAMILIAL HYPOBETALIPOPROTEINEMIA 171
Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature 170
INTERACTION OF THE INTRACELLULAR DOMAIN OF THE LOW DENSITY LIPOPROTEIN (LDL) RECPTOR WITH METALLOTHIONEIN2 (MT2). 168
A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE 165
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia 160
IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA 159
SHORT APOB TRUNCATIONS SHOW IMPAIRE CHYLOMICRON EXPORT AND ENTEROCYTE TRIGLYCERIDE ACCUMULATION. IN VIVO AND IN VITRO EVIDENCE ON A APOB 28.25 STABLE-TRANSFECTED ENTEROCYTE CELL LINE 156
VARIABLE PHENOTYPIC ESPRESSION IN A LIPID ABSORPTION DISORDER DUE TO A MOLECULAR DEFECT IN THE SARA2 GENE 156
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 150
I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. 146
VASCULOPROTECTIVE FUNCTION OF HDL FROM CETP-DEFICIENT SUBJECTS 142
Totale 11.622
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Categoria #
all - tutte 34.306
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 34.306
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022539 19 129 7 13 12 21 13 26 79 78 21 121
2022/2023792 96 96 24 80 98 142 61 65 93 4 28 5
2023/2024501 18 75 31 75 27 120 49 29 5 7 10 55
2024/20251.181 9 66 68 85 66 35 133 95 124 116 169 215
2025/20264.413 363 138 207 269 373 740 572 467 291 696 119 178
2026/2027107 107 0 0 0 0 0 0 0 0 0 0 0
Totale 11.622