statistiche ricercatore

Continente	#
NA - Nord America	1.388
AS - Asia	475
EU - Europa	394
SA - Sud America	87
Continente sconosciuto - Info sul continente non disponibili	52
AF - Africa	13
OC - Oceania	2
Totale	2.411

Nazione	#
US - Stati Uniti d'America	1.356
CN - Cina	173
SG - Singapore	170
UA - Ucraina	104
BR - Brasile	69
IT - Italia	58
DE - Germania	54
FI - Finlandia	42
GB - Regno Unito	36
HK - Hong Kong	36
FR - Francia	34
VN - Vietnam	33
IE - Irlanda	17
TR - Turchia	16
CA - Canada	14
IN - India	14
RU - Federazione Russa	12
MX - Messico	8
AR - Argentina	7
BD - Bangladesh	6
PL - Polonia	6
SE - Svezia	6
JP - Giappone	5
IQ - Iraq	4
NP - Nepal	4
ZA - Sudafrica	4
BE - Belgio	3
CO - Colombia	3
CZ - Repubblica Ceca	3
ES - Italia	3
LT - Lituania	3
NG - Nigeria	3
NI - Nicaragua	3
SV - El Salvador	3
AT - Austria	2
AU - Australia	2
BG - Bulgaria	2
BO - Bolivia	2
CH - Svizzera	2
EC - Ecuador	2
ID - Indonesia	2
NL - Olanda	2
SA - Arabia Saudita	2
UZ - Uzbekistan	2
VE - Venezuela	2
AZ - Azerbaigian	1
CL - Cile	1
CR - Costa Rica	1
CW - ???statistics.table.value.countryCode.CW???	1
DO - Repubblica Dominicana	1
DZ - Algeria	1
EE - Estonia	1
GT - Guatemala	1
HU - Ungheria	1
IR - Iran	1
KE - Kenya	1
KG - Kirghizistan	1
KZ - Kazakistan	1
LA - Repubblica Popolare Democratica del Laos	1
LV - Lettonia	1
MA - Marocco	1
MT - Malta	1
MU - Mauritius	1
OM - Oman	1
PK - Pakistan	1
PS - Palestinian Territory	1
PY - Paraguay	1
SC - Seychelles	1
SI - Slovenia	1
TN - Tunisia	1
TT - Trinidad e Tobago	1
Totale	2.360

Nome	#
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease	219
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity	213
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation.	206
BAFF-R mutations in Good's syndrome.	205
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family.	184
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.	171
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects	167
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers	165
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency.	159
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a.	154
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency	150
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation.	146
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations	140
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency.	132
Totale	2.411

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	105	0	0	0	0	0	4	3	11	6	21	21	39
2022/2023	167	19	0	1	14	18	32	0	32	33	1	5	12
2023/2024	156	9	4	18	10	8	46	5	8	25	3	2	18
2024/2025	276	1	5	2	42	24	23	10	16	36	21	50	46
2025/2026	596	57	65	54	89	72	49	107	15	20	47	14	7
2026/2027	148	14	21	26	87	0	0	0	0	0	0	0	0
Totale													2.411