Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

FAYER, Francesca
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 8.601
EU - Europa 4.200
AS - Asia 3.277
SA - Sud America 557
Continente sconosciuto - Info sul continente non disponibili 383
AF - Africa 81
OC - Oceania 12
Totale 17.111
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 8.399
SG - Singapore 1.186
RU - Federazione Russa 1.151
CN - Cina 853
IT - Italia 794
FI - Finlandia 587
BR - Brasile 437
VN - Vietnam 338
UA - Ucraina 317
DE - Germania 311
HK - Hong Kong 295
PL - Polonia 200
FR - Francia 183
GB - Regno Unito 171
IE - Irlanda 165
JP - Giappone 135
CA - Canada 98
BD - Bangladesh 88
SE - Svezia 83
IN - India 76
KR - Corea 58
BE - Belgio 55
MX - Messico 45
RO - Romania 45
NL - Olanda 40
TR - Turchia 35
IQ - Iraq 34
AR - Argentina 29
AT - Austria 25
EC - Ecuador 21
VE - Venezuela 21
ZA - Sudafrica 21
PK - Pakistan 19
UZ - Uzbekistan 19
ES - Italia 18
PH - Filippine 16
CI - Costa d'Avorio 15
IR - Iran 13
JO - Giordania 13
MA - Marocco 13
CO - Colombia 12
NP - Nepal 12
AU - Australia 11
CL - Cile 11
MY - Malesia 11
AZ - Azerbaigian 10
CR - Costa Rica 10
ID - Indonesia 10
LT - Lituania 10
PY - Paraguay 10
JM - Giamaica 9
SA - Arabia Saudita 9
AE - Emirati Arabi Uniti 8
CH - Svizzera 8
EG - Egitto 8
HN - Honduras 7
IL - Israele 7
PE - Perù 7
BO - Bolivia 6
GR - Grecia 6
KE - Kenya 6
KZ - Kazakistan 6
TH - Thailandia 6
BH - Bahrain 5
DO - Repubblica Dominicana 5
DZ - Algeria 5
NI - Nicaragua 5
PT - Portogallo 5
SN - Senegal 5
TT - Trinidad e Tobago 5
BB - Barbados 4
CZ - Repubblica Ceca 4
GT - Guatemala 4
MK - Macedonia 4
PA - Panama 4
AL - Albania 3
BY - Bielorussia 3
KW - Kuwait 3
MD - Moldavia 3
NG - Nigeria 3
PR - Porto Rico 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
BS - Bahamas 1
GF - Guiana Francese 1
GY - Guiana 1
KG - Kirghizistan 1
LB - Libano 1
LC - Santa Lucia 1
LK - Sri Lanka 1
Totale 16.722
Salva come PNG Salva come JPEG
Città #
Ashburn 1.202
Singapore 758
Fairfield 663
San Jose 538
Chandler 464
Woodbridge 380
Houston 310
Wilmington 296
Hong Kong 285
Seattle 276
Ann Arbor 247
Cambridge 230
Moscow 199
Council Bluffs 174
Jacksonville 168
Palermo 168
Dublin 161
Zgierz 157
Beijing 151
New York 146
Los Angeles 143
Medford 130
Tokyo 130
Ho Chi Minh City 123
Dallas 121
Des Moines 104
Santa Clara 100
Boardman 95
Frankfurt am Main 92
Nanjing 80
Princeton 80
Lauterbourg 70
Hanoi 65
Helsinki 63
Altamura 59
Brussels 54
São Paulo 49
Tulsa 49
San Diego 47
Orem 44
Chicago 43
The Dalles 43
Hefei 41
Lawrence 41
London 38
Milan 37
Buffalo 35
Tianjin 33
Dearborn 31
Nanchang 31
Munich 30
Atlanta 29
Montreal 29
Shenyang 29
Jinan 27
Venice 26
Denver 25
Toronto 24
Changsha 23
Phoenix 23
Rome 22
Hebei 21
Stockholm 21
San Francisco 20
Warsaw 20
Amsterdam 19
Brooklyn 19
Düsseldorf 19
Ningbo 19
Jiaxing 18
Washington 18
Chennai 17
Columbus 17
Da Nang 17
Falls Church 17
Seongnam 17
Shanghai 17
Haiphong 16
Izmir 16
Ludwigshafen am Rhein 16
Tashkent 16
Abidjan 15
Hangzhou 15
Johannesburg 15
Kraków 15
Manchester 15
Zhengzhou 15
Baghdad 14
Bologna 13
Kumar 13
San Mateo 13
Dhaka 12
Guangzhou 12
Lanzhou 12
Turku 12
Boston 11
Verona 11
Mexico City 10
Redwood City 10
Rio de Janeiro 10
Totale 9.934
Salva come PNG Salva come JPEG
Nome #
Frequency and clinical aspects of neurological and psychiatric symptoms in patients with non-celiac wheat sensitivity 596
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 396
Persistence of Nonceliac Wheat Sensitivity, Based on Long-term Follow-up 352
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA 301
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 298
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 294
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA 281
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA 274
Contact dermatitis due to nickel allergy in patients suffering from non-celiac wheat sensitivity 272
Duodenal and Rectal Mucosa Inflammation in Patients With Non-celiac Wheat Sensitivity 271
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 268
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography 267
Predominance of Type 1 Innate Lymphoid Cells in the Rectal Mucosa of Patients With Non-Celiac Wheat Sensitivity: Reversal After a Wheat-Free Diet 267
Autoimmunity Features in Patients With Non-Celiac Wheat Sensitivity 264
Clinical symptoms in celiac patients on a gluten-free diet. 262
FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease 257
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study 251
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 249
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 237
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS 236
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 236
INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY 235
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 232
Body Mass Index and Associated Clinical Variables in Patients with Non-Celiac Wheat Sensitivity 232
Apolipoprotein AI and HDL are reduced in stable cirrhotic patients with adrenal insufficiency: A possible role in glucocorticoid deficiency 225
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing 225
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). 221
LE IPERCOLESTEROLEMIE PRIMITIVE 219
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 219
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 217
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. 217
Metabolomic analysis of plasma from Alzheimer disease patients 216
Obesity and the metabolic syndrome in a student cohort from Southern Italy 213
FAMILIAL LIGAND-DEFECTIVE APOLIPOPROTEIN B: IDENTIFICATION OF A FAMILY HARBOURING THE ARG3531CYS (FDB3531) OF THE APOB GENE 212
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 212
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. 207
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 204
COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE. 201
Genetic epidemiology of ARH in Sicily 200
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. 199
PREVALENCE OF ANGPTL3 AND APOB GENE MUTATIONS IN SUBJECTS WITH COMBINED HYPOLIPIDEMIA 198
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects 196
NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 195
Le ipocolesterolemie primitive 194
Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore 194
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS 194
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. 193
Predominance of type 1 innate lymphoid cells in the rectal mucosa of patients with non-celiac wheat sensitivity: reversal after a wheat-free diet 191
Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia 189
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography 189
DETECTION OF NEW GENES RESPONSIBLE OF FAMILIAL RECESSIVE HYPERCHOLESTEROLEMIA: PRELIMINARY DATA FROM AN EXOME SEQUENCING APPROACH 187
LIPIDOMICS OF HUMAN SKIN FIBROBLASTS IN NEIMANN-PICK DISEASE TYPE C 186
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 184
ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS. 184
FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION. 184
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 183
THE METABOLIC SYNDROME IS A PREDICTOR OF CARDIOVASCULAR EVENTS IN A SICILIAN POPULATION. RESULT OF A 15 YEARS FOLLOW UP 179
Wheat Consumption Leads to Immune Activation and Symptom Worsening in Patients with Familial Mediterranean Fever: A Pilot Randomized Trial 177
RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues 175
TNF-α, IL-17 AND IL-22 PRODUCTION IN THE RECTAL MUCOSA OF NON-CELIAC WHEAT SENSITIVITY PATIENTS: ROLE OF ADAPTIVE IMMUNITY 175
Gynecological Disorders in Patients with Non-celiac Wheat Sensitivity 173
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia 169
NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS. 168
Metabolic disturbances and risk of cancer in the 25 years follow-up of the “Ventimiglia Heart Study” epidemiological project 168
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia 167
Genetic heterogeneity of familial hypercholesterolemia in Sicily 166
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) 165
IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA 164
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 164
Rectal mucosa inflammation in non-celiac wheat sensitivity: comparison with duodenal histology. 163
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 156
Evaluation of tolerability of “ancient” grains in patients with NCGS. 154
DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis 150
I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. 149
IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING IN THE LDL-R GENE AND IN THE PCSK9 GENE 144
PCSK9-D374Y MEDIATED LDL-R DEGRADATION CAN BE FUNCTIONALLY INHIBITED BY EGF-A AND TRUNCATED EGF-A PEPTIDES. AN IN VITRO STUDY 138
MUTATION IN CANDIDATE GENES ACCOUNT FOR A SMALL MINORITY OF HYPOBETALIPOPROTEINEMIAS AND NGS ANALYSIS SUPPORT POLYGENICITY IN MUTATION-NEGATIVE PATIENTS 136
MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH "EXTREME LDL-C PHENOTYPES" 132
IDENTIFICATION OF P.LEU167DEL APOE GENE MUTATION BY NEXT GENERATION SEQUENCING IN A LARGE HYPERCHOLESTEROLEMIC FAMILY 117
Searching for wheat plants with low toxicity in celiac disease: Between direct toxicity and immunologic activation. 94
Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia 92
Totale 17.111
Salva come PNG Salva come JPEG
Categoria #
all - tutte 53.537
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 53.537
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022763 0 0 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
2026/20271.481 574 611 296 0 0 0 0 0 0 0 0 0
Totale 17.111