Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

FAYER, Francesca
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 7.245
EU - Europa 4.163
AS - Asia 3.228
SA - Sud America 539
AF - Africa 81
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 8
Totale 15.276
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 7.115
SG - Singapore 1.181
RU - Federazione Russa 1.151
CN - Cina 852
IT - Italia 773
FI - Finlandia 586
BR - Brasile 431
VN - Vietnam 336
UA - Ucraina 317
DE - Germania 311
HK - Hong Kong 294
PL - Polonia 199
FR - Francia 181
GB - Regno Unito 166
IE - Irlanda 165
JP - Giappone 129
SE - Svezia 81
IN - India 75
BD - Bangladesh 73
BE - Belgio 53
CA - Canada 51
KR - Corea 50
RO - Romania 45
MX - Messico 43
NL - Olanda 38
TR - Turchia 35
IQ - Iraq 34
AR - Argentina 28
AT - Austria 25
ZA - Sudafrica 21
VE - Venezuela 20
PK - Pakistan 19
UZ - Uzbekistan 19
EC - Ecuador 17
ES - Italia 17
CI - Costa d'Avorio 15
PH - Filippine 15
IR - Iran 13
JO - Giordania 13
MA - Marocco 13
AU - Australia 11
CL - Cile 11
NP - Nepal 11
AZ - Azerbaigian 10
LT - Lituania 10
MY - Malesia 10
PY - Paraguay 10
SA - Arabia Saudita 9
AE - Emirati Arabi Uniti 8
CH - Svizzera 8
CO - Colombia 8
EG - Egitto 8
IL - Israele 7
PE - Perù 7
GR - Grecia 6
ID - Indonesia 6
KE - Kenya 6
KZ - Kazakistan 6
BO - Bolivia 5
CR - Costa Rica 5
DZ - Algeria 5
HN - Honduras 5
JM - Giamaica 5
NI - Nicaragua 5
PT - Portogallo 5
SN - Senegal 5
BH - Bahrain 4
CZ - Repubblica Ceca 4
DO - Repubblica Dominicana 4
MK - Macedonia 4
PA - Panama 4
TH - Thailandia 4
AL - Albania 3
BB - Barbados 3
BY - Bielorussia 3
KW - Kuwait 3
MD - Moldavia 3
NG - Nigeria 3
TT - Trinidad e Tobago 3
XK - ???statistics.table.value.countryCode.XK??? 3
EU - Europa 2
HU - Ungheria 2
MM - Myanmar 2
OM - Oman 2
SI - Slovenia 2
SX - ???statistics.table.value.countryCode.SX??? 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
GT - Guatemala 1
GY - Guiana 1
KG - Kirghizistan 1
LB - Libano 1
LK - Sri Lanka 1
ME - Montenegro 1
MT - Malta 1
MU - Mauritius 1
NZ - Nuova Zelanda 1
Totale 15.266
Salva come PNG Salva come JPEG
Città #
Ashburn 1.110
Singapore 754
Fairfield 663
Chandler 464
San Jose 428
Woodbridge 380
Houston 305
Wilmington 296
Hong Kong 284
Seattle 274
Ann Arbor 247
Cambridge 230
Moscow 199
Jacksonville 168
Palermo 167
Dublin 161
Zgierz 157
Beijing 151
Medford 130
New York 126
Tokyo 126
Ho Chi Minh City 123
Los Angeles 112
Council Bluffs 106
Des Moines 104
Frankfurt am Main 92
Boardman 91
Santa Clara 87
Nanjing 80
Princeton 80
Dallas 74
Lauterbourg 70
Hanoi 64
Helsinki 63
Altamura 59
Brussels 52
São Paulo 49
Tulsa 49
San Diego 46
The Dalles 43
Hefei 41
Lawrence 41
Orem 38
London 35
Buffalo 33
Milan 33
Tianjin 33
Dearborn 31
Nanchang 31
Chicago 30
Munich 30
Shenyang 29
Jinan 27
Venice 25
Changsha 23
Hebei 21
Rome 21
Düsseldorf 19
Ningbo 19
Stockholm 19
Warsaw 19
Amsterdam 18
Jiaxing 18
Da Nang 17
Falls Church 17
Seongnam 17
Shanghai 17
Chennai 16
Columbus 16
Haiphong 16
Izmir 16
Ludwigshafen am Rhein 16
Montreal 16
Tashkent 16
Abidjan 15
Hangzhou 15
Johannesburg 15
Kraków 15
Phoenix 15
Washington 15
Zhengzhou 15
Atlanta 14
Baghdad 14
Bologna 13
Kumar 13
Manchester 13
Dhaka 12
Guangzhou 12
Lanzhou 12
San Mateo 12
Turku 12
Brooklyn 11
Denver 11
Verona 11
Redwood City 10
Rio de Janeiro 10
Taiyuan 10
Amman 9
Baku 9
Belo Horizonte 9
Totale 9.400
Salva come PNG Salva come JPEG
Nome #
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 289
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA 280
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA 266
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA 265
Contact dermatitis due to nickel allergy in patients suffering from non-celiac wheat sensitivity 264
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 263
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 263
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography 260
Clinical symptoms in celiac patients on a gluten-free diet. 257
Predominance of Type 1 Innate Lymphoid Cells in the Rectal Mucosa of Patients With Non-Celiac Wheat Sensitivity: Reversal After a Wheat-Free Diet 256
Duodenal and Rectal Mucosa Inflammation in Patients With Non-celiac Wheat Sensitivity 256
Persistence of Nonceliac Wheat Sensitivity, Based on Long-term Follow-up 255
FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease 254
Autoimmunity Features in Patients With Non-Celiac Wheat Sensitivity 253
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study 242
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 239
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 233
INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY 229
Body Mass Index and Associated Clinical Variables in Patients with Non-Celiac Wheat Sensitivity 227
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 222
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 219
Apolipoprotein AI and HDL are reduced in stable cirrhotic patients with adrenal insufficiency: A possible role in glucocorticoid deficiency 218
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). 217
LE IPERCOLESTEROLEMIE PRIMITIVE 215
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. 214
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 210
Metabolomic analysis of plasma from Alzheimer disease patients 209
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 206
Low-density lipoproteins generated during an oral fat load in mild hypertriglyceridemic and healthy subjects are smaller, denser, and have an increased low-density lipoprotein receptor binding affinity. 205
FAMILIAL LIGAND-DEFECTIVE APOLIPOPROTEIN B: IDENTIFICATION OF A FAMILY HARBOURING THE ARG3531CYS (FDB3531) OF THE APOB GENE 205
Obesity and the metabolic syndrome in a student cohort from Southern Italy 204
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
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 196
Genetic epidemiology of ARH in Sicily 196
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. 193
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. 191
NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 190
Le ipocolesterolemie primitive 190
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects 189
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia 188
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. 186
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS 184
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography 184
Predominance of type 1 innate lymphoid cells in the rectal mucosa of patients with non-celiac wheat sensitivity: reversal after a wheat-free diet 182
FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION. 178
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH 178
MALABSORPTION OF FAT IN CELIAC DISEASE DURING AN ORAL FAT LOAD. KINETIC STUDY OF CHYLOMICRONS AND REMNANTS AND CORRELATION WITH THE STAGE OF THE DISEASE 176
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 176
ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS. 174
Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore 174
LIPIDOMICS OF HUMAN SKIN FIBROBLASTS IN NEIMANN-PICK DISEASE TYPE C 174
RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues 173
THE METABOLIC SYNDROME IS A PREDICTOR OF CARDIOVASCULAR EVENTS IN A SICILIAN POPULATION. RESULT OF A 15 YEARS FOLLOW UP 170
Wheat Consumption Leads to Immune Activation and Symptom Worsening in Patients with Familial Mediterranean Fever: A Pilot Randomized Trial 169
Gynecological Disorders in Patients with Non-celiac Wheat Sensitivity 164
NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS. 163
Metabolic disturbances and risk of cancer in the 25 years follow-up of the “Ventimiglia Heart Study” epidemiological project 159
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia 159
IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA 158
Genetic heterogeneity of familial hypercholesterolemia in Sicily 158
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia 157
Erratum: FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease (Analytical and Bioanalytical Chemistry DOI: 10.1007/s00216-015-9229-6) 155
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 154
Rectal mucosa inflammation in non-celiac wheat sensitivity: comparison with duodenal histology. 154
TNF-α, IL-17 AND IL-22 PRODUCTION IN THE RECTAL MUCOSA OF NON-CELIAC WHEAT SENSITIVITY PATIENTS: ROLE OF ADAPTIVE IMMUNITY 153
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 149
I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. 144
Evaluation of tolerability of “ancient” grains in patients with NCGS. 144
DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis 144
Frequency and clinical aspects of neurological and psychiatric symptoms in patients with non-celiac wheat sensitivity 143
Whole cow’s milk but not lactose can induce symptoms in patients with self‐reported milk intolerance: evidence of cow’s milk sensitivity in adults 137
IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING IN THE LDL-R GENE AND IN THE PCSK9 GENE 134
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 130
MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH "EXTREME LDL-C PHENOTYPES" 125
IDENTIFICATION OF P.LEU167DEL APOE GENE MUTATION BY NEXT GENERATION SEQUENCING IN A LARGE HYPERCHOLESTEROLEMIC FAMILY 109
Searching for wheat plants with low toxicity in celiac disease: Between direct toxicity and immunologic activation. 89
Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia 84
Totale 15.651
Salva come PNG Salva come JPEG
Categoria #
all - tutte 50.362
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 50.362
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022962 25 174 25 36 29 55 52 51 145 167 40 163
2022/20231.267 153 203 22 139 152 214 80 99 142 7 50 6
2023/2024746 23 105 41 127 47 179 65 36 3 11 13 96
2024/20251.548 33 67 75 108 74 58 137 127 163 169 253 284
2025/20265.951 491 141 274 395 559 1.000 789 617 420 852 154 259
2026/202721 21 0 0 0 0 0 0 0 0 0 0 0
Totale 15.651