Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

SPINA, Rossella
 Distribuzione geografica
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Continente #
NA - Nord America 4.022
EU - Europa 2.202
AS - Asia 1.876
SA - Sud America 334
AF - Africa 57
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.497
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Nazione #
US - Stati Uniti d'America 3.938
SG - Singapore 708
RU - Federazione Russa 664
IT - Italia 514
CN - Cina 477
BR - Brasile 264
FI - Finlandia 241
HK - Hong Kong 161
VN - Vietnam 155
PL - Polonia 134
DE - Germania 132
FR - Francia 107
GB - Regno Unito 86
IE - Irlanda 83
UA - Ucraina 75
JP - Giappone 66
BD - Bangladesh 51
IN - India 42
BE - Belgio 39
CA - Canada 37
KR - Corea 37
AR - Argentina 28
MX - Messico 28
TR - Turchia 28
IQ - Iraq 25
AT - Austria 23
SE - Svezia 19
ES - Italia 18
NL - Olanda 18
PK - Pakistan 14
RO - Romania 14
ZA - Sudafrica 12
CL - Cile 11
AZ - Azerbaigian 10
CI - Costa d'Avorio 10
IR - Iran 9
AE - Emirati Arabi Uniti 8
EC - Ecuador 8
ID - Indonesia 8
LT - Lituania 8
MY - Malesia 8
NP - Nepal 8
CO - Colombia 7
KE - Kenya 7
MA - Marocco 7
SA - Arabia Saudita 7
DZ - Algeria 6
JO - Giordania 6
PH - Filippine 6
PY - Paraguay 6
UZ - Uzbekistan 6
GR - Grecia 5
TN - Tunisia 5
VE - Venezuela 5
CH - Svizzera 4
CZ - Repubblica Ceca 4
HN - Honduras 4
HU - Ungheria 4
IL - Israele 4
JM - Giamaica 4
LB - Libano 4
AU - Australia 3
BH - Bahrain 3
CR - Costa Rica 3
KZ - Kazakistan 3
LK - Sri Lanka 3
MM - Myanmar 3
PE - Perù 3
SN - Senegal 3
BG - Bulgaria 2
BY - Bielorussia 2
EG - Egitto 2
ET - Etiopia 2
GE - Georgia 2
KG - Kirghizistan 2
KW - Kuwait 2
PA - Panama 2
SY - Repubblica araba siriana 2
TG - Togo 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
UY - Uruguay 2
AO - Angola 1
BB - Barbados 1
BS - Bahamas 1
DO - Repubblica Dominicana 1
EU - Europa 1
GT - Guatemala 1
HR - Croazia 1
LV - Lettonia 1
MD - Moldavia 1
ME - Montenegro 1
MN - Mongolia 1
NZ - Nuova Zelanda 1
PS - Palestinian Territory 1
PT - Portogallo 1
QA - Qatar 1
RS - Serbia 1
TJ - Tagikistan 1
Totale 8.496
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Città #
Ashburn 576
Singapore 457
Chandler 321
Fairfield 317
San Jose 277
Houston 171
Woodbridge 157
Hong Kong 156
Seattle 150
Wilmington 144
Ann Arbor 124
Moscow 120
Cambridge 109
Palermo 104
Zgierz 102
Council Bluffs 100
Beijing 98
New York 93
Medford 83
Dublin 81
Santa Clara 58
Ho Chi Minh City 57
Los Angeles 55
Tokyo 55
Des Moines 53
Altamura 49
Princeton 47
Dallas 45
Lauterbourg 44
Jacksonville 38
Brussels 37
Nanjing 37
Boardman 34
Hanoi 33
Helsinki 33
Lawrence 32
San Diego 28
São Paulo 28
Orem 27
Rome 26
Frankfurt am Main 25
Venice 22
Buffalo 20
Chennai 18
Milan 18
Changsha 17
London 17
Izmir 15
Tulsa 15
Warsaw 15
Jiaxing 14
Manchester 14
Munich 14
Nanchang 14
Phoenix 14
Atlanta 13
Hefei 13
The Dalles 13
Tianjin 13
Brooklyn 12
Chicago 12
Denver 12
Düsseldorf 12
Jinan 12
Kraków 12
Shenyang 12
Baghdad 11
Dearborn 11
Minamiyukigaya 11
Zhengzhou 11
Abidjan 10
Bremen 10
Hebei 10
Lappeenranta 10
Ludwigshafen am Rhein 10
Nuremberg 10
Stockholm 10
Amsterdam 9
Baku 9
Boston 9
Da Nang 9
Johannesburg 9
Montreal 9
Redwood City 9
San Giorgio delle Pertiche 9
Vienna 9
Memphis 8
Rio de Janeiro 8
Shanghai 8
Turku 8
Haiphong 7
Nairobi 7
Ningbo 7
Paris 7
Seongnam 7
Veracruz 7
Washington 7
Brasília 6
Fairhope 6
Lomazzo 6
Totale 5.238
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Nome #
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 265
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 250
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN) 246
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study 242
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 226
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS 224
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 222
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. 218
Metabolomic analysis of plasma from Alzheimer disease patients 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 208
A novel mutation in the Lipase Maturaction Factor 1 (LMF-1)gene responsible for severe hypertriglyceridemia 201
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
Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia 197
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study 192
Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia 190
Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia 190
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia 188
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS 186
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography 184
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL 180
Automated untargeted stable isotope assisted lipidomics of liver cells on high glucose shows alteration of sphingolipid kinetics 180
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH 178
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 176
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). 167
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia 160
Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome 156
Le ipertrigliceridemie severe primitive: studio biochimico e genetico-molecolare 147
Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients 145
DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis 144
Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects: Polygenic hypocholesterolemias 142
APOC-III: a Gatekeeper in Controlling Triglyceride Metabolism 139
VASCULOPROTECTIVE FUNCTION OF HDL FROM CETP-DEFICIENT SUBJECTS 139
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study 139
PCSK9-D374Y MEDIATED LDL-R DEGRADATION CAN BE FUNCTIONALLY INHIBITED BY EGF-A AND TRUNCATED EGF-A PEPTIDES. AN IN VITRO STUDY 134
MUTATION IN CANDIDATE GENES ACCOUNT FOR A SMALL MINORITY OF HYPOBETALIPOPROTEINEMIAS AND NGS ANALYSIS SUPPORT POLYGENICITY IN MUTATION-NEGATIVE PATIENTS 131
Do genetically determined very high and very low LDL levels contribute to Lp(a) plasma concentration? 126
MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH "EXTREME LDL-C PHENOTYPES" 126
TGF-β/VEGF-A Genetic Variants Interplay in Genetic Susceptibility to Non-Melanocytic Skin Cancer 123
PREVALENCE OF STATIN INTOLERANCE IN A COHORT OF OUTPATIENTS IN A LIPID CLINIC 119
EFFECTIVENESS AND SAFETY OF LOMITAPIDE IN A PATIENT WITH FAMILIAL CHYLOMICRONEMIA SYNDROME 111
IDENTIFICATION OF P.LEU167DEL APOE GENE MUTATION BY NEXT GENERATION SEQUENCING IN A LARGE HYPERCHOLESTEROLEMIC FAMILY 111
Genetically determined hypercholesterolaemia results into premature leucocyte telomere length shortening and reduced haematopoietic precursors 111
Lifestyle versus ezetimibe plus lifestyle in patients with biopsy-proven non-alcoholic steatohepatitis (LISTEN): A double-blind randomised placebo-controlled trial 104
Echocardiographic Calcium Score of Aortic Valve Correlates with Coronary Artery Calcium Score in Heterozygous Familial Hypercholesterolemia 91
Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia 84
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 70
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 46
Totale 8.819
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Categoria #
all - tutte 30.534
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 30.534
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2024/20251.035 8 89 102 70 36 48 107 79 71 126 127 172
2025/20263.601 271 125 163 301 415 594 479 378 268 315 117 175
2026/202744 44 0 0 0 0 0 0 0 0 0 0 0
Totale 8.819