statistiche ricercatore

Continente	#
NA - Nord America	1.444
AS - Asia	532
EU - Europa	438
SA - Sud America	72
AF - Africa	15
Continente sconosciuto - Info sul continente non disponibili	2
Totale	2.503

Nazione	#
US - Stati Uniti d'America	1.433
SG - Singapore	217
CN - Cina	151
GB - Regno Unito	146
DE - Germania	54
SE - Svezia	53
VN - Vietnam	53
BR - Brasile	39
HK - Hong Kong	37
IT - Italia	37
FR - Francia	30
FI - Finlandia	27
UA - Ucraina	24
RU - Federazione Russa	23
CL - Cile	18
TR - Turchia	16
KR - Corea	15
NL - Olanda	11
BG - Bulgaria	9
BE - Belgio	8
IN - India	8
BD - Bangladesh	7
CZ - Repubblica Ceca	6
ZA - Sudafrica	6
ID - Indonesia	5
AR - Argentina	4
PK - Pakistan	4
AE - Emirati Arabi Uniti	3
CA - Canada	3
EC - Ecuador	3
ES - Italia	3
MX - Messico	3
UZ - Uzbekistan	3
AZ - Azerbaigian	2
BO - Bolivia	2
CO - Colombia	2
IQ - Iraq	2
JM - Giamaica	2
JO - Giordania	2
JP - Giappone	2
MA - Marocco	2
PE - Perù	2
PL - Polonia	2
SA - Arabia Saudita	2
TN - Tunisia	2
XK - ???statistics.table.value.countryCode.XK???	2
AT - Austria	1
CR - Costa Rica	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
UY - Uruguay	1
Totale	2.503

Nome	#
Lysosomal lipase deficiency: Molecular characterization of eleven patients with Wolman or cholesteryl ester storage disease	405
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol	399
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol.	306
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients	290
Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency	283
Multiple abnormally spliced ABCA1 mRNAs caused by a novel splice site mutation of ABCA1 gene in a patient with Tangier disease.	282
Functional lecithin: Cholesterol acyltransferase Is not required for efficient atheroprotection in humans	273
Severe HDL deficiency due to novel defects in the ABCA1 transporter	268
Totale	2.506

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	41	0	0	0	0	0	0	0	0	0	25	11	5
2021/2022	191	4	37	36	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	917	72	30	57	142	317	65	89	26	56	63	0	0
Totale													2.506