statistiche ricercatore

Nome	#
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy	156
Selection of multipotent cells and enhanced muscle reconstruction by myogenic macrophage-secreted factors.	126
Mutations in the area composita protein alphaT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy	121
Autosomal dominant lateral temporal epilepsy (ADLTE): Novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras	116
A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signaling and miRNA dysregulation.	104
CNTNAP2 mutations and autosomal dominant epilepsy with auditory features	98
Pericentriolar material analyses in normal esophageal mucosa, Barrett's metaplasia and adenocarcinoma	82
Study of the molecular pathogenesis of arrhythmogenic cardiomyopathy due to Desmoglein-2 mutations: the zebrafish helps the mouse	59
Analisi di parametri della proliferazione e del differenziamento cellulare in due modelli post-infiammatori: Metaplasia di Barrett e Rigenerazione muscolare.	41
Totale	903

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	96	0	0	0	0	0	0	14	21	21	19	17	4
2020/2021	140	7	4	7	1	43	3	3	8	19	17	22	6
2021/2022	129	2	14	22	10	6	10	3	19	1	1	9	32
2022/2023	127	20	15	1	26	19	19	1	7	11	3	4	1
2023/2024	88	8	7	13	6	10	19	6	7	0	4	3	5
2024/2025	86	0	19	9	15	37	6	0	0	0	0	0	0
Totale													903