statistiche ricercatore

Nome	#
Remittent C1-inhibitor deficiency due to Arg378Cys mutation	258
Molecular mechanism for the pathogenicity of the human C1-inhibitor Arg378Cys variant	185
Structural and functional characterization of mutations in C1-ihn responsible for hereditary angioedema	178
Gene regulation in the pathogenesis of angioedema due to inherited c1 inhibitor deficiency (hereditary angioedema)	174
Angioedema without urticaria : a large clinical survey	171
Use of C1 inhibitor concentrate for treatment of angioedema attacks in patients with C1 inhibitor deficiency : survey of 1102 infusions in 503 patients	150
Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency	143
Ricerca e valutazione di marker plasmatici indicativi di stato di malattia in pazienti con deficit di C1 inibitore	142
Identification of variables causing different clinical expression of inherited c1-inh deficiency (hereditary angioedema)	138
Natural history and clinical impact of cryoglobulins in chronic hepatitis C : 10-year prospective study of 343 patients	117
Plasmatic markers of acute attack in patients with angioedemadue to C1 inhibitor deficiency	114
Complement and contact system activation in acute congestive heart failure patients	107
Hereditary angioedema-induced acute pancreatitis : clinical picture and effect of C1-esterase inhibitor replacement	96
Structural and functional characterization of mutations in C1-inh responsible for hereditary angioedema	49
Totale	2.022

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	148	0	0	0	10	10	27	17	2	47	25	7	3
2020/2021	230	10	26	16	6	19	13	10	35	23	16	54	2
2021/2022	151	11	1	3	3	10	18	15	11	19	15	13	32
2022/2023	253	37	31	40	28	21	47	0	15	19	2	11	2
2023/2024	155	4	13	16	5	72	10	2	7	3	6	11	6
2024/2025	75	21	37	8	9	0	0	0	0	0	0	0	0
Totale													2.022

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