Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

FAYER, Francesca
 Distribuzione geografica
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Continente #
NA - Nord America 7.571
EU - Europa 4.176
AS - Asia 3.240
SA - Sud America 543
AF - Africa 81
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 8
Totale 15.631
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Nazione #
US - Stati Uniti d'America 7.413
SG - Singapore 1.183
RU - Federazione Russa 1.151
CN - Cina 852
IT - Italia 781
FI - Finlandia 587
BR - Brasile 432
VN - Vietnam 336
UA - Ucraina 317
DE - Germania 311
HK - Hong Kong 295
PL - Polonia 200
FR - Francia 181
GB - Regno Unito 167
IE - Irlanda 165
JP - Giappone 129
SE - Svezia 83
BD - Bangladesh 77
IN - India 76
CA - Canada 72
KR - Corea 54
BE - Belgio 53
RO - Romania 45
MX - Messico 44
NL - Olanda 38
TR - Turchia 35
IQ - Iraq 34
AR - Argentina 28
AT - Austria 25
VE - Venezuela 21
ZA - Sudafrica 21
EC - Ecuador 19
PK - Pakistan 19
UZ - Uzbekistan 19
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
HN - Honduras 7
IL - Israele 7
PE - Perù 7
CR - Costa Rica 6
GR - Grecia 6
ID - Indonesia 6
JM - Giamaica 6
KE - Kenya 6
KZ - Kazakistan 6
BO - Bolivia 5
DZ - Algeria 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
PR - Porto Rico 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
Totale 15.620
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Città #
Ashburn 1.163
Singapore 755
Fairfield 663
Chandler 464
San Jose 444
Woodbridge 380
Houston 307
Wilmington 296
Hong Kong 285
Seattle 275
Ann Arbor 247
Cambridge 230
Moscow 199
Jacksonville 168
Palermo 168
Dublin 161
Zgierz 157
Beijing 151
New York 139
Medford 130
Los Angeles 128
Tokyo 126
Ho Chi Minh City 123
Council Bluffs 106
Des Moines 104
Dallas 98
Frankfurt am Main 92
Boardman 91
Santa Clara 89
Nanjing 80
Princeton 80
Lauterbourg 70
Hanoi 64
Helsinki 63
Altamura 59
Brussels 52
São Paulo 49
Tulsa 49
San Diego 47
The Dalles 43
Hefei 41
Lawrence 41
Orem 41
London 36
Chicago 35
Milan 34
Buffalo 33
Tianjin 33
Dearborn 31
Nanchang 31
Munich 30
Shenyang 29
Jinan 27
Venice 25
Montreal 24
Atlanta 23
Changsha 23
Hebei 21
Rome 21
Stockholm 21
Warsaw 20
Denver 19
Düsseldorf 19
Ningbo 19
Amsterdam 18
Brooklyn 18
Jiaxing 18
Chennai 17
Da Nang 17
Falls Church 17
Phoenix 17
Seongnam 17
Shanghai 17
Washington 17
Columbus 16
Haiphong 16
Izmir 16
Ludwigshafen am Rhein 16
Tashkent 16
Abidjan 15
Hangzhou 15
Johannesburg 15
Kraków 15
Zhengzhou 15
Baghdad 14
Bologna 13
Kumar 13
Manchester 13
Dhaka 12
Guangzhou 12
Lanzhou 12
San Mateo 12
Turku 12
Toronto 11
Verona 11
Mexico City 10
Redwood City 10
Rio de Janeiro 10
Taiyuan 10
Amman 9
Totale 9.584
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Nome #
Frequency and clinical aspects of neurological and psychiatric symptoms in patients with non-celiac wheat sensitivity 342
CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE 290
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA 286
A NOVEL APOB MUTATION IDENTIFIED BY EXOME SEQUENCING COSEGREGATES WITH STEATOSIS, LIVER CANCER AND HYPOCHOLESTEROLEMIA 274
IL GENE PCSK9: UN NUOVO GENE IMPLICATO NEL CONTROLLO DELLA COLESTEROLEMIA 272
A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA 266
Contact dermatitis due to nickel allergy in patients suffering from non-celiac wheat sensitivity 265
A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 264
Duodenal and Rectal Mucosa Inflammation in Patients With Non-celiac Wheat Sensitivity 264
Interleukin 6 plasma levels predict with high sensitivity and specificity coronary stenosis detected by coronary angiography 261
Predominance of Type 1 Innate Lymphoid Cells in the Rectal Mucosa of Patients With Non-Celiac Wheat Sensitivity: Reversal After a Wheat-Free Diet 261
Clinical symptoms in celiac patients on a gluten-free diet. 258
Autoimmunity Features 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
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study 243
PREVALENCE OF APOB VARIANTS IN A SAMPLE OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 240
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia. 234
INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY 231
LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTY ACIDS 227
Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily 227
Body Mass Index and Associated Clinical Variables in Patients with Non-Celiac Wheat Sensitivity 227
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE 226
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing 220
Apolipoprotein AI and HDL are reduced in stable cirrhotic patients with adrenal insufficiency: A possible role in glucocorticoid deficiency 219
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). 218
LE IPERCOLESTEROLEMIE PRIMITIVE 215
Plasma non-cholesterol sterols: a useful diagnostic tool in pediatric hypercholesterolemia. 215
Metabolomic analysis of plasma from Alzheimer disease patients 212
HYPOBETALIPOPROTEINEMIA AND FATTY LIVER: WHO IS THE CULPRIT 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 210
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. 206
FAMILIAL LIGAND-DEFECTIVE APOLIPOPROTEIN B: IDENTIFICATION OF A FAMILY HARBOURING THE ARG3531CYS (FDB3531) OF THE APOB GENE 206
Obesity and the metabolic syndrome in a student cohort from Southern Italy 206
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 198
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. 194
GLI ACIDI GRASSI SATURI ED INSATURI MODULANO L’UPTAKE DELLE LIPOPROTEINE HDL IN UN MODELLO DI CELLULE EPATICHE IN COLTURA. 192
NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS 192
Le ipocolesterolemie primitive 190
A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects 190
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. 187
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS 186
Predominance of type 1 innate lymphoid cells in the rectal mucosa of patients with non-celiac wheat sensitivity: reversal after a wheat-free diet 186
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography 185
ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS? 179
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 178
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
LIPIDOMICS OF HUMAN SKIN FIBROBLASTS IN NEIMANN-PICK DISEASE TYPE C 177
ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS. 176
Le LDL generate in fase post-prandiale dopo carico grasso presentano maggiore densita’, minore size e maggiore affinita’ per il recettore 175
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 170
TNF-α, IL-17 AND IL-22 PRODUCTION IN THE RECTAL MUCOSA OF NON-CELIAC WHEAT SENSITIVITY PATIENTS: ROLE OF ADAPTIVE IMMUNITY 169
Gynecological Disorders in Patients with Non-celiac Wheat Sensitivity 165
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 163
Genetic heterogeneity of familial hypercholesterolemia in Sicily 160
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia 160
Plasma non-cholesterol sterols in primary hypobetalipoproteinemia 160
IPERCOLESTEROLEMIA AUTOSOMICA DOMINANTE IN SICILIA 159
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) 158
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 156
Rectal mucosa inflammation in non-celiac wheat sensitivity: comparison with duodenal histology. 156
PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA 150
I LIVELLI DI CISTATINA C SONO RIDOTTI NELL’INFARTO MIOCARDIO ACUTO. EFFETTO DEL POLIMORFISMO G73A SUI LIVELLI PLASMATICI. 146
DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis 145
Evaluation of tolerability of “ancient” grains in patients with NCGS. 144
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 142
IDENTIFICATION OF A HETEROZYGOUS COMPOUND INDIVIDUAL WITH AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA HARBOURING IN THE LDL-R GENE AND IN THE PCSK9 GENE 137
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
MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH "EXTREME LDL-C PHENOTYPES" 128
IDENTIFICATION OF P.LEU167DEL APOE GENE MUTATION BY NEXT GENERATION SEQUENCING IN A LARGE HYPERCHOLESTEROLEMIC FAMILY 111
Searching for wheat plants with low toxicity in celiac disease: Between direct toxicity and immunologic activation. 90
Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia 84
Totale 16.006
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Categoria #
all - tutte 51.135
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 51.135
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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
2026/2027376 376 0 0 0 0 0 0 0 0 0 0 0
Totale 16.006