statistiche ricercatore

Nome	#
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease	139
BAFF-R mutations in Good's syndrome.	122
A CXCR1 haplotype hampers HIV-1 matrix protein p17 biological activity	120
Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation.	115
A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family.	113
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects	113
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.	97
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a.	97
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers	97
B cell responses to CpG correlate with CXCL16 expression levels in common variable immunodeficiency.	94
Successful Anti-TNF-α Treatment in a Girl with LAD-1 Disease and Autoimmune Manifestations	77
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency	77
Autosomal Recessive Agammaglobulinemia: The Third Case of Igβ Deficiency Due to a Novel Non-sense Mutation.	71
Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency.	67
Totale	1.399

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	304	0	0	13	46	21	40	33	39	26	54	11	21
2020/2021	210	2	25	3	20	4	22	7	20	31	23	48	5
2021/2022	140	11	12	5	7	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	8	1	5	2	0	0	0	0	0	0	0	0	0
Totale													1.399