Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

VALENTI, Vincenza
 Distribuzione geografica
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Continente #
NA - Nord America 4.898
EU - Europa 3.220
AS - Asia 2.467
SA - Sud America 442
AF - Africa 77
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 3
Totale 11.114
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Nazione #
US - Stati Uniti d'America 4.824
SG - Singapore 860
RU - Federazione Russa 828
CN - Cina 744
FI - Finlandia 547
IT - Italia 511
BR - Brasile 349
UA - Ucraina 306
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
IN - India 53
KR - Corea 48
BE - Belgio 43
CA - Canada 36
TR - Turchia 33
AR - Argentina 29
BD - Bangladesh 29
MX - Messico 28
NL - Olanda 27
RO - Romania 22
ZA - Sudafrica 22
AT - Austria 21
IQ - Iraq 18
PK - Pakistan 17
CL - Cile 15
MA - Marocco 15
VE - Venezuela 15
EC - Ecuador 14
CI - Costa d'Avorio 13
ES - Italia 13
MY - Malesia 13
IR - Iran 12
UZ - Uzbekistan 12
NP - Nepal 11
JO - Giordania 9
AE - Emirati Arabi Uniti 8
CO - Colombia 8
SA - Arabia Saudita 8
AZ - Azerbaigian 7
ID - Indonesia 7
PY - Paraguay 7
CH - Svizzera 6
LT - Lituania 6
PH - Filippine 6
AU - Australia 5
DZ - Algeria 5
EG - Egitto 5
BH - Bahrain 4
IL - Israele 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
PT - Portogallo 3
SI - Slovenia 3
TN - Tunisia 3
AL - Albania 2
AO - Angola 2
BG - Bulgaria 2
HN - Honduras 2
HU - Ungheria 2
JM - Giamaica 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
CR - Costa Rica 1
CZ - Repubblica Ceca 1
EU - Europa 1
GE - Georgia 1
GM - Gambi 1
HR - Croazia 1
KG - Kirghizistan 1
LB - Libano 1
MD - Moldavia 1
MU - Mauritius 1
NG - Nigeria 1
NI - Nicaragua 1
OM - Oman 1
PE - Perù 1
PS - Palestinian Territory 1
RS - Serbia 1
Totale 11.111
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Città #
Ashburn 751
Singapore 560
Fairfield 367
Chandler 275
Woodbridge 240
San Jose 232
Houston 228
Hong Kong 218
Wilmington 208
Ann Arbor 191
Seattle 166
Jacksonville 161
Dublin 137
Cambridge 128
Beijing 126
Moscow 123
Zgierz 111
Medford 96
Tokyo 93
New York 92
Council Bluffs 91
Nanjing 87
Santa Clara 86
Des Moines 85
Palermo 80
Ho Chi Minh City 77
Los Angeles 75
Frankfurt am Main 73
Dallas 66
Princeton 57
Lauterbourg 50
Boardman 45
Tulsa 45
Hanoi 43
Hefei 42
Brussels 40
Helsinki 40
The Dalles 32
Buffalo 30
Tianjin 30
Orem 28
Altamura 27
Nanchang 27
Jinan 25
Milan 25
São Paulo 25
Changsha 24
Venice 24
San Diego 23
Düsseldorf 21
Shenyang 21
Dearborn 20
Hebei 20
Chicago 19
Warsaw 19
Munich 18
Johannesburg 17
Lawrence 17
Rome 17
Jiaxing 16
Haiphong 15
San Mateo 15
London 14
Ningbo 14
Seongnam 14
Abidjan 13
Ludwigshafen am Rhein 13
Amsterdam 12
Atlanta 12
Da Nang 12
Guangzhou 12
Izmir 12
Kraków 12
Stockholm 12
Brooklyn 11
Verona 11
Zhengzhou 11
Auburn Hills 10
Kumar 10
Manchester 10
Montreal 10
Phoenix 10
Shanghai 10
Tashkent 10
Brasília 9
Hangzhou 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
Toronto 8
Vienna 8
Baku 7
Totale 6.525
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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 293
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 288
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
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
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
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
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 236
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 231
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
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS 217
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
LE IPERCOLESTEROLEMIE PRIMITIVE 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
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 208
Metabolomic analysis of plasma from Alzheimer disease patients 206
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
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
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
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. 192
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. 189
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. 186
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia 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
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
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 175
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH 175
FUNCTIONAL CHARACTERIZATION OF NOVEL AMINO ACID VARIANTS IN APOB IN FAMILIAL HYPOBETALIPOPROTEINEMIA 174
ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS. 173
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL 173
Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore 170
MUTAZIONI DEL GENE DELL’APOB RESPONSABILI DI IPOBETALIPOPROTEINEMIA FAMILIARE IN SICILIA 169
HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY 169
A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL 169
FUNCTIONAL EFFECT OF NOVEL AMINO ACID VARIANTS OF APOLIPOPROTEIN B IN FAMILIAL HYPOBETALIPOPROTEINEMIA 165
INTERACTION OF THE INTRACELLULAR DOMAIN OF THE LOW DENSITY LIPOPROTEIN (LDL) RECPTOR WITH METALLOTHIONEIN2 (MT2). 164
A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE 162
IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA 156
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia 155
Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature 154
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 151
VARIABLE PHENOTYPIC ESPRESSION IN A LIPID ABSORPTION DISORDER DUE TO A MOLECULAR DEFECT IN THE SARA2 GENE 150
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 144
I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. 142
VASCULOPROTECTIVE FUNCTION OF HDL FROM CETP-DEFICIENT SUBJECTS 133
Totale 11.317
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Categoria #
all - tutte 32.970
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 32.970
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021156 0 0 0 0 0 0 0 0 0 0 75 81
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
2025/20264.215 363 138 207 269 373 740 572 467 291 696 99 0
Totale 11.317