statistiche ricercatore

Continente	#
NA - Nord America	1.627
AS - Asia	553
EU - Europa	459
SA - Sud America	73
AF - Africa	15
Continente sconosciuto - Info sul continente non disponibili	5
Totale	2.732

Nazione	#
US - Stati Uniti d'America	1.608
SG - Singapore	219
CN - Cina	153
GB - Regno Unito	147
DE - Germania	54
IT - Italia	53
SE - Svezia	53
VN - Vietnam	53
BR - Brasile	40
HK - Hong Kong	40
FR - Francia	30
FI - Finlandia	27
UA - Ucraina	24
RU - Federazione Russa	23
BD - Bangladesh	18
CL - Cile	18
KR - Corea	16
TR - Turchia	16
NL - Olanda	12
BG - Bulgaria	9
BE - Belgio	8
IN - India	8
CA - Canada	7
CZ - Repubblica Ceca	7
ID - Indonesia	6
ZA - Sudafrica	6
AR - Argentina	4
ES - Italia	4
PK - Pakistan	4
AE - Emirati Arabi Uniti	3
CR - Costa Rica	3
EC - Ecuador	3
JM - Giamaica	3
JP - Giappone	3
MX - Messico	3
PL - Polonia	3
UZ - Uzbekistan	3
AZ - Azerbaigian	2
BO - Bolivia	2
CO - Colombia	2
IQ - Iraq	2
JO - Giordania	2
MA - Marocco	2
PE - Perù	2
SA - Arabia Saudita	2
TN - Tunisia	2
XK - ???statistics.table.value.countryCode.XK???	2
AT - Austria	1
DZ - Algeria	1
EG - Egitto	1
GA - Gabon	1
HN - Honduras	1
HR - Croazia	1
IE - Irlanda	1
LB - Libano	1
LC - Santa Lucia	1
LY - Libia	1
NG - Nigeria	1
PH - Filippine	1
PY - Paraguay	1
RS - Serbia	1
SK - Slovacchia (Repubblica Slovacca)	1
TH - Thailandia	1
TT - Trinidad e Tobago	1
UY - Uruguay	1
Totale	2.729

Nome	#
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease	419
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol	417
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol.	331
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients	321
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans	321
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease.	319
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency	305
Severe HDL deficiency due to novel defects in the ABCA1 transporter	299
Totale	2.732

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	114	0	0	0	8	6	3	12	11	17	6	35	16
2022/2023	171	18	22	8	9	30	27	1	15	22	1	4	14
2023/2024	89	4	6	8	12	17	6	13	5	3	0	2	13
2024/2025	345	6	1	10	23	65	63	23	27	26	11	40	50
2025/2026	990	72	30	57	142	317	65	89	26	56	72	46	18
2026/2027	153	30	29	33	61	0	0	0	0	0	0	0	0
Totale													2.732