statistiche ricercatore

Continente	#
NA - Nord America	509
AS - Asia	355
EU - Europa	305
SA - Sud America	42
AF - Africa	21
Continente sconosciuto - Info sul continente non disponibili	8
Totale	1.240

Nazione	#
US - Stati Uniti d'America	489
CN - Cina	191
IE - Irlanda	78
SG - Singapore	76
FI - Finlandia	42
DE - Germania	40
RU - Federazione Russa	36
BR - Brasile	33
HK - Hong Kong	31
UA - Ucraina	29
IT - Italia	20
VN - Vietnam	19
FR - Francia	18
GB - Regno Unito	18
SE - Svezia	12
ZA - Sudafrica	12
IN - India	11
CA - Canada	6
JP - Giappone	5
MX - Messico	5
AT - Austria	3
HN - Honduras	3
IQ - Iraq	3
PL - Polonia	3
AR - Argentina	2
AZ - Azerbaigian	2
BD - Bangladesh	2
CO - Colombia	2
DO - Repubblica Dominicana	2
ES - Italia	2
ID - Indonesia	2
LB - Libano	2
MA - Marocco	2
MU - Mauritius	2
PH - Filippine	2
PK - Pakistan	2
TN - Tunisia	2
AO - Angola	1
BH - Bahrain	1
BJ - Benin	1
BO - Bolivia	1
CL - Cile	1
CW - ???statistics.table.value.countryCode.CW???	1
EC - Ecuador	1
GP - Guadalupe	1
GT - Guatemala	1
HT - Haiti	1
IL - Israele	1
JO - Giordania	1
KE - Kenya	1
LT - Lituania	1
NL - Olanda	1
PE - Perù	1
PR - Porto Rico	1
PT - Portogallo	1
RO - Romania	1
SA - Arabia Saudita	1
SY - Repubblica araba siriana	1
TR - Turchia	1
UZ - Uzbekistan	1
VE - Venezuela	1
Totale	1.233

Nome	#
Bioinformatic Analysis of Pathogenic Missense Mutationsof Activin Receptor Like Kinase 1 Ectodomain	170
Bioinformatics as a Starting Point for the Analysis of ALK1 Missense Mutations	140
Immunohistochemical analysis of a merkeloma observed in a patient affected byhereditary haemorrhagic telangiectasia.	139
Argon plasma coagulation is an effective treatment for hereditary hemorrhagic telangiectasia patients with severe nosebleeds.	131
Rendu-Osler-Weber patients have an increasd frequency of mature endothelial cells in peripheral blood	126
Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion in ACVRL1 Suggests the Causing Mechanism.	124
STRUCTURAL MODELLING OF ALK1 ECTO-DOMAIN	122
Natural history and outcome of hepatic ascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia	115
Structural Evolution of Solid Phenanthrene at High Pressures	94
Modelling of ALK1 ectodomain and ALK1-ActRIIA-BMP9 receptor complex: hints from Type 2 Hereditary Haemorrhagic Telangiectasia	79
Totale	1.240

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	38	0	0	0	0	0	0	0	3	2	2	7	24
2022/2023	185	13	21	3	17	19	19	0	4	85	1	2	1
2023/2024	61	10	12	0	5	2	10	2	12	1	2	2	3
2024/2025	179	2	11	6	5	11	3	7	6	52	6	27	43
2025/2026	393	24	18	58	59	61	21	62	16	32	34	6	2
2026/2027	101	9	16	22	35	19	0	0	0	0	0	0	0
Totale													1.240