Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

VALENTI, Vincenza
 Distribuzione geografica
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Continente #
NA - Nord America 3.513
EU - Europa 1.857
AS - Asia 607
SA - Sud America 16
AF - Africa 12
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 1
Totale 6.011
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Nazione #
US - Stati Uniti d'America 3.499
FI - Finlandia 513
IT - Italia 452
CN - Cina 367
UA - Ucraina 294
SG - Singapore 156
IE - Irlanda 131
DE - Germania 115
GB - Regno Unito 78
SE - Svezia 56
FR - Francia 47
RU - Federazione Russa 46
BE - Belgio 41
IN - India 24
RO - Romania 22
KR - Corea 20
PL - Polonia 18
NL - Olanda 17
TR - Turchia 13
IR - Iran 12
BR - Brasile 11
CI - Costa d'Avorio 11
MX - Messico 10
CH - Svizzera 6
AU - Australia 4
ES - Italia 4
VN - Vietnam 4
LK - Sri Lanka 3
AT - Austria 2
BG - Bulgaria 2
CA - Canada 2
CL - Cile 2
GR - Grecia 2
JP - Giappone 2
MK - Macedonia 2
PA - Panama 2
PK - Pakistan 2
SK - Slovacchia (Repubblica Slovacca) 2
UZ - Uzbekistan 2
AR - Argentina 1
BO - Bolivia 1
CO - Colombia 1
DK - Danimarca 1
EU - Europa 1
HK - Hong Kong 1
HU - Ungheria 1
LV - Lettonia 1
MD - Moldavia 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
RS - Serbia 1
SI - Slovenia 1
ZA - Sudafrica 1
Totale 6.011
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Città #
Ashburn 377
Fairfield 367
Chandler 288
Woodbridge 238
Houston 218
Wilmington 208
Ann Arbor 191
Seattle 162
Jacksonville 161
Dublin 131
Cambridge 128
Singapore 113
Medford 97
Nanjing 87
Des Moines 80
Palermo 70
New York 67
Princeton 58
Boardman 45
Tulsa 45
Brussels 39
Altamura 29
Tianjin 28
Nanchang 27
Jinan 25
Venice 24
Changsha 23
San Diego 23
Beijing 22
Santa Clara 22
Shenyang 21
Dearborn 20
Düsseldorf 20
Hebei 20
Lawrence 18
Milan 18
Helsinki 15
San Mateo 15
Ningbo 14
Seongnam 14
Jiaxing 13
Ludwigshafen am Rhein 13
Izmir 12
Kraków 12
Rome 12
Abidjan 11
Guangzhou 11
Zhengzhou 11
Auburn Hills 10
Kumar 10
London 8
Munich 8
Saint Petersburg 8
Tehran 8
Verona 8
Fairhope 7
Hangzhou 7
Kunming 7
Lanzhou 7
Los Angeles 7
Shanghai 7
Taizhou 7
Groningen 6
Haikou 6
Redwood City 6
Taiyuan 6
Veracruz 6
Washington 6
Kolkata 5
Pune 5
Stockholm 5
Alcamo 4
Catania 4
Kiev 4
North Brunswick 4
Norwalk 4
Phoenix 4
Arzano 3
Belfast 3
Bologna 3
Chengdu 3
Colombo 3
Columbus 3
Den Haag 3
Edinburgh 3
Hanoi 3
Indiana 3
Madrid 3
Moscow 3
Naples 3
Napoli 3
Orange 3
Sydney 3
Barrafranca 2
Bergamo 2
Bratislava 2
Casavatore 2
Dallas 2
Durham 2
Florence 2
Totale 3.909
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Nome #
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 193
A novel mutation of the extracellular matrix protein 1 gene (ECM1) in a patient with lipoid proteinosis (Urbach-Wiethe disease) from Sicily 166
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred 163
Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population 162
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent 160
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. 154
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 152
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 150
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA 144
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 143
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 137
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 137
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 137
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 136
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing 136
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 132
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE 130
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 129
LE IPERCOLESTEROLEMIE PRIMITIVE 126
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). 119
HETEROGENITY OF AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA IN SICILY 115
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS 113
Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature 113
A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. 111
MISSENSE MUTATION ALA34VAL IN EXON 2 OF THE LIPOPROTEIN LIPASE GENE IN A YOUNG MAN WITH CHYLOMICRONEMIA. 110
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia 108
IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING A MUTATION IN THE LDL-R GENE AND IN THE PCSK9 GENE 100
Metabolomic analysis of plasma from Alzheimer disease patients 100
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 99
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 96
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 96
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. 94
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 92
A metallothionein family member interacts with the intracellular domain of the low density lipoprotein (ldl) receptor. 90
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. 86
INTERACTION OF THE INTRACELLULAR DOMAIN OF THE LOW DENSITY LIPOPROTEIN (LDL) RECPTOR WITH METALLOTHIONEIN2 (MT2). 86
VARIABLE PHENOTYPIC ESPRESSION IN A LIPID ABSORPTION DISORDER DUE TO A MOLECULAR DEFECT IN THE SARA2 GENE 83
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects 82
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia 82
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH 81
A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL 79
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. 79
ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS. 78
MUTAZIONI DEL GENE DELL’APOB RESPONSABILI DI IPOBETALIPOPROTEINEMIA FAMILIARE IN SICILIA 75
FUNCTIONAL EFFECT OF NOVEL AMINO ACID VARIANTS OF APOLIPOPROTEIN B IN FAMILIAL HYPOBETALIPOPROTEINEMIA 75
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 74
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS 72
I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. 71
A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE 70
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL 70
FUNCTIONAL CHARACTERIZATION OF NOVEL AMINO ACID VARIANTS IN APOB IN FAMILIAL HYPOBETALIPOPROTEINEMIA 67
IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA 66
Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore 61
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 60
VASCULOPROTECTIVE FUNCTION OF HDL FROM CETP-DEFICIENT SUBJECTS 54
The PCSK9 gene: a new gene controlling cholesterolemia 52
Totale 6.219
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Categoria #
all - tutte 20.430
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 20.430
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020911 0 0 0 0 146 160 154 70 135 43 152 51
2020/2021707 24 73 53 72 56 27 65 42 89 50 75 81
2021/2022556 19 129 7 13 12 21 13 26 90 78 25 123
2022/2023816 97 103 24 82 100 147 61 67 98 4 28 5
2023/2024509 18 76 32 76 28 122 49 29 6 7 10 56
2024/2025249 9 68 68 86 18 0 0 0 0 0 0 0
Totale 6.219