Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

MINA', Mariangela
 Distribuzione geografica
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Continente #
NA - Nord America 1.676
EU - Europa 949
AS - Asia 221
OC - Oceania 1
SA - Sud America 1
Totale 2.848
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Nazione #
US - Stati Uniti d'America 1.676
FI - Finlandia 296
UA - Ucraina 209
CN - Cina 182
IT - Italia 171
DE - Germania 54
IE - Irlanda 53
GB - Regno Unito 35
FR - Francia 32
SE - Svezia 30
RU - Federazione Russa 22
KR - Corea 15
PL - Polonia 14
RO - Romania 14
IN - India 13
BE - Belgio 9
TR - Turchia 7
NL - Olanda 5
IR - Iran 3
CH - Svizzera 2
AR - Argentina 1
AT - Austria 1
AU - Australia 1
BG - Bulgaria 1
GR - Grecia 1
UZ - Uzbekistan 1
Totale 2.848
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Città #
Ashburn 192
Fairfield 161
Chandler 124
Woodbridge 122
Jacksonville 113
Houston 106
Wilmington 103
Ann Arbor 92
Seattle 74
Cambridge 60
Dublin 53
Medford 49
Nanjing 40
New York 32
Boardman 30
Princeton 29
Des Moines 28
Tulsa 25
Jinan 16
Seongnam 15
Beijing 13
Nanchang 13
Kraków 12
Palermo 12
San Diego 12
Tianjin 12
Dearborn 11
Shenyang 11
Altamura 10
Changsha 10
Hebei 10
San Mateo 10
Brussels 9
Düsseldorf 9
Venice 9
Milan 8
Ningbo 8
Auburn Hills 7
Izmir 7
Kumar 7
Lanzhou 7
Lawrence 6
Ludwigshafen am Rhein 6
Verona 6
Groningen 5
Guangzhou 5
Helsinki 5
Kunming 5
Taizhou 5
Zhengzhou 5
Haikou 4
Hangzhou 4
Naples 4
Pune 4
Catania 3
Saint Petersburg 3
Shanghai 3
Taiyuan 3
Tehran 3
Bologna 2
Edinburgh 2
Hefei 2
Jiaxing 2
Kiev 2
Los Angeles 2
Mehlingen 2
Rome 2
Turin 2
Washington 2
Cisano Bergamasco 1
Durham 1
Florence 1
Horia 1
Islington 1
Kolkata 1
London 1
Messina 1
Moscow 1
Mountain View 1
Munich 1
Norwalk 1
Paris 1
Parma 1
Polistena 1
Ripe 1
Sofia 1
Southend 1
Stockholm 1
Walnut 1
Zurich 1
Totale 1.791
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Nome #
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 187
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography 155
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 145
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 145
INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY 137
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. 134
Obesity and the metabolic syndrome in a student cohort from Southern Italy 132
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 131
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA 128
CLINICAL AND MOLECULAR CHARACTERIZATION OF HYPERCHOLESTEROLEMIC SICILIAN FAMILIES AND DESCRIPTION OF 3 NOVEL MUTATIONS IN THE LDLR GENE 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). 112
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 94
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 94
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 92
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. 84
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. 81
THE METABOLIC SYNDROME IS A PREDICTOR OF CARDIOVASCULAR EVENTS IN A SICILIAN POPULATION. RESULT OF A 15 YEARS FOLLOW UP 80
USE OF THE DRUG ELUTING STENTS WITH RAPAMICIN IN PATIENTS WITH ANATOMICAL OR CLINICAL PATTERNS FAVOURING RESTENOSIS: RESULTS OF A 6-MONTHS FOLLOW-UP ON THE FIRST 100 PATIENS. 79
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. 78
FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION. 77
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects 76
ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS. 75
MUTAZIONI DEL GENE DELL’APOB RESPONSABILI DI IPOBETALIPOPROTEINEMIA FAMILIARE IN SICILIA 71
NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS. 71
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 70
I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. 68
IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA 62
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 58
Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore 51
Totale 2.893
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Categoria #
all - tutte 8.102
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 8.102
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019128 0 0 0 0 0 0 0 0 0 0 53 75
2019/2020708 90 37 60 58 84 75 85 30 73 19 59 38
2020/2021375 7 44 22 38 36 20 44 14 52 20 39 39
2021/2022252 6 69 0 3 3 5 8 9 44 40 7 58
2022/2023341 50 31 4 35 51 60 20 30 40 4 15 1
2023/2024234 5 40 21 38 11 61 40 16 0 1 1 0
Totale 2.893