FRESA, RAFFAELE
 Distribuzione geografica
Continente #
EU - Europa 1.055
AS - Asia 126
NA - Nord America 52
SA - Sud America 12
AF - Africa 4
Totale 1.249
Nazione #
IT - Italia 1.037
US - Stati Uniti d'America 47
SG - Singapore 42
VN - Vietnam 30
CN - Cina 28
BD - Bangladesh 8
FR - Francia 8
BR - Brasile 7
HK - Hong Kong 6
MX - Messico 3
AR - Argentina 2
CA - Canada 2
DE - Germania 2
IN - India 2
KR - Corea 2
NL - Olanda 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
AT - Austria 1
CL - Cile 1
CM - Camerun 1
DZ - Algeria 1
FI - Finlandia 1
GB - Regno Unito 1
IQ - Iraq 1
JP - Giappone 1
KE - Kenya 1
NA - Namibia 1
NP - Nepal 1
PE - Perù 1
TH - Thailandia 1
TR - Turchia 1
TW - Taiwan 1
UA - Ucraina 1
VE - Venezuela 1
Totale 1.249
Città #
Genova 610
Genoa 272
Rapallo 78
Vado Ligure 71
Singapore 18
San Jose 14
Hanoi 9
Lauterbourg 7
Beijing 6
Hong Kong 6
Ashburn 4
Ho Chi Minh City 4
New York 4
Bordighera 2
Da Nang 2
Frankfurt am Main 2
Los Angeles 2
Riyadh 2
San Diego 2
Santa Clara 2
Amsterdam 1
Ankara 1
Banfield 1
Bangkok 1
Barreiras 1
Boardman 1
Brantford 1
Bratislava 1
Buffalo 1
Bình Dương 1
Can Tho 1
Caracas 1
City of London 1
Ciudad López Mateos 1
Conway 1
Dallas 1
Douala 1
Fort Myers 1
Greenwood 1
Ha Long 1
Hangzhou 1
Helsinki 1
Hải Dương 1
Marseille 1
Mexico City 1
Minaçu 1
Mirassol 1
Mosul 1
New Delhi 1
New Orleans 1
New Rochelle 1
North Bend 1
Northwest Harwich 1
Odesa 1
Paulista 1
Phoenix 1
Phú Thọ 1
Phủ Lý 1
Quilmes Oeste 1
Quảng Ngãi 1
Rio de Janeiro 1
Rome 1
Sainte-Agathe-des-Monts 1
Santiago 1
Seongdong-gu 1
Shanghai 1
São João de Meriti 1
São Paulo 1
Taipei 1
Tifton 1
Tokyo 1
Van Nuys 1
Vienna 1
Windhoek 1
Yichun 1
Yongin-si 1
Totale 1.173
Nome #
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia 212
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla) 207
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients. 186
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia 185
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene. 172
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy. 151
Evaluation of the efficacy of plant sterols supplement sterolip® ESI in patients with type IIA hypercholesterolemia in relation to Genetic variants modulating intestinal absorption of cholesterol 101
Hypoalpha-hypobetalipoproteinemia (Familial Combined Hypolipidemia) caused by loss of function mutations of ANGPTL3 gene. 57
Totale 1.271
Categoria #
all - tutte 3.978
article - articoli 3.978
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 7.956


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20217 0 0 0 0 0 0 0 0 0 0 0 7
2021/2022102 3 3 18 8 2 12 7 18 8 8 4 11
2022/202396 8 6 3 11 15 17 0 7 17 1 9 2
2023/202483 4 8 0 13 8 27 0 3 0 0 7 13
2024/2025180 7 8 6 19 17 24 13 27 6 3 26 24
2025/2026283 39 3 15 15 57 15 47 9 18 31 31 3
Totale 1.271