Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

SPINA, Rossella
 Distribuzione geografica
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Continente #
NA - Nord America 2.697
EU - Europa 1.103
AS - Asia 533
SA - Sud America 78
AF - Africa 18
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.432
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Nazione #
US - Stati Uniti d'America 2.684
IT - Italia 440
CN - Cina 222
SG - Singapore 222
FI - Finlandia 211
DE - Germania 85
IE - Irlanda 79
BR - Brasile 71
UA - Ucraina 69
GB - Regno Unito 46
BE - Belgio 37
FR - Francia 25
RU - Federazione Russa 24
TR - Turchia 17
AT - Austria 15
PL - Polonia 14
RO - Romania 14
JP - Giappone 13
KR - Corea 12
MX - Messico 10
NL - Olanda 10
IR - Iran 9
SE - Svezia 9
CI - Costa d'Avorio 8
IN - India 8
HK - Hong Kong 6
ES - Italia 5
GR - Grecia 5
CH - Svizzera 4
CZ - Repubblica Ceca 4
MA - Marocco 4
BD - Bangladesh 3
CL - Cile 3
PK - Pakistan 3
UZ - Uzbekistan 3
VN - Vietnam 3
BG - Bulgaria 2
CA - Canada 2
CO - Colombia 2
HU - Ungheria 2
IQ - Iraq 2
KZ - Kazakistan 2
TN - Tunisia 2
AR - Argentina 1
AU - Australia 1
EC - Ecuador 1
EU - Europa 1
GE - Georgia 1
KE - Kenya 1
KG - Kirghizistan 1
LB - Libano 1
LK - Sri Lanka 1
LV - Lettonia 1
MD - Moldavia 1
MN - Mongolia 1
MY - Malesia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PA - Panama 1
PH - Filippine 1
RS - Serbia 1
SN - Senegal 1
TG - Togo 1
ZA - Sudafrica 1
Totale 4.432
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Città #
Chandler 321
Fairfield 317
Ashburn 271
Houston 160
Woodbridge 155
Singapore 153
Seattle 148
Wilmington 144
Ann Arbor 124
Cambridge 109
Palermo 94
Medford 82
Dublin 77
New York 58
Des Moines 52
Altamura 49
Princeton 47
Jacksonville 38
Brussels 37
Nanjing 37
Santa Clara 37
Lawrence 32
San Diego 28
Venice 22
Rome 19
Beijing 17
Boardman 17
Changsha 16
Helsinki 16
Izmir 15
Tulsa 15
Nanchang 14
Milan 13
Council Bluffs 12
Jiaxing 12
Kraków 12
Shenyang 12
Dearborn 11
Jinan 11
London 11
Minamiyukigaya 11
Tianjin 11
Bremen 10
Hebei 10
Ludwigshafen am Rhein 10
Zhengzhou 10
Redwood City 9
San Giorgio delle Pertiche 9
Abidjan 8
Düsseldorf 7
Ningbo 7
Seongnam 7
Shanghai 7
Vienna 7
Fairhope 6
Veracruz 6
Cagliari 5
Haikou 5
Lappeenranta 5
Munich 5
Nuremberg 5
Phoenix 5
Saint Petersburg 5
San Paolo di Civitate 5
São Paulo 5
Washington 5
Alcamo 4
Guangzhou 4
Hong Kong 4
Kunming 4
Rio de Janeiro 4
Amsterdam 3
Belfast 3
Casablanca 3
Catania 3
Catanzaro 3
Falkenstein 3
Hangzhou 3
Hanoi 3
Kolkata 3
Madrid 3
Moscow 3
Norwalk 3
Pune 3
Redmond 3
Taiyuan 3
Tehran 3
Athens 2
Baghdad 2
Bari 2
Belo Horizonte 2
Bogotá 2
Brasília 2
Caivano 2
Castell'Umberto 2
Ceglie Messapica 2
Columbus 2
Diso 2
Durham 2
Ferrara 2
Totale 3.094
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Nome #
Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population 170
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred 167
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study 158
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 156
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 151
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 146
PREVALENCE OF ANGPTL3 AND APOB GENE MUTATIONS IN SUBJECTS WITH COMBINED HYPOLIPIDEMIA 145
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE 142
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 142
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing 139
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia 138
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia 136
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 136
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 134
A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia. 122
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia 120
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS 117
Homozygous familial hypobetalipoproteinemia: Two novel mutations in the splicing sites of apolipoprotein B gene and review of the literature 116
Metabolomic analysis of plasma from Alzheimer disease patients 113
Automated untargeted stable isotope assisted lipidomics of liver cells on high glucose shows alteration of sphingolipid kinetics 112
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia 111
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 101
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 101
Le ipertrigliceridemie severe primitive: studio biochimico e genetico-molecolare 100
INTERACTION OF THE INTRACELLULAR DOMAIN OF THE LOW DENSITY LIPOPROTEIN (LDL) RECPTOR WITH METALLOTHIONEIN2 (MT2). 91
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia 90
Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome 89
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH 88
A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia 83
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study 83
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL 79
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS 79
Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects: Polygenic hypocholesterolemias 72
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography 65
DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis 62
VASCULOPROTECTIVE FUNCTION OF HDL FROM CETP-DEFICIENT SUBJECTS 61
Lifestyle versus ezetimibe plus lifestyle in patients with biopsy-proven non-alcoholic steatohepatitis (LISTEN): A double-blind randomised placebo-controlled trial 61
Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients 60
PREVALENCE OF STATIN INTOLERANCE IN A COHORT OF OUTPATIENTS IN A LIPID CLINIC 56
Genetically determined hypercholesterolaemia results into premature leucocyte telomere length shortening and reduced haematopoietic precursors 55
PCSK9-D374Y MEDIATED LDL-R DEGRADATION CAN BE FUNCTIONALLY INHIBITED BY EGF-A AND TRUNCATED EGF-A PEPTIDES. AN IN VITRO STUDY 51
EFFECTIVENESS AND SAFETY OF LOMITAPIDE IN A PATIENT WITH FAMILIAL CHYLOMICRONEMIA SYNDROME 49
MUTATION IN CANDIDATE GENES ACCOUNT FOR A SMALL MINORITY OF HYPOBETALIPOPROTEINEMIAS AND NGS ANALYSIS SUPPORT POLYGENICITY IN MUTATION-NEGATIVE PATIENTS 46
APOC-III: a Gatekeeper in Controlling Triglyceride Metabolism 41
Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia 40
IDENTIFICATION OF P.LEU167DEL APOE GENE MUTATION BY NEXT GENERATION SEQUENCING IN A LARGE HYPERCHOLESTEROLEMIC FAMILY 38
TGF-β/VEGF-A Genetic Variants Interplay in Genetic Susceptibility to Non-Melanocytic Skin Cancer 37
MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH "EXTREME LDL-C PHENOTYPES" 36
Twelve Variants Polygenic Score for Low-Density Lipoprotein Cholesterol Distribution in a Large Cohort of Patients With Clinically Diagnosed Familial Hypercholesterolemia With or Without Causative Mutations 32
Do genetically determined very high and very low LDL levels contribute to Lp(a) plasma concentration? 24
Six genetic variants are associated with cardiovascular disease independently from canonical risk factors: a new method to refine GWAS results based on the UKBiobank phenotype database 8
Totale 4.749
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Categoria #
all - tutte 20.889
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 20.889
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020148 0 0 0 0 0 0 0 0 0 35 95 18
2020/2021512 20 34 48 35 31 26 97 32 39 45 53 52
2021/2022560 15 78 28 8 10 19 20 25 69 120 40 128
2022/2023848 79 159 22 90 87 130 44 77 94 6 43 17
2023/2024398 17 59 24 70 22 98 28 18 3 1 5 53
2024/2025610 8 89 102 70 36 48 107 79 71 0 0 0
Totale 4.749