MONTALI, Anna
 Distribuzione geografica
Continente #
NA - Nord America 451
EU - Europa 136
AS - Asia 38
SA - Sud America 12
AF - Africa 5
Continente sconosciuto - Info sul continente non disponibili 1
Totale 643
Nazione #
US - Stati Uniti d'America 446
IT - Italia 76
CN - Cina 25
CZ - Repubblica Ceca 14
DE - Germania 10
SE - Svezia 9
BR - Brasile 7
ES - Italia 6
TW - Taiwan 6
DK - Danimarca 5
GB - Regno Unito 5
AR - Argentina 3
CA - Canada 3
NL - Olanda 3
TR - Turchia 3
ZA - Sudafrica 3
CL - Cile 2
EG - Egitto 2
GR - Grecia 2
MX - Messico 2
RU - Federazione Russa 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
FI - Finlandia 1
FR - Francia 1
HK - Hong Kong 1
IE - Irlanda 1
IR - Iran 1
JP - Giappone 1
UA - Ucraina 1
Totale 643
Città #
Fairfield 52
Santa Cruz 42
Rome 40
Buffalo 33
Ashburn 32
Woodbridge 30
Cambridge 29
Houston 28
Seattle 24
Wilmington 14
Nanjing 11
Las Vegas 8
Milan 7
Ann Arbor 6
Chicago 6
Des Moines 6
Stockholm 6
Taipei 6
Copenhagen 5
Fleming Island 5
Clearwater 4
Dallas 4
Brooklyn 3
Buenos Aires 3
Cheyenne 3
Duncan 3
Henderson 3
Huddinge 3
Muizenberg 3
Phoenix 3
San Diego 3
São Paulo 3
Torre Del Greco 3
Wuhan 3
Altafulla 2
Beckenham 2
Beijing 2
Boardman 2
Civitavecchia 2
Dokki 2
Lake Forest 2
Los Angeles 2
Manchester 2
Mountain View 2
Nanchang 2
Redmond 2
Riva 2
San Francisco 2
San Jose 2
Thessaloníki 2
Toronto 2
University Park 2
Bevagna 1
Central District 1
Chengdu 1
Ciudad Nezahualcoyotl 1
Council Bluffs 1
Crugers 1
Denver 1
Dortmund 1
Dublin 1
Easton 1
Esslingen am Neckar 1
Frankfurt Am Main 1
Granada Hills 1
Hanover 1
Jinan 1
Kashan 1
Lanciano 1
Latina 1
London 1
Marano Di Napoli 1
Milpitas 1
New York 1
Newmarket 1
Providence 1
Reston 1
Rio De Janeiro 1
Salt Lake City 1
San Giorgio di Nogaro 1
Santa Clara 1
Shanghai 1
Soleto 1
South Bend 1
Tokyo 1
Urgnano 1
Vicenza 1
Totale 505
Nome #
Spectrum of mutations and long-term clinical outcomes in genetic chylomicronemia syndromes, file e3835324-3de1-15e8-e053-a505fe0a3de9 204
Atherogenic dyslipidemia in children: evaluation of clinical, biochemical and genetic aspects., file e3835318-77d3-15e8-e053-a505fe0a3de9 133
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN), file e3835318-762c-15e8-e053-a505fe0a3de9 105
Evaluation of polygenic determinants of non-alcoholic fatty liver disease (NAFLD) by a candidate genes resequencing strategy, file e3835319-be70-15e8-e053-a505fe0a3de9 104
Effects of angiopoietin-like protein 3 deficiency on postprandial lipid and lipoprotein metabolism, file e383532a-104e-15e8-e053-a505fe0a3de9 68
Circulating miR-33a and miR-33b increase in familial hypercholesterolemia in paediatric age, file e383532b-00ea-15e8-e053-a505fe0a3de9 12
A polymorphism in the cyclooxygenase 2 gene as an inherited protective factor against myocardial infarction and stroke, file e3835311-af60-15e8-e053-a505fe0a3de9 7
A common mutation in the insulin receptor substrate-1 gene is a genetic marker for the insulin resistance syndrome in patients with coronary artery disease, file e383532d-a11e-15e8-e053-a505fe0a3de9 6
PON1 L55M polymorphism is not a predictor of coronary atherosclerosis either alone or in combination with Q192R polymorphism in an Italian population, file e3835311-8e9a-15e8-e053-a505fe0a3de9 5
Non-alcoholic fatty liver disease and subclinical atherosclerosis: a comparison of metabolically- versus genetically-driven excess fat hepatic storage, file e3835318-8f1c-15e8-e053-a505fe0a3de9 5
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study, file e3835318-ba77-15e8-e053-a505fe0a3de9 5
Association of RXR-Gamma Gene Variants with Familial Combined Hyperlipidemia: Genotype and Haplotype Analysis, file e3835312-2dcf-15e8-e053-a505fe0a3de9 4
C242T polymorphism of NADPH oxidase p22phox and recurrence of cardiovascular events in coronary artery disease, file e3835311-b090-15e8-e053-a505fe0a3de9 3
The cholesterol ester transfer protein (CETP) TaqIB variant, HDL cholesterol levels, cardiovascular risk and the efficacy of pravastatin treatment – an individual patient meta-analisis of 13,677 subjects, file e3835311-af61-15e8-e053-a505fe0a3de9 2
Angptl3 deficiency is associated with increased insulin sensitivity, lipoprotein lipase activity, and decreased serum free fatty acids, file e3835314-6468-15e8-e053-a505fe0a3de9 2
A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large family, file e3835322-0d76-15e8-e053-a505fe0a3de9 2
Evolving trend in the management of heterozygous familial hypercholesterolemia in Italy: a retrospective, single center, observational study, file e3835327-811e-15e8-e053-a505fe0a3de9 2
Analysis of Children and Adolescents with Familial Hypercholesterolemia, file e3835317-8cba-15e8-e053-a505fe0a3de9 1
Genetic variants in adipose triglyceride lipase influence lipid levels in familial combined hyperlipidemia, file e383531d-9781-15e8-e053-a505fe0a3de9 1
Contribution of mutations in low density lipoprotein receptor (LDLR) and lipoprotein lipase (LPL) genes to familial combined hyperlipidemia (FCHL): A reappraisal by using a resequencing approach, file e3835329-c98c-15e8-e053-a505fe0a3de9 1
Totale 672
Categoria #
all - tutte 1027
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 1027


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201964 2002 63 10 5111717
2019/2020133 7464 116 1714 15161815
2020/2021213 10231417 1313 88 1765223
2021/2022116 51143 122 49 654213
2022/2023142 153719 916 719 711110
Totale 672